Capecitabine is indicated for the treatment of: - for the adjuvant treatment of patients following surgery of stage III (Dukes' stage C) colon cancer (see section 5.1). - metastatic colorectal cancer (see section 5.1). - first-line treatment of advanced gastric cancer in combination with a platinum-based regimen (see section 5.1).

- in combination with docetaxel (see section 5.1) for the treatment of patients with locally advanced or metastatic breast cancer after failure of cytotoxic chemotherapy. Previous therapy should have included an anthracycline. - as monotherapy for the treatment of patients with locally advanced or metastatic breast cancer after failure of taxanes and an anthracycline containing chemotherapy regimen or for whom further anthracycline therapy is not indicated.

 

 Capecitabine should only be prescribed by a qualified physician experienced in the utilisation of anti-neoplastic medicinal products. Careful monitoring during the first cycle of treatment is recommended for all patients. Treatment should be discontinued if progressive disease or intolerable toxicity is observed. Standard and reduced dose calculations according to body surface area for starting doses of Capecitabine of 1250 mg/m2 and 1000 mg/m2 are provided in tables 1 and 2, respectively.

 Posology

Recommended posology (see section 5.1):

Monotherapy

Colon, colorectal and breast cancer Given as monotherapy, the recommended starting dose for capecitabine in the adjuvant treatment of colon cancer, in the treatment of metastatic colorectal cancer or of locally advanced or metastatic breast cancer is 1250 mg/m2 administered twice daily (morning and evening; equivalent to 2500 mg/m2 total daily dose) for 14 days followed by a 7-day rest period. Adjuvant treatment in patients with stage III colon cancer is recommended for a total of 6 months.

Combination therapy

Colon, colorectal and gastric cancer

In combination treatment, the recommended starting dose of capecitabine should be reduced to 800 – 1000 mg/m2 when administered twice daily for 14 days followed by a 7-day rest period, or to 625 mg/m 2 twice daily when administered continuously (see section 5.1). For combination with irinotecan, the recommended starting dose is 800 mg/m² when administered twice daily for 14 days followed by a 7-day rest period combined with irinotecan 200 mg/m² on day 1. The inclusion of bevacizumab in a combination regimen has no effect on the starting dose of capecitabine. Premedication to maintain adequate hydration and anti-emesis according to the cisplatin summary of product characteristics should be started prior to cisplatin administration for patients receiving the capecitabine plus cisplatin combination. Premedication with antiemetics according to the oxaliplatin summary of product characteristics is recommended for patients receiving the capecitabine plus oxaliplatin combination. Adjuvant treatment in patients with stage III colon cancer is recommended for a duration of 6 months.

Breast cancer

In combination with docetaxel, the recommended starting dose of capecitabine in the treatment of metastatic breast cancer is 1250 mg/m2 twice daily for 14 days followed by a 7-day rest period, combined with docetaxel at 75 mg/m2 as a 1 hour intravenous infusion every 3 weeks. Premedication with an oral corticosteroid such as dexamethasone according to the docetaxel summary of product characteristics should be started prior to docetaxel administration for patients receiving the capecitabine plus docetaxel combination

Capecitabine Dose Calculations

Table 1 Standard and reduced dose calculations according to body surface area for a starting

dose of capecitabine of 1250 mg/m2

 

Dose level 1250 mg/m2 (twice daily)
	Full dose 1250 mg/m2	Number of 150 mg tablets and/or 500 mg tablets per administration (each administration to be given morning and evening)		Reduced dose (75%) 950 mg/m2	Reduced dose (50%) 625 mg/m2
Body Surface Area (m2 )	Dose per administration (mg)	150 mg	500 mg	Dose per administration (mg)	Dose per administration (mg)
≤1.26	1500	-	3	1150	800
1.27 - 1.38	1650	1	3	1300	800
1.39 - 1.52	1800	2	3	1450	950
1.53 - 1.66	2000	-	4	1500	1000
1.67 - 1.78	2150	1	4	1650	1000
1.79 - 1.92	2300	2	4	1800	1150
1.93 - 2.06	2500	-	5	1950	1300
2.07 - 2.18	2650	1	5	2000	1300
≥2.19	2800	2	5	2150	1450

 

Table 2 Standard and reduced dose calculations according to body surface area for a starting dose of capecitabine of 1000 mg/m2

Dose level 1000 mg/m2 (twice daily)
	Full dose 1000 mg/m2	Number of 150 mg tablets and/or 500 mg tablets per administration (each administration to be given morning and evening)		Reduced dose (75%) 750 mg/m2	Reduced dose (50%) 500 mg/m2
Body Surface Area (m2 )	Dose per administration (mg)	150 mg	500 mg	Dose per administration (mg)	Dose per administration (mg)
≤1.26	1150	1	2	800	600
1.27 - 1.38	1300	2	2	1000	600
1.39 - 1.52	1450	3	2	1100	750
1.53 - 1.66	1600	4	2	1200	800
1.67 - 1.78	1750	5	2	1300	800
1.79 - 1.92	1800	2	3	1400	900
1.93 - 2.06	2000	-	4	1500	1000
2.07 - 2.18	2150	1	4	1600	1050
≥2.19	2300	2	4	1750	1100

Posology adjustments during treatment:

 General

 Toxicity due to capecitabine administration may be managed by symptomatic treatment and/or modification of the dose (treatment interruption or dose reduction). Once the dose has been reduced, it should not be increased at a later time. For those toxicities considered by the treating physician to be unlikely to become serious or life-threatening, e.g. alopecia, altered taste, nail changes, treatment can be continued at the same dose without reduction or interruption. Patients taking capecitabine should be informed of the need to interrupt treatment immediately if moderate or severe toxicity occurs. Doses of capecitabine omitted for toxicity are not replaced. The following are the recommended dose modifications for toxicity:

Table 3 Capecitabine dose reduction schedule (3-weekly cycle or continuous treatment)

Toxicity grades*	Dose changes within a treatment cycle	Dose adjustment for next cycle/dose (% of starting dose)
• Grade 1	Maintain dose level
• Grade 2
-1st appearance	Interrupt until resolved to grade 0-1	100%
-2nd appearance		75%
-3rd appearance		50%
-4th appearance	Discontinue treatment permanently	Not applicable
• Grade 3
-1st appearance	Interrupt until resolved to grade 0-1	75%
-2nd appearance		50%
-3rd appearance	Discontinue treatment permanently	Not applicable
• Grade 4
-1st appearance	Discontinue permanently Or If physician deems it to be in the patient's best interest to continue, interrupt until resolved to grade 0-1	50%
2nd appearance	Discontinue permanently	Not applicable

*According to the National Cancer Institute of Canada Clinical Trial Group (NCIC CTG) Common Toxicity Criteria (version 1) or the Common Terminology Criteria for Adverse Events (CTCAE) of the Cancer Therapy Evaluation Program, US National Cancer Institute, version 4.0. For hand-foot syndrome and hyperbilirubinemia, see section 4.4.

Haematology

Patients with baseline neutrophil counts of <1.5 x 109

/L and/or thrombocyte counts of <100 x

109

/L should not be treated with Capecitabine. If unscheduled laboratory assessments during

a treatment cycle show that the neutrophil count drops below 1.0 x 109

/L or that the platelet

count drops below 75 x 109

/L, treatment with Capecitabine should be interrupted.

Dose modifications for toxicity when Capecitabine is used as a 3 weekly cycle in combination

with other medicinal products

Dose modifications for toxicity when Capecitabine is used as a 3 weekly cycle in combination

with other medicinal products should be made according to Table 3 above for Capecitabine and

according to the appropriate summary of product characteristics for the other medicinal

product(s).

At the beginning of a treatment cycle, if a treatment delay is indicated for either Capecitabine

or the other medicinal product(s), then administration of all therapy should be delayed until the

requirements for restarting all medicinal products are met.

During a treatment cycle for those toxicities considered by the treating physician not to be

related to Capecitabine, Capecitabine should be continued and the dose of the other medicinal

product should be adjusted according to the appropriate Prescribing Information.

If the other medicinal product(s) have to be discontinued permanently, Capecitabine treatment

can be resumed when the requirements for restarting Capecitabine are met.

This advice is applicable to all indications and to all special populations.

Dose modifications for toxicity when Capecitabine is used continuously in Combination with

other medicinal products:

Dose modifications for toxicity when Capecitabine is used continuously in combination with

other medicinal products should be made according to Table 3 above for Capecitabine and

according to the appropriate summary of product characteristics for the other medicinal

product(s).

Posology adjustments for special populations:

Hepatic impairment

Insufficient safety and efficacy data are available in patients with hepatic impairment to provide

a dose adjustment recommendation. No information is available on hepatic impairment due to

cirrhosis or hepatitis.

Renal impairment

Capecitabine is contraindicated in patients with severe renal impairment (creatinine clearance

below 30 ml/min [Cockcroft and Gault] at baseline). The incidence of grade 3 or 4 adverse

reactions in patients with moderate renal impairment (creatinine clearance 30-50 ml/min at

baseline) is increased compared to the overall population. In patients with moderate renal

impairment at baseline, a dose reduction to 75% for a starting dose of 1250 mg/m2 is

recommended. In patients with moderate renal impairment at baseline, no dose reduction is

required for a starting dose of 1000 mg/m 2

. In patients with mild renal impairment (creatinine

clearance 51-80 ml/min at baseline) no adjustment of the starting dose is recommended.

