Risdiplam

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Risdiplam
Risdiplam.svg
Clinical data
Trade namesEvrysdi
Other namesRG7916; RO7034067
AHFS/Drugs.comMonograph
License data
Routes of
administration		By mouth
ATC code
Legal status
Legal status
Identifiers
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
Chemical and physical data
FormulaC22H23N7O
Molar mass401.474 g·mol−1
3D model (JSmol)

Risdiplam, sold under the brand name Evrysdi, is a medication used to treat spinal muscular atrophy (SMA)[2][3] and the first oral medication approved to treat this disease.[2][3]

Risdiplam is a survival of motor neuron 2-directed RNA splicing modifier.[2][1][4]

In clinical trials, the most common adverse events included fever, diarrhea, rash, ulcers of the mouth area, joint pain (arthralgia) and urinary tract infections.[2][1] Additional adverse events observed in the infantile-onset population included upper respiratory tract infection, pneumonia, constipation and vomiting.[2][1]

Risdiplam was approved by the US Food and Drug Administration (FDA) in August 2020, for the treatment of adults and children two months of age or older.[2][5] Developed in association with PTC Therapeutics and the ,[3][5] it is marketed in the US by Genentech,[2] a subsidiary of Roche.[5]

Medical uses[]

In the United States, risdiplam is indicated to treat people two months of age and older with spinal muscular atrophy.[2][1]

Adverse effects[]

In two clinical trials, the following adverse events occurred at least 5% more frequently in patients treated with risdiplam than in the placebo group: fever, diarrhoea, rash, ulcers of the mouth area, joint pain (arthralgia) and urinary tract infections.[2][1] Additional adverse events for the infantile-onset population included upper respiratory tract infection, pneumonia, constipation and vomiting.[2][1]

Risdiplam should not be taken together with medications that are multidrug and toxin extrusion (MATE) substrates because risdiplam may increase plasma concentrations of these drugs.[2][1]

Pharmacology[]

Mechanism of action[]

Risdiplam addresses the underlying cause of SMA: a reduced amount of survival motor neuron (SMN) protein. The protein is encoded by the SMN1 and SMN2 genes. SMA is caused by mutations in SMN1 that code for inactive forms of the protein. The activity of the SMN2 gene, which produces much smaller quantities of SMN, tends to determine the severity of disease.[3][6]

The compound is a pyridazine derivative that modifies the splicing of SMN2 messenger RNA to include exon 7,[7][4][8] resulting in an increase in the concentration of the functional SMN protein in vivo.[9]

Nusinersen, the first drug approved to treat SMA, an anti-sense oligonucleotide targetting intronic splicing silencer N1 (ISS-N1), also alters mRNA splicing of SMN2.[10]

Efficacy[]

The safety and efficacy of risdiplam in infantile-onset and later-onset SMA has been evaluated in ongoing clinical trials.[3][11] [12]

In the infantile-onset SMA study, an open-label trial with 41 participants, efficacy was established based on the ability to sit without support for at least five seconds. After 12 months of treatment, 29% of participants were able to sit independently for more than five seconds. After 23 or more months of treatment, 81% of participants were alive without permanent ventilation. Although the study did not perform direct comparisons against children receiving a placebo (inactive treatment), these results compare favourably with the typical course of the untreated disease.[11][2]

The study of later-onset SMA was a randomised controlled trial that enrolled 180 participants, aged between 2 and 25 years, with less severe forms of the disease. Participants treated with risdiplam for 12 months showed improvements in motor function compared to participants given a placebo.[12][2][3]

An open-label phase II-III study enrolled 21 infants age 1 month to 7 months and concluded its dose-determination and safety initial phase in 2021. Retinotoxicity, a side effect seen in animal models, was not observed in the study population. It also showed an increase in blood levels of functional SMN protein.[8]

Society and culture[]

Legal status[]

The US Food and Drug Administration (FDA) awarded marketing approval to Genentech on August 7, 2020. The FDA earlier granted the application for risdiplam fast track, priority review, and orphan drug designations.[2][3][5] Genentech was also awarded a rare pediatric disease priority review voucher.[2]

The European Medicines Agency (EMA) awarded risdiplam a priority medicine designation in 2018[5][13][14] and an orphan drug designation in 2019.[5][15]

As of August 2020, Roche has applied for marketing authorisation in Brazil, Chile, China, the European Union, Indonesia, Russia, South Korea and Taiwan.[5][16]

