MTPA announces long-term findings from post-marketing safety study of Radicava
Analysis of Post-Marketing Safety Data Shows Consistent Findings with Safety Profile Reported in Clinical Trials of Edaravone
Analysis of Post-Marketing Safety Data Shows Consistent Findings with Safety Profile Reported in Clinical Trials of Edaravone
Radicava ORS was approved by the U.S. Food and Drug Administration (FDA) on May 12, 2022
CB03 is a candidate drug for the treatment of refractory epilepsy, independently developed by Zhimeng
CLNK is a biotechnology research and development company that utilizes umbilical cord blood as the raw material to develop innovative, allogeneic, off-the-shelf, cell based therapeutic products
Around 85% of ALS patients suffer from a progressive loss of bulbar functionality
he financing was significantly oversubscribed with high demand from both existing and new investors.
AMX0035 is an investigational therapy for the treatment of amyotrophic lateral sclerosis (ALS).
Nearly 6,000 patients have been treated with the drug since 2017
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