Stage IVA Cervical Cancer AJCC v8

3

Review clinical trials related to Stage IVA Cervical Cancer AJCC v8. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Personalized Neoantigen Peptide-Based Vaccine in Combination With Pembrolizumab for Treatment of Advanced Solid Tumors

This phase I/II trial tests the safety and tolerability of an experimental personalized vaccine when given by itself and with pembrolizumab in treating patients with solid tumor cancers that have spread to other places in the body (advanced). The experimental vaccine is designed target certain proteins (neoantigens) on individuals' tumor cells. 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. Giving the personalized neoantigen peptide-based vaccine with pembrolizumab may be safe and effective in treating patients with advanced solid tumors.

Participants needed: 132
Trial details
Phase: Phase 1, Phase 2Age: 16+Biological sex: AllType: InterventionalSponsor: Mayo ClinicUpdated: Jun 23, 2026Locations: 1
Eligibility criteria

Willing to provide tissue specimens per protocol [+82]

Pregnant person [+63]

Status: Recruiting

Talazoparib and Radiation Therapy in Treating Patients With Locally Recurrent Gynecologic Cancers

This phase I trial studies the side effects and best dose of talazoparib in combination with radiation therapy and to see how well they work in treating patients with gynecologic cancers that have come back after previous treatment (recurrent). Talazoparib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Radiation therapy uses high energy x-rays to kill tumor cells and shrink tumors. Giving talazoparib in combination with radiation therapy may work better in treating patients with gynecologic cancers.

Participants needed: 24
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: M.D. Anderson Cancer CenterUpdated: Mar 11, 2026Locations: 2
Eligibility criteria

Provision of informed consent prior to any study specific procedures [+18]

Ascites, peritoneal carcinomatosis, hepatic metastases [+20]

Status: Recruiting

Establishing a Tumor Registry for Patients With Neuroendocrine Carcinoma of the Cervix

This study collects information and data on patients with neuroendocrine cervical cancer. Information from this study may be used to better understand the correlation between clinical data, such as patient characteristics, treatment, and disease outcomes, and overall patient outcomes.

Participants needed: 750
Trial details
Biological sex: AllType: ObservationalSponsor: M.D. Anderson Cancer CenterUpdated: Mar 5, 2026Locations: 1
Eligibility criteria

Small cell neuroendocrine carcinoma [+10]

Patients with other histologic subtypes of NEC of the cervix including typical a...