Hematological Disorders

Takeda’s ADZYNMA gains Japanese approval for cTTP treatment

Takeda has announced that the Japanese Ministry of Health, Labour and Welfare (MHLW) has approved ADZYNMA Intravenous Injection 1500 (apadamtase…

BMS’ cell therapy Abecma gains EC approval for multiple myeloma

The European Commission (EC) has approved Bristol Myers Squibb’s (BMS) cell therapy Abecma (idecabtagene vicleucel; ide-cel) to treat adults with relapsed…

Akums introduces Hydroxyurea oral suspension for sickle cell disease

Indian company Akums Drugs and Pharmaceuticals has introduced Hydroxyurea oral suspension, the country’s first room temperature-stable drug for treating sickle…

FDA committee endorses Johnson & Johnson’s multiple myeloma therapy

The US Food and Drug Administration's (FDA) Oncologic Drugs Advisory Committee (ODAC) has recommended Johnson & Johnson’s Carvykti (ciltacabtagene autoleucel,…

MHRA authorises Daiichi Sankyo quizartinib for AML for marketing

The UK Medicines and Healthcare products Regulatory Agency (MHRA) has granted marketing authorisation to Daiichi Sankyo for quizartinib (Vanflyta) for…

CARsgen’s CAR-T therapy for multiple myeloma gains NMPA approval

The National Medical Products Administration (NMPA) of China has approved CARsgen Therapeutics' new drug application for zevorcabtagene autoleucel to treat…

EMA CHMP recommends AstraZeneca’s Voydeya for PNH treatment

The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency has recommended AstraZeneca's oral Factor D…

MHRA revokes Novartis’ Adakveo authorisation for sickle cell disease

The UK Medicines and Healthcare products Regulatory Agency (MHRA) has revoked a conditional marketing authorisation for Novartis Pharmaceuticals' Adakveo 10mg/ml…

Grifols gears up for FDA approval of fibrinogen replacement therapy

Spanish pharmaceutical company Grifols has reported positive Phase III trial data for its fibrinogen concentrate, AdFIrst (BT524) as a treatment…

Regeneron’s linvoseltamab application accepted for review

Regeneron Pharmaceuticals marketing authorisation application (MAA) for linvoseltamab has received acceptance for review from the European Medicines Agency (EMA) to…

close

Sign up to the newsletter: In Brief

Your corporate email address *
First name *
Last name *
Company name *
Job title *
Visit our Privacy Policy for more information about our services, how we may use, process and share your personal data, including information of your rights in respect of your personal data and how you can unsubscribe from future marketing communications. Our services are intended for corporate subscribers and you warrant that the email address submitted is your corporate email address.

Thank you for subscribing

View all newsletters from across the GlobalData Media network.

close