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Clinical trial intelligence report
A Randomized, Placebo-Controlled, Double-Blind, Parallel-Group Study Evaluating the Efficacy, Safety, and Pharmacokinetics of Daily Administrations of the GLP-1 Analogue ROSE-010 on Appetite and Food Intake in Overweight and Obese Subjects
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Aug 04, 2026
Report code
NCT06621017-Aug 04, 2026
NCT ID
NCT06621017
Status
COMPLETED
Phase
Phase 2
Sponsor
Rose Pharma Inc
Executive brief
Investment-Ready Snapshot
ROSE-010, a GLP-1 analogue, targets appetite regulation in overweight and obese female subjects. The obesity treatment market is expanding, driven by increasing prevalence and demand for effective weight management solutions. Competitive landscape includes established GLP-1 receptor agonists like liraglutide and semaglutide, as well as emerging therapies. Successful trial outcomes could position Rose Pharma Inc favorably within this lucrative market, but potential regulatory hurdles and market access strategies will require careful consideration.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT06621017
Indication
Obesity; Overweight
Modality
small molecule
Target
GLP-1 receptor
Intervention
ROSE-010 99 mcg, Placebo, ROSE-010 150 mcg
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.