A Phase 2b, Multi-Center, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Once-Weekly MET097 in Adults With Obesity or Overweight, and Type 2 Diabetes Mellitus (VESPER-2)

Status: Recruiting
Location: See all (5) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This study is designed to test how well once-weekly MET097 (an ultra-long-acting GLP-1 receptor agonist) works to treat adults with obesity or overweight and type 2 diabetes mellitus (T2DM) compared to placebo. MET097 or placebo will be administered to individuals via subcutaneous injection once weekly for 28 weeks. If an individual is randomly assigned to MET097 they will receive one of four different dose regimens.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• BMI ≥27.0 kg/m2 to ≤50.0 kg/m2 at screening

• Type 2 diabetes mellitus (\*T2DM) for at least 3 months before screening

• Glycated hemoglobin (HbA1c) value between ≥7.0% (53.0 mmol/mol) and ≤10.5% (91.3 mmol/mol) at Screening and treated with stable therapy for at least 30 days prior to Screening/Visit 1 (diet and exercise alone or in combination with metformin monotherapy and/or SGLT-2)

• Stable body weight (increase or decrease ≤5 kg) within 3 months prior to screening

Locations
United States
Florida
Research Site 097202-001001
RECRUITING
Hollywood
Research Site 097202-001003
RECRUITING
Tampa
Georgia
Research Site 097202-001002
RECRUITING
Decatur
Research Site 097202-001005
RECRUITING
Savannah
Ohio
Research Site 097202-001010
RECRUITING
Cincinnati
Contact Information
Primary
Metsera Recruiting
clinicaltrials@metsera.com
888-746-7403
Time Frame
Start Date: 2025-03-14
Estimated Completion Date: 2026-06
Participants
Target number of participants: 125
Treatments
Experimental: MET097 Active with titration
Placebo_comparator: Placebo
Experimental: MET097 Active without titration
Related Therapeutic Areas
Sponsors
Leads: Metsera

This content was sourced from clinicaltrials.gov

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