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A study comparing capecitabine oral granules 500 mg per packet to capecitabine tablets 500 mg in patients with breast cancer or colorectal cancer

Not Applicable
Conditions
Health Condition 1: C509- Malignant neoplasm of breast of unspecified site
Registration Number
CTRI/2019/10/021793
Lead Sponsor
Intas Pharmaceuticals Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Patient and /or LAR willing to give written informed consent for participation in the trial.

2. Male or Female >=18 years and <= 65 years of age and having a Body Mass Index (BMI) at least 17 calculated as weight in kg / height in m2.

3. Patients must have/have had histopathologically /cytologically confirmed breast cancer or colorectal cancer.

4. Patients with

a. Dukes C colon cancer patients who have undergone complete resection of the primary tumour when treatment with fluoropyrimidine therapy alone is preferred. OR

b. Metastatic colorectal carcinoma when treatment with fluoropyrimidine therapy alone is preferred. OR

c. Metastatic breast cancer resistant to chemotherapy regimens with paclitaxel and anthracycline-resistant or paclitaxel for patients in whom additional therapy with an anthracycline is not indicated.

5. Patients who require a daily dose of capecitabine monotherapy, who are stabilized

on twice daily dosing for at least one cycle of chemotherapy before randomization and who are eligible to receive a dose of 2500 mg/m2/day.

6. Patients should have their BSA between 1.26-1.91 (Both inclusive).

7. Eastern Cooperative Oncology Group (ECOG) performance status <= 2.

8. Patient with adequate bone marrow, renal and hepatic function.

9. Adequate cardiac function (left ventricular ejection fraction [LVEF] >=50%).

10. Patient should have recovered from any toxic effects of previous chemotherapy as

judged by the Investigator.

11. Patients with life expectancy of at least 3 months (as per the Investigators

discretion).

12. Able to comply with study requirement in opinion of Investigator.

13. Able to give written informed consent for participation in the trial.

14. In case of female patient the serum pregnancy test at screening visit and urine

pregnancy test at day 0 must be negative.

15. Sexually active women, unless surgically sterile (at least 6 months prior to Study

drug administration) or postmenopausal for at least 12 consecutive months, must use an effective method of avoiding pregnancy (including oral, transdermal, or implanted contraceptives [any hormonal method in conjunction with a secondary method], intrauterine device, female condom with spermicide, diaphragm with spermicide, absolute sexual abstinence, use of condom with spermicide by sexual partner or sterile [at least 6 months prior to Study drug administration] sexual partner) for at least 4 weeks prior to study drug administration, during study and up to 180 days after the last dose of study drug. Cessation of birth control after this point should be discussed with a responsible physician.

16. In case of male patients: Either partner or patient must use an effective method of

avoiding pregnancy for at least 4 weeks prior to study drug administration, during

study and up to 90 days after the last dose of study drug. Cessation of birth control

after this point should be discussed with a responsible physician.

Exclusion Criteria

1. Prior unanticipated severe reaction to fluoropyrimidine therapy, or known sensitivity to 5-fluorouracil, or known DPD (Dihydropyrimidine Dehydrogenase) deficiency.

2. Pregnant or breast-feeding female.

3. Any of the following cardiac conditions:

Unstable angina.

Myocardial infarction within the past 6 months.

NYHA (New York State Heart Association) class II-IV heart failure.

Severe uncontrolled ventricular arrhythmias.

Clinically significant pericardial disease.

Electrocardiographic evidence of acute ischemic or active conduction system abnormalities.

Any other cardiac illness that could lead to a safety risk to the patient in case of enrolment in the study.

4. History of drug/alcohol addiction.

5. Known brain metastasis.

6. Pre-existing motor or sensory neurotoxicity of a severity >= grade 2 by NCI CTCAE criteria.

7. A positive hepatitis screen including hepatitis B surface antigen and HCV antibodies.

8. Patients with HIV infection.

9. Patients found positive on urine scan for drugs of abuse and/or breath test for alcohol consumption at screening or baseline.

10. The receipt of an investigational medicinal product or participation in other drug research study within a period of 30 days (or 5 half-lives, whichever is longer) prior to the first dose of investigational medicinal product for the current study.

11. Any other condition that, in the investigators judgment, might increase the risk to the patient or decrease the chance of obtaining satisfactory data needed to achieve

the objectives of the study.

12. Abnormal baseline findings considered by the investigator to indicate conditions that might affect study endpoints.

13. Donation of blood (1 unit or 350 ml) within 90 days prior to receiving the first dose of investigational medicinal product for the current study.

14. Known, existing uncontrolled coagulopathy.

Study & Design

Study Type
BA/BE
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To characterise the pharmacokinetic profile of the sponsors test formulation <br/ ><br>[capecitabine oral granules 500 mg per packet (Manufactured by Intas Pharmaceuticals Ltd, India)] relative to that of reference formulation [Xeloda® (capecitabine) tablets 500 mg (Distributed by: Genentech USA, Inc., A member of the Roche group, 1 DNA Way, South san Francisco, CA 94080-4990)] in patients of metastatic breast cancer or metastatic colorectal cancer under fed condition and to assess the bioequivalence.Timepoint: Pre-dose and 0.167, 0.333, <br/ ><br>0.500, 0.750, 1.000, 1.250, 1.500, 1.750, 2.000, 2.250, 2.500, 2.750, 3.000, 3.333, <br/ ><br>3.667, 4.000, 4.500, 5.000, 6.000, 7.000 and 8.000 hour post-dose
Secondary Outcome Measures
NameTimeMethod
Safety of the patientsTimepoint: Through out the study
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