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Tag: novartis

You Searched For "novartis"
Novartis bolsters Neuroscience pipeline

Novartis Gets CDSCO Panel Nod to study Remibrutinib to treat chronic spontaneous urticaria

Dr. Divya Colin8 Dec 2023 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...
Caplin Steriles gets USFDA nod for Procainamide Hydrochloride Injection for treating abnormal heart rhythm

Novartis gets USFDA nod for Fabhalta for adults with paroxysmal nocturnal hemoglobinuria

Ruchika Sharma7 Dec 2023 11:43 AM IST
Basel: Novartis has announced that the U.S. Food and Drug Administration (FDA) has approved Fabhalta (iptacopan) as the first oral monotherapy for the...
Novartis oral Fabhalta gets USFDA nod for adults with C3 glomerulopathy

Novartis raises sales growth target to 5 percent a year through 2027

Ruchika Sharma28 Nov 2023 3:30 PM IST
Frankfurt: Novartis has dialled up its sales growth target to 5% per year until 2027, citing demand for innovative drugs after the spin off of...
Atrasentan found superior to placebo for proteinuria reduction in the Phase 3 Trial for IgA Nephropathy.

Atrasentan found superior to placebo for proteinuria reduction in the Phase 3 Trial for IgA Nephropathy.

Dr Kartikeya Kohli4 Nov 2023 11:15 AM IST
IgA nephropathy (IgAN) is an autoimmune disorder wherein clusters of antibodies get deposited in the kidneys, leading to inflammation and damage to...
Novartis wins USFDA nod for Cosentyx to treat hidradenitis suppurativa in adults

Novartis wins USFDA nod for Cosentyx to treat hidradenitis suppurativa in adults

Ruchika Sharma1 Nov 2023 2:00 PM IST
Basel: Novartis has announced that the US Food and Drug Administration (FDA) has approved Cosentyx (secukinumab) to treat moderate to severe...
Novartis bolsters Neuroscience pipeline

CDSCO Panel approves Novartis proposal to update package insert of Secukinumab

Dr. Divya Colin25 Oct 2023 6:00 PM IST
New Delhi: The Subject Expert Committee (SEC) functional under the Center Drug Standard Control Organisation (CDSCO) has granted approval to drug...
FDA approves intravenous Secukinumab for Rheumatic diseases

FDA approves intravenous Secukinumab for Rheumatic diseases

Dr. Kamal Kant Kohli11 Oct 2023 11:45 AM IST
The US Food and Drug Administration (FDA) has approved an intravenous formulation of Secukinumab for patients with psoriatic arthritis, ankylosing...
Novartis oral Fabhalta gets USFDA nod for adults with C3 glomerulopathy

Novartis Cosentyx IV formulation for rheumatic diseases bags USFDA okay

Ruchika Sharma10 Oct 2023 1:30 PM IST
The IV formulation of Cosentyx offers patients a monthly 30-minute, weight-based dosing option, requiring no pre-medication and no lab monitoring.
Novartis concludes Sandoz spin-off

Novartis concludes Sandoz spin-off

Ruchika Sharma5 Oct 2023 10:30 AM IST
Basel: Novartis has completed the Spin-off of Sandoz, its Generics and Biosimilars business, through a dividend-in-kind distribution to holders of...
Novartis oral Fabhalta gets USFDA nod for adults with C3 glomerulopathy

BeiGene regains full rights from Novartis for Anti-PD-1 antibody Tevimbra

Ruchika Sharma20 Sept 2023 5:31 PM IST
Basel: BeiGene, Ltd., a global biotechnology company, has announced that it has entered into an agreement with Novartis to regain worldwide...
Novartis oral Fabhalta gets USFDA nod for adults with C3 glomerulopathy

Novartis Kisqali reduced cancer recurrence risk while maintaining quality of life in patients diagnosed with early breast cancer

Ruchika Sharma18 Sept 2023 12:30 PM IST
Basel: Novartis has presented new patient-reported outcomes (PRO) data from the Phase III NATALEE trial at the European Society for Medical Oncology...
Novartis bolsters Neuroscience pipeline

Novartis shareholders approve proposed 100 percent Spinoff of Sandoz

Ruchika Sharma16 Sept 2023 3:30 PM IST
Basel: Novartis shareholders approved the proposed 100% Spin-off of Sandoz, the Generics and Biosimilars business of Novartis in an Extraordinary...
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