Trial Of Erlotinib With Or Without PF-3512676 In Advanced Non Small Cell Lung Cancer
Part of paid clinical trials in Daphne, Alabama.
- Sponsor
- Pfizer
- Study ID
- NCT00321815
- Phase
- PHASE2
- Status
- Completed
Conditions
- Carcinoma, Non-Small-Cell Lung
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- PF-3512676 + Erlotinib — DRUGPF-3512676 0.2 mg/kg subcutaneously on days 1, 8 and 15 of each 21 day cycle until disease progression or unacceptable toxicity. Erlotinib 150 mg orally daily (21 day cycles) until disease progression or unacceptable toxicity
- Erlotinib — DRUGErlotinib 150 mg orally daily (21 day cycles) until disease progression or unacceptable toxicity
Study Details
To assess the efficacy and safety of PF-3512676 administered in combination with erlotinib in patients with advanced EGFR-positive non-small cell lung cancer after failure of at least one prior chemotherapy regimen.
Key Dates
- First listed
- May 4, 2006
- Start date
- Aug 31, 2006
- Status verified
- Dec 2010
- Primary completion
- Jun 30, 2010
- Completion
- Jun 30, 2010
Study Design
- Enrollment
- 43 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: AStandard of Care chemotherapy plus experimental intervention (PF-3512676)
- Active Comparator: BStandard of Care chemotherapy
Primary Outcome Measure
Progression-Free Survival [ Time Frame: 50Events ]
Locations (35)
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