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New data from Japan shows early resolution of common Covid-19 symptoms - Vimarsana News

New data from Japan shows early resolution of common Covid-19 symptoms

Japanese pharmaceutical company Shionogi has announced the first peer-reviewed publication of its phase 3 study investigating ensitrelvir to treat patients with mild to moderate COVID-19 in Japan, South Korea and Vietnam.

Shionogi Announces New Phase 3 Data Showing Early Resolution of Many Common COVID-19 Symptoms in JAMA Network Open - Vimarsana News

Shionogi Announces New Phase 3 Data Showing Early Resolution of Many Common COVID-19 Symptoms in JAMA Network Open

Shionogi & Co., Ltd. (Head Office: Osaka, Japan; Chief Executive Officer: Isao Teshirogi, Ph.D.; hereafter "Shionogi") announced the first peer-reviewed publication of the Phase 3 portion of its pivotal, double-blind, randomized, placebo-controlled...

Funds needed for 17-month-old with rare genetic condition - Vimarsana News

Funds needed for 17-month-old with rare genetic condition

Singapore News - When their son started gagging and refusing his food at about eight months old, the first-time parents knew something was amiss. A month later, Baby Shamel was not able to sit up and showed no signs of being able to put weight on his legs. Soon after, he lost the... Read more at www.tnp.sg

Anonymous donor gives S$1.5 million to baby with rare disorder in S'pore for treatment - Vimarsana News

Anonymous donor gives S$1.5 million to baby with rare disorder in S'pore for treatment

The disorder may affect one's ability to swallow, suck, and breathe.

'Most expensive drug in the world': $3 million raised for infant in NUH with rare genetic disorder - Vimarsana News

'Most expensive drug in the world': $3 million raised for infant in NUH with rare genetic disorder

A five-month-old boy facing immobility or even death because of a rare genetic disorder may get a new lease of life after his parents successfully raised the $3 million needed for a drug to treat his condition. Baby Zayn - who was diagnosed with Type 1 spinal muscular atrophy (SMA) at about five weeks old - will be able to...