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A Master Protocol for Orforglipron in Participants With Obstructive Sleep Apnea and Obesity or Overweight

← catalyst calendar

NCT06649045 · readout ≤ 103 d

Sponsored by Eli Lilly and Company (industry) · LLY — their whole pipeline →.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
600estimated
Sites
66
Countries
Argentina, Brazil, China +6

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2024-10-22actualWhen the study began enrolling
Primary completionNov 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionJan 2027estimatedThe whole study's end, after follow-up
First posted2024-10-18actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-09-29actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • OSA
  • Overweight or Obesity

Interventions

  • Drug: Orforglipron — also filed as LY3502970
  • Drug: Placebo

Primary outcome

what the primary-completion date above is the date OF
Change from Baseline in Apnea-Hypopnea Index (AHI)
measured Baseline to Week 52

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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