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Real-World Analysis Sheds Light on Safety and Efficacy of Teclistamab in R/R Multiple Myeloma

The T-cell redirecting bispecific antibody teclistamab-cqyv demonstrated efficacy and a tolerable safety profile in a real-world population of patients with relapsed/refractory multiple myeloma consistent with that of those enrolled in the phase 2 MajesTEC-1 trial.

Ohio
United-states
Danai-dima
Taussig-cancer-center
Department-of-hematology
Janssen-pharmaceutical-companies-of-johnson
Cleveland-clinic
Hispanic-black
Janssen-pharmaceutical-companies
Teclistamab
Majestec-1-trial
Multiple-myeloma

Nasal Spray Shows Promise in Major Depression Treatment

A recent study demonstrated that esketamine nasal spray, used in conjunction with standard antidepressants, could significantly improve outcomes in patients with treatment-resistant depression.

Frankfurt
Brandenburg
Germany
Fraunhofer-institute-for-translational-medicine
Janssen-pharmaceutical-companies-of-johnson
University-hospital-frankfurt
Janssen-pharmaceutical-companies
University-hospital
New-england-journal
Fraunhofer-institute
Translational-medicine

HIV vaccine trial in Africa ends after data shows it wouldn't work

An experimental HIV vaccine trial that took place in Uganda, Tanzania and South Africa was halted after preliminary data suggested it wasn't effective.

Uganda
South-africa
Tanzania
Eugene-ruzagira
Pontiano-kaleebu
London-school-of-hygiene
Uganda-virus-research-institute
Johnson
Janssen-pharmaceutical-companies
Reuters
London-school
Tropical-medicine

Johnson & Johnson Vs. Pfizer: Better Pharma Stock? (NYSE:JNJ)

Johnson & Johnson Vs. Pfizer: Better Pharma Stock? (NYSE:JNJ)
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United-kingdom
Eli-lilly
Eli-lilly-mounjaro
Becton-dickinson-lutonix
Albert-bourla
Momenta-pharmaceuticals
Jp-morgan
Cancer-research-united-kingdom
Company-data
Product-development
Mckesson
Product-development-comparison

Janssen submits application to EMA for amivantamab-based lung cancer regimen in new indication

Today, the Janssen Pharmaceutical Companies of Johnson & Johnson announced the submission of a type II extension of indication application to the European Medicines Agency (EMA) seeking approval of RYBREVANT®▼ (amivantamab) in combination with chemotherapy for the treatment of adult patients with advanced no.

European-medicines-agency
Janssen-pharmaceutical-companies-of-johnson
Janssen-pharmaceutical-companies
Late-breaking-presidential-symposium

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