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UF Health successfully implements genomic medicine program

GAINESVILLE, Fla. — At the conclusion of the first year of UF Health’s Personalized Medicine Program, the results are in: The program has successfully implemented a process for genetic testing that helps cardiologists identify which patients may benefit from...

GSK and MMV initiate Phase III programme for development of malaria drug

GlaxoSmithKline (GSK) and Medicines for Malaria Venture (MMV) have initiated a Phase III global programme to assess the efficacy and safety of tafenoquine, an investigational medicine, being developed for the treatment and relapse prevention (radical cure) of Plasmodium vivax...

Ohr Pharma completes patient enrolment in Phase II trial of macular degeneration drug

US-based Ohr Pharmaceutical has completed patient enrolment in its OHR-002 Phase II clinical trial evaluating Squalamine Eye Drops for treatment of the wet form of age related macular degeneration (wet-AMD). A total of 142 treatment naive...

European Commission grants marketing approval for Teva’s DuoResp Spiromax

Teva Pharmaceutical has obtained marketing authorisation approval from European Commission for its DuoResp Spiromax for treatment of patients with asthma and chronic obstructive pulmonary disease (COPD) when a combination inhaled corticosteroid and long-acting beta(2) adrenoceptor agonist is appropriate. ...

Bavarian Nordic doses first patient in Phase II trial of CV-301 to treat bladder cancer

Denmark-based biotechnology firm Bavarian Nordic has dosed first patient in a randomised, prospective Phase II trial of its active immunotherapy product candidate CV-301 for treatment of bladder cancer. In the trial, which is sponsored by the...

Janssen’s type 2 diabetes drug Vokanamet gets European Commission approval in EU

Janssen-Cilag International (Janssen) has received approval from the European Commission (EC) for use of Vokanamet in the European Union (EU) as a treatment for adults with type 2 diabetes mellitus to improve glycaemic control. Vokanamet is...

Alexion begins multinational registration trials of eculizumab to treat NMO and MG

US-based Alexion Pharmaceuticals has started a single, multinational, placebo-controlled trial designed to assess the safety and efficacy of eculizumab (Soliris) in patients with relapsing neuromyelitis optica (NMO), a life-threatening, ultra-rare neurologic disorder. Primary objective of the...

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