Cell therapies trial planned for COVID-19 – Mirage News

More than 200,000 people have died from COVID-19 since January 2020. While Australia has been relatively spared from the onslaught of infections and deaths, our nations scientists need to be part of the global effort to address this pandemic. Research Group Head, Amnion Cell Biology There is no effective treatment to address the ongoing damage caused by for severe COVID-19 infections, said Associate Professor Rebecca Lim, Research Group Head of Amnion Cell Biology at Hudson Institute.

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UAE stem cell therapy: Revolutionary treatment helps cure COVID-19 patients – Gulf News

Members of the research team at the Abu Dhabi Stem Cell Center, United Arab Emirates. Image Credit: WAM / Gulf News DUBAI: Adult stem cell therapy is dubbed as the new healing force of the 21st century, much as theinternet revolutionised the past century. Now, UAE researchers have demonstrated they're in the leading edge of this breakthrough in medicine.

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Athersys and University Hospitals Cleveland Medical Center Announce Activation of the First Clinical Site for the MACOVIA Study, a Pivotal Phase 2/3…

CLEVELAND--(BUSINESS WIRE)--Athersys, Inc. (NASDAQ: ATHX) and University Hospitals Cleveland Medical Center (UH Cleveland) announced today that UH Cleveland is now open as the first clinical site for the MACOVIA (MultiStem Administration for COVID-19 Induced Acute Respiratory Distress Syndrome) trial. On April 13, 2020, Athersys announced authorization from the U.S

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US Food and Drug Administration Approves DARZALEX FASPRO (daratumumab and hyaluronidase-fihj), a New Subcutaneous Formulation of Daratumumab in the…

DetailsCategory: AntibodiesPublished on Saturday, 02 May 2020 12:42Hits: 411 - Innovative, fixed-dose formulation significantly reduces treatment time from hours to minutes and demonstrates consistent efficacy with a reduction in administration-related reactions compared to DARZALEX (daratumumab) for approved indications - DARZALEX FASPRO is the only subcutaneous CD38-directed antibody approved in the treatment of multiple myeloma HORSHAM, PA, USA I May 1, 2020 I The Janssen Pharmaceutical Companies of Johnson & Johnson announced today the U.S. Food and Drug Administration (FDA) approved DARZALEX FASPRO (daratumumab and hyaluronidase-fihj), a new subcutaneous formulation of daratumumab. DARZALEX FASPRO is approved in four regimens across five indications in multiple myeloma patients, including newly diagnosed, transplant-ineligible patients as well as relapsed or refractory patients.As a fixed-dose formulation, DARZALEX FASPRO can be administered over approximately three to five minutes, significantly less time than DARZALEX,which is given intravenously over hours

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