πŸ›οΈ 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

πŸ”΅ Active, Not Recruiting Phase2 πŸ’Š Investigational Drug / Biologic Sponsor: Novartis Pharmaceuticals

🩺 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

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ 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

πŸ’° 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.

Explore by condition: All Melanoma clinical trials

πŸ’‘ 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.
πŸ›οΈ View Official NIH Record β†—