setrusumab: Clinical Trials

10 trials of setrusumab, newest first

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

4 completed, 3 active not recruiting, 2 withdrawn, 1 terminated. 8 Phase 2, 3 Phase 3.

By phase and status

PhaseTrialsStatus
Phase 28Completed 4, Withdrawn 2, Active not recruiting 1, Terminated 1
Phase 33Active not recruiting 3

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Trials newest first · largest first

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
Setrusumab in Pediatric Japanese Subjects With Osteogenesis Imperfecta
setrusumab - Osteogenesis Imperfecta
Phase 3Active not recruitingUltragenyx Pharmaceutical Inc62024-10-252026-09-28
Setrusumab vs Bisphosphonates in Pediatric Subjects With Osteogenesis Imperfecta
Bisphosphonate, Setrusumab - Osteogenesis Imperfecta
Phase 3Active not recruitingUltragenyx Pharmaceutical Inc692023-06-142026-10-20
Long-term Extension Study of Setrusumab in Adults With Type I, III, or IV Osteogenesis Imperfecta
Setrusumab - Osteogenesis Imperfecta
Phase 2TerminatedUltragenyx Pharmaceutical Inc22022-04-282025-07-23
Setrusumab vs Placebo for Osteogenesis Imperfecta
Setrusumab, Placebo - Osteogenesis Imperfecta
Phase 2 / Phase 3Active not recruitingUltragenyx Pharmaceutical Inc1832022-02-212026-10-20
An Exploratory Study of BPS804 Treatment in Adult Patients With Type I, III or IV Osteogenesis Imperfecta
BPS804 - Osteogenesis Imperfecta
Phase 2WithdrawnUltragenyx Pharmaceutical Inc2017-10-312023-07-03
A Study in Adult Patients With Type I, III or IV Osteogenesis Imperfecta Treated With BPS804
setrusumab, Calcium, Vitamin D - Osteogenesis Imperfecta, Type I, Osteogenesis Imperfecta Type III
Phase 2CompletedUltragenyx Pharmaceutical Inc1122017-09-112023-07-05
Study of Safety and Tolerability of BPS804 in Patients With Late-stage Chronic Kidney Disease
BPS804, Placebo - Chronic-kidney Disease Stage 5D on Stable Hemodialysis
Phase 2WithdrawnUltragenyx Pharmaceutical Inc2013-08-012022-09-14
Dose Escalation Study to Evaluate the Safety and Tolerability of Multiple Infusions of BPS804 in Adults With Hypophosphatasia (HPP)
BPS804 - Hypophosphatasia
Phase 2CompletedUltragenyx Pharmaceutical Inc82011-07-012022-09-16
Safety and Efficacy of Multiple Dosing Regimens of BPS804 in Post Menopausal Women With Low Bone Mineral Density
BPS804 20mg/Kg, Placebo to 20mg/Kg BPS804 - Osteopenia, Osteoporosis
Phase 2CompletedUltragenyx Pharmaceutical Inc442011-07-012022-09-15
Safety, Pharmacokinetics and Pharmacodynamics of BPS804 in Osteogenesis Imperfecta
BPS804 - Osteogenesis Imperfecta
Phase 2CompletedUltragenyx Pharmaceutical Inc102011-06-012021-05-11

Conditions studied

Osteogenesis Imperfecta (7)  ·  Bone Diseases, Metabolic (1)  ·  Connective Tissue Diseases (1)  ·  Fractures, Bone (1)  ·  Hypophosphatasia (1)  ·  Osteogenesis imperfecta, type 3 (1)  ·  Osteoporosis (1)

Sponsors

Ultragenyx Pharmaceutical Inc (10)

Countries

United States (7)  ·  Canada (4)  ·  France (3)  ·  Germany (3)  ·  Italy (2)  ·  Netherlands (2)  ·  Poland (2)  ·  United Kingdom (2)  ·  Australia (1)  ·  Belgium (1)  ·  Brazil (1)  ·  Denmark (1)  ·  Japan (1)  ·  Portugal (1)  ·  Turkey (Türkiye) (1)

Results publications

PMID 42470570, PMID 28436937, PMID 39012717

NIH funding

2016 (1), 2023 (1)