BAY63-2521:Long-term Extension Study in Patients With Pulmonary Arterial Hypertension

Completed · Phase 3

Conditions studied: Hypertension, Pulmonary

In brief

Patients who have completed the 12 weeks treatment of the PATENT-1 trial (study number 12934) will be asked to participate in this long term extension study with BAY63-2521.

Key facts

Study ID

NCT00863681

Run by

Bayer

People needed

396

Starts

2009-03-12

Expected to finish

2019-08-19

Last updated by the study team

2023-11-07

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients who have completed 12 weeks of treatment in the double blind trial PATENT 1

You may not qualify if…

• Patients who have an ongoing serious adverse event from PATENT 1 that is assessed as related to BAY63-2521 are not allowed to participate in the extension trial.

Where it is running

• Study site — Sacramento, California, United States
• Study site — Aurora, Colorado, United States
• Study site — Boston, Massachusetts, United States
• Study site — Boston, Massachusetts, United States
• Study site — Omaha, Nebraska, United States
• Study site — Cleveland, Ohio, United States
• Study site — Columbus, Ohio, United States
• Study site — Fairfield, Ohio, United States
• Study site — Dallas, Texas, United States
• Study site — El Paso, Texas, United States
• Study site — Capital Federal, Argentina
• Study site — Darlinghurst, New South Wales, Australia
• Study site — Auchenflower, Queensland, Australia
• Study site — Herston, Queensland, Australia
• Study site — Hobart, Tasmania, Australia
• Study site — Prahran, Victoria, Australia
• Study site — Linz, Upper Austria, Austria
• Study site — Innsbruck, Austria
• Study site — Vienna, Austria
• Study site — Bruxelles - Brussel, Belgium
• Study site — Leuven, Belgium
• Study site — Porto Alegre, Rio Grande do Sul, Brazil
• Study site — São Paulo, São Paulo, Brazil
• Study site — São Paulo, São Paulo, Brazil
• Study site — Los Angeles, California, United States

Full record on ClinicalTrials.gov

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