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NCT05861986RecruitingPhase 4

A Study Evaluating the Effectiveness and Safety of Risdiplam Administered as an Early Intervention in Pediatric Participants With Spinal Muscular Atrophy After Gene Therapy

A Phase IV Open-Label Study Evaluating the Effectiveness and Safety of Risdiplam Administered as an Early Intervention in Pediatric Patients With Spinal Muscular Atrophy After Gene Therapy

Source: ClinicalTrials.gov · Last updated 30 Oct 2026

Brief summary (registry, in English)

This is an open-label, single-arm, multicenter clinical study to evaluate the effectiveness and safety of risdiplam administered as an early intervention in pediatric participants with spinal muscular atrophy (SMA) and 2 SMN2 copies who have previously received onasemnogene abeparvovec. Participants are children \< 2 years of age genetically diagnosed with SMA.

Status (registry)
Recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
28 (estimated)
First submitted
8 May 2023
Start date
May 2024
Primary completion date
Mar 2028
Lead sponsor
Hoffmann-La Roche
NCT number
NCT05861986
EU CT number
2023-504508-26-00

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 28
  • From May 2024 to the primary completion date, Mar 2028
  • 16 sites in 4 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous or current enrolment in investigational study prior to initiation of study treatment
  • Concomitant or previous administration of an SMN2-targeting antisense oligonucleotide
  • Concomitant or previous use of an anti-myostatin agent
  • Any major illness requiring hospitalization within 1 month before the screening examination or any febrile illness within 1 week prior to screening and up to first dose administration.

Lab values

  • Any unresolved standard-of-care laboratory abnormalities per the onasemnogene abeparvovec prescribing information

Other

  • Participants requiring invasive ventilation or tracheostomy
  • Participants requiring awake non-invasive ventilation or with awake hypoxemia (Arterial Oxygen Saturation \[SaO2\] \<95%) with or without ventilator support
  • Presence of feeding tube and an OrSAT score of 0
  • Hospitalization for pulmonary event within the last 2 months, or any planned hospitalization at the time of screening

Who the study is looking for

  • \<2 years of age at the time of informed consent
  • Confirmed diagnosis of 5q-autosomal recessive SMA, including genetic confirmation of homozygous deletion or compound heterozygosity predictive of loss of function of the Survival of Motor Neuron 1 (SMN1) gene
  • Confirmed presence of two SMN2 gene copies as documented through laboratory testing
  • Administration of onasemnogene abeparvovec pre-symptomatically or post-symptomatically
  • Has received onasemnogene abeparvovec for SMA no less than 13 weeks, but not more than months 30 weeks, prior to enrollment
  • If treated with risdiplam prior to onasemnogene abeparvovec, risdiplam treatment must not have exceeded 3 weeks and must be discontinued 1 day prior to onasemnogene abeparvovec administration
  • Has, in the opinion of the investigator, not experienced clinically significant decline in function from the time of onasemnogene abeparvovec administration

Age in the registry: 3 months to 24 months · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (16)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Charite Universitaetsmedizin Berlin KöR
Coordinator of this site? Confirm its status
BerlinGermanyRecruiting
Justus-Liebig-Universitaet Giessen
Coordinator of this site? Confirm its status
GiessenGermanyRecruiting
Great Ormond Street Hospital for Children
Coordinator of this site? Confirm its status
LondonUnited KingdomRecruiting
Uniwersyteckie Centrum Kliniczne
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GdanskPolandActive, not recruiting
Instytut Pomnik Centrum Zdrowia Dziecka
Coordinator of this site? Confirm its status
WarsawPolandActive, not recruiting
Children's Healthcare of Atlanta Center for Advanced Pediatrics
Coordinator of this site? Confirm its status
AtlantaUnited StatesRecruiting
Children's Hospital of Colorado
Coordinator of this site? Confirm its status
AuroraUnited StatesRecruiting
Ann and Robert H. Lurie Children Hospital of Chicago
Coordinator of this site? Confirm its status
ChicagoUnited StatesWithdrawn
The University of Texas Southwestern Medical Center at Dallas
Coordinator of this site? Confirm its status
DallasUnited StatesRecruiting
Cook Children's Jane and John Justin Neurosciences Center
Coordinator of this site? Confirm its status
Fort WorthUnited StatesRecruiting
University of Florida Pediatrics
Coordinator of this site? Confirm its status
GainesvilleUnited StatesRecruiting
Helen DeVos Children's Hospital at Spectrum Health
Coordinator of this site? Confirm its status
Grand RapidsUnited StatesWithdrawn
University of Arkansas for Medical Sciences
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Little RockUnited StatesRecruiting
Columbia University Medical Center
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New YorkUnited StatesWithdrawn
Children's Hospital of The King's Daughter
Coordinator of this site? Confirm its status
NorfolkUnited StatesWithdrawn
Children's Hospital of Philadelphia
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PhiladelphiaUnited StatesWithdrawn

This page is information, not medical advice. Discuss any trial with your doctor.