 

Careful monitoring and prompt treatment interruption is recommended if the patient develops

a grade 2, 3 or 4 adverse event during treatment and subsequent dose adjustment as outlined in

Table 3 above. If the calculated creatinine clearance decreases during treatment to a value below

30 ml/min, Capecitabine should be discontinued. These dose adjustment recommendations for

renal impairment apply both to monotherapy and combination use (see also section “Elderly”

below).

Elderly

During Capecitabine monotherapy, no adjustment of the starting dose is needed. However,

grade 3 or 4 treatment related adverse reactions were more frequent in patients ≥60 years of age

compared to younger patients.

When Capecitabine was used in combination with other medicinal products, elderly patients

(≥65 years) experienced more grade 3 and grade 4 adverse drug reactions, including those

leading to discontinuation, compared to younger patients. Careful monitoring of patients ≥60

years of age is advisable.

In combination with docetaxel: an increased incidence of grade 3 or 4 treatment related adverse

reactions and treatment related serious adverse reactions were observed in patients 60 years of

age or more (see section 5.1). For patients 60 years of age or more, a starting dose reduction of

Capecitabine to 75% (950 mg/m2 twice daily) is recommended. If no toxicity is observed in

patients ≥60 years of age treated with a reduced Capecitabine starting dose in combination with

docetaxel, the dose of Capecitabine may be cautiously escalated to 1250 mg/m2 twice daily.

Paediatric population

There is no relevant use of capecitabine in the paediatric population in the indications colon,

colorectal, gastric and breast cancer.

Method of administration

Capecitabine tablets should be swallowed with water within 30 minutes after a meal.

• History of severe and unexpected reactions to fluoropyrimidine therapy, • Hypersensitivity to the capecitabine or to any of the excipients listed in section 6.1 or fluorouracil, • • In patients with known complete absence of dihydropyrimidine dehydrogenase (DPD) activity (see section 4.4), • During pregnancy and lactation, • In patients with severe leukopenia, neutropenia, or thrombocytopenia, • In patients with severe hepatic impairment, • In patients with severe renal impairment (creatinine clearance below 30 ml/min), • Recent or concomitant treatment with brivudine (see section 4.4 and 4.5 for drug-drug interaction), • If contraindications exist to any of the medicinal products in the combination regimen, that medicinal product should not be used.

Dose limiting toxicities include diarrhoea, abdominal pain, nausea, stomatitis and hand-foot syndrome (hand-foot skin reaction, palmar-plantar erythrodysesthesia). Most adverse reactions are reversible and do not require permanent discontinuation of therapy, although doses may need to be withheld or reduced. Diarrhoea. Patients with severe diarrhoea should be carefully monitored and given fluid and electrolyte replacement if they become dehydrated. Standard antidiarrhoeal treatments (e.g. loperamide) may be used. NCIC CTC grade 2 diarrhoea is defined as an increase of 4 to 6 stools/day or nocturnal stools, grade 3 diarrhoea as an increase of 7 to 9 stools/day or incontinence and malabsorption. Grade 4 diarrhoea is an increase of ≥10 stools/day or grossly bloody diarrhoea or the need for parenteral support. Dose reduction should be applied as necessary (see section 4.2). Dehydration. Dehydration should be prevented or corrected at the onset. Patients with anorexia, asthenia, nausea, vomiting or diarrhoea may rapidly become dehydrated. Dehydration may cause acute renal failure, especially in patients with pre-existing compromised renal function or when capecitabine is given concomitantly with known nephrotoxic medicinal products. Acute renal failure secondary to dehydration might be potentially fatal. If grade 2 (or higher) dehydration occurs, capecitabine treatment should be immediately interrupted and the dehydration corrected. Treatment should not be restarted until the patient is rehydrated and any precipitating causes have been corrected or controlled. Dose modifications applied should be applied for the precipitating adverse event as necessary (see section 4.2). Hand-foot syndrome (also known as hand-foot skin reaction or palmar-plantar erythrodysesthesia or chemotherapy induced acral erythema). Grade 1 hand-foot syndrome is defined as numbness, dysesthesia/paresthesia, tingling, painless swelling or erythema of the hands and/or feet and/or discomfort which does not disrupt the patient’s normal activities. Grade 2 hand- foot syndrome is painful erythema and swelling of the hands and/or feet and/or discomfort affecting the patient’s activities of daily living. Grade 3 hand- foot syndrome is moist desquamation, ulceration, blistering and severe pain of the hands and/or feet and/or severe discomfort that causes the patient to be unable to work or perform activities of daily living. Persistent or severe hand-foot syndrome (Grade 2 and above) can eventually lead to loss of fingerprints which could impact patient identification. If grade 2 or 3 hand- foot syndrome occurs, administration of capecitabine should be interrupted until the event resolves or decreases in intensity to grade 1. Following grade 3 hand-foot syndrome, subsequent doses of capecitabine should be decreased. When capecitabine and cisplatin are used in combination, the use of vitamin B6 (pyridoxine) is not advised for symptomatic or secondary prophylactic treatment of hand-foot syndrome, because of published reports that it may decrease the efficacy of cisplatin. There is some evidence that dexpanthenol is effective for hand-foot syndrome prophylaxis in patients treated with capecitabine. Cardiotoxicity. Cardiotoxicity has been associated with fluoropyrimidine therapy, including myocardial infarction, angina, dysrhythmias, cardiogenic shock, sudden death and electrocardiographic changes (including very rare cases of QT prolongation). These adverse reactions may be more common in patients with a prior history of coronary artery disease. Cardiac arrhythmias (including ventricular fibrillation, torsade de pointes, and bradycardia), angina pectoris, myocardial infarction, heart failure and cardiomyopathy have been reported in patients receiving capecitabine. Caution must be exercised in patients with history of significant cardiac disease, arrhythmias and angina pectoris (see section 4.8). Hypo- or hypercalcaemia. Hypo- or hypercalcaemia has been reported during capecitabine treatment. Caution must be exercised in patients with pre-existing hypo- or hypercalcaemia (see section 4.8). Central or peripheral nervous system disease. Caution must be exercised in patients with central or peripheral nervous system disease, e.g. brain metastasis or neuropathy (see section 4.8). Diabetes mellitus or electrolyte disturbances. Caution must be exercised in patients with diabetes mellitus or electrolyte disturbances, as these may be aggravated during capecitabine treatment. Coumarin-derivative anticoagulation. In a interaction study with single-dose warfarin administration, there was a significant increase in the mean AUC (+57%) of S-warfarin. These results suggest an interaction, probably due to an inhibition of the cytochrome P450 2C9 isoenzyme system by capecitabine. Patients receiving concomitant capecitabine and oral coumarin-derivative anticoagulant therapy should have their anticoagulant response (INR or prothrombin time) monitored closely and the anticoagulant dose adjusted accordingly (see section 4.5). Brivudine. Brivudine must not be administered concomitantly with capecitabine. Fatal cases have been reported following this drug interaction. There must be at least a 4-week waiting period between end of treatment with brivudine and start of capecitabine therapy. Treatment with brivudine can be started 24 hours after the last dose of capecitabine (see section 4.3 and 4.5). In the event of accidental administration of brivudine to patients being treated with capecitabine, effective measures should be taken to reduce the toxicity of capecitabine. Immediate admission to hospital is recommended. All measures should be initiated to prevent systemic infections and dehydration. Hepatic impairment. In the absence of safety and efficacy data in patients with hepatic impairment, Capecitabine use should be carefully monitored in patients with mild to moderate liver dysfunction, regardless of the presence or absence of liver metastasis. Administration of capecitabine should be interrupted if treatment-related elevations in bilirubin of >3.0 x ULN or treatment-related elevations in hepatic aminotransferases (ALT, AST) of >2.5 x ULN occur. Treatment with capecitabine monotherapy may be resumed when bilirubin decreases to ≤3.0 x ULN or hepatic aminotransferases decrease to ≤ 2.5 x ULN. Renal impairment. The incidence of grade 3 or 4 adverse reactions in patients with moderate renal impairment (creatinine clearance 30-50 ml/min) is increased compared to the overall population (see sections 4.2 and 4.3). Dihydropyrimidine dehydrogenase (DPD) deficiency: Rarely, unexpected, severe toxicity (e.g. stomatitis, diarrhoea, mucosal inflammation, neutropenia and neurotoxicity) associated with 5- FU has been attributed to a deficiency of DPD activity

