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  • johnson and johnson

Tag: johnson and johnson

You Searched For "johnson and johnson"
GSK Nucala wins USFDA OK for use in adults with COPD

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 commercial partner launches psoriatic arthritis injection in Japan

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 Imaavy gets USFDA okay for generalized myasthenia gravis

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 Imaavy gets USFDA okay for generalized myasthenia gravis

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...
JnJ to resume US VARIPULSE cases

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...
Icotrokinra results show significant skin clearance in patients with difficult to treat scalp, genital psoriasis: JnJ

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...
Alembic Pharma gets USFDA EIR for Panelav facility

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...
First subjects dosed in Phase-1 clinical trial of Cognitive Disorder drug

Shockwave Medical concludes enrollment in all-female coronary IVL study

Ruchika Sharma2 Nov 2024 2:16 PM IST
Santa Clara: Shockwave Medical, Inc., part of Johnson & Johnson MedTech has announced the completion of enrollment in EMPOWER CAD, the first...
Alkem Labs completes acquisition of 100% stake in Adroit Biomed

JnJ completes acquisition of V Wave

Ruchika Sharma10 Oct 2024 12:34 PM IST
New Brunswick: Johnson & Johnson has announced that it has successfully completed the acquisition of V-Wave Ltd., a privately-held company...
Icotrokinra results show significant skin clearance in patients with difficult to treat scalp, genital psoriasis: JnJ

JnJ to discontinue Phase 2 Field Study evaluating investigational antiviral for Dengue prevention

Ruchika Sharma8 Oct 2024 4:50 PM IST
Raritan: Johnson & Johnson has announced it is discontinuing the Phase 2 field study (NCT05201794) evaluating the efficacy of investigational...
Icotrokinra results show significant skin clearance in patients with difficult to treat scalp, genital psoriasis: JnJ

JnJ seeks USFDA nod for Darzalex Faspro-based quadruplet regimen for newly diagnosed multiple myeloma patients for whom transplant is not planned

Ruchika Sharma6 Oct 2024 10:30 AM IST
Raritan: Johnson & Johnson has announced the submission of a supplemental Biologics License Application (sBLA) to the U.S. Food and Drug...
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