Combination Pembrolizumab, Chemotherapy and Bevacizumab in Patients With Cervical Cancer
Part of paid clinical trials in Miami, Florida.
- Sponsor
- University of Miami
- Study ID
- NCT03367871
- Phase
- PHASE2
- Status
- Terminated
Conditions
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Pembrolizumab — DRUGIV
- Paclitaxel — DRUGAdministered intravenously (IV) on day 1
- Cisplatin — DRUGAdministered intravenously (IV) on day 1
- Carboplatin — DRUGAdministered intravenously (IV) on day 1
- Bevacizumab — DRUGAdministered intravenously (IV) on day 1
Study Details
The investigators propose to evaluate the efficacy of the combination of standard chemotherapy with bevacizumab with Pembrolizumab in women with recurrent, persistent, or metastatic cervical cancer.
Key Dates
- First listed
- Dec 11, 2017
- Start date
- Sep 6, 2018
- Status verified
- May 2024
- Primary completion
- Jan 30, 2023
- Completion
- Jan 30, 2023
Study Design
- Enrollment
- 17 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Pembrolizumab, Chemotherapy, BevacizumabOn day 1 of each 21 day cycle, participants will be administered Pembrolizumab 200mg (IV); Chemotherapy including Paclitaxel 175mg/m2 or 135 mg/m2 (IV), and Cisplatin 50mg/m2 (IV) or Carboplatin area under the curve (AUC) 5; and Bevacizumab 15mg/kg (IV).
Primary Outcome Measure
Objective Response (OR) [ Time Frame: Up to 24 months ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Miami | Miami | Florida | 33136 | - |
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