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A multicentre, randomized, A cmparision between two Gemcitabine formulation to prove ithe equivalence in patients with Pancreatic or Ovarian Cancer

Not Applicable
Conditions
Health Condition 1: C259- Malignant neoplasm of pancreas, unspecified
Registration Number
CTRI/2012/03/002482
Lead Sponsor
Intas Pharmaceuticals Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
66
Inclusion Criteria

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

2.Male and female patients between the ages of 18 and 65 years.

3.Patients with Histo-pathologically or through Fine Needle Aspiration Cytology (FNAC) confirmed

ï?§Locally Advanced (non-resectable Stage II or Stage III) or Metastatic (Stage IV) Adenocarcinoma of the Pancreas (Gemcitabine as first line treatment)

â??ORâ??

ï?§Pancreatic cancer patients previously treated with 5-Fluorouracil

â??ORâ??

ï?§Advanced Ovarian cancer that has relapsed at least 6 months after completion of platinum-based therapy (Gemcitabine in combination with Carboplatin)

4.Recovered from any toxic effects of previous chemotherapy as judged by the Investigator.

5.Patients if already on Radiotherapy, a gap of at least one week shall be maintained between the last day of radiotherapy and the day of screening

6.Patients with life expectancy of at least 2 months

7.Able to comply with study requirement in opinion of Principal Investigator.

8.Adequate hepatic, renal and hematopoietic function.

Exclusion Criteria

1.Known hypersensitivity reaction to Gemcitabine and any ingredient of the formulation.

2.Use of any recreational drugs or history of drug addiction.

3.History of psychiatric disorders.

4.A positive hepatitis screen including hepatitis B surface antigen, HCV and HAV antibodies.

5.Known case of HIV infection.

6.Pregnant or breast-feeding women.

7.The receipt of an investigational drug or product, or participation in a drug research study within a period of 60 days prior to the first dose of investigational Product (Elimination half-life of the study drug should be taken into consideration for inclusion of the patient in the study).

Study & Design

Study Type
BA/BE
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To characterize the pharmacokinetic profile of the sponsorâ??s test formulation relative to that of reference formulation in patients and to assess the bioequivalenceTimepoint: Day 7 of the patients PK analysis
Secondary Outcome Measures
NameTimeMethod
To monitor the safety of the patients, who are exposed to the Investigational Medicinal Product.Timepoint: up to 30 days afgter last study drug administration
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