๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-02-12

Study of RP1 Monotherapy and RP1 in Combination With Nivolumab (IGNYTE) (NCT03767348)

An Open-Label, Multicenter, Phase 1/2 Study of RP1 as a Single Agent and in Combination With PD1 Blockade in Patients With Solid Tumors [IGNYTE]

๐Ÿ”ต Active, Not Recruiting Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Replimune, Inc.

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

The Phase 2 study is a multicenter, open-label study of RP1 to further investigate safety and to estimate the efficacy of RP1 at the RP2D in combination with nivolumab in patients with Stage IIIb-IV unresectable melanoma, microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) solid tumors, non-melanoma skin cancer (NMSC), and non-small cell lung cancer (NSCLC).

Who can join: Review the eligibility criteria below.

Location: University of Birmingham Alabama 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 (51 Sites)

Showing the first 25 of 51 sites.

  • University of Birmingham Alabama โ€” Birmingham, Alabama
  • Banner MD Anderson Cancer Center โ€” Gilbert, Arizona
  • Mayo Clinic โ€” Phoenix, Arizona
  • Carti Cancer Center โ€” Little Rock, Arkansas
  • UC San Diego โ€” La Jolla, California
  • University of Southern California โ€” Los Angeles, California
  • UCLA โ€” Los Angeles, California
  • University of California, Irvine โ€” Orange, California
  • University of California- San Francisco โ€” San Francisco, California
  • Sylvester Comprehensive Cancer Center- University of Miami โ€” Miami, Florida
  • University of Iowa-Cancer Center Research โ€” Iowa City, Iowa
  • James Graham Brown Cancer Center- University of Louisville โ€” Louisville, Kentucky
  • Mayo Clinic โ€” Rochester, Minnesota
  • New York University Clinical Cancer Center โ€” New York, New York
  • Weill Cornell Medical College โ€” New York, New York
  • University of Rochester Medical Center โ€” Rochester, New York
  • Duke Cancer Center โ€” Durham, North Carolina
  • University of Cincinnati Medical Center โ€” Cincinnati, Ohio
  • Providence Portland Medical Center โ€” Portland, Oregon
  • MUSC Health โ€” Charleston, South Carolina
  • West Cancer Center โ€” Germantown, Tennessee
  • The University of Texas MD Anderson Cancer Center โ€” Houston, Texas
  • Eccles Outpatient Care Center- Oncology Clinical Trials โ€” Murray, Utah
  • Intermountain Cancer Center- Saint George Cancer Center โ€” St. George, Utah
  • Seattle Cancer Care Alliance- University of Washington โ€” Seattle, Washington

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†—