Patients with low or absent DPD activity, an enzyme involved in fluorouracil degradation, are at increased risk for severe, life-threatening, or fatal adverse reactions caused by fluorouracil. Although DPD deficiency cannot be precisely defined, it is known that patients with certain homozygous or certain compound heterozygous mutations in the DPYD gene locus (e.g. DPYD*2A, c.1679T>G, c.2846A>T and c.1236G>A/HapB3 variants), which can cause complete or near complete absence of DPD enzymatic activity (as determined from laboratory assays), have the highest risk of life-threatening or fatal toxicity and should not be treated with capecitabine (see section 4.3). No dose has been proven safe for patients with complete absence of DPD activity. Patients with certain heterozygous DPYD variants (including DPYD*2A, c.1679T>G, c.2846A>T and c.1236G>A/HapB3 variants) have been shown to have increased risk of severe toxicity when treated with capecitabine. The frequency of the heterozygous DPYD*2A genotype in the DPYD gene in Caucasian patients is around 1%, 1.1% for c.2846A>T, 2.6-6.3% for c.1236G>A/HapB3 variants and 0.07 to 0.1% for c.1679T>G. Genotyping for these alleles is recommended to identify patients at increased risk for severe toxicity. Data on the frequency of these DPYD variants in other populations than Caucasian is limited. It cannot be excluded that other rare variants may also be associated with an increased risk of severe toxicity. For patients with partial DPD deficiency (such as those with heterozygous mutations in the DPYD gene) and where the benefits of capecitabine are considered to outweigh the risks (taking into account the suitability of an alternative non-fluoropyrimidine chemotherapeutic regimen), these patients must be treated with extreme caution and frequent monitoring with dose adjustment according to toxicity. A reduction of the starting dose in these patients may be considered to avoid serious toxicity. There is insufficient data to recommend a specific dose in patients with partial DPD activity as measured by specific test. It has been reported that the DPYD*2A, c.1679T>G variants lead to a greater reduction in enzymatic activity than the other variants with a higher risk of side effects. The consequences of a reduced dose for efficacy are currently uncertain. Therefore, in the absence of serious toxicity the dose could be increased while carefully monitoring the patient. The patients who are tested negative for the above-mentioned alleles may still have a risk of severe adverse events. In patients with unrecognised DPD deficiency treated with capecitabine as well as in those patients who test negative for specific DPYD variations, life-threatening toxicities manifesting as acute overdose may occur (see section 4.9). In the event of grade 2-4 acute toxicity, treatment must be discontinued immediately. Permanent discontinuation should be considered based on clinical assessment of the onset, duration and severity of the observed toxicities. Ophthalmologic complications: Patients should be carefully monitored for ophthalmological complications such as keratitis and corneal disorders, especially if they have a prior history of eye disorders. Treatment of eye disorders should be initiated as clinically appropriate. Severe skin reactions: Capecitabine can induce severe skin reactions such as Stevens-Johnson syndrome and Toxic Epidermal Necrolysis. Capecitabine should be permanently discontinued in patients who experience a severe skin reaction during treatment.

As this medicinal product contains anhydrous lactose as an excipient, patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption should not take this medicine. Catabina tablets should not be crushed or cut. In case of exposure of either patient or caregiver to crushed or cut Catabina tablets adverse drug reactions could occur (see Section 4.8).

Interaction studies have only been performed in adults. Interaction with other medicinal products: Brivudine: a clinically significant interaction between brivudine and fluoropyrimidines (e.g. capecitabine, 5-Fluorouracil, tegafur), resulting from the inhibition of dihydropyrimidine dehydrogenase by brivudine, has been described. This interaction, which leads to increased fluoropyrimidine toxicity, is potentially fatal. Therefore, brivudine must not be administered concomitantly with capecitabine (see section 4.3 and 4.4). There must be at least a 4-week waiting period between end of treatment with brivudine and start of capecitabine therapy. Treatment with brivudine can be started 24 hours after the last dose of capecitabine. Cytochrome P-450 2C9 substrates: Other than warfarin, no formal interaction studies between capecitabine and other CYP2C9 substrates have been conducted. Care should be exercised when capecitabine is co-administered with 2C9 substrates (e.g., phenytoin). See also interaction with coumarin-derivative anticoagulants below, and section 4.4. Coumarin-derivative anticoagulants: altered coagulation parameters and/or bleeding have been reported in patients taking capecitabine concomitantly with coumarin-derivative anticoagulants such as warfarin and phenprocoumon. These reactions occurred within several days and up to several months after initiating capecitabine therapy and, in a few cases, within one month after stopping capecitabine. In a clinical pharmacokinetic interaction study, after a single 20 mg dose of warfarin, capecitabine treatment increased the AUC of S-warfarin by 57% with a 91% increase in INR value. Since metabolism of R -warfarin was not affected, these results indicate that capecitabine down-regulates isozyme 2C9, but has no effect on isozymes 1A2 and 3A4. Patients taking coumarin-derivative anticoagulants concomitantly with capecitabine should be monitored regularly for alterations in their coagulation parameters (PT or INR) and the anticoagulant dose adjusted accordingly. Phenytoin: increased phenytoin plasma concentrations resulting in symptoms of phenytoin intoxication in single cases have been reported during concomitant use of capecitabine with phenytoin. Patients taking phenytoin concomitantly with capecitabine should be regularly monitored for increased phenytoin plasma concentrations. Folinic acid/folic acid: a combination study with capecitabine and folinic acid indicated that folinic acid has no major effect on the pharmacokinetics of capecitabine and its metabolites. However, folinic acid has an effect on the pharmacodynamics of capecitabine and its toxicity may be enhanced by folinic acid: the maximum tolerated dose (MTD) of capecitabine alone using the intermittent regimen is 3000 mg/m2 per day whereas it is only 2000 mg/m2 per day when capecitabine was combined with folinic acid (30 mg orally bid). The enhanced toxicity may be relevant when switching from 5-FU/LV to a capecitabine regimen. This may also be relevant with folic acid supplementation for folate deficiency due to the similarity between folinic acid and folic acid. Sorivudine and analogues: a clinically significant drug-drug interaction between sorivudine and 5-FU, resulting from the inhibition of dihydropyrimidine dehydrogenase by sorivudine, has been described. This interaction, which leads to increased fluoropyrimidine toxicity, is potentially fatal. Therefore, capecitabine must not be administered concomitantly with sorivudine or its chemically related analogues, such as brivudine (see section 4.3). There must be at least a 4-week waiting period between end of treatment with sorivudine or its chemically related analogues such as brivudine and start of capecitabine therapy. Antacid: the effect of an aluminium hydroxide and magnesium hydroxide-containing antacid on the pharmacokinetics of capecitabine was investigated. There was a small increase in plasma concentrations of capecitabine and one metabolite (5’-DFCR); there was no effect on the 3 major metabolites (5’- DFUR, 5-FU and FBAL). Allopurinol: interactions with allopurinol have been observed for 5-FU; with possible decreased efficacy of 5-FU. Concomitant use of allopurinol with capecitabine should be avoided. Interferon alpha: the MTD of capecitabine was 2000 mg/m2 per day when combined with interferon alpha- 2a (3 MIU/m2 per day) compared to 3000 mg/m2 per day when capecitabine was used alone. Radiotherapy: the MTD of capecitabine alone using the intermittent regimen is 3000 mg/m2 per day, whereas, when combined with radiotherapy for rectal cancer, the MTD of capecitabine is 2000 mg/m2 per day using either a continuous schedule or given daily Monday through Friday during a 6-week course of radiotherapy. Oxaliplatin: no clinically significant differences in exposure to capecitabine or its metabolites, free platinum or total platinum occurred when capecitabine was administered in combination with oxaliplatin or in combination with oxaliplatin and bevacizumab. Bevacizumab: there was no clinically significant effect of bevacizumab on the pharmacokinetic parameters of capecitabine or its metabolites in the presence of oxaliplatin. Food interaction In all clinical trials, patients were instructed to administer capecitabine within 30 minutes after a meal. Since current safety and efficacy data are based upon administration with food, it is recommended that capecitabine be administered with food. Administration with food decreases the rate of capecitabine absorption (see section 5.2).

Women of childbearing potential/Contraception in males and females

Women of childbearing potential should be advised to avoid becoming pregnant while receiving treatment with capecitabine. If the patient becomes pregnant while receiving capecitabine, the potential hazard to the foetus must be explained. An effective method of contraception should be used during treatment and for 6 months after the last dose of capecitabine. Based on genetic toxicity findings, male patients with female partners of reproductive potential should use effective contraception during treatment and for 3 months following the last dose of capecitabine.

Pregnancy

There are no studies in pregnant women using capecitabine; however, it should be assumed that capecitabine may cause foetal harm if administered to pregnant women. In reproductive toxicity studies in animals, capecitabine administration caused embryolethality and teratogenicity. These findings are expected effects of fluoropyrimidine derivatives. Capecitabine is contraindicated during pregnancy.

Breast-feeding

It is not known whether capecitabine is excreted in human breast milk. No studies have been conducted to assess the impact of capecitabine on milk production or its presence in human breast milk. In lactating mice, considerable amounts of capecitabine and its metabolites were found in milk. As the potential for harm to the nursing infant is unknown, breast-feeding should be discontinued while receiving treatment with capecitabine and for 2 weeks after the final dose. Fertility There is no data on capecitabine and impact on fertility. The capecitabine pivotal studies included females of childbearing potential and males only if they agreed to use an acceptable method of birth control to avoid pregnancy for the duration of the study and for a reasonable period thereafter.

In animal studies effects on fertility were observed (see section 5.3).

Capecitabine has minor or moderate influence on the ability to drive and use machines. Capecitabine may cause dizziness, fatigue and nausea.

Summary of the safety profile

The overall safety profile of capecitabine is based on data from over 3000 patients treated with

capecitabine as monotherapy or capecitabine in combination with different chemotherapy

regimens in multiple indications. The safety profiles of capecitabine monotherapy for the

metastatic breast cancer, metastatic colorectal cancer and adjuvant colon cancer populations are

comparable. See section 5.1 for details of major studies, including study designs and major

efficacy results.

The most commonly reported and/or clinically relevant treatment-related adverse drug reactions

(ADRs) were gastrointestinal disorders (especially diarrhoea, nausea, vomiting, abdominal

pain, stomatitis), hand-foot syndrome (palmar-plantar erythrodysesthesia), fatigue, asthenia,

anorexia, cardiotoxicity, increased renal dysfunction on those with preexisting compromised

renal function, and thrombosis/embolism.

