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FDA approves novel gene therapy for rare neurometabolic disorder
The FDA has approved an adeno-associated virus vector-based gene therapy to treat both adult and pediatric patients with aromatic L-amino acid decarboxylase deficiency.
Pfizer
Pfizer explores sale of hospital drugs unit amid activist investor’s call for accountability: Reuters
Evaxion
Evaxion announces positive preclinical data for cytomegalovirus (CMV) vaccine program EVX-V
Drug R&D
With high hopes for the economy, AstraZeneca adds $2B to US investment in manufacturing, R&D
FDA grants breakthrough status to J&J’s nipocalimab for SjD treatment
The US Food and Drug Administration (FDA) has awarded the second breakthrough therapy designation (BTD) to Johnson & Johnson‘s (J&J) nipocalimab for treating individuals with...
International Congress for Ataxia Research
Preclinical + International Congress for Ataxia Research
FDA Takes Step Toward Removal of Ineffective Decongestants From the Market
FDA Takes Step Toward Removal of Ineffective Decongestants From the Market
Eisai
Eisai lowers Leqembi revenue forecast after rocky entry to market
Mustang Bio’s MB-108
Mustang Bio’s MB-108 receives FDA orphan drug status for glioma treatment
VitalityXtra
VitalityXtra may be harmful due to hidden drug ingredient
Lupin
Lupin Secures Tentative U.S. FDA Approval For Generic HIV Drug Raltegravir
SITC
Werewolf Therapeutics, Inc., an innovative biopharmaceutical company pioneering the development of conditionally activated therapeutics engineered to stimulate the body’s immune system for the treat...
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