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NCT00239174COMPLETEDanonymous

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Fixed-Dose, Multi-Center Study Evaluating the Efficacy and Safety of Four Doses of SR147778 in Obese Patients

Sponsor

Source record

Sanofi

Phase

Source record

Phase 2

Modality

AI-normalized

small molecule

Target

AI-normalized

Not specified in the provided data; further investigation required to determine the precise molecular or mechanistic target profile of SR147778.

Indication / condition

AI-normalized

Obesity

Intervention

Source record

SR147778

Source & freshness

Source record

NCT ID

NCT00239174

Original source

ClinicalTrials.gov

Source last updated

Dec 10, 2008

Ingested at

Jun 13, 2026

Internal sync

Jun 13, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

Open original registry record
View original source fields

NCT ID

NCT00239174

Title

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Fixed-Dose, Multi-Center Study Evaluating the Efficacy and Safety of Four Doses of SR147778 in Obese Patients

Sponsor

Sanofi

Status

COMPLETED

Phase

Phase 2

Condition raw

Obesity

Condition normalized

Obesity

Modality raw

small molecule

Modality normalized

small molecule

Target raw

Not specified in the provided data; further investigation required to determine the precise molecular or mechanistic target profile of SR147778.

Target normalized

Not specified in the provided data; further investigation required to determine the precise molecular or mechanistic target profile of SR147778.

Interventions

SR147778

Public preview

Source record

SR147778, developed by Sanofi, is currently in Phase 2 clinical trials aimed at evaluating its efficacy and safety in promoting weight loss in obese patients. Given the increasing prevalence of obesity and associated metabolic disorders, this asset addresses a significant market need. The obesity treatment market is highly competitive, with established players and emerging therapies vying for market share. Successful outcomes from this trial could position Sanofi favorably against competitors, particularly if SR147778 demonstrates superior efficacy or safety profiles. Diligence implications include assessing the competitive landscape, potential partnerships, and market entry strategies post-trial completion.

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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