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On Medicine - Insights and opinion on the latest medical research, clinical practices, and developments in the field

On Medicine In response to the COVID-19 pandemic, rapid sharing of information about planned clinical trials investigating treatments and vaccines was necessary. In this blog… Read more » Rachel Todd discusses the CO2 study registered at the ISRCTN registry. In the second part of a two-part blog for Clinical Trials Day 2021 we look back at a year of COVID-19 studies registered at the ISRCTN registry, focusing on vaccine… Read more »

Two Families Grapple with Rare Disease Diagnosis, Finding Treatments

By Dana Talesnik Isabella and Julia Flysjo, age 4, are part of a first-in-human gene therapy trial at the Clinical Center for their rare disease. Photo: Niclas Flysjo It’s agonizing for parents to watch their children suffer and not know how to help them. When parents learn their child has a rare disease, consumed with grief and fear, they try to navigate the confusing medical lingo for diseases that have limited resources and few, if any, effective treatments. Two families were among those who shared their rare disease journeys during NIH’s Rare Disease Day virtual event on Mar. 1. In both cases, their babies were born seemingly healthy. Then, around age 2, worrisome symptoms appeared that led these families to seek a medical evaluation.

Pharmaceutical Market Europe - April 2021

Pharmaceutical Market Europe - April 2021
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W Va Legislature: Senate Calendar and Committee Schedule for Friday, April 2, 2021

W Va Legislature: Senate Calendar and Committee Schedule for Friday, April 2, 2021
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