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Workforce Development Team Aids in COVID-19 Vaccine Trials

Rutgers University Rutgers has been instrumental in getting the coronavirus vaccines to the public – most recently leading one of the largest phase 3 clinical trials sites in the world for the newly approved Johnson & Johnson vaccine, which is expected to play a pivotal role in stemming the pandemic. Behind the university’s crucial efforts at New Jersey Medical School and Robert Wood Johnson Medical school is a Rutgers-led collaborative established two years ago to create clinical trial innovations that can speed the translation of research discoveries into improved patient care. “Who could have imagined this would be needed so quickly?” said Barbara Tafuto, instructor in the health informatics department at the Rutgers University School of Health Professions and member of workforce development for the NJ Alliance for Clinical and Translational Science’s $29 million grant program known as NJACTS.

Rutgers universityNew jerseyUnited statesPrinceton universityNew jersey institute of technologyRobert wood johnsonDoreen lechnerLauren aleksunesLauren castelliBarbara gladsonReynolda panettieri jrNj alliance for clinicalHealth scienceJersey institute of technologyRutgers institute for translational medicineErnest mario school of pharmacy

We give medicine to more than two hundred countries, our two cities are called Vaccine City | दो सौ से ज्यादा देशों को हम मेडिसिन देते हैं, हमारे दो शहर कहलाते हैं वैक्सीन सिटी

We give medicine to more than two hundred countries, our two cities are called Vaccine City | दो सौ से ज्यादा देशों को हम मेडिसिन देते हैं, हमारे दो शहर कहलाते हैं वैक्सीन सिटी
bhaskar.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from bhaskar.com Daily Mail and Mail on Sunday newspapers.

Andhra pradeshManufacturing associationLife sciencesIt life sciencesInternational marketClinical research managementCompanies coronaCity newNational president maheshPharmaceutical industryIndustry indiaIndia bhutanIndian marketIndian pharmaceuticalGlobal pharmaIndia world

Lupus Research Alliance Hails Approval of Aurinia s Lupkynis(TM) (voclosporin)

Lupus Research Alliance Hails Approval of Aurinia s Lupkynis(TM) (voclosporin) First Oral Treatment for Lupus Nephritis; Second Lupus Treatment to Receive FDA Approval in Past Month News provided by Share this article Share this article NEW YORK, Jan. 22, 2021 /PRNewswire/ The Lupus Research Alliance (LRA) is excited to share that the U.S. Food and Drug Administration (FDA) approved the use of Aurinia Pharmaceuticals Lupkynis TM (voclosporin) as the first oral treatment developed specifically for adults with active lupus nephritis (LN) in combination with standard of care. Voclosporin follows the recent approval of belimumab by the FDA as new therapies indicated for lupus nephritis – both within the past month.

United statesBrad rovinKennethm farberLupus research alliance board of directorsNational institute of diabetesLupus research allianceAurinia pharmaceuticals incOhio state universityDrug administrationDivision of nephrologyClinical research managementNational institutes of health accelerating medicines partnershipNational kidney foundationAurinia pharmaceuticalsWexner medical centerAurinia pharmaceutical

Coronavirus Vaccine India Update; Bharat Biotech COVAXIN | Ground Report From Hyderabad Genome Valley | 15 हजार वैज्ञानिक, 200 कंपनियां, सालभर में बनते हैं वैक्सीन के 6 अरब डोज

Coronavirus Vaccine India Update; Bharat Biotech COVAXIN | Ground Report From Hyderabad Genome Valley | 15 हजार वैज्ञानिक, 200 कंपनियां, सालभर में बनते हैं वैक्सीन के 6 अरब डोज
bhaskar.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from bhaskar.com Daily Mail and Mail on Sunday newspapers.

Andhra pradeshNarendra modiLife sciencesIt life sciencesRhea developmentClinical research managementCompanies coronaIndia biotech the companya factoryGround reportIndia biotechGuest houseValley cityEmployee foodRegulatory endValley asiaஆந்திரா பிரதேஷ்

FDA approves GSK s BENLYSTA as the first medicine for adult patients with active lupus nephritis in the US

FDA approves GSK s BENLYSTA as the first medicine for adult patients with active lupus nephritis in the US Approval builds on nearly 10 years of experience in lupus News provided by Share this article Share this article LONDON, Dec. 17, 2020 /PRNewswire/ GlaxoSmithKline plc (LSE/NYSE: GSK) announced the US Food and Drug Administration (FDA) has approved BENLYSTA (belimumab) for the treatment of adult patients with active lupus nephritis (LN) who are receiving standard therapy. Lupus nephritis is a serious inflammation of the kidneys caused by systemic lupus erythematosus (SLE), the most common form of lupus, which can lead to end-stage kidney disease, requiring dialysis or a kidney transplant. The approval extends the current indication in the US to include both SLE and LN for both the intravenous and subcutaneous formulations.

United kingdomUnited statesCity ofUnited kingdom generalBrad rovinSarah elton farrKathleen quinnJeff mclaughlinSimon steelSonya ghobrialRichard furieTim foleyJames dodwellHal barronKristen neeseDivision of rheumatology