Atezolizumab and Bevacizumab in Treating Patients With Recurrent, Persistent, or Metastatic Cervical Cancer
Part of paid clinical trials in Los Angeles, California.
- Sponsor
- National Cancer Institute (NCI)
- Study ID
- NCT02921269
- Phase
- PHASE2
- Status
- Completed
Conditions
- Cervical Adenocarcinoma
- Cervical Adenosquamous Carcinoma
- Cervical Squamous Cell Carcinoma, Not Otherwise Specified
- Recurrent Cervical Carcinoma
- Stage IV Cervical Cancer AJCC v6 and v7
- Stage IVA Cervical Cancer AJCC v6 and v7
- Stage IVB Cervical Cancer AJCC v6 and v7
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Atezolizumab — DRUGGiven IV
- Bevacizumab — BIOLOGICALGiven IV
- Laboratory Biomarker Analysis — OTHERCorrelative studies
Study Details
This phase II trial studies how well atezolizumab and bevacizumab work in treating patients with cervical cancer that has come back, remains despite treatment, or has spread to other places in the body. Monoclonal antibodies, such as atezolizumab and bevacizumab, may shrink tumor cell and interfere with the ability of tumor cells to grow and spread.
Key Dates
- Start date
- Mar 10, 2017
- Status verified
- Jan 2023
- Primary completion
- Oct 1, 2020
- Completion
- Jan 13, 2021
Study Design
- Enrollment
- 11 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Treatment (atezolizumab, bevacizumab)Patients receive atezolizumab IV over 30-60 minutes and bevacizumab IV over 30-90 minutes on day 1. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.
Primary Outcome Measure
Number of Participants With Objective Response Rate (ORR, Either Partial or Complete Response) Defined by Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1 Criteria [ Time Frame: Up to 2 years ]
Locations (22)
Find similar trials in Los Angeles, CA
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