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
- Diseases
- Spinal muscular atrophy
- 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
Sites (16)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Charite Universitaetsmedizin Berlin KöR Coordinator of this site? Confirm its status | Berlin | Germany | Recruiting |
| Justus-Liebig-Universitaet Giessen Coordinator of this site? Confirm its status | Giessen | Germany | Recruiting |
| Great Ormond Street Hospital for Children Coordinator of this site? Confirm its status | London | United Kingdom | Recruiting |
| Uniwersyteckie Centrum Kliniczne Coordinator of this site? Confirm its status | Gdansk | Poland | Active, not recruiting |
| Instytut Pomnik Centrum Zdrowia Dziecka Coordinator of this site? Confirm its status | Warsaw | Poland | Active, not recruiting |
| Children's Healthcare of Atlanta Center for Advanced Pediatrics Coordinator of this site? Confirm its status | Atlanta | United States | Recruiting |
| Children's Hospital of Colorado Coordinator of this site? Confirm its status | Aurora | United States | Recruiting |
| Ann and Robert H. Lurie Children Hospital of Chicago Coordinator of this site? Confirm its status | Chicago | United States | Withdrawn |
| The University of Texas Southwestern Medical Center at Dallas Coordinator of this site? Confirm its status | Dallas | United States | Recruiting |
| Cook Children's Jane and John Justin Neurosciences Center Coordinator of this site? Confirm its status | Fort Worth | United States | Recruiting |
| University of Florida Pediatrics Coordinator of this site? Confirm its status | Gainesville | United States | Recruiting |
| Helen DeVos Children's Hospital at Spectrum Health Coordinator of this site? Confirm its status | Grand Rapids | United States | Withdrawn |
| University of Arkansas for Medical Sciences Coordinator of this site? Confirm its status | Little Rock | United States | Recruiting |
| Columbia University Medical Center Coordinator of this site? Confirm its status | New York | United States | Withdrawn |
| Children's Hospital of The King's Daughter Coordinator of this site? Confirm its status | Norfolk | United States | Withdrawn |
| Children's Hospital of Philadelphia Coordinator of this site? Confirm its status | Philadelphia | United States | Withdrawn |
This page is information, not medical advice. Discuss any trial with your doctor.