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  • johnson and johnson...

Tag: johnson and johnson news

You Searched For "johnson and johnson news"
Imbruvica gets positive EMA Committee opinion for untreated mantle cell lymphoma eligible for Stem Cell Transplant: Janssen-Cilag International

JnJ to acquire Intra-Cellular Therapies for USD 14.6 billion

Ruchika Sharma15 Jan 2025 11:30 AM IST
New Brunswick: Johnson & Johnson and Intra-Cellular Therapies, Inc. have announced that they have entered into a definitive agreement under...
ORSL Stall at Pedicon Conference

Promotion of Sugary Drinks? ORSL Stall at Pedicon Conference Leads to Controversy

Barsha Misra14 Jan 2025 5:34 PM IST
Hyderabad: The recently held annual conference of the Indian Academy of Pediatrics (IAP) led to a controversy after the event included an...
USFDA nod to JnJ Tremfya for Crohns disease

JnJ Nipocalimab gets USFDA Priority Review designation for generalized myasthenia gravis

Ruchika Sharma12 Jan 2025 3:30 PM IST
Spring House: Johnson & Johnson has announced the nipocalimab Biologics License Application (BLA) has received Priority Review designation...
JnJ Tremfya gets USFDA approval for subcutaneous induction in adults with ulcerative colitis

JnJ temporarily pauses rollout of Varipulse heart device in US

Ruchika Sharma11 Jan 2025 5:35 PM IST
Johnson & Johnson has announced a temporarily pause in the rollout of its Varipulse heart device in the United States as it investigates four...
USFDA nod to JnJ Tremfya for Crohns disease

JnJ Posdinemab gets USFDA Fast Track Designation for treatment of Alzheimer's disease

Ruchika Sharma9 Jan 2025 1:30 PM IST
Posdinemab is an investigational monoclonal antibody that targets the mid-domain of Alzheimer's disease-specific phosphorylated tau.
JnJ seeks indication extension of Akeega from EMA for adults with metastatic hormone-sensitive prostate cancer, HRR gene alterations

JnJ enters licensing agreement for global development, manufacturing, commercialization of STAT6 program from Kaken Pharma

Ruchika Sharma27 Dec 2024 10:00 AM IST
New Brunswick: Johnson & Johnson has announced that it has entered into an exclusive licensing agreement for the global...
USFDA warns pharma cos to remove misleading ads

JnJ seeks USFDA approval for Simponi to treat pediatric ulcerative colitis

Ruchika Sharma19 Dec 2024 12:42 PM IST
Developed by Johnson & Johnson, SIMPONI is an anti-TNF biologic medicine that targets and blocks a protein called TNF-alpha.
JnJ seeks indication extension of Akeega from EMA for adults with metastatic hormone-sensitive prostate cancer, HRR gene alterations

JnJ seeks USFDA nod for Tremfya for treatment of plaque psoriasis, juvenile psoriatic arthritis in children

Ruchika Sharma3 Dec 2024 12:30 PM IST
Spring House: Johnson & Johnson has announced the submission of two supplemental Biologics License Applications (sBLAs) to the U.S. Food and...
Imbruvica gets positive EMA Committee opinion for untreated mantle cell lymphoma eligible for Stem Cell Transplant: Janssen-Cilag International

JnJ seeks USFDA approval for subcutaneous induction regimen of Tremfya in ulcerative colitis

Ruchika Sharma29 Nov 2024 11:30 AM IST
Spring House: Johnson & Johnson has announced the submission of a supplemental Biologics License Application (sBLA) to the U.S. Food and Drug...
Darzalex receives positive EMA Committee opinion for high-risk smouldering multiple myeloma: Janssen-Cilag International

JnJ MedTech gets IDE approval for OTTAVA Robotic Surgical System

Ruchika Sharma15 Nov 2024 5:05 PM IST
New Brunswick: Johnson & Johnson MedTech has announced that the U.S. Food & Drug Administration (USFDA) has approved the OTTAVA...
AbbVie seeks USFDA nod for combination regimen of Venclexta, Acalabrutinib

USFDA grants Breakthrough Therapy Designation to Nipocalimab for treatment of adults with moderate-to-severe Sjögren's disease: JnJ

Ruchika Sharma12 Nov 2024 1:00 PM IST
Spring House: Johnson & Johnson has announced that the U.S. Food and Drug Administration (FDA) has granted nipocalimab Breakthrough Therapy...
USFDA nod to JnJ Tremfya for Crohns disease

JnJ seeks approval from USFDA, EMA for DARZALEX FASPRO as subcutaneous monotherapy for high-risk smoldering multiple myeloma

Ruchika Sharma10 Nov 2024 4:15 PM IST
Raritan: Johnson & Johnson has announced the submission of regulatory applications to the U.S. Food and Drug Administration (FDA) and...
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