280 Participants Needed

VK2735 for Obesity

Recruiting at 14 trial locations
BS
SH
Overseen ByStephanie Herman
Age: 18+
Sex: Any
Trial Phase: Phase 2
Sponsor: Viking Therapeutics, Inc.
Prior Safety DataThis treatment has passed at least one previous human trial

Trial Summary

Will I have to stop taking my current medications?

The trial does not specify if you need to stop taking your current medications, but you cannot have used any GLP-1 receptor agonists or weight loss medications within 6 months before the screening.

What is the purpose of this trial?

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.

Eligibility Criteria

This trial is for adults who are obese with a BMI of 30 or higher, or overweight with a BMI of at least 27 and have one weight-related health issue. Key eligibility details aren't provided, so interested individuals should inquire further about specific inclusion and exclusion criteria.

Inclusion Criteria

My BMI is between 27 and 50, and I may have a condition like high blood pressure or sleep apnea.

Exclusion Criteria

I have been diagnosed with diabetes.
I have been diagnosed with chronic pancreatitis.
I haven't taken any GLP-1 drugs in the last 6 months.
See 4 more

Timeline

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive VK2735 or placebo daily for weight management over 13 weeks

13 weeks

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

Treatment Details

Interventions

  • VK2735
Trial Overview The study tests VK2735 against a placebo to see if it helps with weight loss. Participants will be randomly assigned to receive either the drug or placebo once daily for 13 weeks in this double-blind study where neither they nor the researchers know who gets what.
Participant Groups
7Treatment groups
Experimental Treatment
Placebo Group
Group I: Active Assignment (Dose #6)Experimental Treatment1 Intervention
VK2735 is a peptide GLP-1 and GIP dual agonist administered Daily
Group II: Active Assignment (Dose #5)Experimental Treatment1 Intervention
VK2735 is a peptide GLP-1 and GIP dual agonist administered Daily
Group III: Active Assignment (Dose #4)Experimental Treatment1 Intervention
VK2735 is a peptide GLP-1 and GIP dual agonist administered Daily
Group IV: Active Assignment (Dose #3)Experimental Treatment1 Intervention
VK2735 is a peptide GLP-1 and GIP dual agonist administered Daily
Group V: Active Assignment (Dose #2)Experimental Treatment1 Intervention
VK2735 is a peptide GLP-1 and GIP dual agonist administered Daily
Group VI: Active Assignment (Dose #1)Experimental Treatment1 Intervention
VK2735 is a peptide GLP-1 and GIP dual agonist administered Daily
Group VII: Placebo AssignmentPlacebo Group1 Intervention
VK2735 (Placebo) administered Daily

Find a Clinic Near You

Who Is Running the Clinical Trial?

Viking Therapeutics, Inc.

Lead Sponsor

Trials
7
Recruited
990+
Unbiased ResultsWe believe in providing patients with all the options.
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