Tabulated list of adverse reactions

ADRs considered by the investigator to be possibly, probably, or remotely related to the

administration of capecitabine are listed in table 4 for capecitabine given as a monotherapy

and in Table 5 for capecitabine given in combination with different chemotherapy regimens in

multiple indications. The following headings are used to rank the ADRs by frequency: very

common (≥ 1/10), common (≥ 1/100 to < 1/10), uncommon (≥ 1/1,000 to < 1/100), rare

(≥1/10,000 to <1/1,000), very rare (<1/10,000). Within each frequency grouping, ADRs are

presented in order of decreasing seriousness.

Capecitabine Monotherapy:

Table 4 lists ADRs associated with the use of capecitabine monotherapy based on a pooled

analysis of safety data from three major studies including over 1900 patients (studies M66001,

SO14695, and SO14796). ADRs are added to the appropriate frequency grouping according to

the overall incidence from the pooled analysis.

Table 4 Summary of related ADRs reported in patients treated with capecitabine monotherapy

 

Body System	Very Common All grades	Common All grades	Uncommon Severe and/or Life threatening (grade 3-4) or considered medically relevant	Rare/Very Rare (Post-Marketing Experience)
Infections and Infestations	-	Herpes viral infection , Nasopharyngitis, Lower respiratory tract infection	Sepsis, Urinary tract infection, Cellulitis Tonsillitis, Pharyngitis, Oral candidiasis, Influenza, Gastroenteritis, Fungal infection, Infection, Tooth abscess
Neoplasm benign, malignant and unspecified	-	-	Lipoma
Blood and lymphatic system disorders		Neutropenia Anaemia	Febrile neutropenia, Pancytopenia, Granulocytopenia, Thrombocytopenia, Leukopenia, Haemolytic anaemia, International Normalised Ratio (INR) increased/Prothrombin time prolonged
Immune system disorders	-	-	Hypersensitivity
Metabolism and nutrition disorders	Anorexia	Dehydration, Weight decreased	Diabetes, Hypokalaemia, Appetite disorder, Malnutrition, Hypertriglyceridaemia,
Psychiatric disorders	-	Insomnia, Depression	Confusional state, Panic attack, Depressed mood, Libido decreased
Nervous system disorders	-	Headache, Lethargy Dizziness, Parasthesia Dysgeusia	Aphasia, Memory impairment, Ataxia, Syncope, Balance disorder, Sensory disorder, Neuropathy peripheral	Toxic leukoencephalopathy (very rare)
Eye disorders	-	Lacrimation increased Conjunctivitis, Eye irritation	Visual acuity reduced Diplopia	Lacrimal duct stenosis (rare), Cornea disorders(rare), keratitis (rare), punctate keratitis (rare)
Ear and labyrinth disorders	-	-	Vertigo, Ear pain
Cardiac disorders	-	-	Angina unstable, Angina pectoris, Myocardial ischaemia/ infarction, Atrial fibrillation, Arrhythmia, Tachycardia, Sinus tachycardia, Palpitations	Ventricular fibrillation (rare), QT prolongation (rare), Torsade de pointes (rare), Bradycardia (rare), Vasospasm (rare)
Vascular disorders	-	Thrombophlebitis	Deep vein thrombosis Hypertension, Petechiae, Hypotension, Hot flush, Peripheral coldness
Respiratory, thoracic and mediastinal disorders		Dyspnoea, Epistaxis, Cough, Rhinorrhoea	Pulmonary embolism, Pneumothorax Haemoptysis, Asthma, Dyspnoea exertional
Gastrointestinal disorders	Diarrhoea Vomiting Nausea Stomatitis, Abdominal pain	Gastrointestinal haemorrhage Constipation, Upper abdominal pain, Dyspepsia, Flatulence, Dry mouth	Intestinal obstruction, Ascites, Enteritis Gastritis, Dysphagia, Abdominal pain lower, Oesophagitis Abdominal discomfort, Gastrooesophageal reflux disease, Colitis, Blood in stool
Hepatobiliary Disorders	-	Hyperbilirubinemia, Liver function test abnormalities	Jaundice	Hepatic failure (rare), Cholestatic hepatitis (rare)
Skin and subcutaneous tissue disorders	Palmar-plantar Erythrodysaesthesia syndrome**	Rash, Alopecia, Erythema, Dry skin, Pruritus, Skin hyper- pigmentation, Rash macular, Skin desquamation, Dermatitis, Pigmentation disorder, Nail disorder	Blister, Skin ulcer, Rash, Urticaria Photosensitivity reaction, Palmar erythema, Swelling face, Purpura, Radiation recall syndrome	Cutaneous lupus erythematosus (rare), Severe skin reactions such as Stevens-Johnson Syndrome and toxic Epidermal Necrolysis (very rare) (see section 4.4.)
Muskuloskeletal and connective tissue disorders	-	Pain in extremity Back pain, Arthralgia	Joint swelling, Bone pain, Facial pain, Musculoskeletal stiffness, Muscular weakness
Renal and urinary - disorders	-	-	Hydronephrosis, Urinary incontinence, Haematuria, Nocturia, Blood creatinine increased
Reproductive system and breast disorders	-	-	Vaginal haemorrhage
General disorders and administration site conditions	Fatigue, Asthenia	Pyrexia, Oedema peripheral, Malaise, Chest pain	Oedema, Chills, Influenza like illness, Rigors, Body temperature increased

** Based on the post-marketing experience, persistent or severe palmar-plantar erythrodysaesthesia syndrome can eventually lead to loss of fingerprints (see section 4.4)

Capecitabine in combination therapy:

Table 5 lists ADRs associated with the use of capecitabine in combination with different

chemotherapy regimens in multiple indications based on safety data from over 3000 patients.

ADRs are added to the appropriate frequency grouping (Very common or Common) according

to the highest incidence seen in any of the major clinical trials and are only added when they

were seen in addition to those seen with capecitabine monotherapy or seen at a higher

frequency grouping compared to capecitabine monotherapy (see Table 4). Uncommon ADRs

reported for capecitabine in combination therapy are consistent with the ADRs reported for

capecitabine monotherapy or reported for monotherapy with the combination medicinal product

(in literature and/or respective summary of product characteristics).

Some of the ADRs are reactions commonly seen with the combination medicinal product (e.g.

peripheral sensory neuropathy with docetaxel or oxaliplatin, hypertension seen with

bevacizumab); however an exacerbation by capecitabine therapy cannot be excluded.

Table 5 Summary of related ADRs reported in patients treated with Capecitabine in

combination treatment in addition to those seen with capecitabine monotherapy or seen at a

higher frequency grouping compared to capecitabine monotherapy

 

Body System	Very Common All grades	Common All grades	Rare/Very Rare (Post-Marketing Experience)
Infections and Infestations	-	Herpes zoster, Urinary tract infection, Oral candidiasis, Upper respiratory tract infection, Rhinitis, Influenza, +Infection, Oral herpes
Blood and lymphatic system disorders	+Neutropenia, +Leukopenia, +Anaemia, +Neutropenic fever Thrombocytopenia	Bone marrow depression, +Febrile Neutropenia
Immune system disorders	-	Hypersensitivity
Metabolism and nutrition disorders	Appetite decreased	Hypokalaemia, Hyponatraemia, Hypomagnesaemia, Hypocalcaemia, Hyperglycaemia
Psychiatric disorders	-	Sleep disorder, Anxiety
Nervous system disorders	Paraesthesia, Dysaesthesia, Peripheral neuropathy, Peripheral sensory neuropathy, Dysgeusia Headache	Neurotoxicity, Tremor, Neuralgia, Hypersensitivity reaction Hypoaesthesia
Eye disorders	Lacrimation increased	Visual disorders, Dry eye, Eye pain, Visual impairment, Vision blurred
Ear and labyrinth disorders	-	Tinnitus, Hypoacusis
Cardiac disorders	-	Atrial fibrillation, Cardiac ischaemia/infarction
Vascular disorders	Lower limb oedema, Hypertension +Embolism and thrombosis	Flushing, Hypotension, Hypertensive crisis, Hot flush, Phlebitis
Respiratory, thoracic and mediastinal disorders	Sore throat, Dysaesthesia pharynx	Hiccups, Pharyngolaryngeal pain, Dysphonia
Gastrointestinal disorders	Constipation, Dyspepsia	Upper gastrointestinal haemorrhage, Mouth ulceration, Gastritis, Abdominal distension, Gastroesophageal reflux disease, Oral pain, Dysphagia, Rectal haemorrhage, Abdominal pain lower, Oral dysaesthesia, Paraesthesia oral, Hypoaesthesia oral, Abdominal discomfort
Hepatobiliary Disorders	-	Hepatic function abnormal
Skin and subcutaneous tissue disorders	Alopecia, Nail disorder	Hyperhidrosis, Rash erythematous, Urticaria, Night sweats
Muskuloskeletal and connective tissue disorders	Myalgia, Arthralgia, Pain in extremity	Pain in jaw , Muscle spasms, Trismus, Muscular weakness
Renal and urinary disorders	-	Haematuria, Proteinuria, Creatinine renal clearance decreased, Dysuria	Acute renal failure secondary to dehydration (rare)
General disorders and administration site conditions	Pyrexia, Weakness, +Lethargy, Temperature intolerance	Mucosal inflammation, Pain in limb, Pain, Chills, Chest pain, Influenza-like illness, +Fever, Infusion related reaction, Injection site reaction, Infusion site pain, Injection site pain
Injury, poisoning and procedural complications	-	Contusion

+ For each term, the frequency count was based on ADRs of all grades. For terms marked with

a “+”, the frequency count was based on grade 3-4 ADRs. ADRs are added according to the

highest incidence seen in any of the major combination trials.

