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Latest Industry News - Page 598

Gilead Sciences bags European Commission nod for HIV drug Sunlenca

Gilead Sciences bags European Commission nod for HIV drug Sunlenca

Ruchika Sharma23 Aug 2022 1:30 PM IST
Sunlenca is indicated in the European Union for the treatment of adults with multi-drug resistant HIV infection in combination with other...
Unichem Labs anticonvulsant drug Carbamazepine gets USFDA okay

Unichem Labs anticonvulsant drug Carbamazepine gets USFDA okay

Ruchika Sharma23 Aug 2022 12:32 PM IST
Carbamazepine Tablets are indicated for use as an anticonvulsant drug and in the treatment of the pain associated with true trigeminal neuralgia.
Pfizer, BioNTech seek USFDA emergency use nod for Omicron adapted COVID booster dose for 12 years of age and older

Pfizer, BioNTech seek USFDA emergency use nod for Omicron adapted COVID booster dose for 12 years of age and older

Ruchika Sharma23 Aug 2022 11:32 AM IST
The bivalent vaccine contains mRNA encoding the original SARS-CoV-2 spike protein, which is present in the original Pfizer-BioNTech COVID-19 Vaccine,...
Cognota Healthcare secures USFDA nod for blood pressure monitor device

Cognota Healthcare secures USFDA nod for blood pressure monitor device

Ruchika Sharma22 Aug 2022 2:31 PM IST
Pune: Healthtech company Cognota Healthcare has announced that the United States Food and Drug Administration (US FDA) has approved the company's...
Novavax COVID vaccine Nuvaxovid gets provisional nod in New Zealand for adolescents aged 12 through 17

Novavax COVID vaccine Nuvaxovid gets provisional nod in New Zealand for adolescents aged 12 through 17

Ruchika Sharma22 Aug 2022 1:45 PM IST
Nuvaxovid (NVX-CoV2373) is a protein-based vaccine engineered from the genetic sequence of the first strain of SARS-CoV-2, the virus that causes...
Novavax COVID vaccine Adjuvanted gets USFDA emergency use authorization for adolescents aged 12 through 17

Novavax COVID vaccine Adjuvanted gets USFDA emergency use authorization for adolescents aged 12 through 17

Ruchika Sharma22 Aug 2022 12:15 PM IST
NVX-CoV2373 is a protein-based vaccine engineered from the genetic sequence of the first strain of SARS-CoV-2, the virus that causes COVID-19 disease.
Cipla, Glenmark and 1 other recall products in US over manufacturing issues

Cipla, Glenmark and 1 other recall products in US over manufacturing issues

Ruchika Sharma22 Aug 2022 11:23 AM IST
As per the USFDA, homegrown drug major Cipla is recalling 7,992 bottles of Difluprednate Ophthalmic Emulsion, used to treat swelling and pain after...
Moderna to supply 12 million doses of Omicron containing bivalent COVID booster vaccines to Govt of Canada

Moderna to supply 12 million doses of Omicron containing bivalent COVID booster vaccines to Govt of Canada

Ruchika Sharma22 Aug 2022 9:30 AM IST
Cambridge: Moderna, Inc., a biotechnology company pioneering messenger RNA (mRNA) therapeutics and vaccines, today announced that the Government...
Mifepristone manufacturer GenBioPro drops legal challenge to Mississippi ban

Mifepristone manufacturer GenBioPro drops legal challenge to Mississippi ban

Ruchika Sharma21 Aug 2022 5:45 PM IST
New Delhi: A manufacturer of mifepristone, a drug used in medication abortions, on Thursday dropped its legal fight to sell the drug in Mississippi...
Regenerons Inmazeb and Ridgeback Bios Ebanga recommended by WHO for Ebola

Regeneron's Inmazeb and Ridgeback Bio's Ebanga recommended by WHO for Ebola

Ruchika Sharma21 Aug 2022 3:30 PM IST
Geneva: The World Health Organization (WHO) has recommended two monoclonal antibody treatments against Ebola, saying the use of such drugs combined...
Bayer begins Phase I study with GIRK4 inhibitor for atrial fibrillation

Bayer Mirena gets USFDA nod for extended use as contraceptive

Ruchika Sharma21 Aug 2022 1:15 PM IST
LNG-IUS is one of the most effective birth control methods as it does not require user interventions such as daily dosing or monthly re-fills.
Test second Paxlovid course in patients with COVID rebound: USFDA asks Pfizer

Test second Paxlovid course in patients with COVID rebound: USFDA asks Pfizer

Ruchika Sharma21 Aug 2022 11:30 AM IST
Bengaluru: The U.S. Food and Drug Administration (USFDA) has asked Pfizer Inc to test the effects of an additional course of its antiviral Paxlovid...
PrevNext

Editorial

ROBUST Study Released: One of the Largest Beta-Blocker KAP Study Captures Place of Beta Blockers in Indian Real-World Practice

ROBUST Study Released: One of the Largest Beta-Blocker KAP Study Captures Place of Beta Blockers in...

Obesity-Prediabetes Duo: Why Clinicians Must Intervene Early?

Obesity-Prediabetes Duo: Why Clinicians Must Intervene Early?

SURPASS-2- Tirzepatide vs Semaglutide in Type 2 Diabetes

SURPASS-2- Tirzepatide vs Semaglutide in Type 2 Diabetes

Efficacy and Safety of Dapagliflozin-Vildagliptin in Indian T2DM Patients with CV Risk Factors

Efficacy and Safety of Dapagliflozin-Vildagliptin in Indian T2DM Patients with CV Risk Factors

SURPASS-2: Superior HbA1c and Weight Reduction With Tirzepatide vs. Semaglutide

SURPASS-2: Superior HbA1c and Weight Reduction With Tirzepatide vs. Semaglutide

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Journal Club Today

MRI Study Maps Brain Growth Across the Perinatal Period

MRI Study Maps Brain Growth Across the Perinatal Period

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Health News Today

Health Bulletin 07/February/2026

Health Bulletin 07/February/2026

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