Biopharma

Short-Term Limited Duration Insurance Plans Tied to Inc...

FRIDAY, March 21, 2025 -- Loosening restrictions on short-term limited duration...

ACP Issues Clinical Guideline for Pharmacologic Treatme...

FRIDAY, March 21, 2025 -- In a clinical guideline issued by the American Colleg...

Nvidia outlines new AI projects in robotic surgery, aut...

At its GTC conference in San Jose, Nvidia outlined collaborations with several m...

Speed, Scale, and Success – The Rise of Bispecific Anti...

Bispecific antibodies are revolutionizing targeted therapies, enabling dual-targ...

Alnylam enters the ATTR-CM drug race

Today in "The Readout" newsletter: Alnylam's Amvuttra enters ATTR-CM drug race, ...

J&J boosts US manufacturing as big pharma reshores

Following big announcements from Lilly and Merck, J&J is pledging $55 billion ov...

AstraZeneca deepens China investment; Editas loses CFO ...

The pharma is spending $2.5 billion on an R&D center in Beijing. Elsewhere, Adap...

Delayed CDC meeting on vaccines is rescheduled to April

A panel of CDC advisers, who had originally been set to meet in February, will d...

Novartis links music and science in corporate campaign ...

A Big Pharma may seem like an incongruous choice of sponsor for a global music c...

Fierce Biotech Layoff Tracker 2025: Elevation eliminate...

As always, if you know of layoffs occurring at a biotech, please reach out to th...

Alnylam prices heart drug at premium to rivals

Initially, Amvuttra’s annual list price will be nearly double the yearly cost of...

J&J touts $55B in planned US investments over 4 years, ...

Johnson & Johnson will invest $55 billion in the U.S. over the next four years. ...

Adaptimmune, after bringing cell therapy to market, que...

Despite a historic FDA approval last year, Adaptimmune Therapeutics is expressin...

European countries, universities implement initiatives ...

As the U.S. cuts federal research funding and infrastructure, European countries...

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EMEA-003520-PIP01-23

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EMEA-003225-PIP01-22

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Opinion/decision on a Paediatric investigation plan (PI...

Opinion/decision on a Paediatric investigation plan (PIP): Rinvoq, upadacitinib,...

Human medicines European public assessment report (EPAR...

Human medicines European public assessment report (EPAR): Veoza, fezolinetant, D...

Human medicines European public assessment report (EPAR...

Human medicines European public assessment report (EPAR): Buvidal, buprenorphine...

Novartis snags FDA nod for Fabhalta in another kidney d...

Novartis' Fabhalta has become the first treatment approved by the FDA for the ul...

UPDATE: Director of National Human Genome Research Inst...

"Eric Green, M.D. Ph.D., is no longer serving as director of NIH’s National Huma...

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