risdiplam   Click here for help

GtoPdb Ligand ID: 11170

Synonyms: compound 1 [PMID: 30044619] | Evrysdi® | RG-7916 | RG7916 | RO-7034067 | RO7034067
Approved drug
risdiplam is an approved drug (FDA (2020), EMA (2021))
Compound class: Synthetic organic
Comment: Risdiplam is a first-in-class, orally bioavailable splicing modifier [3]. Like nusinersen, it is intended to improve the efficiency of SMN2 (HGNC ID 11118; Uniprot Q16637) gene transcription in patients with spinal muscular atrophy (SMA) [2].
2D Structure
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Physico-chemical Properties
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Hydrogen bond acceptors 5
Hydrogen bond donors 1
Rotatable bonds 2
Topological polar surface area 79.83
Molecular weight 401.2
XLogP 3.52
No. Lipinski's rules broken 0
SMILES / InChI / InChIKey
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Canonical SMILES Cc1cn2c(n1)c(C)cc(n2)c1cc(=O)n2c(n1)ccc(c2)N1CCNC2(C1)CC2
Isomeric SMILES Cc1cn2c(n1)c(C)cc(n2)c1cc(=O)n2c(n1)ccc(c2)N1CCNC2(C1)CC2
InChI InChI=1S/C22H23N7O/c1-14-9-18(26-29-11-15(2)24-21(14)29)17-10-20(30)28-12-16(3-4-19(28)25-17)27-8-7-23-22(13-27)5-6-22/h3-4,9-12,23H,5-8,13H2,1-2H3
InChI Key ASKZRYGFUPSJPN-UHFFFAOYSA-N
No information available.
Summary of Clinical Use Click here for help
The EMA granted risdiplam orphan drug designation for the treatment of SMA in 2019. Favourable efficacy and safety for risdiplam were established in the FIREFISH and SUNFISH trials. Risdiplam was FDA approved in August 2020, and EMA authorisation followed in early 2021. It is indicated for use in SMA patients ≥2 months of age.
Clinical Trials
Clinical Trial ID Title Type Source Comment References
NCT02913482 Investigate Safety, Tolerability, PK, PD and Efficacy of Risdiplam (RO7034067) in Infants With Type1 Spinal Muscular Atrophy Phase 2/Phase 3 Interventional Hoffmann-La Roche This is the FIREFISH trial.
NCT02908685 A Study to Investigate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Efficacy of Risdiplam (RO7034067) in Type 2 and 3 Spinal Muscular Atrophy (SMA) Participants Phase 2/Phase 3 Interventional Hoffmann-La Roche This is the SUNFISH trial.