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US FDA approves Regeneron's blood cancer therapy
Regeneron Pharmaceuticals said on Wednesday the U.S. Food and Drug Administration has approved its drug for a type of blood ...
UroGen Pharma Receives FDA Approval for ZUSDURI for Recurrent Bladder Cancer
UroGen Pharma Ltd. (NASDAQ:URGN) is one of the best hot stocks to buy according to Wall Street analysts. In mid-June, UroGen ...
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Dizal set to bring lung cancer drug Zegfrovy to US
Dizal will market sunvozertinib in the US under the Zegfrovy brand name, entering a market for EGFR inhibitors currently dominated by AstraZeneca's Tagrisso (osimertinib) but currently being shaken up ...
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Lupin receives FDA approval for Loteprednol Etabonate Ophthalmic Gel, 0.38%
Lupin Limited secures FDA approval for Loteprednol Etabonate Ophthalmic Gel, enhancing treatment options for postoperative ...
US approves twice-yearly injection for HIV prevention. What you need to know about lenacapavir
The US Food and Drug Administration (FDA) has approved lenacapavir, an injectable drug that offers long-lasting protection ...
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Thermo Fisher Scientific’s NGS assay, Oncomine Dx Express Test receives US FDA approval as a companion diagnostic for Dizal’s Zegfrovy
Carlsbad, California Saturday, July 5, 2025, 16:00 Hrs [IST] ...
US FDA eliminates risk evaluation, mitigation strategies for CAR-T cancer therapies
The U.S. Food and Drug Administration said on Friday it had eliminated risk evaluation and mitigation strategies (REMS), a ...
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FDA approves Takeda’s Gammagard liquid ERC for primary immunodeficiency
The US Food and Drug Administration (FDA) has approved Takeda’s new immunoglobulin (IG) therapy, Gammagard liquid ERC [immune ...
Moderna RSV Vaccine Gains Expanded FDA Approval for Younger Adults
This builds upon its initial approval in May 2024 for adults aged 60 years and older, which makes mRESVIA the second approved ...
Telix Pharmaceuticals (TLX) Announces That US FDA Approves Label Expansion for Illuccix
Telix Pharmaceuticals Limited (NASDAQ: TLX) is one of the 7 Best ASX Stocks to Buy Now. On June 23, the company announced ...
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Sobi’s Gamifant receives US FDA approval for first-ever treatment for adults and children with MAS in Still's disease
Stockholm, Sweden Monday, June 30, 2025, 10:00 Hrs [IST] ...