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News

FDA rejects Novartis' cholesterol drug after factory inspect...

Novartis’ cholesterol drug inclisiran has hit a speed bump with the FDA, which has rejected the potential blockbuster because a manufacturing facility has yet to be inspected.

News

FDA approves Alnylam's ultra-rare disease drug Oxlumo

The FDA has approved Alnylam’s gene silencing drug Oxlumo, the first treatment for primary hyperoxaluria type 1 (PH1), an ultra-rare and life-threatening genetic disorder.

News

Sanofi/Alnylam's haemophilia drug hits another safety speed-...

Sanofi’s attempt to take on Roche with a ground-breaking approach to treating haemophilia has hit a setback after the company voluntarily placed its late-stage trials of fitusiran on hold b

R&D

Alnylam, gene-silencing and biotech in 2020: the pharmaphoru...

Alnylam's Brendan Martin joined the pharmaphorum podcast for episode 23 to talk about his company's work in gene-silencing and how it could offer a route to target the current coronavirus p

Views & Analysis

Alnylam’s Anant Murthy on making it as a US biotech in Europ...

Alnylam’s European head of market access and GM of mid-size markets, Anant Murthy, shares his perspective on how a US biotech can adapt to the many unique challenges of the EU market.

News

UK patients get early access to Alnylam's ultra-rare disease...

The UK's regulator has granted early access to Alnylam's ultra-rare disease drug lumasiran, allowing patients with primary hyperoxaluria type 1 to gain access ahead of a regulatory decision

FDA rejects Novartis' cholesterol drug after factory inspect...

FDA approves Alnylam's ultra-rare disease drug Oxlumo

Sanofi/Alnylam's haemophilia drug hits another safety speed-...

Alnylam, gene-silencing and biotech in 2020: the pharmaphoru...

Alnylam’s Anant Murthy on making it as a US biotech in Europ...

UK patients get early access to Alnylam's ultra-rare disease...

Is Martin Makary Trump's pick for FDA Commissioner?

Coming soon: The Life Sciences Industry Report 2025 – insigh...

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