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)

Medpace CPU

Cincinnati, Ohio, United States

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NCT07444294


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