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Looking for participantsPhase3

A Study of Orforglipron (LY3502970) on Cardiovascular Outcomes in Adults With Atherosclerotic Cardiovascular Disease and/or Chronic Kidney Disease (ATTAIN-Outcomes)

Sponsor: Eli Lilly and Company

NCT ID: NCT07241390

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Orforglipron (drug), Placebo (drug)
How long the study runs
Study runs about 68 months (dates as stated)
About the drug or intervention
Orforglipron — drug: Administered orally · Placebo — drug: Administered orally
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
50 Years and over
Who
All
Number of participants
7,140
Started
2025-12-01
Last checked
2026-10

Plain English Summary

What is this study?

  • • Testing a new treatment for atherosclerosis cardiovascular disease
  • • Phase3 - 7,140 participants
  • • The purpose of this study is to measure cardiovascular outcomes with orforglipron compared with placebo in participants with atherosclerotic cardiovascular disease (ASCVD) and/or chronic kidney disease (CKD)

Who can take part?

  • • Ages 50 Years and over
  • • Diagnosed with atherosclerosis cardiovascular disease

Where?

  • • Birmingham - FutureMeds - Birmingham
  • • Blackpool - Layton Medical Centre
  • • Bromborough - FutureMeds - Liverpool
  • • Newcastle - Futuremeds-Newcastle
  • • +4 more UK sites

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

The purpose of this study is to measure cardiovascular outcomes with orforglipron compared with placebo in participants with atherosclerotic cardiovascular disease (ASCVD) and/or chronic kidney disease (CKD). Participation in the study will last about 5 years.

Atherosclerosis Cardiovascular DiseaseChronic Kidney Disease

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 50 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓Have established ASCVD and/or CKD

Who cannot take part

  • ✗Have type 1 diabetes
  • ✗Have had a major heart condition within 60 days prior to screening
  • ✗Have New York Heart Association Functional Classification Class IV heart failure
See the full criteria
Inclusion Criteria: * Have established ASCVD and/or CKD Exclusion Criteria: * Have type 1 diabetes * Have had a major heart condition within 60 days prior to screening * Have New York Heart Association Functional Classification Class IV heart failure

Where Is This Study? (8 UK sites)

FutureMeds - Birmingham

Birmingham B21 9RY, United Kingdom

Recruiting
Site contact (verified)
Tehmina AhmedPrincipal Investigator

Layton Medical Centre

Blackpool FY3 7EN, United Kingdom

Recruiting
Site contact (verified)
Rebecca ClarkPrincipal Investigator

FutureMeds - Liverpool

Bromborough CH62 6EE, United Kingdom

Recruiting
Site contact (verified)
Connor McGladderyPrincipal Investigator

Futuremeds-Newcastle

Newcastle NE6 1SG, United Kingdom

Recruiting
Site contact (verified)
Anneliese FlattPrincipal Investigator

Newquay Health Centre

Newquay TR7 1RU, United Kingdom

Recruiting
Site contact (verified)
Rutesh PatelPrincipal Investigator

The Adam Practice

Poole BH16 5PW, United Kingdom

Recruiting
Site contact (verified)
Patrick MoorePrincipal Investigator

Clifton Medical Centre

Rotherham S65 1DA, United Kingdom

Recruiting
Site contact (verified)
Matthew CapehornPrincipal Investigator

Rame Group Practice

Torpoint PL11 2TB, United Kingdom

Recruiting
Site contact (verified)
Susan KeastPrincipal Investigator

How to Get in Touch

Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or

Sponsor contact

CONTACT

317-615-4559 LillyTrials@Lilly.com

Physicians interested in becoming principal investigators please contact

Sponsor contact

CONTACT

clinical_inquiry_hub@lilly.com
Data sourced from ClinicalTrials.gov · Last verified: 2026-10