LivingGLP1
Study S003266

A Multicenter, Randomized, Double-blind, Placebo-controlled Phase II Study to Evaluate the Efficacy and Safety of VCT220 in Participants With Hypertension and Obesity or Overweight.

Registration

Registration
NCT07360275
Acronym
VICTOR-HTN
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
DOUBLE
Status
ACTIVE_NOT_RECRUITING
Enrollment
160
Start
2026-03-01
Primary completion
2026-10-30
Lead sponsor
Vincentage Pharma Co., Ltd
Conditions
Hypertension
Interventions
DRUG:VCT220 Tablet; DRUG:VCT220 Placebo Tablet
Results posted
FALSE

Registered primary outcomes

  • Change from baseline in office seated systolic blood pressure (SBP) at Week 20 [From baseline to week 20]

Linked records (0)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.

No records link to this registration yet.