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
Wave Life Sciences USA, Inc.
296 participants
Jan 31, 2025
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
Plain Language Summary
Simplified for easier understanding
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Interventions
Stereopure siRNA oligonucleotide
Locations(6)
View Full Details on ClinicalTrials.gov
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NCT06842186