ποΈ Verified NIH Record β’ Updated 2026-03-11
Study of Efficacy and Safety of LXH254 Combinations in Patients With Previously Treated Unresectable or Metastatic Melanoma (NCT04417621)
A Randomized, Open-label, Multi-arm, Two-part, Phase II Study to Assess Efficacy and Safety of Multiple LXH254 Combinations in Patients With Previously Treated Unresectable or Metastatic BRAFV600 or NRAS Mutant Melanoma
π΅ Active, Not Recruiting Phase2 π Investigational Drug / Biologic Sponsor: Novartis Pharmaceuticals
π©Ί Plain-English Summary (8th-Grade Level)
The primary purpose of this study is to evaluate the efficacy of LXH254 combinations in previously treated unresectable or metastatic melanoma
Who can join: Review the eligibility criteria below.
Location: The Angeles Clinic and Research Institute β Los Angeles, California
Age range: 12 Years to 120 Years
π§ͺ Interventions in This Study
π "Do I Qualify?" β 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria β
π All Participating Trial Locations (36 Sites)
Showing the first 25 of 36 sites.
- The Angeles Clinic and Research Institute β Los Angeles, California
- UCSF Medical Center β San Francisco, California
- Florida Cancer Specialists β Fort Myers, Florida
- H Lee Moffitt Cancer Center and Research Institute β Tampa, Florida
- Massachusetts General Hospital β Boston, Massachusetts
- Dana Farber Cancer Institute β Boston, Massachusetts
- Mayo Clinic Mayo Rochester β Rochester, Minnesota
- Mayo Clinic Rochester β Rochester, Minnesota
- NYU Laura and Isaac Perlmutter Cancer Center β New York, New York
- Memorial Sloan Kettering β New York, New York
- University of Pittsburgh Med Center β Pittsburgh, Pennsylvania
- Univ of TX MD Anderson Cancer Cntr β Houston, Texas
- Novartis Investigative Site β CABA, Buenos Aires
- Novartis Investigative Site β North Sydney, New South Wales
- Novartis Investigative Site β Wooloongabba, Queensland
- Novartis Investigative Site β Subiaco, Western Australia
- Novartis Investigative Site β Leuven,
- Novartis Investigative Site β Wilrijk,
- Novartis Investigative Site β Lille,
- Novartis Investigative Site β Marseille,
- Novartis Investigative Site β Paris,
- Novartis Investigative Site β Pierre-BΓ©nite,
- Novartis Investigative Site β Toulouse,
- Novartis Investigative Site β Villejuif,
- Novartis Investigative Site β Dresden, Saxony
π° 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 Β§ 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 Melanoma
- Randomized Study Comparing Two Dosing Schedules for Hypofractionated Image-Guided Radiation Therapy β San Francisco, California
- An Efficacy Study of Adjuvant Treatment With the Personalized Cancer Vaccine mRNA-4157 and Pembrolizumab in Participants With High-Risk Melanoma (KEYNOTE-942) β Tucson, Arizona
- Adjuvant Encorafenib and Binimetinib in High-risk Stage II Melanoma With a BRAF Mutation. β CABA, Buenos Aires
- Phase 2 Trial of Voyager V1 in Combination With Cemiplimab in Cancer Patients β Santa Monica, California
- NeoVax + CDX-301 and Nivolumab or Pembrolizumab in Melanoma β Boston, Massachusetts
- A Clinical Trial of Three Study Medicines (Encorafenib, Binimetinib, and Pembrolizumab) in Patients With Advanced or Metastatic Melanoma β Orlando, Florida
Explore by condition: All Melanoma clinical trials
π‘ How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.