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Taking people in United StatesPhase 2

ALV-100 for keeping weight off in adults with overweight or obesity

Tests ALV-100 in adults with overweight or obesity after earlier weight loss.

Plain-language title generated from the registry record
Registry title: Study to Assess the Effect and Safety of ALV-100 on Maintenance of Weight Loss

Key facts

Where
Birmingham, Bradenton, Champaign, Doral, Farmington Hills, Gretna, Irving, Nashville, New York, Oceanside, Oklahoma City, Orlando, San Antonio, South Jordan, Sun City, Tempe, Tomball, Wilmington, and Woodstock, United StatesSee the 20 sites
Phase
Phase 2

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 75 years old?

Source: NCT07837973, who can take part

Where in United States

  • University of Alabama BirminghamBirmingham, United StatesTaking people
  • DM Clinical ResearchBradenton, United StatesTaking people
  • Christie ClinicChampaign, United StatesTaking people
  • DM Clinical ResearchDoral, United StatesTaking people
  • Profound ResearchFarmington Hills, United StatesTaking people
  • BRCR Global LouisianaGretna, United StatesTaking people
  • DM Clinical ResearchIrving, United StatesTaking people
  • AMR ClinicalNashville, United StatesTaking people
  • ALSA Research-ManhattanNew York, United StatesTaking people
  • Profound ResearchOceanside, United StatesTaking people
  • Lynn Health Science InstituteOklahoma City, United StatesTaking people
  • Clinical Neuroscience SolutionsOrlando, United StatesTaking people
  • DM Clinical Research - Dominion Family HealthcareSan Antonio, United StatesTaking people
  • Tekton ResearchSan Antonio, United StatesTaking people
  • AMR ClinicalSouth Jordan, United StatesTaking people
  • DM Clinical ResearchSun City, United StatesTaking people
  • AMR ClinicalTempe, United StatesTaking people
  • DM Clinical ResearchTomball, United StatesTaking people
  • TMA HeadlandsWilmington, United StatesTaking people
  • North Georgia Clinical ResearchWoodstock, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Alveus Therapeutics, Inc.
Trial code
NCT07837973
Record updated
26 October 2026
Original description
A study of ALV-100 to assess efficacy, safety and tolerability among participants with overweight or obesity who have previously achieved a body weight reduction of ≥10% while treated with incretin-based therapies.Read full original descriptionShow less

A Double-Blind, Randomized, Multi-Center, Dose-Ranging, Phase 2 Study of the Efficacy and Safety of ALV-100 Versus Placebo for Maintenance of Weight Loss in Patients Previously Treated With Incretin-Based Therapies

A study of ALV-100 to assess efficacy, safety and tolerability among participants with overweight or obesity who have previously achieved a body weight reduction of ≥10% while treated with incretin-based therapies.

Inclusion: Adult male and female participants, aged ≥18 to ≤75; BMI ≥23 kg/m2 at screening; Has been treated with incretin-based therapy for weight management at a stable dose for at least 3 continuous months prior to screening; Tolerating incretin-based therapy at the discretion of the investigator; WL of at least 10% while on incretin-based therapy and with stable BW for at least 3 months prior to screening; Willing to maintain their current general diet and physical activity regimen throughout the study.

Exclusion: Prior obesity treatment with surgery or a weight loss device; Current or history of (within 3 months prior to screening) treatment with medications that may cause significant weight gain; Lifetime history of Type 1 or Type 2 diabetes; Obesity caused by known endocrinologic disorders or by known congenital or acquired hypothalamic disease or monogenetic or syndromic forms of obesity; Family or personal history of MTC or MEN 2; Presence or history of malignant neoplasms within the past 5 years prior to screening.

ClinicalTrials.gov NCT07837973