Description of selected adverse reactions

Hand-foot syndrome (see section 4.4):

For the capecitabine dose of 1250 mg/m2 twice daily on days 1 to 14 every 3 weeks, a frequency

of 53% to 60% of all- grades HFS was observed in capecitabine monotherapy trials (comprising

studies in adjuvant therapy in colon cancer, treatment of metastatic colorectal cancer, and

treatment of breast cancer) and a frequency of 63% was observed in the capecitabine/docetaxel

arm for the treatment of metastatic breast cancer. For the capecitabine dose of 1000 mg/m2

twice daily on days 1 to 14 every 3 weeks, a frequency of 22% to 30% of all-grade HFS was

observed in capecitabine combination therapy

A meta-analysis of 14 clinical trials with data from over 4700 patients treated with capecitabine

monotherapy or capecitabine in combination with different chemotherapy regimens in multiple

indications (colon, colorectal, gastric and breast cancer) showed that HFS (all grades) occurred

in 2066 (43%) patients after a median time of 239 [95% CI 201, 288] days after starting

treatment with capecitabine. In all studies combined, the following covariates were statistically

significantly associated with an increased risk of developing HFS: increasing capecitabine

starting dose (gram), decreasing cumulative capecitabine dose (0.1*kg), increasing relative dose

intensity in the first six weeks, increasing duration of study treatment (weeks), increasing age

(by 10 year increments), female gender, and good ECOG performance status at baseline (0

versus ≥1).

Diarrhoea (see section 4.4): Capecitabine can induce the occurrence of diarrhoea, which has been observed in up to 50% of patients. The results of a meta-analysis of 14 clinical trials with data from over 4700 patients treated with capecitabine showed that in all studies combined, the following covariates were statistically significantly associated with an increased risk of developing diarrhoea: increasing capecitabine starting dose (gram), increasing duration of study treatment (weeks), increasing age (by 10 year increments), and female gender. The following covariates were statistically significantly associated with a decreased risk of developing diarrhoea: increasing cumulative capecitabine dose (0.1*kg) and increasing relative dose intensity in the first six weeks. Cardiotoxicity (see section 4.4) : In addition to the ADRs described in tables 4 and 5, the following ADRs with an incidence of less than 0.1% were associated with the use of capecitabine monotherapy based on a pooled analysis from clinical safety data from 7 clinical trials including 949 patients (2 phase III and 5 phase II clinical trials in metastatic colorectal cancer and metastatic breast cancer): cardiomyopathy, cardiac failure, sudden death, and ventricular extrasystoles. Encephalopathy: In addition to the ADRs described in tables 4 and 5, and based on the above pooled analysis from clinical safety data from 7 clinical trials, encephalopathy was also associated with the use of Capecitabine monotherapy with an incidence of less than 0.1%. Exposure to crushed or cut capecitabine tablets: In the instance of exposure to crushed or cut capecitabine tablets, the following adverse drug reactions have been reported: eye irritation, eye swelling, skin rash, headache, paresthesia, diarrhea, nausea, gastric irritation, and vomiting. Special populations Elderly patients (see section 4.2): An analysis of safety data in patients ≥60 years of age treated with capecitabine monotherapy and an analysis of patients treated with capecitabine plus docetaxel combination therapy showed an increase in the incidence of treatment-related grade 3 and 4 adverse reactions and treatment related serious adverse reactions compared to patients

associated with an increased risk of developing HFS and diarrhoea and with a decreased risk of

developing neutropenia.

Patients with renal impairment (see section 4.2, 4.4, and 5.2):

An analysis of safety data in patients treated with capecitabine monotherapy (colorectal cancer)

with baseline renal impairment showed an increase in the incidence of treatment-related grade 3

and 4 adverse reactions compared to patients with normal renal function (36% in patients

without renal impairment n=268, vs. 41% in mild n=257 and 54% in moderate n=59,

respectively) (see section 5.2). Patients with moderately impaired renal function show an

increased rate of dose reduction (44%) vs. 33% and 32% in patients with no or mild renal

impairment and an increase in early withdrawals from treatment (21% withdrawals during the

first two cycles) vs. 5% and 8% in patients with no or mild renal impairment.

Reporting of suspected adverse reactions

To report any side effect(s): • The National Pharmacovigilance and Drug Safety Centre (NPC) Fax: +966-11-205-7662 Call NPC at: +966-11-2038222 Exts: 2317-2356-2353- 2354-2334-2340.  Toll free phone: 8002490000 E-mail: npc.drug@sfda.gov.sa Website: www.sfda.gov.sa/npc

The manifestations of acute overdose include nausea, vomiting, diarrhoea, mucositis, gastrointestinal irritation and bleeding, and bone marrow depression. Medical management of overdose should include customary therapeutic and supportive medical interventions aimed at correcting the presenting clinical manifestations and preventing their possible complications.

Pharmacotherapeutic group: cytostatic (antimetabolite), ATC code: L01BC06

Capecitabine is a non-cytotoxic fluoropyrimidine carbamate, which functions as an orally

administered precursor of the cytotoxic moiety 5-fluorouracil (5- FU). Capecitabine is activated

via several enzymatic steps (see section 5.2). The enzyme involved in the final conversion to 5-

FU, thymidine phosphorylase (ThyPase), is found in tumour tissues, but also in normal tissues,

albeit usually at lower levels. In human cancer xenograft models capecitabine demonstrated a

synergistic effect in combination with docetaxel, which may be related to the upregulation of

thymidine phosphorylase by docetaxel.

There is evidence that the metabolism of 5-FU in the anabolic pathway blocks the methylation

reaction of deoxyuridylic acid to thymidylic acid, thereby interfering with the synthesis of

deoxyribonucleic acid (DNA). The incorporation of 5-FU also leads to inhibition of RNA and

protein synthesis. Since DNA and RNA are essential for cell division and growth, the effect of 5- FU may be to create a thymidine deficiency that provokes unbalanced growth and death of a cell.

The effects of DNA and RNA deprivation are most marked on those cells which proliferate more

rapidly and which metabolise 5-FU at a more rapid rate.

Colon and colorectal cancer:

Monotherapy with capecitabine in adjuvant colon cancer

Data from one multicentre, randomised, controlled phase III clinical trial in patients with stage

III (Dukes’ C) colon cancer supports the use of capecitabine for the adjuvant treatment of patients

with colon cancer (XACT Study; M66001). In this trial, 1987 patients were randomised to

treatment with capecitabine (1250 mg/m2 twice daily for 2 weeks followed by a 1-week rest

period and given as 3-week cycles for 24 weeks) or 5-FU and leucovorin (Mayo Clinic regimen:

20 mg/m2 leucovorin IV followed by 425 mg/m2 intravenous bolus 5-FU, on days 1 to 5, every

28 days for 24 weeks). capecitabine was at least equivalent to IV 5-FU/LV in disease-free survival

in per protocol population (hazard ratio 0.92; 95% CI 0.80- 1.06). In the all-randomised

population, tests for difference of Capecitabine vs 5-FU/LV in disease -free and overall survival

showed hazard ratios of 0.88 (95% CI 0.77 – 1.01; p = 0.068) and 0.86 (95% CI 0.74 – 1.01; p =

0.060), respectively. The median follow up at the time of the analysis was 6.9 years. In a

preplanned multivariate Cox analysis, superiority of capecitabine compared with bolus 5- FU/LV

was demonstrated. The following factors were pre-specified in the statistical analysis plan for

inclusion in the model: age, time from surgery to randomization, gender, CEA levels at baseline,

lymph nodes at baseline, and country. In the all-randomised population, capecitabine was shown

to be superior to 5FU/LV for disease-free survival (hazard ratio 0.849; 95% CI 0.739 - 0.976; p

= 0.0212), as well as for overall survival (hazard ratio 0.828; 95% CI 0.705 - 0.971; p = 0.0203).

Combination therapy in adjuvant colon cancer

Data from one multicentre, randomised, controlled phase 3 clinical trial in patients with stage

III (Dukes’ C) colon cancer supports the use of capecitabine in combination with oxaliplatin

(XELOX) for the adjuvant treatment of patients with colon cancer (NO16968 study). In this trial,

944 patients were randomised to 3-week cycles for 24 weeks with capecitabine (1000 mg/m2

twice daily for 2 weeks followed by a 1-week rest period) in combination with oxaliplatin (130

mg/m2 intravenous infusion over 2-hours on day 1 every 3 weeks); 942 patients were randomized

to bolus 5-FU and leucovorin. In the primary analysis for DFS in the ITT population, XELOX

was shown to be significantly superior to 5-FU/LV (HR=0.80, 95% CI=[0.69; 0.93]; p=0.0045).

The 3 year DFS rate was 71% for XELOX versus 67% for

5-FU/LV. The analysis for the secondary endpoint of RFS supports these results with a HR of

0.78 (95% CI=[0.67; 0.92]; p=0.0024) for XELOX vs. 5- FU/LV. XELOX showed a trend

towards superior OS with a HR of 0.87 (95% CI=[0.72; 1.05]; p=0.1486) which translates into a

13% reduction in risk of death. The 5 year OS rate was 78% for XELOX versus 74% for 5-

FU/LV. The efficacy data is based on a median observation time of 59 months for OS and 57

months for DFS. The rate of withdrawal due to adverse events was higher in the XELOX

combination therapy arm (21%) as compared with that of the 5- FU/LV monotherapy arm (9%)

in the ITT population.

