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Brief Title: Dostarlimab and Cobolimab in Advanced Cervical Cancer
Official Title: A Phase 2 Study of Dostarlimab in Combination With Cobolimab in Advanced Cervical Cancer
Study ID: NCT06238635
Brief Summary: This research is being done to determine how effective dostarlimab in combination with cobolimab is in metastatic or recurrent cervical cancer.
Detailed Description: This is a non-randomized, open-label, two-arm phase 2 trial of dostarlimab and cobolimab for participants with metastatic or recurrent cervical cancer who have or have not been treated with immunotherapy previously. The names of the study drugs involved in this study are: * Cobolimab (a type of monoclonal antibody) * Dostarllimab (a type of monoclonal antibody) The U.S. Food and Drug Administration (FDA) has not approved cobolimab as a treatment for cervical cancer. The FDA has not approved dostarlimab for cervical cancer but it has been approved for other uses. The study procedures including, screening for eligibility, treatment visits, blood tests, x-rays, Computerized Tomograph (CT) scans, Magnetic Resonance Imaging (MRI) scans, or Positron Emission Tomograph (PET) scans. Participants will be followed for up to 7 years. It is expected that about 66 people will take part in this research study. GlaxoSmithKline is funding this research study by providing funding and the study drugs.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: FEMALE
Healthy Volunteers: No
Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States
Dana-Farber Cancer Institute, Boston, Massachusetts, United States
Massachusetts General Hospital Cancer Center, Boston, Massachusetts, United States
Name: Meghan Shea, MD
Affiliation: Beth Israel Deaconess Medical Center
Role: PRINCIPAL_INVESTIGATOR