Petrelintide
DrugPetrelintide will be taken by participants once weekly subcutaneously.
Other names: ZP8396
NCT Number: NCT06926842
The main purpose of this study is to investigate efficacy and safety of three doses of petrelintide versus placebo in participants with overweight or obesity and type 2 diabetes.
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Notify Me18 year and older
All sexes
Interventional
Phase 2
Cullman Clinical Trials - Family Medicine, Cullman, Alabama, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Main Inclusion Criteria:
Main Exclusion Criteria:
Petrelintide will be taken by participants once weekly subcutaneously.
Other names: ZP8396
Matching placebo to petrelintide will be taken by participants once weekly subcutaneously.
Time frame: From Baseline (Day 1) to Weeks 28
Time frame: From Baseline (Day 1) to Weeks 28
Time frame: From Baseline (Day 1) to Weeks 28
Time frame: From Baseline (Day 1) to Weeks 28
Time frame: From Baseline (Day 1) to Weeks 28
Time frame: From Baseline (Day 1) to Weeks 28
Time frame: From Baseline (Day 1) to Weeks 28
Time frame: From Baseline (Day 1) to Weeks 28
Time frame: From Baseline (Day 1) to Weeks 28
Time frame: From Baseline (Day 1) to Weeks 28
Time frame: From Baseline (Day 1) to Weeks 38
Time frame: From Baseline (Day 1) to Weeks 38
Time frame: From Baseline (Day 1) to Weeks 38
Time frame: From Baseline (Day 1) to Week 38
Time frame: From Baseline (Day 1) to Week 38
Time frame: From Baseline (Day 1) to Week 38
Zealand Pharma
Industry
A Randomized, Double-Blind, Phase 2 Trial of Once-Weekly Petrelintide Compared With Placebo in Participants With Overweight or Obesity and Type 2 Diabetes
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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