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Oak Hill Bio and Chiesi Group Announce First Patient Enrolled in the Resumed Phase 2b Clinical Study Evaluating OHB-607 for the Prevention of Bronchopulmonary Dysplasia, the Most Common Cause of Chronic Lung Disease in Premature Infants

Published: May 18, 2024

Design of the multi-center study is based on Phase 2a clinical data, which showed a decrease in the occurrence of severe bronchopulmonary dysplasia (BPD), a condition for which there are

Source: tigersroar.com

Enzyme replacement therapy approved for Fabry disease

Published: May 8, 2023

The European Commission (EC) has given approval to the first PEGylated enzyme replacement therapy to treat Fabry disease.

Source: europeanpharmaceuticalreview.com

Chiesi Global Rare Diseases and Protalix BioTherapeutics Announce European Commission Authorization of PRX-102 (pegunigalsidase alfa) for the Treatment of Fabry Disease

Published: May 5, 2023

/PRNewswire/ -- Chiesi Global Rare Diseases, a business unit of the Chiesi Group established to deliver innovative therapies and solutions for people affected...

Source: prnewswire.com