Cisplatin, Pemetrexed and Bevacizumab for Untreated Malignant Mesothelioma
Part of paid clinical trials in Dallas, Texas.
- Sponsor
- University of Texas Southwestern Medical Center
- Study ID
- NCT00295503
- Phase
- PHASE2
- Status
- Completed
Conditions
- Mesothelioma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- bevacizumab — DRUG15 mg/kg IV every 3 weeks
- cisplatin — DRUG75 mg/m2 IV every 3 weeks
- pemetrexed — DRUG500 mg/m2 every 3 weeks
Study Details
To estimate the time to progression of cancer in patients with previously untreated mesothelioma receiving cisplatin, pemetrexed and bevacizumab
Key Dates
- First listed
- Feb 23, 2006
- Start date
- Feb 28, 2006
- Status verified
- Sep 2020
- Primary completion
- Jun 30, 2010
- Completion
- Aug 31, 2010
Study Design
- Enrollment
- 53 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: 1cisplatin, pemetrexed, and bevacizumab
Primary Outcome Measure
Progression Free Survival Rate at 6 Months [ Time Frame: patients progression free at 6 months ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Texas Southwestern Medical Center | Dallas | Texas | 75390-8852 | - |
Find similar trials in Dallas, TX
By research site
Related Studies
- VMD-928 Monotherapy and in Combination With Pembrolizumab to Treat TrkA Overexpression Driven Solid Tumors or LymphomaPHASE1/PHASE2 · Recruiting · VM Oncology, LLC · Santa Rosa, California
- Study to Evaluate VT3989 in Patients With Metastatic Solid TumorsPHASE1/PHASE2 · Recruiting · Vivace Therapeutics, Inc · San Francisco, California
- Solid Tumor Analysis for HLA Loss of Heterozygosity (LOH) and Apheresis for CAR T- Cell ManufacturingRecruiting · A2 Biotherapeutics Inc. · Gilbert, Arizona
- Phase 1 Study of MRTX1719 in Solid Tumors With MTAP DeletionPHASE1 · Recruiting · Bristol-Myers Squibb · Phoenix, Arizona