Biopharma

Cancellation of NIH summer internships disrupts ‘vital’ training program for U.S. scientists

Cancellation of NIH summer internships disrupts ‘vital’...

Mar 5, 2025 0

The NIH cancelled an internship program that gave more than 1,000 college studen...

Opinion: Former chairs of the Advisory Committee on Immunization Practices on the panel’s role

Opinion: Former chairs of the Advisory Committee on Imm...

Mar 5, 2025 0

Six former chairs of the U.S. Advisory Committee on Immunization Practices expla...

NIH cancels grants for LGBTQ+ health research effective immediately: Stat

NIH cancels grants for LGBTQ+ health research effective...

Mar 5, 2025 0

Several scientists studying LGBTQ+ health issues have had their grants from the ...

STAT+: Even critics of the scientific establishment give Trump’s drama-filled weeks mixed reviews

STAT+: Even critics of the scientific establishment giv...

Mar 5, 2025 0

STAT interviews two dozen scientists and researchers who support some of Trump's...

Union Product Database: release notes

Union Product Database: release notes

Mar 5, 2025 0

Union Product Database: release notes

BMS pushes Fulcrum off its list of partners, scrapping MyoKardia heart muscle pact

BMS pushes Fulcrum off its list of partners, scrapping ...

Mar 5, 2025 0

Bristol Myers Squibb is levering Fulcrum Therapeutics out of its life. MyoKardia...

BioNTech's RNA malaria vaccine trial hit by FDA hold

BioNTech's RNA malaria vaccine trial hit by FDA hold

Mar 5, 2025 0

The FDA has placed a hold on BioNTech’s phase 1/2a trial, pausing the company’s ...

Human medicines European public assessment report (EPAR): Alimta, pemetrexed, Date of authorisation: 20/09/2004, Revision: 28, Status: Authorised

Human medicines European public assessment report (EPAR...

Mar 5, 2025 0

Human medicines European public assessment report (EPAR): Alimta, pemetrexed, Da...

Vitrolife IVF media - Procedural steps and scientific i...

Mar 5, 2025 0

Vitrolife IVF media - Procedural steps and scientific information after initial ...

Human medicines European public assessment report (EPAR): Inrebic, fedratinib, Date of authorisation: 08/02/2021, Revision: 7, Status: Authorised

Human medicines European public assessment report (EPAR...

Mar 5, 2025 0

Human medicines European public assessment report (EPAR): Inrebic, fedratinib, D...

Human medicines European public assessment report (EPAR): ReFacto AF, moroctocog alfa, Date of authorisation: 13/04/1999, Revision: 41, Status: Authorised

Human medicines European public assessment report (EPAR...

Mar 5, 2025 0

Human medicines European public assessment report (EPAR): ReFacto AF, moroctocog...

BioNTech’s RNA malaria vaccine trial hit by FDA hold

BioNTech’s RNA malaria vaccine trial hit by FDA hold

Mar 5, 2025 0

The FDA has placed a hold on BioNTech’s phase 1/2a trial, pausing the company’s ...

Protein project uses AI to boost disease treatment

Protein project uses AI to boost disease treatment

Mar 5, 2025 0

UK initiative to harness big biological data sets and look deeper into how the h...

Cingulate Reports Safety Results from Final Phase 3 Trials for Lead ADHD Asset CTx-1301

Cingulate Reports Safety Results from Final Phase 3 Tri...

Mar 5, 2025 0

KANSAS CITY, Kan., March 04, 2025 (GLOBE NEWSWIRE) -- Cingulate Inc. (NASDAQ: CI...

Tevimbra Approved in U.S. for First-line Treatment of Advanced Esophageal Squamous Cell Carcinoma in Combination with Chemotherapy

Tevimbra Approved in U.S. for First-line Treatment of A...

Mar 5, 2025 0

SAN MATEO, Calif.--(BUSINESS WIRE) Mar 04, 2025 -- BeiGene, Ltd. (NASDAQ: ONC; H...

FDA Grants Orphan Drug Designation for Bexmarilimab in MDS

FDA Grants Orphan Drug Designation for Bexmarilimab in MDS

Mar 5, 2025 0

TURKU, Finland March 3, 2025 – Faron Pharmaceuticals Ltd. (AIM: FARN, First Nort...

FDA Approves Stoboclo (denosumab-bmwo), a Biosimilar to Prolia

FDA Approves Stoboclo (denosumab-bmwo), a Biosimilar to...

Mar 5, 2025 0

JERSEY CITY, N.J., March 3, 2025 /PRNewswire/ -- Celltrion today announced that ...

FDA Approves Osenvelt (denosumab-bmwo), a Biosimilar to Xgeva

FDA Approves Osenvelt (denosumab-bmwo), a Biosimilar to...

Mar 5, 2025 0

JERSEY CITY, N.J., March 3, 2025 /PRNewswire/ -- Celltrion today announced that ...

High Levels of Perimenopause-Related Symptoms Seen in Younger Women

High Levels of Perimenopause-Related Symptoms Seen in Y...

Mar 5, 2025 0

TUESDAY, March 4, 2025 -- A significant number of individuals aged 30 to 45 yea...

1990 to 2021 Saw Global Decline in Mortality Rate for Suicide

1990 to 2021 Saw Global Decline in Mortality Rate for S...

Mar 5, 2025 0

TUESDAY, March 4, 2025 -- The age-standardized mortality rate for suicide decre...

STAT+: To fight U.S. tariffs, Canada should suspend U.S. patents on medicines, one expert argues

STAT+: To fight U.S. tariffs, Canada should suspend U.S...

Mar 4, 2025 0

To fight U.S. tariffs, the Canadian government should consider suspending patent...

FDA Roundup: March 4, 2025

FDA Roundup: March 4, 2025

Mar 4, 2025 0

The U.S. Food and Drug Administration is providing an at-a-glance summary of new...

DOGE terminates leases for 30 FDA sites across 23 states

DOGE terminates leases for 30 FDA sites across 23 states

Mar 4, 2025 0

Under President Donald Trump’s administration, DOGE has reportedly terminated le...

Blackstone buys majority stake in CMIC, Japan's largest contract research organization

Blackstone buys majority stake in CMIC, Japan's largest...

Mar 4, 2025 0

Private equity giant Blackstone is going big on Japan, acquiring a majority stak...

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