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A Randomized, Double-Blind, Placebo Controlled, Multicenter, 12-week Phase 3 Study to Evaluate Efficacy and Safety of ALS-L1023 Tablet in Patients With Abdominal Obesity of Metabolic Syndrome
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 17, 2026
NCT ID
NCT01872182
Status
TERMINATED
Phase
PHASE3
Sponsor
Hanmi Pharmaceutical Company Limited
Executive brief
Investment-Ready Snapshot
The main objective of this study is to evaluate efficacy and safety of ALS-L1023 tablet in patients with abdominal obesity of metabolic syndrome.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT01872182
Indication
Abdominal Obesity Metabolic Syndrome
Modality
small molecule
Target
ALS-L1023, placebo
Intervention
ALS-L1023, placebo
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.