Pancreatic Cancer Clinical Trial
Official title:
An Open Label Study to Evaluate the Effect of First Line Treatment With Tarceva in Combination With Gemcitabine on Overall Survival and Disease Progression in Patients With Locally Advanced, Unresectable or Metastatic Pancreatic Cancer
This single arm study will assess the efficacy and safety of Tarceva + gemcitabine in patients with locally advanced, unresectable or metastatic pancreatic cancer. Patients will receive Tarceva 100mg po daily, in combination with gemcitabine 1000mg/m2 iv weekly for 8 weeks, followed by weekly for 3 weeks of each 4 week cycle. The anticipated time on study treatment is until disease progression, and the target sample size is <100 individuals.
Status | Terminated |
Enrollment | 6 |
Est. completion date | April 2009 |
Est. primary completion date | April 2009 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - adult patients, >=18 years of age; - pancreatic cancer, surgically unresectable or with metastases; - no previous chemotherapy (except concomitant with radiotherapy); - ECOG 0-2. Exclusion Criteria: - pancreatic cancer without histologic or cytologic confirmation; - surgical resection possible; - previous chemotherapy not concomitant with radiotherapy; - ECOG 3-4. |
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Hoffmann-La Roche |
Mexico,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Overall survival; time to progression | 6 months | No | |
Secondary | Duration of response; disease-free survival | Event driven | No | |
Secondary | AEs, lab parameters | Throughout study | No |
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