Monotherapy with capecitabine in metastatic colorectal cancer

Data from two identically-designed, multicentre, randomised, controlled phase III clinical trials

(SO14695; SO14796) support the use of capecitabine for first line treatment of metastatic

colorectal cancer. In these trials, 603 patients were randomised to treatment with capecitabine

(1250 mg/m2 twice daily for 2 weeks followed by a 1-week rest period and given as 3-week

cycles). 604 patients were randomised to treatment with 5-FU and leucovorin (Mayo regimen: 20

mg/m2 leucovorin IV followed by 425 mg/m2 IV bolus 5-FU, on days 1 to 5, every 28 days). The

overall objective response rates in the all randomised, population (investigator assessment) were

25.7% (capecitabine) vs. 16.7% (Mayo regimen); p <0.0002. The median time to progression was

140 days (capecitabine) vs. 144 days (Mayo regimen). Median survival was 392 days

(capecitabine) vs. 391 days (Mayo regimen). Currently, no comparative data are available on

capecitabine monotherapy in colorectal cancer in comparison with first line combination

regimens.

Combination therapy in first-line treatment of metastatic colorectal cancer

Data from a multicentre, randomised, controlled phase III clinical study (NO16966) support the

use of Capecitabine in combination with oxaliplatin or in combination with oxaliplatin and

bevacizumab for the first -line treatment of metastatic colorectal cancer. The study contained

two parts: an initial 2-arm part in which 634 patients were randomised to two different

treatment groups, including XELOX or FOLFOX-4, and a subsequent 2x2 factorial part in

which 1401 patients were randomised to four different treatment groups, including XELOX

plus placebo, FOLFOX-4 plus placebo, XELOX plus bevacizumab, and FOLFOX-4 plus

bevacizumab. See Table 6 for treatment regimens. Table 6 Treatment regimens in study

NO16966 (mCRC)

 

	Treatment	Starting Dose	Schedule
FOLFOX-4 Or FOLFOX-4 + Bevacizumab	Oxaliplatin	85 mg/m2 intravenous 2 hr.	Oxaliplatin on Day 1, every 2 weeks Leucovorin on Days 1 and 2, every 2 weeks 5-fluorouracil intravenous bolus/infusion, each on Days 1 and 2, every 2 weeks
	Leucovorin	200 mg/m2 intravenous 2 hr.
	5-Fluorouracil	400 mg/m2 intravenous bolus, followed by 600 mg/m2 intravenous 22 hr.
	Placebo or Bevacizumab	5 mg/kg intravenous 30-90 mins	Day 1, prior to FOLFOX-4, every 2 weeks
XELOX Or XELOX+ Bevacizumab	Oxaliplatin	130 mg/m2 intravenous 2 hr.	Oxaliplatin on Day 1, every 3 weeks capecitabine oral twice daily for 2 weeks (followed by 1 week off treatment)
	Capecitabine	1000 mg/m2 oral twice daily
	Placebo or Bevacizumab	7.5 mg/kg intravenous 30-90 mins	Day 1, prior to XELOX, every 3 weeks
5-Fluorouracil: IV bolus injection immediately after leucovorin

Non-inferiority of the XELOX-containing arms compared with the FOLFOX- 4-containing arms in the overall comparison was demonstrated in terms of progression-free survival in the eligible patient population and the intent-to treat population (see table 7). The results indicate that XELOX is equivalent to FOLFOX-4 in terms of overall survival (see table 7). A comparison of XELOX plus bevacizumab versus FOLFOX-4 plus bevacizumab was a pre-specified exploratory analysis. In this treatment subgroup comparison, XELOX plus bevacizumab was similar compared to FOLFOX- 4 plus bevacizumab in terms of progression-free survival (hazard ratio 1.01; 97.5% CI 0.84 - 1.22). The median follow up at the time of the primary analyses in the intent-to-treat population was 1.5 years; data from analyses following an additional 1 year of

follow up are also included in ta ble 7. However, the on treatment PFS analysis did not confirm

the results of the general PFS and OS analysis: the hazard ratio of XELOX versus FOLFOX-4

was 1.24 with 97.5% CI 1.07 - 1.44. Although sensitivity analyses show that differences in

regimen schedules and timing of tumor assessments impact the on-treatment PFS analysis, a full

explanation for this result has not been found.

Table 7 Key efficacy results for the non-inferiority analysis of Study NO16966

 

PRIMARY ANALYSIS
XELOX/XELOX+P/XELOX+BV (EPP*: N=967; ITT**: N=1017)		FOLFOX-4/FOLFOX-4+P/FOLFOX-4+BV (EPP*: N = 937; ITT**: N= 1017)
Population	Median Time to Event (Days)		HR (97.5% CI)
Parameter: Progression-free Survival
EPP	241	259	1.05 (0.94; 1.18)
ITT	244	259	1.04 (0.93; 1.16)
Parameter: Overall Survival
EPP	577	549	0.97 (0.84; 1.14)
ITT	581	553	0.96 (0.83; 1.12)
ADDITIONAL 1 YEAR OF FOLLOW UP
Population	Median Time to Event (Days)		HR (97.5% CI)
Parameter: Progression-free Survival
EPP	242	259	1.02 (0.92; 1.14)
ITT	244	259	1.01 (0.91; 1.12)
Parameter: Overall Survival
EPP	600	594	1.00 (0.88; 1.13)
ITT	602	596	0.99 (0.88; 1.12)

*EPP=eligible patient population; **ITT=intent-to-treat population

In a randomised, controlled phase III study (CAIRO), the effect of using capecitabine at a starting dose of 1000 mg/m2 for 2 weeks every 3 weeks in combination with irinotecan for the first-line treatment of patients with metastatic colorectal cancer was studied. 820 Patients were randomized to receive either sequential treatment (n=410) or combination treatment (n=410). Sequential treatment consisted of first-line capecitabine (1250 mg/m2 twice daily for 14 days), second-line irinotecan (350 mg/m2 on day1), and third-line combination of capecitabine (1000 mg/m2 twice daily for 14 days) with oxaliplatin (130 mg/m2 on day 1). Combination treatment consisted of first-line capecitabine (1000 mg/m2 twice daily for 14 days) combined with irinotecan (250 mg /m2 on day 1) (XELIRI) and second-line capecitabine (1000 mg/m2 twice daily for 14 days) plus oxaliplatin (130 mg/m2 on day 1). All treatment cycles were administered at intervals of 3 weeks. In first -line treatment the median progression-free survival in the intentto-treat population was 5.8 months (95%CI 5.1 - 6.2 months) for capecitabine monotherapy and 7.8 months (95%CI 7.0 - 8.3 months; p=0.0002) for XELIRI. However this was associated with an increased incidence of gastrointestinal toxicity and neutropenia during first-line treatment with XELIRI (26% and 11% for XELIRI and first line capecitabine respectively). The XELIRI has been compared with 5-FU + irinotecan (FOLFIRI) in three randomised studies in patients with metastatic colorectal cancer. The XELIRI regimens included capecitabine 1000 mg/m2 twice daily on days 1 to 14 of a three-week cycle combined with irinotecan 250 mg/m2 on day1. In the largest study (BICC-C), patients were randomised to receive either open label FOLFIRI (n=144), bolus 5-FU (mIFL) (n=145) or XELIRI (n=141) and were additionally randomised to receive either double-blind treatment with celecoxib or placebo. Median PFS was 7.6 months for FOLFIRI, 5.9 months for mIFL (p=0.004) for the

comparison with FOLFIRI), and 5.8 months for XELIRI (p=0.015). Median OS was 23.1

months for FOLFIRI, 17.6 months for mIFL (p=0.09), and 18.9 months for XELIRI (p=0.27).

Patients treated with XELIRI experienced excessive gastrointestinal toxicity compared with

FOLFIRI (diarrhoea 48% and 14% for XELIRI and FOLFIRI respectively).

In the EORTC study patients were randomised to receive either open label FOLFIRI (n=41) or

XELIRI (n=44) with additional randomisation to either double-blind treatment with celecoxib

or placebo. Median PFS and overall survival (OS) times were shorter for XELIRI versus

FOLFIRI (PFS 5.9 versus 9.6 months and OS 14.8 versus 19.9 months), in addition to which

excessive rates of diarrhoea were reported in patients receiving the XELIRI regimen (41%

XELIRI, 5.1% FOLFIRI).

In the study published by Skof et al, patients were randomised to receive either FOLFIRI or

XELIRI. Overall response rate was 49% in the XELIRI and 48% in the FOLFIRI arm (p=0.76).

At the end of treatment, 37% of patients in the XELIRI and 26% of patients in the FOLFIRI

arm were without evidence of the disease (p=0.56). Toxcity was similar between treatments

with the exception of neutropenia reported mor e commonly in patients treated with FOLFIRI.

Montagnani et al used the results from the above three studies to provide an overall analysis of

randomised studies comparing FOLFIRI and XELIRI treatment regimens in the treatment of

mCRC. A significant reduction in the risk of progression was associated with FOLFIRI (HR,

0.76; 95%CI, 0.62- 0.95; P <0.01), a result partly due to poor tolerance to the XELIRI regimens

used.

Data from a randomised clinical study (Souglakos et al, 2012) comparing FOLFIRI + bevacizumab

with XELIRI + bevacizumab showed no significant differences in PFS or OS between treatments.

Patients were randomised to receive either FOLFIRI plus bevacizumab (Arm-A, n=167) or XELIRI

plus bevacizumab (Arm-B, n-166). For Arm B, the XELIRI regimen used capecitabine 1000 mg/m2

twice daily for 14 days +irinotecan 250 mg/m2 on day

1. Median progression-free survival (PFS) was 10.0 and 8.9 months; p=0.64, overall survival

25.7 and 27.5 months; p=0.55 and response rates 45.5 and 39.8%; p=0.32 for FOLFIRI-Bev

and XELIRI-Bev, respectively. Patients treated with XELIRI + bevacizumab reported a

significantly higher incidence of diarrhoea, febrile neutropenia and hand-foot skin reactions

than patients treated with FOLFIRI + bevacizumab with significantly increased treatment

delays, dose reductions and treatment discontinuations.

