NRG-GY037

Open to Accrual

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Protocol Information

Tab containing protocol details, study design, and eligibility criteria
Tab containing study documents, informed consent forms, and study materials
Tab containing information for potential study participants

A Phase III Study of Induction Pembrolizumab and Chemotherapy Followed by Chemoradiation and Pembrolizumab vs Chemoradiation and Pembrolizumab Both Followed by Pembrolizumab for High Risk Locally Advanced Cervical Cancer

Principal Investigator

Jyoti Mayadev, MD

Co-Principal Investigator(s)

Dmitriy Zamarin, MD

Status

Open to Accrual

Date Opened To Accrual

September 29, 2025


Disease Site

Gynecologic [GY] Cervix

Phase

III

Developmental Therapeutics

No

Primary Objective

To determine whether induction IO and chemotherapy prior to CRT+IO improves progression-free survival (PFS) compared to CRT+IO alone.

 

Patient Population

Patients must have pathologically confirmed newly diagnosed cervical cancer. Eligible pathologic types: squamous cell carcinoma, adenocarcinoma, adenosquamous cell carcinoma.

Target Accrual

336

Protocol Documents

Available via the National Cancer Institute (NCI) Cancer Trials Support Unit (CTSU) website.


Patient Study Webpage

There is no available patient study webpage available for this trial at this time.