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orforglipron

orforglipron: 25 clinical trials tracked.

orforglipron evidence translation

What we can confirm

25 tracked trials

No verified listed developer

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about orforglipron, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence8 indications · 1 study sponsors
Clinical Trials (25)showing 10 most recent

A Phase 3, Randomized, Double-Blind Study to Investigate the Efficacy and Safety of Once- Daily Oral Orforglipron Compared With Placebo in Chinese Adult Participants With Obesity or Overweight With Weight-Related Comorbidities

NCT07790861·Phase 3·LLY
Not yet recruiting

Primary endpoint: Mean Percent Change From Baseline in Body Weight

InterventionalRandomizeddouble192 targetStarted 2026-12Completion 2028-0313 sites · ChinaEli Lilly and Company

A Phase 3, Randomized, Open-Label Study to Investigate the Efficacy, Safety, and Pharmacokinetics of Once-Daily Oral Orforglipron Compared With Once-Weekly Dulaglutide in Pediatric Participants 10 to Less Than 18 Years of Age With Type 2 Diabetes

NCT07668336·Phase 3·LLY
Not yet recruiting

Primary endpoint: Change from Baseline in Hemoglobin A1c (HbA1c)

InterventionalRandomizedopen170 targetStarted 2026-09Completion 2030-0350 sites · Belgium, Brazil, India, Italy…Eli Lilly and Company

A Phase 3b, Multicenter, Multi-Country, Open-Label, Single-Arm Study to Investigate the Efficacy and Safety of Orforglipron in Adult Participants With Type 2 Diabetes Who Observe Ramadan Fasting (ACHIEVE-RAM)

NCT07613307·Phase 3·LLY
Recruiting

Primary endpoint: Change from Baseline in Hemoglobin A1C (HbA1c)

Interventionalopen130 targetStarted 2026-07Completion 2027-0540 sites · India, Saudi Arabia, South Africa, United Arab EmiratesEli Lilly and Company

A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Event-Driven Study to Investigate the Effect of Orforglipron on the Incidence of Major Adverse Cardiovascular Events in Participants With Established Atherosclerotic Cardiovascular Disease and/or Chronic Kidney Disease

NCT07241390·Phase 3·LLY
Recruiting

Primary endpoint: Time to First Occurrence of Composite Endpoint of Major Cardiovascular Events

InterventionalRandomizeddouble7,140 targetStarted 2025-12Completion 2031-0850 sites · ArgentinaEli Lilly and Company

A Study to Investigate the Efficacy and Safety of Orforglipron Once Daily in Participants With Peripheral Artery Disease: A Randomized, Double-Blind, Placebo Controlled Trial

NCT07223593·Phase 3·LLY
Recruiting

Primary endpoint: Percent Change from Baseline in Maximum Walking Distance

InterventionalRandomizeddouble1,205 targetStarted 2025-10Completion 2028-0650 sites · Argentina, Australia, United StatesEli Lilly and Company

A Master Protocol to Investigate the Efficacy and Safety of Orforglipron Tablet Once Daily Compared With Placebo in Female Participants With Stress Urinary Incontinence Who Have Obesity or Overweight

NCT07202884·Phase 3·LLY
Recruiting

Primary endpoint: Change from Baseline in Incontinence Episode Frequency (IEF)

InterventionalRandomizeddouble1,000 targetStarted 2025-09Completion 2028-0350 sites · Canada, China, United StatesEli Lilly and Company

A Phase 3 Study to Investigate the Efficacy and Safety of Orforglipron Once Daily in Participants Who Have Obesity or Overweight and Osteoarthritis of the Knee: A Multicenter, Randomized, Double-Blind, Parallel-Arm, Placebo-Controlled Trial

NCT07153471·Phase 3·LLY
Recruiting

Primary endpoint: Change from Baseline in the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Pain Subscale Score

InterventionalRandomizedsingle800 targetStarted 2025-09Completion 2028-0550 sites · Canada, China, United StatesEli Lilly and Company

A Master Protocol to Investigate the Efficacy and Safety of Orforglipron Tablet Once Daily Compared With Placebo in Participants With Obesity or Overweight With and Without Type 2 Diabetes

NCT06993792·Phase 3·LLY
Active, not recruiting

Primary endpoint: Number of Participants Allocated to Each Study

InterventionalRandomizeddouble1,400 targetStarted 2025-05Completion 2027-0850 sites · Argentina, China, United StatesEli Lilly and Company

A Master Protocol to Investigate the Efficacy and Safety of Orforglipron Tablet Once Daily Compared With Placebo in Participants With Obesity or Overweight With and Without Type 2 Diabetes

NCT06972459·Phase 3·LLY
Active, not recruiting

Primary endpoint: Percent Change from Baseline in Body Weight

InterventionalRandomizeddouble800 targetStarted 2025-05Completion 2027-0850 sites · Argentina, China, United StatesEli Lilly and Company

A Master Protocol to Investigate the Efficacy and Safety of Orforglipron Once Daily in Participants With Hypertension and Obesity or Overweight: Randomized, Double-Blind, Placebo-Controlled Trials (ATTAIN-HYPERTENSION)

NCT06948435·Phase 3·LLY
Active, not recruiting

Primary endpoint: Change from Baseline in office Systolic Blood Pressure (SBP)

InterventionalRandomizeddouble487 targetStarted 2025-04Completion 2027-0950 sites · Argentina, China, Czechia, United StatesEli Lilly and Company