Data from a multicentre, randomised, controlled phase II study (AIO KRK 0604) supports the

use of capecitabine at a starting dose of 800 mg/m2 for 2 weeks every 3 weeks in combination

with irinotecan and bevacizumab for the first-line treatment of patients with metastatic

colorectal cancer. 120 Patients were randomised to a modified XELIRI regimen with

capecitabine 800 mg/m2 twice daily for two weeks followed by a 7-day rest period), irinotecan

(200 mg/m2 as a 30 minute infusion on day 1 every 3 weeks), and bevacizumab (7.5 mg/kg as

a 30 to 90 minute infusion on day 1 every 3 weeks) ; 127 patients were randomised to treatment

with capecitabine (1000 mg/m2 twice daily for two weeks followed by a 7-day rest period),

oxaliplatin (130 mg/m2 as a 2 hour infusion on day 1 every 3 weeks), and bevacizumab (7.5

mg/kg as a 30 to 90 minute infusion on day 1 every 3 weeks). Following a mean duration of

follow-up for the study population of 26.2 months, treatment responses were as shown below:

Table 8 Key efficacy results for AIO KRK study

 

	XELOX + bevacizumab (ITT: N=127)	Modified XELIRI+ bevacizumab (ITT: N= 120)	Hazard ratio 95% CI P value
Progression-free Survival after 6 months
ITT 95% CI	76% 69 - 84%	84% 77 - 90%	-
Median progression free survival
ITT 95% CI	10.4 months 9.0 - 12.0	12.1 months 10.8 - 13.2	0.93 0.82 - 1.07 P=0.30
Median overall survival
ITT 95% CI	24.4 months 19.3 - 30.7	25.5 months 21.0 - 31.0	0.90 0.68 - 1.19 P=0.45

Combination therapy in second-line treatment of metastatic colorectal cancer

Data from a multicentre, randomised, controlled phase III clinical study (NO16967) support the

use of capecitabine in combination with oxaliplatin for the second-line treatment of metastastic

colorectal cancer. In this trial, 627 patients with metastatic colorectal carcinoma who have

received prior treatment with irinotecan in combination with a fluoropyrimidine regimen as first

line therapy were randomised to treatment with XELOX or FOLFOX-4. For the dosing

schedule of XELOX and FOLFOX-4 (without addition of placebo or bevacizumab), refer to

table 6. XELOX was demonstrated to be non-inferior to FOLFOX-4 in terms of progressionfree survival in the per protocol population and intent-to-treat population (see table 9). The

results indicate that XELOX is equivalent to FOLFOX-4 in terms of overall survival (see table

10). The median follow up at the time of the primary analyses in the intent-to-treat population

was 2.1 years; data from analyses following an additional 6 months of follow up are also

included in Table 9.

Table 9 Key efficacy results for the non-inferiority analysis of Study NO16967

 

 

PRIMARY ANALYSIS
XELOX (PPP*: N=251; ITT**: N=313)		FOLFOX-4 (PPP*: N = 252; ITT**: N= 314)
Population	Median Time to Event (Days)		HR (95% CI)
Parameter: Progression-free Survival
PPP ITT	154 144	168 146	1.03 (0.87; 1.24) 0.97 (0.83; 1.14)
Parameter: Overall Survival
PPP ITT	388 363	401 382	1.07 (0.88; 1.31) 1.03 (0.87; 1.23)
ADDITIONAL 6 MONTHS OF FOLLOW UP
Population	Median Time to Event (Days)		HR (95% CI)
Parameter: Progression-free Survival
PPP ITT	154 143	166 146	1.04 (0.87; 1.24) 0.97 (0.83; 1.14)
Parameter: Overall Survival
PPP ITT	393 363	402 382	1.05 (0.88; 1.27) 1.02 (0.86; 1.21)

*PPP=per-protocol population; **ITT=intent-to-treat population

Advanced gastric cancer:

 

Data from a multicentre, randomised, controlled phase III clinical trial in patients with advanced gastric cancer supports the use of capecitabine for the first-line treatment of advanced gastric cancer (ML17032). In this trial, 160 patients were randomised to treatment with Capecitabine (1000 mg/m2 twice daily for 2 weeks followed by a 7-day rest period) and cisplatin (80 mg/m2 as a 2-hour infusion every 3 weeks). A total of 156 patients were randomised to treatment with 5-FU (800 mg/m2 per day, continuous infusion on days 1 to 5 every 3 weeks) and cisplatin (80 mg/m2 as a 2-hour infusion on day 1, every 3 weeks). capecitabine in combination with cisplatin was non-inferior to 5-FU in combination with cisplatin in terms of progression-free survival in the per protocol analysis (hazard ratio 0.81; 95% CI 0.63 - 1.04). The median progression-free survival was 5.6 months (capecitabine + cisplatin) versus 5.0 months (5-FU + cisplatin). The hazard ratio for duration of survival (overall survival) was similar to the hazard ratio for progression-free survival (hazard ratio 0.85; 95% CI 0.64 - 1.13). The median duration of survival was 10.5 months (capecitabine + cisplatin) versus 9.3 months (5-FU + cisplatin). Data from a randomised multicentre, phase III study comparing capecitabine to 5-FU and oxaliplatin to cisplatin in patients with advanced gastric cancer supports the use of Capecitabine for the first-line treatment of advanced gastric cancer (REAL-2). In this trial, 1002 patients were randomised in a 2x2 factorial design to one of the following 4 arms:

 

ECF: epirubicin (50 mg/ m2 as a bolus on day 1 every 3 weeks), cisplatin (60 mg/m2

As a two hour infusion on day 1 every 3 weeks) and 5-FU (200 mg/m2 daily given by continuous infusion via a central line).

 ECX: epirubicin (50 mg/m2 as a bolus on day 1 every 3 weeks), cisplatin (60 mg/m2 as a two hour infusion on day 1 every 3 weeks), and capecitabine (625 mg/m2 twice daily continuously).

 EOF: epirubicin (50 mg/m2 as a bolus on day 1 every 3 weeks), oxaliplatin (130 mg/m2

given as a 2 hour infusion on day 1 every three weeks), and 5-FU (200 mg/m2 daily

given by continuous infusion via a central line).

 EOX: epirubicin (50 mg/m2 as a bolus on day 1 every 3 weeks), oxaliplatin (130 mg/m2 given as a 2 hour infusion on day 1 every three weeks), and capecitabine (625 mg/m2 twice daily continuously). The primary efficacy analyses in the per protocol population demonstrated non-inferiority in overall survival for capecitabine- vs 5-FU-based regimens (hazard ratio 0.86; 95% CI 0.8 - 0.99) and for oxaliplatin- vs cisplatin-based regimens (hazard ratio 0.92; 95% CI 0.80 - 1.1). The median overall survival was 10.9 months in capecitabine-based regimens and 9.6 months in 5- FU based regimens. The median overall survival was 10.0 months in cisplatinbased regimens and 10.4 months in oxaliplatin-based regimens. Capecitabine has also been used in combination with oxaliplatin for the treatment of advanced gastric cancer. Studies with capecitabine monotherapy indicate that capecitabine has activity in advanced gastric cancer

 

Colon, colorectal and advanced gastric cancer:

meta-analysis A meta-analysis of six clinical trials (studies SO14695, SO14796, M66001, NO16966, NO16967, M17032) supports capecitabine replacing 5-FU in mono- and combination treatment in gastrointestinal cancer. The pooled analysis includes 3097 patients treated with capecitabine -containing regimens and 3074 patients treated with 5-FU-containing regimens. Median overall survival time was 703 days (95% CI: 671; 745) in patients treated with capecitabine -containing regimens and 683 days (95% CI: 646; 715) in patients treated with 5-FU-containing regimens. The hazard ratio for overall survival was 0.94 (95% CI: 0.89; 1.00, p=0.0489) indicating that capecitabine -containing regimens are non-inferior to 5-FU-containing regimens.

Breast cancer:

Combination therapy with capecitabine and docetaxel in locally advanced or metastatic breast cancer

Data from one multicentre, randomised, controlled phase III clinical trial support the use of capecitabine in combination with docetaxel for treatment of patients with locally advanced or metastatic breast cancer after failure of cytotoxic chemotherapy, including an anthracycline. In this trial, 255 patients were randomised to treatment with capecitabine (1250 mg/m2 twice daily for 2 weeks followed by 1-week rest period and docetaxel 75 mg/m2 as a 1 hour intravenous infusion every 3 weeks). 256 patients were randomised to treatment with docetaxel alone (100 mg/m2 as a 1 hour intravenous infusion every 3 weeks). Survival was superior in the capecitabine + docetaxel combination arm (p=0.0126). Median survival was 442 days (capecitabine + docetaxel) vs. 352 days (docetaxel alone). The overall objective response rates in the all-randomised population (investigator assessment) were 41.6% (capecitabine + docetaxel) vs. 29.7% (docetaxel alone); p = 0.0058. Time to progressive disease was superior in the capecitabine + docetaxel combination arm (p<0.0001). The median time to progression

was 186 days (capecitabine + docetaxel) vs. 128 days (docetaxel alone). Monotherapy with capecitabine after failure of taxanes, anthracycline containing chemotherapy, and for whom anthracycline therapy is not indicated Data from two multicentre phase II clinical trials support the use of capecitabine monotherapy for treatment of patients after failure of taxanes and an anthracycline-containing chemotherapy regimen or for whom further anthracycline therapy is not indicated. In these trials, a total of 236 patients were treated with capecitabine (1250 mg/m2 twice daily for 2 weeks followed by 1-week rest period). The overall objective response rates (investigator assessment) were 20% (first trial) and 25% (second trial). The median time to progression was 93 and 98 days. Median survival was 384 and 373 days

All indications:

A meta-analysis of 14 clinical trials with data from over 4700 patients treated with capecitabine monotherapy or capecitabine in combination with different chemotherapy regimens in multiple indications (colon, colorectal, gastric and breast cancer) showed that patients on capecitabine who developed hand-foot syndrome (HFS) had a longer overall survival compared to patients who did not develop HFS: median overall survival 1100 days (95% CI 1007;1200) vs 691 days (95% CI 638;754) with a hazard ratio of 0.61 (95% CI 0.56; 0.66).

