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Pfizer acquires spinal muscular atrophy research programme

Gains rights to drug candidate RG3039 in deal with Repligen that could be worth up to $70m

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India’s Supreme Court wants tighter clinical trial regulation

Justice Lodha says illegal studies of investigational medicines causing “havoc to human life”

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EMA to focus on efficiency, transparency and new legislation in 2013

Regulator also plans significant staff reorganisation

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Eliquis and Ryzodeg feature among Japan’s year-end approvals

Actonel and Neupro also given green light

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FDA clears six new drugs in time for the new year

Brings 2012 tally to 39 – the highest for more than 15 years

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ViiV submits dolutegravir for approval to treat HIV in US, EU and Canada

GSK-Pfizer joint venture takes next step towards commercialisation

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Year-end FDA approvals for Novartis, GSK drugs

Agency gives go-ahead to Cushing’s disease treatment Signifor and raxibacumab for inhalational anthrax

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Early FDA approval for Ariad’s leukaemia drug Iclusig

Available in US three months ahead of schedule

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Eliquis meets targets as long-term VTE therapy

Pfizer and BMS report positive phase III data for the Factor Xa inhibitor

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EMA: move to greater clinical trial transparency ‘irreversible’

New Europe data rules could be ready by 2014

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Pfizer set for negative NICE decision on Inlyta

Institute's draft guidance doesn't recommend drug for advanced kidney cancer

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Pfizer reports strong data with new breast cancer candidate

Phase II results suggest progression-free survival benefits for PD-0332991

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