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Tag: Takeda

You Searched For "takeda"
Eris Lifesciences designates Gopal Agrawal, Nita Borkar in leadership roles

Eris Lifesciences designates Gopal Agrawal, Nita Borkar in leadership roles

Ruchika Sharma2 April 2025 1:16 PM IST
Mumbai: Eris Lifesciences Limited, an Indian branded formulations manufacturing company, has designated Gopal Agrawal and Nita Borkar in...
Takeda gets EMA nod for additional subcutaneous administration of Takhzyro in  Hereditary Angioedema patients

Takeda gets EMA nod for additional subcutaneous administration of Takhzyro in Hereditary Angioedema patients

Ruchika Sharma25 Feb 2025 10:30 AM IST
Zurich: Takeda has announced that the European Medicines Agency (EMA) has given approval for an additional 2 mL pre-filled pen option for...
Julie Kim to succeed Christophe Weber as CEO of Takeda

Julie Kim to succeed Christophe Weber as CEO of Takeda

Ruchika Sharma30 Jan 2025 5:06 PM IST
Osaka: Takeda has announced that its Board of Directors made the decision unanimously to appoint Julie Kim, currently president of Takeda's...
Innocan Pharma granted patent in India for Liposomal CBD Injection

Takeda gets Japenese nod for Hyqvia 10% SC injection set for Agammaglobulinemia

Ruchika Sharma27 Dec 2024 12:32 PM IST
Osaka: Takeda has announced that the Japanese Ministry of Health, Labour and Welfare has approved the use of HYQVIA [Immune Globulin...
Submit Separate Retrospective, Prospective Study data of subjects: CDSCO Panel Tells Takeda on Velaglucerase alfa study

Submit Separate Retrospective, Prospective Study data of subjects: CDSCO Panel Tells Takeda on Velaglucerase alfa study

Dr. Divya Colin15 July 2024 6:00 PM IST
New Delhi: Regarding the post-marketing surveillance study of the drug major Takeda Pharmaceutical's Velaglucerase alfa injection, the Subject Expert...
Takeda gets European Commission approval for Fruzaqla for previously treated metastatic Colorectal cancer

Takeda gets European Commission approval for Fruzaqla for previously treated metastatic Colorectal cancer

Ruchika Sharma23 Jun 2024 12:00 PM IST
FRUZAQLA is a selective oral inhibitor of all three VEGF receptors (-1, -2 and -3). VEGFR inhibitors play a pivotal role in blocking tumor...
Takeda gets EMA nod for additional subcutaneous administration of Takhzyro in  Hereditary Angioedema patients

Takeda announces Phase 3 topline results for Soticlestat in patients with Dravet Syndrome, Lennox-Gastaut Syndrome

Ruchika Sharma18 Jun 2024 4:14 PM IST
Osaka: Takeda has announced topline data from its SKYLINE and SKYWAY studies. SKYLINE (TAK-935-3001) was a multicenter, randomized, double-blind...
Takeda gets EMA nod for additional subcutaneous administration of Takhzyro in  Hereditary Angioedema patients

Takeda signs option agreement with Ascentage Pharma to enter into exclusive global license for Olverembatinib

Ruchika Sharma16 Jun 2024 10:30 AM IST
Japan: Takeda has announced the signing of an option agreement with Ascentage Pharma to enter into an exclusive license agreement for...
Takeda Biopharma names Annapurna Das as General Manager for India Operations

Takeda Biopharma names Annapurna Das as General Manager for India Operations

Ruchika Sharma17 May 2024 11:36 AM IST
Mumbai: Takeda Biopharmaceuticals India Pvt Ltd (formerly known as Baxalta Bioscience India Private Limited), part of a global values-based,...
First subjects dosed in Phase-1 clinical trial of Cognitive Disorder drug

India becoming attractive for clinical trials: Pharma industry leaders

Ruchika Sharma29 April 2024 2:33 PM IST
New Delhi: Experts from the pharmaceutical sector have noted that over the last decade, clinical trials in India have undergone significant...
Takeda gets EMA nod for additional subcutaneous administration of Takhzyro in  Hereditary Angioedema patients

Takeda gets USFDA nod for Entyvio subcutaneous administration for Crohn's disease

Ruchika Sharma21 April 2024 10:00 AM IST
Osaka: Takeda has announced that the U.S. Food and Drug Administration (FDA) has approved ENTYVIO (vedolizumab) subcutaneous (SC)...
Alembic Pharma secures USFDA final nod for anticonvulsant drug Carbamazepine

Takeda bags accelerated USFDA nod for Iclusig with chemotherapy in adult patients with newly diagnosed Ph+ ALL

Ruchika Sharma22 March 2024 11:57 AM IST
Osaka: Takeda has announced that the U.S. Food and Drug Administration (FDA) has approved the supplemental New Drug Application (sNDA) for...
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