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Study identifier: NCT07359820 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Study of Lirafugratinib in Non-CCA Solid Tumors With FGFR2 Fusion or Rearrangement

Condition: FGFR2 Gene Fusion/Rearrangement · Other Solid Tumors, Adult  ·  Sponsor: Elevar Therapeutics

PhasePhase 2
Planned participants30
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this clinical trial is to evaluate if lirafugratinib is efficacious and safe to treat adult patients with previously treated, unresectable, locally advanced or metastatic solid tumors (excluding cholangiocarcinoma) harboring FGFR2 fusion or rearrangement. Participants will: * Take lirafugratinib regularly as instructed by their study doctor. * Visit the clinic as instructed for checkups and tests. * Keep a diary recording each time a dose of lirafugratinib is taken.

This description comes directly from the study's public registry record.

Talk to the study team

Jacki Dillingham  ·  +1 (385) 276-3611  ·  jdillingham@elevartx.com

Lissa Nazal  ·  +1 (385) 276-3621  ·  lnazal@elevartx.com

Always discuss trial participation with your own doctor first.

Locations (19)

Mayo ClinicPhoenix, Arizona, United StatesNot Yet Recruiting
Mayo ClinicJacksonville, Florida, United StatesNot Yet Recruiting
Moffitt Cancer CenterTampa, Florida, United StatesRecruiting
University of Chicago Medical CenterChicago, Illinois, United StatesRecruiting
Massachusetts General HospitalBoston, Massachusetts, United StatesRecruiting
Mayo ClinicRochester, Minnesota, United StatesNot Yet Recruiting
The University of Texas M.D. Anderson Cancer CenterHouston, Texas, United StatesRecruiting
Institut BergonieBordeaux, FranceNot Yet Recruiting
Centre Georges François LeclercDijon, FranceNot Yet Recruiting
Centre Leon BerardLyon, FranceNot Yet Recruiting
Gustave Roussy Cancer CampusParis, FranceNot Yet Recruiting
Seoul National University HospitalSeoul, South KoreaRecruiting

+ 7 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07359820