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NCT06445075CompletedPhase 2

Efficacy and Safety of Apitegromab for the Treatment of Adults Who Are Overweight or Obese

A Phase 2 Randomized, Double-blind, Placebo-controlled, Multicenter Study to Evaluate the Efficacy, Safety and Pharmacokinetics of Apitegromab in Overweight and Obese Adult Subjects

Source: ClinicalTrials.gov · Last updated 23 Jan 2026

Brief summary (registry, in English)

A phase 2 study to evaluate the effects of apitegromab as an adjunctive therapy to GLP-1 receptor agonist therapy in subjects with overweight or obesity

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
102 (actual)
First submitted
22 May 2024
Start date
21 May 2024
Primary completion date
4 Mar 2025
Lead sponsor
Scholar Rock, Inc.
Diseases
Obesity
NCT number
NCT06445075

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 102
  • From 21 May 2024 to the primary completion date, 4 Mar 2025
  • 7 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • History of immunosuppressive, chemotherapeutic, or radiation treatment within 12 months prior to Screening
  • History of Type 1 diabetes or active Type 2 diabetes (T2D). If there was a history of T2D and it resolved, then the resolution must have occurred \>12 months prior to Screening. Prediabetes managed with nonpharmacologic approaches (exercise and diet) is not an exclusion

Other illness

  • History of or active cardiovascular, neurovascular, peripheral vascular, pulmonary, hepatic, pancreatic, neuromuscular, and/or psychiatric disease
  • Active malignancy, other than local subcutaneous squamous cell and basal cell carcinomas

Who the study is looking for

  • Able to comprehend the informed consent process and provide written informed consent prior to study enrollment and the conduct of any study-related assessments to study enrollment and the conduct of any study-related assessments
  • Male or female, age ≥ 18 and ≤ 65 years at the time of informed consent
  • Stable body weight (±5 kg) within 90 days of Screening
  • At Screening, a BMI of:
    • ≥30.0 kg/m2 to ≤45.0 kg/m2 or
    • ≥27.0 kg/m2 to \<30.0 kg/m2 with the presence of 1 or more weight-related comorbid condition(s). Note: See exclusion criteria for specific organ class disease parameters

Age in the registry: 18 years to 65 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (7)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Apex Mobile Clinical Research
Coordinator of this site? Confirm its status
BellaireUnited StatesUnknown status
Great Lakes Clinical Trials, LLC d/b/a Flourish Research
Coordinator of this site? Confirm its status
ChicagoUnited StatesUnknown status
ProSciento CRU
Coordinator of this site? Confirm its status
Chula VistaUnited StatesUnknown status
Tandem Clinical Research GI, LLC
Coordinator of this site? Confirm its status
MarreroUnited StatesUnknown status
Alliance for Multispecialty Research, LLC
Coordinator of this site? Confirm its status
NormanUnited StatesUnknown status
AdventHealth Translational Research Institute
Coordinator of this site? Confirm its status
OrlandoUnited StatesUnknown status
Clinical Trials of Texas, LLC., dba Flourish Research
Coordinator of this site? Confirm its status
San AntonioUnited StatesUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.