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GSK malaria drug begins pivotal trials

CDA (chlorproguanil hydrochloride-dapsone-artesunate) is being developed as a fixed-dose combination to meet the urgent need for new malaria treatments in the developing world where multi-drug resistance is contributing

Barr smoothes way for Pliva takeover

Consequently, the company said that it will not include an FTC approval condition in the formal tender offer it intends to file with the Croatian Financial Services Supervisory

Bayer and Onyx’ Nexavar approved in Europe

The Nexavar approval is specifically for the treatment of patients with advanced renal cell carcinoma who have failed prior interferon- alpha or interleukin-2 based therapy or are considered

Study finds Gleevec could damage heart

After studying ten patients who suffered heart failure after taking the drug at University of Texas’ M.D. Anderson Cancer Center, the researchers found that a protein targeted by

Biogen Idec and Elan re-launch Tysabri in US

Tysabri was removed form the market following its original 2004 approval after it was shown to increase the risk of progressive multifocal leukoencephalopathy (PML), an opportunistic viral infection

AstraZeneca’s Symbicort approved in US

Symbicort, which is already approved in Europe, is a twice-daily asthma therapy combining budesonide, an inhaled corticosteroid, and formoterol, a rapid and long-acting beta2-agonist into one inhaler. AstraZeneca