RecruitingPhase 1Phase 2NCT06842186

A Phase 1/2a Study of WVE-007 in Adults Living With Overweight or Obesity

A Phase 1/2a, Randomized, Double-blind, Placebo-controlled Study of Ascending Doses of WVE-007 to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics in Adults Living With Overweight or Obesity


Sponsor

Wave Life Sciences USA, Inc.

Enrollment

296 participants

Start Date

Jan 31, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of ascending doses of WVE-007 when administered subcutaneously (SC) . Part A is a single ascending dose study in adults living with overweight and obesity. The Part B of the study is a repeat dose administration in two adult populations: Pre Type 2 diabetes (Pre T2D) and Type 2 Diabetes (T2D) in adults who are affected by obesity.


Eligibility

Min Age: 18 YearsMax Age: 60 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called WVE-007 for people with overweight and obesity. The study is currently recruiting participants at 6 locations. People eligible for this study include aged 18 Years to 60 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGWVE-007

Stereopure siRNA oligonucleotide


Locations(6)

Parexel International-EPCU Baltimore

Baltimore, Maryland, United States

ARENSIA Research Clinic

Chisinau, Moldova

Arensia Clinics S.R.L.

Bucharest, Romania

Spitalul Clinic Judetean De Urgenta Cluj

Cluj-Napoca, Romania

Parexel International Early Phase Clinical Unit

Harrow, United Kingdom

Simbec-Orion Clinical Pharmacology

Merthyr Tydfil, United Kingdom

View Full Details on ClinicalTrials.gov

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NCT06842186


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