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setrusumab

·Code: BPS-804, UX143

setrusumab: developed by 1 company · 4 clinical trials tracked.

setrusumab evidence translation

What we can confirm

What it means

Source-backed records connect setrusumab to MREO; that link alone does not prove the drug works.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

How could setrusumab → MREO affect its developer, and what evidence supports the link?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence2 indications · 1 study sponsors

Related indications

Osteogenesis imperfecta (OI)Osteogenesis Imperfecta
Development Pipeline (1)
CompanyPhase
Mereo BioPharma Group plc (MREO)
Osteogenesis imperfecta (OI)
Phase 3
Clinical Trials (4)

An Open-label Phase 3 Study of Setrusumab in Pediatric Japanese Subjects With Osteogenesis Imperfecta Type I, III, or IV

NCT06636071·Phase 3·RARE
Active, not recruiting

Primary endpoint: Annualized Rate of All Radiographically-Confirmed Fractures, Including Morphometric Vertebral Fractures During the Treatment Period

Interventionalopen6 targetStarted 2024-10Completion 2028-013 sites · JapanUltragenyx Pharmaceutical Inc

An Open-label, Randomized, Active-Controlled, Phase 3 Study of Setrusumab Compared With Bisphosphonates in Pediatric Subjects With Osteogenesis Imperfecta Types I, III or IV

NCT05768854·Phase 3·RARE
Active, not recruiting

Primary endpoint: Annualized Rate of All Radiographically-Confirmed Fractures, Including Morphometric Vertebral Fractures, at the Primary Analysis

InterventionalRandomizedopen69 targetStarted 2023-06Completion 2027-0420 sites · Brazil, Canada, France, Italy…Ultragenyx Pharmaceutical Inc

A Phase 2b, Multicenter, Long-term Extension Study of Setrusumab in Adults With Type I, III, or IV Osteogenesis Imperfecta

NCT05312697·Phase 2·RARE
Terminated

Primary endpoint: Percentage Change From Retreatment Baseline in Lumbar Spine Bone Mineral Density (BMD) Measured by Dual-Energy X-Ray Absorptiometry (DXA) After 12 Months of Setrusumab

InterventionalRandomizedopen2 targetStarted 2022-04Completion 2022-071 site · United StatesUltragenyx Pharmaceutical Inc

An Operationally Seamless, Randomized Phase 2/3 Study Consisting of a Phase 2 Single-Blind, Dose-Evaluation Phase and a Phase 3 Double-Blind, Placebo-Controlled Phase to Assess the Efficacy and Safety of Setrusumab in Subjects With Osteogenesis Imperfecta

NCT05125809·Phase 2/Phase 3·RARE
Active, not recruiting

Primary endpoint: Phase 2: Percent Change in Serum Amino-terminal Propeptide of Type 1 Procollagen (P1NP) from Baseline at Month 1

InterventionalRandomizedquadruple183 targetStarted 2022-02Completion 2027-0444 sites · Australia, Canada, France, Germany…Ultragenyx Pharmaceutical Inc

Frequently asked questions

Who is developing setrusumab?

setrusumab is being developed by Mereo BioPharma Group plc.

How many clinical trials involve setrusumab?

BioSniper tracks 4 clinical trials involving setrusumab.