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  • johnson and johnson...

Tag: johnson and johnson news

You Searched For "johnson and johnson news"
Caplin Steriles gets USFDA nod for Procainamide Hydrochloride Injection for treating abnormal heart rhythm

USFDA approves Carvykti for patients with Relapsed or Refractory Multiple Myeloma who have received at least one prior line of therapy

Ruchika Sharma7 April 2024 10:00 AM IST
Horsham: Johnson & Johnson has announced that the U.S. Food and Drug Administration (FDA) has approved CARVYKTI (ciltacabtagene...
Darzalex receives positive EMA Committee opinion for high-risk smouldering multiple myeloma: Janssen-Cilag International

USFDA grants Fast Track designation to JnJ nipocalimab to reduce fetal neonatal alloimmune thrombocytopenia risk in alloimmunized pregnant adults

Ruchika Sharma27 March 2024 12:30 PM IST
Spring House: Johnson & Johnson has announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation (FTD) for...
Darzalex receives positive EMA Committee opinion for high-risk smouldering multiple myeloma: Janssen-Cilag International

JnJ gets USFDA nod for Opsynvi for chronic treatment of adults with pulmonary arterial hypertension

Ruchika Sharma23 March 2024 12:23 PM IST
Raritan: Johnson & Johnson has announced that the U.S. Food and Drug Administration (FDA) has approved OPSYNVI - a single-tablet combination...
Darzalex receives positive EMA Committee opinion for high-risk smouldering multiple myeloma: Janssen-Cilag International

USFDA nod to Johnson and Johnson EDURANT PED for certain pediatric patients living with HIV-1

Ruchika Sharma20 March 2024 12:30 PM IST
Titusville: Johnson & Johnson has announced that the U.S. Food and Drug Administration (FDA) has approved EDURANT PED (rilpivirine) for the...
Darzalex receives positive EMA Committee opinion for high-risk smouldering multiple myeloma: Janssen-Cilag International

Johnson & Johnson seeks USFDA nod for Tremfya for ulcerative colitis treatment in adults

Ruchika Sharma12 March 2024 12:39 PM 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

Latest JnJ talc trial ends with hung jury

Ruchika Sharma8 March 2024 1:30 PM IST
New York: The latest trial over claims that Johnson & Johnson's talc products cause cancer ended in a mistrial on Tuesday, as a Florida state...
USFDA nod to JnJ for Rybrevant, Chemotherapy combo for lung cancer treatment

USFDA nod to JnJ for Rybrevant, Chemotherapy combo for lung cancer treatment

Anshika Mishra4 March 2024 5:09 PM IST
Johnson & Johnson has announced that following a priority review, the U.S. Food and Drug Administration (FDA) has approved RYBREVANT...
Health Bulletin 04/ March/ 2024

Health Bulletin 04/ March/ 2024

Anshika Mishra4 March 2024 4:44 PM IST
Here the top health news for the day :Lady hardinge medical college to introduce new DNB and FNB courses soon Bringing good news to the postgraduate...
Darzalex receives positive EMA Committee opinion for high-risk smouldering multiple myeloma: Janssen-Cilag International

Johnson and Johnson gets USFDA approval for Rybrevant, chemotherapy combo for lung cancer treatment

Ruchika Sharma2 March 2024 2:33 PM IST
Raritan: Johnson & Johnson has announced that following a priority review, the U.S. Food and Drug Administration (FDA) has approved RYBREVANT...
Darzalex receives positive EMA Committee opinion for high-risk smouldering multiple myeloma: Janssen-Cilag International

JnJ gets USFDA nod for Bi-weekly dose of blood cancer therapy Tecvayli

Ruchika Sharma21 Feb 2024 11:39 AM IST
United States: The U.S. Food and Drug Administration has approved a bi-weekly dose of Johnson & Johnson's blood cancer therapy Tecvayli, the...
Darzalex receives positive EMA Committee opinion for high-risk smouldering multiple myeloma: Janssen-Cilag International

USFDA grants Breakthrough Therapy Designation for JnJ Nipocalimab for individuals at high risk for severe hemolytic disease of fetus, newborn

Ruchika Sharma10 Feb 2024 12:06 PM IST
Spring House: Johnson & Johnson has announced that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Therapy Designation...
Imbruvica gets positive EMA Committee opinion for untreated mantle cell lymphoma eligible for Stem Cell Transplant: Janssen-Cilag International

JnJ Balversa gets full USFDA nod to treat locally advanced or metastatic Bladder Cancer with Select Genetic Alterations

Ruchika Sharma21 Jan 2024 4:30 PM IST
Raritan: Johnson & Johnson has announced that the U.S. Food and Drug Administration (FDA) has approved a supplemental New Drug Application...
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