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Latest Industry News - Page 201

Merck injectable version of blockbuster cancer therapy Keytruda gets USFDA approval

Alembic Pharma bags USFDA final nod for cancer injection Nelarabine

Ruchika Sharma2 Aug 2024 12:30 PM IST
Vadodara: Alembic Pharmaceuticals Limited today announced that the Company has received final approval from the US Food & Drug...
Darzalex receives positive EMA Committee opinion for high-risk smouldering multiple myeloma: Janssen-Cilag International

JnJ gets USFDA nod for Darzalex Faspro-based quadruplet regimen for newly diagnosed multiple myeloma who are transplant-eligible

Ruchika Sharma2 Aug 2024 11:30 AM IST
Horsham: Johnson & Johnson has announced that the U.S. Food and Drug Administration (FDA) has approved DARZALEX FASPRO (daratumumab and...
CDSCO Panel Approves GSKs Proposal to Double Indian Patient Pool in Dostarlimab Trial

US FDA expands Jemperli plus chemotherapy approval to all adult patients with primary advanced or recurrent endometrial cancer: GSK

Ruchika Sharma2 Aug 2024 10:00 AM IST
London: GSK plc has announced the US Food and Drug Administration (FDA) has approved Jemperli (dostarlimab) in combination with carboplatin and...
Sanofi gets USFDA fast track designation for neovascular age-related macular degeneration gene therapy

Sanofi gets CDSCO marketing nod for RSV treatment Beyfortus in India

Ruchika Sharma1 Aug 2024 5:30 PM IST
Drugmaker, Sanofi India, has received marketing authorisation approval from the Central Drugs Standard Control Organisation (CDSCO) for Beyfortus in...
Shilpa Medicare arm partners with Orion Corporation for Recombinant Human Albumin for European Market

Shilpa Pharma Lifesciences receives certificate of suitability from EDQM for Ursodeoxycholic Acid

Ruchika Sharma1 Aug 2024 2:26 PM IST
Karnataka: Shilpa Medicare Limited's 100 percent subsidiary, Shilpa Pharma Lifesciences Limited has received certificate of suitability (CEP)...
Natco Pharma Independent Director Dr MUR Naidu no more

Natco Pharma Independent Director Dr MUR Naidu no more

Ruchika Sharma1 Aug 2024 12:28 PM IST
Telangana: Natco Pharma has announced the sad demise of Dr M.U.R. Naidu, Independent Director of the Company on 30th July, 2024.Dr. M.U.R....
Insufficient Efficacy, Safety Data: CDSCO Panel Rejects Zydus Phase III CT Waiver Request for Voclosporin

Zydus Lifesciences gets Mexican marketing approval for Mamitra to treat various cancers \

Ruchika Sharma1 Aug 2024 11:46 AM IST
Ahmedabad: Zydus Lifesciences Limited has announced that the Mexican regulatory authority COFEPRIS (Federal Commission for the Protection...
Bayer Elinzanetant recommended for nod in EU for moderate to severe vasomotor symptoms

Bayer submits New Drug Application to USFDA for Elinzanetant for treatment of moderate to severe vasomotor symptoms associated with menopause

Ruchika Sharma1 Aug 2024 10:00 AM IST
Berlin: Bayer has announced that a New Drug Application (NDA) for the investigational compound elinzanetant has been submitted to the U.S. Food...
Novo Nordisk Gets CDSCO Panel Nod for Rybelsus Label Update, Aligned with EMA

CDSCO Panel Approves Novo Nordisk's Protocol Amendment proposal to study Somapacitan

Dr. Divya Colin31 July 2024 6:00 PM IST
New Delhi: The Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organization (CDSCO) has approved the drug major Novo...
Sanofi gets USFDA fast track designation for neovascular age-related macular degeneration gene therapy

Duchenne muscular dystrophy: Sanofi owned biotech company sues Sarepta Therapeutics over patent infringement

Ruchika Sharma31 July 2024 4:02 PM IST
Sanofi-owned biotech company Genzyme has initiated a lawsuit against competitor Sarepta Therapeutics in Delaware federal court, accusing the firm of...
Lupin bags USFDA approval for Multiple myeloma treatment

Lupin bags tentative USFDA nod for HIV-1 infection drugs

Ruchika Sharma31 July 2024 12:30 PM IST
Mumbai: Global pharma major Lupin Limited today announced that it has received tentative approval from the United States Food and Drug...
WHO unveils new guideline to improve global access to controlled medicines

Biological E gets WHO pre-qualification status for oral polio vaccine

Ruchika Sharma31 July 2024 11:38 AM IST
Hyderabad: In a stride towards eradicating polio worldwide, Biological E. Limited (BE), a Hyderabad-based vaccine and pharmaceutical company has...
PrevNext

Editorial

Evidence-Based Recommendation by Indian Pediatric Experts on the Use of Acid-Reducing Medications in Children

Evidence-Based Recommendation by Indian Pediatric Experts on the Use of Acid-Reducing Medications in...

Beta-Blockers After MI in Patients with LVEF Above 40%: Findings of BETAMI-DANBLOCK Trial Presented at ESC Congress 2025

Beta-Blockers After MI in Patients with LVEF Above 40%: Findings of BETAMI-DANBLOCK Trial Presented...

Beta-blockers Reduce Death, MI, Heart Failure 25% in Mildly Reduced LVEF:  Latest Meta-Analysis Presented at ESC Congress 2025

Beta-blockers Reduce Death, MI, Heart Failure 25% in Mildly Reduced LVEF: Latest Meta-Analysis...

From Potential to Global Impact: Strengthening India’s Research Ecosystem through Capacity Building - Dr Prashant Mishra

From Potential to Global Impact: Strengthening India’s Research Ecosystem through Capacity Building...

Exploring Buccal Prochlorperazine: A Targeted Review of Its Pharmacological Profile

Exploring Buccal Prochlorperazine: A Targeted Review of Its Pharmacological Profile

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Journal Club Today

Evidence-Based Recommendation by Indian Pediatric Experts on the Use of Acid-Reducing Medications in Children

Evidence-Based Recommendation by Indian Pediatric Experts on the Use of Acid-Reducing Medications in...

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Health Bulletin 20/September/2025

Health Bulletin 20/September/2025

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