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7 June 2024 | By Catherine Eckford (European Pharmaceutical Review)
The FDA’s regulatory approval of the telomerase inhibitor is welcome, considering the high unmet need for many lower-risk myelodysplastic syndromes (LR-MDS) patients, according to Geron.
1 November 2022 | By Catherine Eckford (European Pharmaceutical Review)
Reblozyl, the first erythroid maturation agent showed increased haemoglobin in transfusion-dependant patients with myelodysplastic syndromes.
5 May 2020 | By Victoria Rees (European Pharmaceutical Review)
The EMA's human medicines committee has adopted a positive opinion for eight medicines, recommending their marketing authorisation.
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