๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2024-03-29

Ramucirumab and Trifluridine/Tipiracil or Paclitaxel for the Treatment of Patients With Previously Treated Advanced Gastric or Gastroesophageal Junction Cancer (NCT04660760)

Ramucirumab Plus Trifluridine/Tipiracil (TAS-102) for Patients With Previously Treated Advanced Gastric or Gastroesophageal Junction Adenocarcinoma: An Investigator-Initiated, Randomized Non-Inferiority Phase 2 Study

๐ŸŸข Recruiting Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Academic and Community Cancer Research United

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

This phase II trial studies the effect of the combination of ramucirumab and trifluridine/tipiracil or paclitaxel in treating patients with previously treated gastric or gastroesophageal junction cancer that has spread to other places in the body (advanced). Ramucirumab may damage tumor cells by targeting new blood vessel formation. Trifluridine/tipiracil is a chemotherapy pill and that may damage tumor cells by damaging their deoxyribonucleic acid (DNA). Paclitaxel may block cell growth by stopping cell division which may kill tumor cells. Giving ramucirumab and trifluridine/tipiracil will not be worse than ramucirumab and paclitaxel in treating gastric or gastroesophageal junction cancer.

Who can join: Review the eligibility criteria below.

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

Age range: 18 Years

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

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

๐Ÿ“ All Participating Trial Locations (15 Sites)

  • University of Alabama at Birmingham Cancer Center โ€” Birmingham, Alabama
  • Mayo Clinic in Arizona โ€” Scottsdale, Arizona
  • Arizona Clinical Research Center โ€” Tucson, Arizona
  • USC / Norris Comprehensive Cancer Center โ€” Los Angeles, California
  • Mayo Clinic in Florida โ€” Jacksonville, Florida
  • Cleveland Clinic-Weston โ€” Weston, Florida
  • Emory University Hospital/Winship Cancer Institute โ€” Atlanta, Georgia
  • Carle Cancer Center NCI Community Oncology Research Program โ€” Urbana, Illinois
  • University of Iowa/Holden Comprehensive Cancer Center โ€” Iowa City, Iowa
  • Cancer Center of Kansas - Wichita โ€” Wichita, Kansas
  • Metro Minnesota Community Oncology Research Consortium โ€” Saint Louis Park, Minnesota
  • University of Nebraska Medical Center โ€” Omaha, Nebraska
  • Vanderbilt University/Ingram Cancer Center โ€” Nashville, Tennessee
  • Saint Vincent Hospital Cancer Center Green Bay โ€” Green Bay, Wisconsin
  • Aurora Cancer Care-Milwaukee West โ€” Wauwatosa, Wisconsin

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†—