Estimation of FMO3 Ontogeny by Mechanistic Population Pharmacokinetic Modelling of Risdiplam and Its Impact on Drug–Drug Interactions in Children

Author:

Cleary YumiORCID,Kletzl Heidemarie,Grimsey Paul,Heinig Katja,Ogungbenro KayodeORCID,Silber Baumann Hanna Elisabeth,Frey Nicolas,Aarons LeonORCID,Galetin Aleksandra,Gertz Michael

Funder

F. Hoffmann-La Roche

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pharmacology

Reference41 articles.

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2. D’Amico A, et al. Spinal muscular atrophy. Orphanet J Rare Dis. 2011;6:71.

3. Ratni H, et al. Discovery of risdiplam, a selective survival of motor neuron-2 ( SMN2) gene splicing modifier for the treatment of spinal muscular atrophy (SMA). J Med Chem. 2018;61(15):6501–17.

4. European Medicines Agency. Evrysdi (risdiplam). 2021. https://www.ema.europa.eu/en/documents/smop-initial/chmp-summary-positive-opinion-evrysdi_en.pdf. Accessed Feb 2022.

5. US FDA. FDA Approves Oral Treatment for Spinal Muscular Atrophy. 2020. https://www.fda.gov/news-events/press-announcements/fda-approves-oral-treatment-spinal-muscular-atrophy. Accessed Nov 2022.

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