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Clinical

Sandoz says Humira biosimilar clears clinical hurdle

Sandoz says Humira biosimilar clears clinical hurdle

Its drug matches the safety and efficacy of AbbVie’s plaque psoriasis blockbuster

Amgen's Mvasi is first FDA-approved cancer biosimilar

Amgen's Mvasi is first FDA-approved cancer biosimilar

Offers prospect of lower-cost alternative to Roche's Avastin

Teva poaches Lundbeck's Schultz as new CEO

Teva poaches Lundbeck's Schultz as new CEO

Shares in Lundbeck fall as two senior posts become vacant

Prix Galien opens for entries with new award

Awards seen as highest accolade for innovation in life sciences

Novartis scores but Roche misses in melanoma trials

Novartis scores but Roche misses in melanoma trials

Phase III trial combo success for Tafinlar/Mekinist “unprecedented”

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reactivating drug research programmes

reactivating drug research programmes

Gene profiling technology offers new avenues for producing precision drugs

Rare diseases: meeting the challenge

Rare diseases: meeting the challenge

Problems with regulating orphan drugs

Japanese pharma pulls no punches with post-Brexit UK

Japanese pharma pulls no punches with post-Brexit UK

Firm want reassurance from the UK on its future in science and innovation

Brexit: Implications for the pharma industry

Brexit: Implications for the pharma industry

From patents to the EMA, data protection to clinical trials, there's a lot that should be a concern

Real-world evidence

Real-world evidence Investigating the sources of evidence as best practice moves from being knowledge-based to evidence-based

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