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Completed Phase 2 Interventional

VK2735 for Weight Management Phase 2 (Venture Oral Dosing)

ClinicalTrials.gov ID: NCT06828055

Public ClinicalTrials.gov record NCT06828055. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 5:22 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2 Randomized, Double-Blind, Placebo-Controlled, 13-week Dose Finding Study of VK2735 Oral Formulation for Weight Management in Subjects Who Are Obese, or Overweight With at Least One Weight-related Comorbid Condition

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a phase 2, 13-week randomized, double-blind, placebo-controlled, parallel arm dose-finding study that will evaluate the safety, tolerability, weight loss efficacy, pharmacodynamic effects, and pharmacokinetics of VK2735 Oral Formulation in adults who are obese (BMI ≥30 kg/m2) or who are overweight (BMI ≥27 kg/m2) with at least one weight-related co-morbid condition. VK2735 or matched placebo will be administered once daily.

Study identification

NCT ID
NCT06828055
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Viking Therapeutics, Inc.
Industry
Enrollment
280 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 17, 2024
Primary completion
Jun 23, 2025
Completion
Aug 14, 2025
Last update posted
Oct 5, 2025

2024 – 2025

United States locations

U.S. sites
15
U.S. states
10
U.S. cities
15
Facility City State ZIP Site status
Viking Clinical Site #111 Peoria Arizona 85381
Viking Clinical Site #105 Lake Forest California 96230
Viking Clinical Site #101 Clearwater Florida 33756
Viking Clinical Site #108 Largo Florida 33777
Viking Clinical Site #107 Ocoee Florida 34761
Viking Clinical Site #102 Port Orange Florida 32127
Viking Clinical Site #100 Indianapolis Indiana 46260
Viking Clinical Site #110 Louisville Kentucky 40213
Viking Clinical Site #114 Marrero Louisiana 70072
Viking Clinical Site #109 City of Saint Peters Missouri 63303
Viking Clinical Site #112 Kansas City Missouri 64131
Viking Clinical Site #113 Butte Montana 59701
Viking Clinical Site #103 Knoxville Tennessee 37909
Viking Clinical Site #104 Austin Texas 78705
Viking Clinical Site #106 San Antonio Texas 78229

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06828055, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 5, 2025 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06828055 live on ClinicalTrials.gov.

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