Setrusumab vs Placebo for Osteogenesis Imperfecta

Running, not enrolling · Phase 2/Phase 3 · Has a placebo group

Conditions studied: Osteogenesis Imperfecta

In brief

The primary objectives of the study are to identify a setrusumab dosing strategy in participants with OI and to evaluate the effect of setrusumab vs placebo on reduction in fracture rate.

Key facts

Study ID: NCT05125809
Run by: Ultragenyx Pharmaceutical Inc
People needed: 183
Starts: 2022-02-21
Expected to finish: 2027-04-01
Last updated by the study team: 2026-02-25

Who can join

Age: 5 and older, up to 25. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Diagnosis of OI Type I, III, or IV as confirmed by identification of pathogenic or likely pathogenic genetic variants in COL1A1 or COL1A2. If a variant of uncertain significance is identified, then clinical presence of the expected phenotype can be used to confirm the diagnosis
≥ 1 fracture in the past 12 months, ≥ 2 fractures in the past 24 months or ≥ 1 tibia, femur or humerus fracture in the past 24 months
Serum 25-hydroxyvitamin D ≥ 20 ng/mL at the Screening Visit. If 25-hydroxyvitamin D levels are below 20 ng/mL, 25-hydroxyvitamin D testing can repeated after a minimum of 14 days of vitamin D supplementation as directed by the treating physician
Willing to not receive bisphosphonate therapy during the study
From the period following informed consent to 60 days after the last dose of the study drug, females of childbearing potential and fertile males must consent to use highly effective contraception. If female, agree not to become pregnant. If male, agree not to father a child or donate sperm
Willing and able to provide informed consent for subjects greater than or equal to 18 years of age, or provide assent (if possible) and have a legally authorized representative provide informed consent, after the nature of the study has been explained and prior to any research-related procedures
Willing to provide access to medical records for the collection of radiographic data, fracture data, growth data, and disease history
Must, in the opinion of the Investigator, be willing and able to complete all aspects of the study, adhere to the study visit schedule, and comply with the assessments

You may not qualify if…

History of skeletal malignancies or bone metastases at any time
History of neural foraminal stenosis (except if due to scoliosis)
Clinical manifestations of Chiari malformation or basilar invagination. Presence of any other neurologic disease that has been unstable within past 2 years requires review by the Medical Monitor
History of or uncontrolled concomitant diseases such as hypo/hyperparathyroidism, Paget's disease, abnormal thyroid function, thyroid disease or other endocrine disorders or conditions that could affect bone metabolism such as Stage IV/V renal disease
Rickets or any skeletal condition (other than OI) leading to long-bone deformities and/or increased risk of fractures
History of stroke, myocardial infarction, transient ischemic attack or angina.
Hypocalcemia, defined as serum calcium levels below the age-adjusted normal limits after a ≥ 4 hour fast
Estimated glomerular filtration rate ≤ 29 mL/min/1.73 m2
Prior treatment with the following:
Teriparatide, growth hormone, bone anabolic, or anti-resorptive medications (other than bisphosphonates) within 6 months of the first dose with study drug (Month 0)
Denosumab within 24 months of Screening
Romosozumab at any time
Documented alcohol and/or drug abuse within 12 months prior to dosing or evidence of such abuse as indicated by the laboratory results during the Screening assessments
Presence or history of any condition that, in the view of the Investigator, would interfere with participation, pose undue risk, or would confound interpretation of results
Known hypersensitivity to setrusumab or excipients that, in the judgment of the Investigator, places the subject at increased risk for adverse effects
History of external radiation therapy
Pregnant or breastfeeding or planning to become pregnant (self or partner) at any time during the study
Use of any investigational product or investigational medical device within 4 weeks or 5 half-lives of investigational drug (whichever is longer) prior to Screening, or during the study (per discretion of the Investigator in consultation with the Medical Monitor)
Concurrent participation in another clinical study without prior approval from the Investigator in consultation with the Medical Monitor
For Phase 2 Only: A history of bone surgery within the previous 6 months prior to Screening or planned bone surgery for the first 3 months of the study

Where it is running

Arkansas Children's Hospital — Little Rock, Arkansas, United States
Children's Hospital Los Angeles — Los Angeles, California, United States
Shriners Hospital for Children - Northern California — Sacramento, California, United States
Children's Hospital Colorado — Aurora, Colorado, United States
Connecticut Children's Medical Center — Hartford, Connecticut, United States
Yale New Haven Hospital — New Haven, Connecticut, United States
Nemours/ Alfred i. duPoint Hospital for Children — Wilmington, Delaware, United States
Children's National Medical Center — Washington D.C., District of Columbia, United States
University of South Florida — Tampa, Florida, United States
Shriners Hospitals for Children - Chicago — Chicago, Illinois, United States
Indiana University Hospital — Indianapolis, Indiana, United States
Kennedy Krieger Institute — Baltimore, Maryland, United States
Boston Children's Hospital — Boston, Massachusetts, United States
Washington University School of Medicine — St Louis, Missouri, United States
Children's Hospital and Medical Center — Omaha, Nebraska, United States
New Mexico Clinical Research & Osteoporosis Center, Inc. — Albuquerque, New Mexico, United States
Atrium Health Levine Children's Hospital — Charlotte, North Carolina, United States
Nationwide Children's Hospital- Ohio State University College of Medicine — Columbus, Ohio, United States
The Children's Hospital of Philadelphia — Philadelphia, Pennsylvania, United States
Vanderbilt University Medical Center — Nashville, Tennessee, United States
Cook Children's Medical Center — Fort Worth, Texas, United States
Baylor College of Medicine — Houston, Texas, United States
UW Health University Hospital — Madison, Wisconsin, United States
Queensland Paediatric Endocrinology — South Brisbane, Queensland, Australia
Royal Children's Hospital — Melbourne, Australia

Full record on ClinicalTrials.gov

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