Names[]

Risdiplam is the International nonproprietary name (INN).[17]

Compassionate use[]

Since late 2019, Roche has been offering the drug globally for free for eligible people through an expanded access program.[18]

References[]

  1. ^ Jump up to: a b c d e f g h Food and Drugs Administration (FDA) (18 August 2020). "Evrysdi- risdiplam powder, for solution". DailyMed. Bethesda, Maryland, United States: MedLine by the National Library of Medicine (NLM) of the United States National Institutes of Health (NIH). Retrieved 24 September 2020.
  2. ^ Jump up to: a b c d e f g h i j k l m n o p O'Keefe, Lindsey (7 August 2020). "FDA Approves Oral Treatment for Spinal Muscular Atrophy" (Press release). Silver Spring, Maryland, United States of America: United States Food and Drug Administration (FDA). FDA Newsroom Department. Archived from the original on 11 August 2020. Retrieved 7 August 2020. Public Domain This article incorporates text from this source, which is in the public domain.
  3. ^ Jump up to: a b c d e f g Food and Drugs Administration (FDA) (7 August 2020). "Evrysdi (Risdiplam) for Spinal Muscular Atrophy". SMA News Today. Pensacola, Florida, United States: BioNews Services (BioNews Services, LLC.). Archived from the original on 21 January 2021. Retrieved 9 June 2021.
  4. ^ Jump up to: a b Zhao X, Feng Z, Ling KK, Mollin A, Sheedy J, Yeh S, et al. (May 2016). "Pharmacokinetics, pharmacodynamics, and efficacy of a small-molecule SMN2 splicing modifier in mouse models of spinal muscular atrophy". Human Molecular Genetics. Oxford, United Kingdom of Great Britain: Oxford University Press (OUP). 25 (10): 1885–1899. doi:10.1093/hmg/ddw062. PMC 5062580. PMID 26931466.
  5. ^ Jump up to: a b c d e f g "FDA Approves Genentech's Evrysdi (risdiplam) for Treatment of Spinal Muscular Atrophy (SMA) in Adults and Children 2 Months and Older". Genentech (Press release). San Francisco, California, United States of America: Genentech, Inc. (Roche Group). Genentech Global Product Development Division. 7 August 2020. Archived from the original on 18 August 2020. Retrieved 7 August 2020.
  6. ^ Ramdas S, Servais L (February 2020). Grech D, Mikhailidis D, Abdollahi M (eds.). "New treatments in spinal muscular atrophy: an overview of currently available data". Expert Opinion on Pharmacotherapy. London, England, United Kingdom of Great Britain: Taylor & Francis (Informa UK Ltd). 21 (3): 307–315. doi:10.1080/14656566.2019.1704732. OCLC 57378019. PMID 31973611. S2CID 210880199.
  7. ^ "RG7916". Pensacola, Florida, United States: BioNews Services (BioNews Services, LLC.). 8 November 2016. Archived from the original on 24 April 2020. Retrieved 9 June 2021.
  8. ^ Jump up to: a b Baranello G, Darras BT, Day JW, Deconinck N, Klein A, Masson R, et al. (March 2021). "Risdiplam in Type 1 Spinal Muscular Atrophy". The New England Journal of Medicine. Boston, Massachusetts, United States of America: NEJM Group (Massachusetts Medical Society). 384 (10): 915–923. doi:10.1056/NEJMoa2009965. ISSN 0028-4793. LCCN 20020456. OCLC 231027780. PMID 33626251.
  9. ^ Ratni H, Ebeling M, Baird J, Bendels S, Bylund J, Chen KS, et al. (August 2018). "Discovery of Risdiplam, a Selective Survival of Motor Neuron-2 ( SMN2) Gene Splicing Modifier for the Treatment of Spinal Muscular Atrophy (SMA)". Journal of Medicinal Chemistry. Washington, D.C. 61 (15): 6501–6517. doi:10.1021/acs.jmedchem.8b00741. ISSN 0022-2623. LCCN a63000643. OCLC 39480771. PMID 30044619.
  10. ^ Zanetta C, Nizzardo M, Simone C, Monguzzi E, Bresolin N, Comi GP, Corti S (January 2014). "Molecular therapeutic strategies for spinal muscular atrophies: current and future clinical trials". Clinical Therapeutics. Philadelphia, Pennsylvania, United States of America: Elsevier. 36 (1): 128–40. doi:10.1016/j.clinthera.2013.11.006. PMID 24360800.
