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NCT05861999Active, not recruitingPhase 4

A Study Evaluating the Effectiveness and Safety of Risdiplam Administered in Pediatric Patients With Spinal Muscular Atrophy Who Experienced a Plateau or Decline in Function After Gene Therapy

A Phase IV Open-Label Study Evaluating the Effectiveness and Safety of Risdiplam Administered in Pediatric Patients With Spinal Muscular Atrophy Who Experienced a Plateau or Decline in Function After Gene Therapy

Source: ClinicalTrials.gov · Last updated 22 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 in pediatric participants with SMA and 2 SMN2 copies who previously received onasemnogene abeparvovec and experience a plateau or decline in function. Participants to be enrolled are children \<2 years of age genetically diagnosed with SMA.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
19 (actual)
First submitted
8 May 2023
Start date
14 Aug 2024
Primary completion date
31 Mar 2028
Lead sponsor
Hoffmann-La Roche
NCT number
NCT05861999
EU CT number
2023-505161-81-00

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 19
  • From 14 Aug 2024 to the primary completion date, 31 Mar 2028
  • 17 sites in 6 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
  • 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 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.
  • In the opinion of the investigator, has demonstrated a plateau or decline in function post-gene therapy (with a duration of 26 weeks or less) documented by 2 individual time points in the functions as follows: swallowing AND one additional function/ability (respiratory, motor function, other) per appropriate expectation.

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

Full criteria on ClinicalTrials.gov

Sites (17)

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
BerlinGermanyActive, not recruiting
Justus-Liebig-Universitaet Giessen
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GiessenGermanyActive, not recruiting
Great Ormond Street Hospital for Children
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LondonUnited KingdomUnknown status
Soroka Medical Center
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BeershebaIsraelUnknown status
Schneider Children's Medical Center of Israel
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Petah TikvaIsraelUnknown status
Sourasky MC, Dana-Dwek Children's Hospital
Coordinator of this site? Confirm its status
Tel AvivIsraelUnknown status
Uniwersyteckie Centrum Kliniczne
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GdanskPolandActive, not recruiting
Instytut Pomnik Centrum Zdrowia Dziecka
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WarsawPolandActive, not recruiting
Sidra Medicine
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Al RayyanQatarUnknown status
Children's Healthcare of Atlanta Center for Advanced Pediatrics
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AtlantaUnited StatesUnknown status
Children's Hospital of Colorado
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AuroraUnited StatesUnknown status
University of Texas Southwestern Medical Center
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DallasUnited StatesUnknown status
University of Florida Pediatrics
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GainesvilleUnited StatesUnknown status
Helen DeVos Children's Hospital at Spectrum Health
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Grand RapidsUnited StatesUnknown status
University of Arkansas for Medical Sciences
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Little RockUnited StatesUnknown status
Valley Children's Hospital
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MaderaUnited StatesUnknown status
Stanford Univ Medical Center
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Palo AltoUnited StatesUnknown status

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