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Clinical trial intelligence report
A Double Blind, Randomized, Placebo Controlled Study to Determine the Physiological Effectiveness of Januvia for Reducing Inflammation and Increasing EPC Number in HIV Infected Men and Women With Insulin Resistance and Central Adiposity.
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 25, 2026
Report code
NCT01552694-Jun 25, 2026
NCT ID
NCT01552694
Status
COMPLETED
Phase
Phase 3
Sponsor
Washington University School of Medicine
Executive brief
Investment-Ready Snapshot
The clinical trial investigates the efficacy of Januvia (sitagliptin) in reducing inflammation and improving endothelial function in HIV-infected individuals with insulin resistance and cardiovascular disease risk factors. Given the high prevalence of diabetes and cardiovascular complications in this population, successful outcomes could position sitagliptin as a novel therapeutic option, expanding its market beyond diabetes management to include HIV-related cardiometabolic complications. This could enhance Merck's portfolio and provide a competitive edge in the growing market for treatments addressing comorbidities in HIV patients. Diligence should focus on the regulatory landscape and potential reimbursement pathways for this indication.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT01552694
Indication
Inflammation
Modality
small molecule
Target
Dipeptidyl peptidase-IV (DPP4)
Intervention
Sitagliptin, 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.