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NCT07622810NOT_YET_RECRUITINGanonymous

BALANCE-OBS: A Multiregional, Randomized, Multicenter, Active-Controlled Confirmatory Phase III Study to Evaluate the Efficacy and Safety of Bofanglutide (GZR18) Versus Semaglutide in Latin American Adults With Overweight or Obesity

Sponsor

Source record

Carnot Laboratories

Phase

Source record

Phase 3

Modality

AI-normalized

small molecule

Target

AI-normalized

GLP-1 receptor agonist

Indication / condition

AI-normalized

Obesity & Overweight

Intervention

Source record

Bofanglutida, Semaglutide

Source & freshness

Source record

NCT ID

NCT07622810

Original source

ClinicalTrials.gov

Source last updated

Jun 03, 2026

Ingested at

Jun 16, 2026

Internal sync

Jun 16, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT07622810

Title

BALANCE-OBS: A Multiregional, Randomized, Multicenter, Active-Controlled Confirmatory Phase III Study to Evaluate the Efficacy and Safety of Bofanglutide (GZR18) Versus Semaglutide in Latin American Adults With Overweight or Obesity

Sponsor

Carnot Laboratories

Status

NOT_YET_RECRUITING

Phase

Phase 3

Condition raw

Obesity & Overweight

Condition normalized

Obesity & Overweight

Modality raw

small molecule

Modality normalized

small molecule

Target raw

GLP-1 receptor agonist

Target normalized

GLP-1 receptor agonist

Interventions

Bofanglutida, Semaglutide

Public preview

Source record

Carnot Laboratories is advancing Bofanglutide (GZR18) through a Phase 3 clinical trial (BALANCE-OBS) aimed at evaluating its efficacy and safety compared to Semaglutide in Latin American adults with overweight or obesity. The trial's focus on metabolic parameters, cardiovascular risk factors, and quality of life positions Bofanglutide as a potential competitor in the growing obesity treatment market. Given the increasing prevalence of obesity and related comorbidities, successful outcomes could lead to significant market penetration. However, the competitive landscape includes established products like Semaglutide, which has demonstrated efficacy and safety. Diligence is warranted regarding regulatory pathways and potential market access challenges in the Latin American region.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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