๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-05-05

Talimogene Laherparepvec and Pembrolizumab in Treating Patients With Stage III-IV Melanoma (NCT02965716)

A Phase II Study of Combining Talimogene Laherparepvec (T-VEC) (NSC-785349) and MK-3475 (Pembrolizumab) (NSC-776864) in Patients With Advanced Melanoma Who Have Progressed on Anti-PD1/L1 Based Therapy

๐Ÿ”ต Active, Not Recruiting Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: National Cancer Institute (NCI)

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

This phase II trial studies how well talimogene laherparepvec and pembrolizumab work in treating patients with stage III-IV melanoma. Biological therapies, such as talimogene laherparepvec, use substances made from living organisms that may stimulate or suppress the immune system in different ways and stop tumor cells from growing. 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 talimogene laherparepvec and pembrolizumab may work better in treating patients with melanoma by shrinking the tumor.

Who can join: Review the eligibility criteria below.

Location: University of South Alabama Mitchell Cancer Institute โ€” Mobile, 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 (20 Sites)

  • University of South Alabama Mitchell Cancer Institute โ€” Mobile, Alabama
  • CTCA at Western Regional Medical Center โ€” Goodyear, Arizona
  • Los Angeles General Medical Center โ€” Los Angeles, California
  • USC / Norris Comprehensive Cancer Center โ€” Los Angeles, California
  • UCLA / Jonsson Comprehensive Cancer Center โ€” Los Angeles, California
  • Keck Medical Center of USC Pasadena โ€” Pasadena, California
  • Loyola University Medical Center โ€” Maywood, Illinois
  • Indiana University/Melvin and Bren Simon Cancer Center โ€” Indianapolis, Indiana
  • University of Kansas Hospital-Westwood Cancer Center โ€” Westwood, Kansas
  • Henry Ford Cancer Institute-Downriver โ€” Brownstown, Michigan
  • Henry Ford Macomb Hospital-Clinton Township โ€” Clinton Township, Michigan
  • Henry Ford Hospital โ€” Detroit, Michigan
  • Allegiance Health โ€” Jackson, Michigan
  • Henry Ford West Bloomfield Hospital โ€” West Bloomfield, Michigan
  • Kansas City Veterans Affairs Medical Center โ€” Kansas City, Missouri
  • University of Cincinnati Cancer Center-UC Medical Center โ€” Cincinnati, Ohio
  • Ohio State University Comprehensive Cancer Center โ€” Columbus, Ohio
  • University of Cincinnati Cancer Center-West Chester โ€” West Chester, Ohio
  • Vanderbilt University/Ingram Cancer Center โ€” Nashville, Tennessee
  • Huntsman Cancer Institute/University of Utah โ€” Salt Lake City, Utah

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†—