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J5P-MC-GZRA: A Master Protocol to Investigate the Efficacy and Safety of Orforglipron Once Daily in Participants Who Have Obstructive Sleep Apnea and Obesity or Overweight: A Randomized, Double-Blind, Placebo-Controlled Trial (ATTAIN-OSA); J5P-MC-GZ01: Participants with OSA unable or unwilling to use PAP therapy; J5P-MC-GZ02: Participants with OSA on PAP therapy

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-515905-25-00
Acronym
J5P-MC-GZRA
Enrollment
118
Registered
2025-01-14
Start date
2025-01-29
Completion date
Unknown
Last updated
2025-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Overweight or Obesity, OSA (Obstructive Sleep Apnea)

Brief summary

Change from Baseline in Apnea-Hypopnea Index (AHI) [Time Frame: Baseline to Week 52]

Interventions

Sponsors

Eli Lilly & Co.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Change from Baseline in Apnea-Hypopnea Index (AHI) [Time Frame: Baseline to Week 52]

Countries

Czechia, Germany

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026