 

Paediatric population:

The European Medicines Agency has waived the obligation to conduct studies with capecitabine in all subsets of the paediatric population in adenocarcinoma of the colon and rectum, gastric adenocarcinoma and breast carcinoma (see section 4.2 for information on paediatric use).

The pharmacokinetics of capecitabine have been evaluated over a dose range of 502-3514 mg/m2 /day. The parameters of capecitabine, 5'-deoxy-5- fluorocytidine (5'-DFCR) and 5'- deoxy-5-fluorouridine (5'-DFUR) measured on days 1 and 14 were similar. The AUC of 5-FU was 30%-35% higher on day 14. Capecitabine dose reduction decreases systemic exposure to 5-FU more than dose-proportionally, due to non-linear pharmacokinetics for the active metabolite.

Absorption:

After oral administration, capecitabine is rapidly and extensively absorbed, followed by extensive conversion to the metabolites, 5'-DFCR and 5'-DFUR. Administration with food decreases the rate of capecitabine absorption, but only results in a minor effect on the AUC of 5'-DFUR, and on the AUC of the subsequent metabolite 5-FU. At the dose of 1250 mg/m2 on day 14 with administration after food intake, the peak plasma concentrations (Cmax in μg/ml) for capecitabine, 5'-DFCR, 5'- DFUR, 5-FU and FBAL were 4.67, 3.05, 12.1, 0.95 and 5.46 respectively. The time to peak plasma concentrations (Tmax in hours) were 1.50, 2.00, 2.00, 2.00 and 3.34. The AUC0- ∞ values in μg•h/ml were 7.75, 7.24, 24.6, 2.03 and 36.3.

Distribution:

In vitro human plasma studies have determined that capecitabine, 5'-DFCR, 5'-DFUR and 5- FU are 54%, 10%, 62% and 10% protein bound, mainly to albumin.

Biotransformation:

Capecitabine is first metabolised by hepatic carboxylesterase to 5'-DFCR, which is then converted to 5'-DFUR by cytidine deaminase, principally located in the liver and tumour tissues. Further catalytic activation of 5'-DFUR then occurs by thymidine phosphorylase (ThyPase). The enzymes involved in the catalytic activation are found in tumour tissues but also in normal tissues, albeit usually at lower levels. The sequential enzymatic biotransformation of capecitabine to 5-FU leads to higher concentrations within tumour tissues. In the case of colorectal tumours, 5-FU generation appears to be in large part localised in tumour stromal cells. Following oral administration of capecitabine to patients with colorectal cancer, the ratio of 5-FU concentration in colorectal tumours to adjacent tissues was 3.2 (ranged from 0.9 to 8.0). The ratio of 5-FU concentration in tumour to plasma was 21.4 (ranged from 3.9 to 59.9, n=8) whereas the ratio in healthy tissues to plasma was 8.9 (ranged from 3.0 to 25.8, n=8). Thymidine phosphorylase activity was measured and found to be 4 times greater in primary colorectal tumour than in adjacent normal tissue. According to immunohistochemical studies, thymidine phosphorylase appears to be in large part localised in tumour stromal cells. 5-FU is further catabolised by the enzyme dihydropyrimidine dehydrogenase (DPD) to the much less toxic dihydro-5-fluorouracil (FUH2). Dihydropyrimidinase cleaves the pyrimidinering to yield 5-fluoro-ureidopropionic acid (FUPA). Finally, β -ureido-propionase cleaves FUPA to α-fluoro-β- alanine (FBAL) which is cleared in the urine. Dihydropyrimidine dehydrogenase (DPD) activity is the rate limiting step. Deficiency of DPD may lead to increased toxicity of capecitabine (see section 4.3 and 4.4).

Elimination:

The elimination half-life (t1/2 in hours) of capecitabine, 5'-DFCR, 5'-DFUR, 5-FU and FBAL were 0.85, 1.11, 0.66, 0.76 and 3.23 respectively. Capecitabine and its metabolites are predominantly excreted in urine; 95.5% of administered capecitabine dose is recovered in urine. Faecal excretion is minimal (2.6%). The major metabolite excreted in urine is FBAL, which represents 57% of the administered dose. About 3% of the administered dose is excreted in urine as unchanged drug.

 

Combination therapy:

Phase I studies evaluating the effect of capecitabine on the pharmacokinetics of either docetaxel or paclitaxel and vice versa showed no effect by capecitabine on the pharmacokinetics of docetaxel or paclitaxel (Cmax and AUC) and no effect by docetaxel or paclitaxel on the pharmacokinetics of 5’-DFUR.

Pharmacokinetics in special populations:

A population pharmacokinetic analysis was carried out after capecitabine treatment of 505 patients with colorectal cancer dosed at 1250 mg/m2 twice daily. Gender, presence or absence of liver metastasis at baseline, Karnofsky Performance Status, total bilirubin, serum albumin, ASAT and ALAT had no statistically significant effect on the pharmacokinetics of 5'-DFUR, 5-FU and FBAL. Patients with hepatic impairment due to liver metastases:According to a pharmacokinetic study in cancer patients with mild to moderate liver impairment due to liver metastases, the bioavailability of capecitabine and exposure to 5-FU may increase compared to patients with no liver impairment. There are no pharmacokinetic data on patients with severe hepatic impairment. Patients with renal impairment: Based on a pharmacokinetic study in cancer patients with mild to severe renal impairment, there is no evidence for an effect of creatinine clearance on the pharmacokinetics of intact drug and 5-FU. Creatinine clearance was found to influence the systemic exposure to 5’- DFUR (35% increase in AUC when creatinine clearance decreases by 50%) and to FBAL (114% increase in AUC when creatinine clearance decreases by 50%). FBAL is a metabolite without antiproliferative activity. Elderly: Based on the population pharmacokinetic analysis, which included patients with a wide range of ages (27 to 86 years) and included 234 (46%) patients greater or equal to 65, age has no influence on the pharmacokinetics of 5'-DFUR and 5-FU. The AUC of FBAL increased with age (20% increase in age results in a 15% increase in the AUC of FBAL). This increase is likely due to a change in renal function. Ethnic factors: Following oral administration of 825 mg/m2 capecitabine twice daily for 14 days, Japanese patients (n=18) had about 36% lower Cmax and 24% lower AUC for capecitabine than Caucasian patients (n=22). Japanese patients had also about 25% lower Cmax and 34% lower AUC for FBAL than Caucasian patients. The clinical relevance of these differences is unknown. No significant differences occurred in the exposure to other metabolites (5'-DFCR, 5'-DFUR, and 5-FU).

In repeat -dose toxicity studies, daily oral administration of capecitabine to cynomolgus monkeys and mice produced toxic effects on the gastrointestinal, lymphoid and haemopoietic systems, typical for fluoropyrimidines. These toxicities were reversible. Skin toxicity, characterised by degenerative/regressive changes, was observed with capecitabine. Capecitabine was devoid of hepatic and CNS toxicities. Cardiovascular toxicity (e.g. PR- and QT-interval prolongation) was detectable in cynomolgus monkeys after intravenous administration (100 mg/kg) but not after repeated oral dosing (1379 mg/m2 /day). A two-year mouse carcinogenicity study produced no evidence of carcinogenicity by capecitabine. During standard fertility studies, impairment of fertility was observed in female mice receiving capecitabine; however, this effect was reversible after a drug- free period. In addition, during a 13-week study, atrophic and degenerative changes occurred in reproductive organs of male mice; however these effects were reversible after a drug-free period (see section 4.6). In embryotoxicity and teratogenicity studies in mice, dose-related increases in foetal resorption and teratogenicity were observed. In monkeys, abortion and embryolethality were observed at high doses, but there was no evidence of teratogenicity. Capecitabine was not mutagenic in vitro to bacteria (Ames test) or mammalian cells (Chinese hamster V79/HPRT gene mutation assay). However, similar to other nucleoside analogues (ie, 5-FU), capecitabine was clastogenic in human lymphocytes (in vitro) and a positive trend occurred in mouse bone marrow micronucleus tests (in vivo).

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This medicinal product must not be mixed with other medicinal products except those mentioned in section 6.6.

24 months

Do not store above 30°C.

Catabina film-coated tablets are available in clear PVC/PVDC - Aluminium foil blister packs. Pack Sizes: Catabina 150 mg film-coated tablets Blister pack: 60 film-coated tablets (6 blisters of 10 tablets). Catabina 500 mg film-coated tablets Blister pack: 120 film-coated tablets (12 blisters of 10 tablets).

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