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Study identifier: NCT07169279 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Interventional Study of Infigratinib in Children < 3 Years Old With Achondroplasia (ACH)

Condition: Achondroplasia  ·  Sponsor: QED Therapeutics, a BridgeBio company

PhasePhase 2
Planned participants77
Who can joinAll sexes, 0 Years to 32 Months
Healthy volunteersNo

About this study

This is a Phase 2, multicenter, randomized, placebo-controlled study to evaluate the safety and efficacy of infigratinib in participants \< 3 years old with ACH. The purposes of the SAD and Phase 2 portions are to identify and confirm the dose of infigratinib to be used in the Phase 2b portion, based on safety and PK. The purpose of the Phase 2b, placebo-controlled portion is to evaluate the safety and efficacy of infigratinib in children \< 3 years old with ACH at the selected dose.

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

Talk to the study team

QED Therapeutics Inc.  ·  18772805655  ·  medinfo@qedtx.com

Always discuss trial participation with your own doctor first.

Locations (12)

UCSF Benioff Children's HospitalOakland, California, United StatesRecruiting
Johns Hopkins UniversityBaltimore, Maryland, United StatesRecruiting
University of Wisconsin Madison - Waisman Center Bone Dysplasia ClinicMadison, Wisconsin, United StatesRecruiting
Murdoch Children's Research InstituteParkville, Victoria, AustraliaRecruiting
Children's Hospital of Eastern Ontario Research InstituteOttawa, Ontario, CanadaRecruiting
Université de Montréal - Centre Hospitalier Universitaire Sainte-JustineMontreal, Quebec, CanadaRecruiting
Paediatric Clinical Research Unit at Oslo University HospitalOslo, NorwayRecruiting
KK Women's and Children's HospitalSingapore, SingaporeRecruiting
Unidad de Cirugía Artroscópica (UCA)Vitoria-Gasteiz, SpainRecruiting
NHS Greater Glasgow and ClydeGlasgow, United KingdomRecruiting
Manchester University NHS Foundation TrustManchester, United KingdomRecruiting
Sheffield Children's NHS Foundation TrustSheffield, United KingdomRecruiting

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Source record: clinicaltrials.gov/study/NCT07169279