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A Multi-center, phase3, Open-label Study to Evaluate the Long Term Safety and Efficacy of DWP16001 in Patients With Type 2 Diabetes Mellitus Inadequately Controlled on Metformin and Gemigliptin
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT06141980-Jul 28, 2026
NCT ID
NCT06141980
Status
UNKNOWN
Phase
Phase 3
Sponsor
Daewoong Pharmaceutical Co. LTD.
Executive brief
Investment-Ready Snapshot
Daewoong Pharmaceutical Co. LTD. is advancing DWP16001 through a Phase 3 clinical trial aimed at demonstrating its long-term safety and efficacy in T2DM patients. The market for diabetes therapeutics is substantial, with increasing prevalence driving demand for effective treatments. DWP16001's positioning as an adjunct therapy for patients inadequately controlled on existing medications may provide a competitive edge, particularly in markets with high unmet needs. The trial's outcomes could significantly influence Daewoong's market share and revenue potential in the diabetes sector, contingent upon successful results and subsequent regulatory approvals.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT06141980
Indication
T2DM (Type 2 Diabetes Mellitus)
Modality
small molecule
Target
DWP16001 is a novel therapeutic agent targeting glucose control mechanisms in Type 2 Diabetes Mellitus (T2DM) patients inadequately controlled on metformin and gemigliptin.
Intervention
DWP16001 0.3 mg
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.