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)
🩺 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 ChecklistFull 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.
More studies in Advanced Melanoma
- Using Biomarkers to Help Guide Safe Immunotherapy Discontinuation in Patients With Unresectable Stage IIIB-IV Melanoma, The PET-Stop Trial — Fairhope, Alabama
- Ipilimumab With or Without Sargramostim in Treating Patients With Stage III or Stage IV Melanoma That Cannot Be Removed by Surgery — Birmingham, Alabama
- Talimogene Laherparepvec and Pembrolizumab in Treating Patients With Stage III-IV Melanoma — Mobile, Alabama
- A Study of Botensilimab (AGEN1181) for the Treatment of Advanced Melanoma — Scottsdale, Arizona
- A Trial of Pembrolizumab and Metformin Versus Pembrolizumab Alone in Advanced Melanoma — Pittsburgh, Pennsylvania
- Memory-Like Natural Killer Cells With Nivolumab and Relatlimab in Advanced or Metastatic Melanoma After Progression on Checkpoint Inhibitors — St Louis, Missouri
Explore by condition: All Advanced Melanoma clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.