🏛️ Verified NIH Record • Updated 2026-05-06

Safety and Efficacy of EIK1001 in Combo With Pembro Versus Placebo and Pembro as First-Line Therapy in Patients With Advanced Melanoma. (NCT06697301)

A Multicenter, Randomized, Double-Blind, Active Comparator-Controlled, Adaptive Phase 2/3 Study to Evaluate the Safety and Efficacy of EIK1001 and Pembrolizumab Versus Placebo and Pembrolizumab as First-Line Therapy in Participants With Advanced Melanoma (TeLuRide-006)

🟢 Recruiting Phase2 / Phase3 💊 Investigational Drug / Biologic Sponsor: Eikon Therapeutics

🩺 Plain-English Summary (8th-Grade Level)

The study is for patients with advanced melanoma who are eligible for standard therapy with Pembrolizumab.

Who can join: Review the eligibility criteria below.

Location: Ironwood Cancer & Research Centers — Chandler, Arizona

Age range: 18 Years

🧪 Interventions in This Study

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (107 Sites)

Showing the first 25 of 107 sites.

  • Ironwood Cancer & Research Centers — Chandler, Arizona
  • Genesis Cancer and Blood Institute — Hot Springs, Arkansas
  • Helios Clinical Research — Los Angeles, California
  • Providence Medical Foundation — Santa Rosa, California
  • UCHealth Memorial Hospital Central — Colorado Springs, Colorado
  • Bioresearch Partner — Hialeah, Florida
  • The Center for Cancer and Blood Disorders — Bethesda, Maryland
  • MidAmerica Cancer Care — Kansas City, Missouri
  • Washington University School of Medicine in St. Louis — St Louis, Missouri
  • Gabrail Cancer Center Research LLC — Canton, Ohio
  • University of Pittsburgh Medical Center(UPMC)-Hillman Cancer Center — Pittsburgh, Pennsylvania
  • Cancer Care Wollongong — Wollongong, New South Wales
  • Icon Cancer Centre Chermside — Chermside, Queensland
  • Southern Adelaide Local Health Network Incorporated Flinders Medical Centre — Bedford Park, South Australia
  • Eastern Health — Box Hill, Victoria
  • Peninsula and South Eastern Haematology and Oncology Group — Frankston, Victoria
  • Universitätsklinikum Graz — Graz, Styria
  • Universitair Ziekenhuis Antwerpen — Edegem, Antwerpen
  • Cliniques Universitaires Saint-Luc — Brussels, Brussels Capital
  • Centre Hospitalier Universitaire Universite Catholique de Louvain - Site Godinne — Yvoir, Namur
  • Universitair Ziekenhuis Leuven - Campus Gasthuisberg — Leuven, Vlaams Brabant
  • Algemeen Ziekenhuis Groeninge - Campus Kennedylaan — Kortrijk, West-Vlaanderen
  • Vitaz Primary Location — Sint-Niklaas,
  • Sunnybrook Research Ins<tute — Toronto, Ontario
  • Masaryk Memorial Cancer Institute — Brno, Brno

📞 Contact the Study Coordinator

Phone: (516) 675-6163

Email: Kazak@eikontx.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 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 § 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.

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  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.
🏛️ View Official NIH Record ↗