Blog Archive
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2008
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October
(25)
- Vision-Sciences : Advanced, Video-Based Bronchosco...
- Varian Medical Systems : Clinicians in Netherlands...
- Quark : Publication of Study on Use of siRNA again...
- Aerovance : Aerovant Inhalation Powder is Well To...
- Aires Pharmaceuticals : Key Technology License Agr...
- Novartis and Nektar Therapeutics Pulmonary Business
- Ranbaxy & GSK : IND APPLICATION TO DCGI FOR RESPIR...
- Bayer Schering Pharma : Progress in Clinical Progr...
- APT Pharmaceuticals : Phase III Trial of Inhaled...
- NeoGenomics Laboratories Extends Its Cancer Testin...
- BioView : Interim Results of Early Detection Lung ...
- Novartis : Early data show potential for imatinib ...
- Alfacell's ONCONASE(R) Targets siRNA : Paper in Ce...
- Neotropix : Expansion of On-going Clinical Trial f...
- Health Hero Network : Recertification from Nationa...
- Teva Pharmaceutical : Proair® HFA, the Market Lead...
- Gemin X : Key U.S. Patent Issued for Obatoclax
- Kuros Biosurgery and Aeris Therapeutics : Exclusiv...
- REGENERX : RGN-457 for Cystic Fibrosis
- Gilead Complete Response Letter from U.S. Food and...
- MD Biosciences : Preclinical Disease Models at the...
- Medical Acoustics : Results on Efficacy of Medical...
- Arriva Pharmaceuticals : Protein Production Patent
- Dynavax Technologies : Milestone from AstraZeneca
- Advanced Life Sciences : NDA Submission for Cethr...
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October
(25)
Oct 16, 2008
Bayer Schering Pharma : Progress in Clinical Program for Riociguat
October 6, 2008 – Based on positive Phase II trial findings, Bayer Schering Pharma will move into Phase III trials with its oral agent riociguat (BAY 63-2521). Riociguat is the first member of a new class of vasodilating agents called soluble guanylate cyclase (sGC) stimulators. It is being investigated as a new approach for the treatment of different forms of pulmonary hypertension. Riociguat demonstrated significantly improved exercise capacity in a Phase II study in patients with chronic thromboembolic pulmonary hypertension (CTEPH) and pulmonary arterial hypertension (PAH) as compared to baseline values. The Phase III program for these indications is planned to be initiated in late 2008... Bayer Schering Pharma's Press Release -