Pembrolizumab in Treating Participants With Unresectable Thymoma or Thymic Cancer
Part of paid clinical trials in Houston, Texas.
- Sponsor
- M.D. Anderson Cancer Center
- Study ID
- NCT03295227
- Phase
- PHASE1
- Status
- Recruiting
Conditions
- Stage III Thymoma AJCC v8
- Stage IIIA Thymoma AJCC v8
- Stage IIIB Thymoma AJCC v8
- Stage IV Thymoma AJCC v8
- Stage IVA Thymoma AJCC v8
- Stage IVB Thymoma AJCC v8
- Unresectable Thymic Carcinoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Pembrolizumab — BIOLOGICALGiven IV
Study Details
This phase I trial studies the sides effects and best dose of pembrolizumab in treating participants with thymoma or thymic cancer that cannot be removed by surgery. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread.
Key Dates
- Start date
- Dec 6, 2017
- Status verified
- Jan 2026
- Primary completion
- Dec 31, 2027
- Completion
- Dec 31, 2027
Study Design
- Enrollment
- 37 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Treatment (pembrolizumab)Participants receive pembrolizumab IV over 30 minutes on day 1. Courses repeat every 21 days for up to 2 years in the absence of disease progression or unacceptable toxicity.
Primary Outcome Measure
Incidence of adverse events [ Time Frame: Up to 3 years ]
Central Contacts
- Anne S. Tsao713-792-6363
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| M D Anderson Cancer Center | Houston | Texas | 77030 | Anne S. Tsao 713-792-6363 Anne S. Tsao (PRINCIPAL_INVESTIGATOR) |
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