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Bayer To Present Data On Investigational Pulmonary Hypertension Compound At CHEST 2012

WAYNE, N.J., Oct. 17, 2012 /PRNewswire/ -- Bayer HealthCare announced today that data on its investigational pulmonary hypertension compound riociguat (BAY 63-2521) will be presented in a scientific forum at the American College of Chest Physicians (ACCP) annual meeting October 20 – 25, in Atlanta, GA.  Data from two pivotal, Phase III trials researching riociguat in patients with for pulmonary arterial hypertension (PAH) and chronic thromboembolic pulmonary hypertension (CTEPH) will be presented as late-breaking abstracts in oral presentation sessions.

"At Bayer, we are dedicated to researching new treatment options for people living with devastating diseases, like pulmonary hypertension," said Pamela A. Cyrus, M.D., Vice President and Head of U.S. Medical Affairs, Bayer HealthCare Pharmaceuticals.  "We are pleased to present top-line results of riociguat and its potential as a treatment option for PAH and CTEPH."

The studies to be presented are:

  • Riociguat for the treatment of inoperable chronic thromboembolic pulmonary hypertension: a randomized, double-blind, placebo-controlled study (CHEST-1)
    • Abstract 1462924; Late Breaking Abstract Session
    • October 23, 2012, 4:30 p.m.5:45 p.m., Convention Center, Room C206
  • Riociguat for the treatment of pulmonary arterial hypertension: a randomized, double-blind, placebo-controlled study (PATENT-1)
    • Abstract 1462799 Late Breaking Abstract Session
    • October 23, 2012, 4:30 p.m.5:45 p.m., Convention Center, Room C206

About Riociguat Riociguat (BAY 63-2521), discovered and developed at the Bayer research laboratories, is an investigational oral soluble guanylate cyclase (sGC) stimulator.  It is currently being developed for its potential to treat patients with various types of PH.

Riociguat is an investigational agent and is not approved by the FDA, EMA or other health authorities.

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