GSK and Theravance file for FF/VI approval in the USA and Europe; Talks with … – The Pharma Letter

GSK and Theravance file for FF/VI approval in the USA and Europe; Talks with
The Pharma Letter
Asthma (100/25mcg and 200/25mcg): The regular treatment of asthma in adults and adolescents aged 12 years and older, where use of a combination product (long-acting beta2-agonist and inhaled corticosteroid) is appropriate. • COPD (100/25mcg): The
GSK, Theravance seek approvals for FF/VI in US, EuropePharmaceutical Business Review
GSK and Theravance file next-generation Advair in USA, EUPharma Times

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GSK and Theravance Announce Regulatory Submissions for FF/VI in the US and … – MarketWatch (press release)

GSK and Theravance Announce Regulatory Submissions for FF/VI in the US and
MarketWatch (press release)
Asthma (100/25mcg and 200/25mcg): The regular treatment of asthma in adults and adolescents aged 12 years and older, where use of a combination product (long-acting beta2-agonist and inhaled corticosteroid) is appropriate. COPD (100/25mcg): The
GSK, Theravance unveil Regulatory Submissions for FF/VI in US, EuropeRTT News
GSK files key new lung drug for regulatory approvalWHTC

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View full post on asthma – Google News

Dose Proportionality Study: Blood Levels of Fluticasone Furoate (FF) and Vilanterol (VI) Following Different Doses of FF/VI Via an Inhaler

Condition:   Asthma
Interventions:   Drug: Fluticasone furoate 50 mcg (4 inhalations);   Drug: Fluticasone furoate 100 mcg (4 inhalations);   Drug: Fluticasone furoate 200 mcg (4 inhalations);   Drug: Vilanterol 25 mcg (4 inhalations)
Sponsor:   GlaxoSmithKline
Not yet recruiting – verified October 2010

View full post on ClinicalTrials.gov: “Asthma” | updated in the last 30 days