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  • johnson and johnson

Tag: johnson and johnson

You Searched For "johnson and johnson"
JnJ Nipocalimab gets USFDA Fast Track designation for Sjogrens disease

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 Nipocalimab gets USFDA Fast Track designation for Sjogrens disease

European Commission approves Janssen-Cilag International Rybrevant, Lazcluze combo for first-line treatment of lung cancer

Ruchika Sharma31 Dec 2024 11:30 AM IST
Belgium: Janssen-Cilag International NV, a Johnson & Johnson company, has announced that the European Commission (EC) has approved a Type II...
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

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.
Biocon Biologics Yesafili gets Health Canada nod for eye diseases

Approval of Biocon Biologics Yesintek recommended by EMA Committee

Ruchika Sharma16 Dec 2024 11:30 AM IST
Bengaluru: Biocon Biologics Ltd, a fully integrated global biosimilars company and subsidiary of Biocon Ltd, has announced that the European...
JnJ seeks indication extension of Akeega from EMA for adults with metastatic hormone-sensitive prostate cancer, HRR gene alterations

Health Ministry Reconstitutes Expert Panel for J&J ASR Hip Implant Compensation

Farhat Nasim6 Dec 2024 4:06 PM IST
New Delhi: The Ministry of Health and Family Welfare has reconstituted its Central Expert Committee to address compensation issues concerning faulty...
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...
USFDA lifts Risk Evaluation and Mitigation Strategies for CAR T cell therapies

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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