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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
Aug 04, 2026
Report code
NCT01872182-Aug 04, 2026
NCT ID
NCT01872182
Status
TERMINATED
Phase
Phase 3
Sponsor
Hanmi Pharmaceutical Company Limited
Executive brief
Investment-Ready Snapshot
The Phase 3 trial of ALS-L1023, sponsored by Hanmi Pharmaceutical Company Limited, aimed to evaluate the efficacy and safety of the drug in patients with abdominal obesity associated with metabolic syndrome. Given the increasing prevalence of metabolic syndrome globally, particularly in developed countries, there is a significant market opportunity for effective treatments. However, the trial's termination raises concerns regarding the drug's viability and may impact Hanmi's competitive positioning in the obesity and metabolic disorder market. Stakeholders should conduct further diligence to assess the reasons for termination and explore alternative strategies or assets within Hanmi's pipeline.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT01872182
Indication
Abdominal Obesity Metabolic Syndrome
Modality
small molecule
Target
Not specified in the provided data; further investigation required to determine the precise molecular or mechanistic target profile of ALS-L1023.
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.