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NCT06015893RECRUITINGanonymous

Semaglutide Therapy for Alcohol Reduction (STAR): A Proof-of-Concept Phase II Clinical Trial

Sponsor

Source record

National Institute on Drug Abuse (NIDA)

Phase

Source record

Phase 2

Modality

AI-normalized

behavioral intervention

Target

AI-normalized

Glucagon-like peptide-1 (GLP-1) receptor

Indication / condition

AI-normalized

Addiction

Intervention

Source record

Take Control, Semaglutide

Source & freshness

Source record

NCT ID

NCT06015893

Original source

ClinicalTrials.gov

Source last updated

May 27, 2026

Ingested at

Jun 16, 2026

Internal sync

Jun 16, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

Open original registry record
View original source fields

NCT ID

NCT06015893

Title

Semaglutide Therapy for Alcohol Reduction (STAR): A Proof-of-Concept Phase II Clinical Trial

Sponsor

National Institute on Drug Abuse (NIDA)

Status

RECRUITING

Phase

Phase 2

Condition raw

Addiction, Alcohol Use Disorder

Condition normalized

Addiction, Alcohol Use Disorder

Modality raw

behavioral intervention

Modality normalized

behavioral intervention

Target raw

Glucagon-like peptide-1 (GLP-1) receptor

Target normalized

Glucagon-like peptide-1 (GLP-1) receptor

Interventions

Take Control, Semaglutide

Public preview

Source record

The STAR trial is investigating Semaglutide, a GLP-1 analogue, as a potential treatment for Alcohol Use Disorder (AUD). Given the limited current pharmacotherapy options for AUD, a successful outcome could position Semaglutide as a novel therapeutic alternative in a market with significant unmet needs. The trial's design includes a robust behavioral therapy component, enhancing its appeal. If proven effective, this could lead to expanded indications for Semaglutide beyond its current use in diabetes and obesity, potentially increasing market share and revenue streams for the sponsor, the National Institute on Drug Abuse (NIDA). The competitive landscape includes existing AUD treatments such as naltrexone and acamprosate, but Semaglutide's unique mechanism may provide a differentiated offering. Diligence should focus on the trial's safety and tolerability outcomes, as adverse events could impact market acceptance.

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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