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Moderna Starts New COVID-19 Vaccine Trial

Moderna Starts New COVID-19 Vaccine Trial by Angela Mohan on  March 17, 2021 at 2:17 PM First participants have been dosed in the Phase 1 study of mRNA-1283, Moderna s next generation COVID-19 vaccine candidate, which will assess the safety and immunogenicity of mRNA-1283. We are pleased to begin this Phase 1 study of our next generation COVID-19 vaccine candidate, mRNA-1283, said Stéphane Bancel, Chief Executive Officer of Moderna. Our investments in our mRNA platform have enabled us to develop this next generation vaccine candidate, which is a potential refrigerator-stable vaccine that could facilitate easier distribution and administration in a wider range of settings, including potentially for developing countries, Bancel added.

Chiasma to Present New Data from Two Phase 3 Trials, CHIASMA OPTIMAL and MPOWERED™, at ENDO 2021

One oral presentation and five late-breaking posters accepted NEEDHAM, Mass., March 10, 2021 (GLOBE NEWSWIRE) Chiasma, Inc. (NASDAQ: CHMA), (“Chiasma” or the “Company”), a commercial-stage biopharmaceutical company utilizing its delivery platform technology to develop and commercialize oral therapies to improve the lives of patients with rare diseases currently treated with burdensome and painful injections, as evidenced by its recent approval of MYCAPSSA as the first and only oral therapy for the treatment of acromegaly, today announced that it will be presenting data from two Phase 3 clinical trials: the open-label extension of the CHIASMA OPTIMAL study and the MPOWERED™ study, at the Endocrine Society’s annual meeting, ENDO 2021. The conference will be held virtually from March 20-23, 2021. Chiasma is proud to be a platinum sponsor of the conference and will have a virtual booth available where registrants can find more information. Th

Process Begins for COVID-19 Vaccine s Emergency Use

Process Begins for COVID-19 Vaccine s Emergency Use by Angela Mohan on  February 22, 2021 at 11:13 AM Dr. Reddy s has started the process with the Drugs Controller General of India (DCGI) for Emergency Use Authorization (EUA) of Russian vaccine candidate, Sputnik V. As part of the review process, Dr Reddy s will present the safety profile of the Phase 2 study, and interim data of the Phase 3 study, which is expected to complete by February 21. Sputnik V, developed by the Gamaleya National Research Institute of Epidemiology and Microbiology, is one of only three vaccines in the world with an efficacy of 91.6 per cent and has most authorizations granted with 26 countries globally.

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