  11. ^ Jump up to: a b Baranello, G.; Servais, L.; Day, J.; Deconinck, N.; Mercuri, E.; Klein, A.; et al. (1 October 2019). "P.353FIREFISH Part 1: 16-month safety and exploratory outcomes of risdiplam (RG7916) treatment in infants with type 1 spinal muscular atrophy". Neuromuscular Disorders. London, United Kingdom of Great Britain: World Muscle Society (WMS)/Elsevier Inc. 29 (Supplement 1): S184. doi:10.1016/j.nmd.2019.06.515. ISSN 0960-8966. OCLC 24318845.
  12. ^ Jump up to: a b Mercuri, Eugenio; Baranello, Giovanni; Kirschner, Janbernd; Servais, Laurent; Goemans, Nathalie; Pera, Maria Carmela; et al. (16 April 2019). "Update from SUNFISH Part 1: Safety, Tolerability and PK/PD from the Dose-Finding Study, Including Exploratory Efficacy Data in Patients with Type 2 or 3 Spinal Muscular Atrophy (SMA) Treated with Risdiplam (RG7916) (S25.007)". Neurology. Minneapolis, Minnesota, United States of America: American Academy of Neurology/Wolters Kluwer. 92 (15 (Supplement)). ISSN 0028-3878. LCCN 55043902. OCLC 960771045. Retrieved 9 June 2021.
  13. ^ Inacio, Patricia (21 December 2018). "Risdiplam Granted EMA's PRIME Designation for Potential in Spinal Muscular Atrophy". SMA News Today. Pensacola, Florida, United States: BioNews Services (BioNews Services, LLC.). Archived from the original on 26 January 2021. Retrieved 9 June 2021.
  14. ^ Roche Group Media Relations Division (17 December 2018). "PRIME designation granted by European Medicines Agency for Roche's risdiplam for treatment of spinal muscular atrophy (SMA)" (Press release). Basel, Switzerland: F. Hoffmann-La Roche Ltd. Group Communications Department (Roche Group Media Relations Division). pp. 1–5. Archived from the original (PDF) on 18 August 2018. Retrieved 9 June 2021.
  15. ^ Stoyanova-Beninska, Violeta (Committee Chair); Schwarzer-Daum, Brigitte (Committee Vice Chair) (26 February 2019). Public summary of opinion on orphan designation: Risdiplam for the treatment of spinal muscular atrophy (PDF). EMA Committee for Orphan Medicinal Products (COMP) (Report). Amsterdam, The Netherlands: European Medicines Agency (EMA Committee for Orphan Medicinal Products). pp. 1–4. Archived (PDF) from the original on 6 May 2020.
  16. ^ PTC Therapeutics (17 August 2020). "PTC Announces the Acceptance of the European Marketing Authorization Application for Evrysdi™ (risdiplam) for the Treatment of Spinal Muscular Atrophy" (Press release). Albuquerque, New Mexico, United States of America: PR Newswire. PTC Therapeutics. Archived from the original on 18 August 2020. Retrieved 9 June 2021.
  17. ^ World Health Organization (2018). "International nonproprietary names for pharmaceutical substances (INN): recommended INN: list 80". WHO Drug Information. 32 (3): 482. hdl:10665/330907.
  18. ^ Petridis F (13 January 2020). "Roche announces global compassionate use programme for Risdiplam" (Press release). Stratford-upon-Avon, England, United Kingdom of Great Britain: Spinal Muscular Atrophy UK ltd. Roche Global SMA Team (F. Hoffmann-La Roche Ltd). Retrieved 9 June 2021.

Further reading[]

External links[]

  • "Risdiplam". Drug Information Portal. U.S. National Library of Medicine.
  • Clinical trial number NCT02913482 for "Investigate Safety, Tolerability, PK, PD and Efficacy of Risdiplam (RO7034067) in Infants With Type1 Spinal Muscular Atrophy (FIREFISH)" at ClinicalTrials.gov
  • Clinical trial number NCT02908685 for "A Study to Investigate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Efficacy of Risdiplam (RO7034067) in Type 2 and 3 Spinal Muscular Atrophy (SMA) Participants (SUNFISH)" at ClinicalTrials.gov
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