๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-07-30

Triapine With Chemotherapy and Radiation Therapy in Treating Patients With IB2-IVA Cervical or Vaginal Cancer (NCT02595879)

Phase I Dose-Escalation Bioavailability Study of Oral Triapine in Combination With Concurrent Chemoradiation for Locally Advanced Cervical Cancer (LACC) and Vaginal Cancer

๐Ÿ”ต Active, Not Recruiting Phase1 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: National Cancer Institute (NCI)

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

This phase I trial studies the side effects and best dose of triapine when given with radiation therapy and cisplatin in treating patients with stage IB2-IVA cervical or vaginal cancer. Triapine may stop the growth of cancer cells by blocking an enzyme needed for cell growth. Cisplatin is a drug used in chemotherapy that kills cancer cells by damaging their deoxyribonucleic acid (DNA) and stopping them from dividing. Radiation therapy uses high-energy x-rays to kill tumor cells and shrink tumors. Adding triapine to standard treatment with cisplatin and radiation therapy may kill more cancer cells.

Who can join: Review the eligibility criteria below.

Location: University of Alabama at Birmingham Cancer Center โ€” Birmingham, Alabama

Age range: 18 Years

๐Ÿงช Interventions in This Study

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (17 Sites)

  • University of Alabama at Birmingham Cancer Center โ€” Birmingham, Alabama
  • Los Angeles General Medical Center โ€” Los Angeles, California
  • USC / Norris Comprehensive Cancer Center โ€” Los Angeles, California
  • Keck Medical Center of USC Pasadena โ€” Pasadena, California
  • University of Kansas Clinical Research Center โ€” Fairway, Kansas
  • University of Kansas Cancer Center โ€” Kansas City, Kansas
  • University of Kansas Hospital-Indian Creek Campus โ€” Overland Park, Kansas
  • University of Kansas Hospital-Westwood Cancer Center โ€” Westwood, Kansas
  • University of Kentucky/Markey Cancer Center โ€” Lexington, Kentucky
  • University of Michigan Rogel Cancer Center โ€” Ann Arbor, Michigan
  • Wayne State University/Karmanos Cancer Institute โ€” Detroit, Michigan
  • Weisberg Cancer Treatment Center โ€” Farmington Hills, Michigan
  • Rutgers Cancer Institute of New Jersey โ€” New Brunswick, New Jersey
  • University of Oklahoma Health Sciences Center โ€” Oklahoma City, Oklahoma
  • UPMC Hillman Cancer Center โ€” Pittsburgh, Pennsylvania
  • University of Virginia Cancer Center โ€” Charlottesville, Virginia
  • VCU Massey Comprehensive Cancer Center โ€” Richmond, Virginia

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Review the official NIH record below to find the coordinating site.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—