RecruitingPhase 1NCT07444294
A Single- and Multiple-Ascending Dose Study of SRK-439 in Healthy Adults
A Phase 1 Single- and Multiple-Ascending Dose Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of SRK-439 in Healthy Adults
Sponsor
Scholar Rock, Inc.
Enrollment
76 participants
Start Date
Nov 21, 2025
Study Type
INTERVENTIONAL
Conditions
Summary
A phase 1 study to assess the safety, tolerability, pharmacokinetics, and pharmacodynamics of SRK-439 in healthy adults
Eligibility
Min Age: 18 YearsMax Age: 55 Years
Inclusion Criteria2
- Male or female participants, ≥18 to ≤55 years of age, at the time of informed consent
- BMI of ≥18 kg/m2 to ≤35 kg/m2 (inclusive) at screening
Exclusion Criteria6
- Previous treatment with SRK-439 or apitegromab, or with other anti-myostatin therapies, including ACTR antagonists.
- History of immunosuppressive, chemotherapeutic, or radiation treatment within 12 months prior to screening.
- Current or prior use of anabolic steroids, growth hormones, or other substances with known effects on muscle.
- Use of therapies with potentially significant muscle effects (eg, insulin-like growth factor, systemic beta-agonist, neurotoxins, or muscle relaxants or muscle-enhancing supplements) in any form within 3 months prior to screening or during the study.
- Any history of exposure to a mAb or Fc domain-bearing recombinant protein within 5 years prior to screening with any prior history of hypersensitivity reactions from exposure
- Treatment with other investigational drugs or devices in a clinical study or exposure to a biologic therapeutic within 3 months or 5 half-lives, whichever is longer, prior to screening.
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Interventions
DRUGPlacebo
Matching placebo to SRK-439, subcutaneous administration
DRUGSRK-439
Single ascending dose, subcutaneous administration
DRUGSRK-439
Multiple ascending dose, subcutaneous administration
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07444294
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