FDA approves Geron’s RYTELO for MDS associated anaemia
The regulatory decision is grounded in the positive results from the IMerge Phase III clinical trial.
07 June 2024
07 June 2024
The regulatory decision is grounded in the positive results from the IMerge Phase III clinical trial.
Keeping high-qualified, experienced clinical trial staff on board plays a crucial role in bringing new drugs to market.
The acquisition follows a successful initial partnership between the two companies which began in July 2023.
An FDA advisory committee voted unanimously in favour of updating Covid-19 vaccines to target the JN.1 variant.
Anti-trust regulator AGCM alleges that the companies colluded to delay the Italian market launch of eye drug Byooviz.
Vanda's board will review Cycle's unsolicited proposal to determine the best course for the company and its shareholders.
Global investment company Temasek spearheaded the funding round.
Moderna is developing mRNA-3705 for methylmalonic acidemia (MMA), and Myrtelle is developing rAAV-Olig001 for Canavan disease (CD).
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