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Taking people in CzechiaPhase 3

Orforglipron and Heart Events in People With Heart Artery Disease or Chronic Kidney Disease

Tests orforglipron against placebo for heart problems in adults with artery or kidney disease.

Plain-language title generated from the registry record
Registry title: A Study of Orforglipron (LY3502970) on Cardiovascular Outcomes in Adults With Atherosclerotic Cardiovascular Disease and/or Chronic Kidney Disease (ATTAIN-Outcomes)

Key facts

Where
Brandýs nad Labem, České Budějovice, Chlumec Nad Cidlinou Iv, Havířov, Jilove U Prahy, Krnov, Ostrava, Poštovní, Prague, Praha 1, and Praha 6, CzechiaSee the 14 sites
Phase
Phase 3

Where in Czechia

  • Diacentrum Brandys n.L. s.r.o.Brandýs nad Labem, CzechiaTaking people
  • KardioInt s.r.o. Lékařský dům GéčkoČeské Budějovice, CzechiaTaking people
  • MUDr. Alena Váchová Diabetologie a obezitologieČeské Budějovice, CzechiaTaking people
  • Kardio Chlumec s.r.o.Chlumec Nad Cidlinou Iv, CzechiaTaking people
  • DIKa centrum s.r.o.Havířov, CzechiaTaking people
  • Diavital Jesenice s.r.o.Jilove U Prahy, CzechiaTaking people
  • MUDr. Tomas Edelsberger DiabetologieKrnov, CzechiaTaking people
  • MUDr. Miroslav Koliba s.r.o.Ostrava, CzechiaTaking people
  • Kardiologie KarMa s.r.o.Poštovní, CzechiaTaking people
  • Centrum kardiovaskularni mediciny s.r.o.Prague, CzechiaTaking people
  • MILAN KVAPIL s.r.o.Prague, CzechiaTaking people
  • Praglandia s.r.o.Prague, CzechiaTaking people
  • MUDr. Jana Parkanyiová Endokrinologie a diabetologiePraha 1, CzechiaTaking people
  • Diabetologie a endokrinologie, J.Venerová s.r.o.Praha 6, CzechiaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Eli Lilly and Company
Trial code
NCT07241390EU 2025-523123-22-00
Record updated
4 November 2026
Original description
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.Read full original descriptionShow less

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

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.

Inclusion: Have established ASCVD and/or CKD.

Exclusion: Have had a major heart condition within 60 days prior to screening; Have type 1 diabetes; Have New York Heart Association Functional Classification Class IV heart failure.

ClinicalTrials.gov NCT07241390 · EU CTIS 2025-523123-22-00