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Tag: novartis

You Searched For "novartis"
CDSCO Panel Asks Novartis to Submit Revised Protocol, Dose Changes for Ianalumab Phase III Trial

Novartis Fabhalta gets positive CHMP opinion as first oral monotherapy for adult patients with paroxysmal nocturnal hemoglobinuria

Ruchika Sharma24 March 2024 2:30 PM IST
Basel: Novartis has announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a...
CDSCO Panel Asks Novartis to Submit Revised Protocol, Dose Changes for Ianalumab Phase III Trial

Submit Interim Safety, Efficacy Data: CDSCO Panel Tells Novartis on Crizanlizumab

Dr. Divya Colin20 March 2024 6:00 PM IST
New Delhi: Reviewing the status of the ongoing studies of Crizanlizumab concentrate for solution for infusion 10mg/mL (100mg/10mL), the Subject Expert...
CDSCO Panel Asks Novartis to Submit Revised Protocol, Dose Changes for Ianalumab Phase III Trial

Modify Clinical study protocol of Iptacopan study in aHUS: CDSCO Panel Tell Novartis

Dr. Divya Colin17 March 2024 5:15 PM IST
New Delhi: Reviewing the Phase IIIb clinical trial study protocol of Iptacopan, the Subject Expert Committee (SEC) functional under the Central...
Former Novartis India Chief Ranjit Shahani no more

Former Novartis India Chief Ranjit Shahani no more

Ruchika Sharma11 March 2024 3:22 PM IST
New Delhi: Former Vice Chairman and Managing Director of Novartis India and Chairman of JB Pharmaceuticals, Ranjit Shahani has passed...
CDSCO Panel Asks Novartis to Submit Revised Protocol, Dose Changes for Ianalumab Phase III Trial

Britain health regulator revokes conditional marketing authorisation for Novartis sickle cell drug Adakveo

Ruchika Sharma22 Feb 2024 11:20 AM IST
Sickle cell disease is a genetic disorder in which misshapen blood cells cause strokes, organ damage, severe pain and early death.
CDSCO Panel Asks Novartis to Submit Revised Protocol, Dose Changes for Ianalumab Phase III Trial

Will Novartis continue business in India? Global Drug major strategic review to decide

Ruchika Sharma17 Feb 2024 2:16 PM IST
Drug major Novartis AG has announced a strategic review of Novartis India Ltd, a public company listed on the BSE.The strategic review will include an...
CDSCO Panel Approves Novartis Protocol Amendment Proposal For Multiple Sclerosis Drug Ofatumumab

CDSCO Panel Approves Novartis Protocol Amendment Proposal For Multiple Sclerosis Drug Ofatumumab

Dr. Divya Colin11 Feb 2024 6:00 PM IST
New Delhi: The Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) has approved the drug major...
Alkem Labs completes acquisition of 100% stake in Adroit Biomed

Novartis to acquire MorphoSys AG for EUR 68 per share or aggregate of EUR 2.7bn in cash

Ruchika Sharma6 Feb 2024 12:30 PM IST
Basel: Novartis has announced that it has entered into an agreement to make a voluntary public takeover offer to acquire MorphoSys AG, a...
CDSCO Panel grants Novartis Protocol Amendment proposal for Remibrutinib study in Relapsing Multiple Sclerosis

CDSCO Panel grants Novartis Protocol Amendment proposal for Remibrutinib study in Relapsing Multiple Sclerosis

Dr. Divya Colin5 Feb 2024 5:30 PM IST
New Delhi: The Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) has approved the drug major...
Novartis Gets CDSCO Panel Nod to Study XXB750 in Patients With Heart Failure

Novartis Gets CDSCO Panel Nod to Study XXB750 in Patients With Heart Failure

Dr. Divya Colin2 Feb 2024 6:00 PM IST
New Delhi: The drug major Novartis has got approval from the Subject Expert Committee (SEC) functional under the Central Drug Standard Control...
CDSCO Panel Grants Novartis Protocol Amendment Proposal For anti-cholesterol drug Inclisiran

CDSCO Panel Grants Novartis Protocol Amendment Proposal For anti-cholesterol drug Inclisiran

Dr. Divya Colin28 Jan 2024 5:30 PM IST
New Delhi: The Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) has approved the drug major...
EU regulator starts safety review of CAR-T cancer cell therapies

EU regulator starts safety review of CAR-T cancer cell therapies

Ruchika Sharma15 Jan 2024 9:00 AM IST
The European Union's drug watchdog has said it had started a review into the safety risks associated with cancer cell therapies made by companies such...
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