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  • johnson and johnson...

Tag: johnson and johnson news

You Searched For "johnson and johnson news"
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...
JnJ seeks USFDA approval for Icotrokinra for plaque psoriasis

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...
USFDA extends review period for Bayer Elinzanetant

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...
58 Unauthorised Clinical Trials Spark DCGI Ban on VS Hospital, Doctors, Pharma Giants Under Fire

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...
Darzalex receives positive EMA Committee opinion for high-risk smouldering multiple myeloma: Janssen-Cilag International

Johnson and Johnson gets European Commission nod for expanded use of HIV 1 therapy Edurant in younger pediatric patients

Ruchika Sharma1 Nov 2024 11:00 AM IST
Beerse: Johnson & Johnson has announced that the European Commission (EC) has approved EDURANT (rilpivirine) for the treatment of HIV-1 infection...
Sanofi to expand respiratory vaccines pipeline with acquisition of Vicebio

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...
Darzalex receives positive EMA Committee opinion for high-risk smouldering multiple myeloma: Janssen-Cilag International

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...
Darzalex receives positive EMA Committee opinion for high-risk smouldering multiple myeloma: Janssen-Cilag International

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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