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
Sites (7)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Apex Mobile Clinical Research Coordinator of this site? Confirm its status | Bellaire | United States | Unknown status |
| Great Lakes Clinical Trials, LLC d/b/a Flourish Research Coordinator of this site? Confirm its status | Chicago | United States | Unknown status |
| ProSciento CRU Coordinator of this site? Confirm its status | Chula Vista | United States | Unknown status |
| Tandem Clinical Research GI, LLC Coordinator of this site? Confirm its status | Marrero | United States | Unknown status |
| Alliance for Multispecialty Research, LLC Coordinator of this site? Confirm its status | Norman | United States | Unknown status |
| AdventHealth Translational Research Institute Coordinator of this site? Confirm its status | Orlando | United States | Unknown status |
| Clinical Trials of Texas, LLC., dba Flourish Research Coordinator of this site? Confirm its status | San Antonio | United States | Unknown status |
Related publications
This page is information, not medical advice. Discuss any trial with your doctor.