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Clinical Trials in the UK / NCT05115110
Active, not recruiting Phase 2/3

A Study to Investigate the Safety and Efficacy of RO7204239 in Combination With Risdiplam (RO7034067) in Participants With Spinal Muscular Atrophy

NCT05115110 · tracked via the Priya Life Science UK tracker
Sponsor
Hoffmann-La Roche
Phase
Phase 2/3
Started
2022-06-02
Last updated
2026-09-09

Condition(s) studied

Spinal Muscular Atrophy (SMA)

Investigational drug(s) / intervention(s)

RO7204239PlaceboRisdiplam

RO7204239: RO7204239 will administered every 4 weeks (Q4W) by subcutaneous (SC) injection into the abdomen. RO7204239 will be investigated at low- and high-dose in Part 1.

Placebo: Placebo will be administered Q4W by SC injection into the abdomen.

Risdiplam: Risdiplam will be administered orally once daily (QD) for the duration of the study.

Study summary

Risdiplam works by helping the body produce more survival motor neuron (SMN) protein throughout the body. This means fewer motor neurons - nerve cells that pass impulses from nerves to muscles to cause movement - are lost, which may improve how well muscles work in people with SMA. RO7204239 is an investigational anti-myostatin antibody that is designed to target myostatin. Myostatin plays an important role in the regulation of skeletal muscle size by controlling growth. Inhibiting myostatin may help muscles grow in size and strength. RO7204239 in combination with risdiplam, which is designed to increase the amount of SMN protein throughout the body, has the potential to further improve motor function and clinical outcomes for people living with SMA.

This trial will study the safety and efficacy of RO7204239 in combination with risdiplam in patients with spinal muscular atrophy (SMA). The trial has two parts; Part 1 is the dose-finding part in SMA patients that are either ambulant (aged 2-10 years) or non-ambulant (aged 5-10 years) within separate cohorts, and Part 2 is the pivotal part in SMA patients aged 2-25 years that are ambulant.

Eligibility

Sex
ALL
Min age
2 Years
Max age
25 Years
Healthy volunteers
No
Inclusion Criteria: * Age at screening: Part 1 Cohorts A (ambulant participants), B (ambulant participants), and D (non-ambulant participants): 5-10 years, inclusive; Part 1 Cohort C (ambulant participants): 2-4 years, inclusive; Part 2 (ambulant participants): 2-25 years, inclusive * Participants who have a confirmed genetic diagnosis of 5q-autosomal recessive SMA * Symptomatic SMA disease, as per investigator's clinical judgement * Participants who have received previous SMA disease-modifying therapies may be included provided that: Onasemnogene abeparvovec was received at least 90 days prior to screening. Participants should be tapered off steroids prior to receiving risdiplam. In addition, participants should have normal levels of liver function tests, coagulatory parameters, platelets, and troponin-I at 90 days after administration of onasemnogene abeparvovec or at least 1 month after tapering off corticosteroids, whichever comes later; Nusinersen last dose was received at least 90 days prior to screening; Risdiplam is switched to the investigational medicinal product (IMP) provided by the site Inclusion Criteria for Part 1 Cohorts A, B, and C and Part 2 only: * Participants who are ambulant, where ambulant is defined as able to walk/run unassisted (i.e., without the use of assistive devices such as canes, walking sticks, crutches, walkers, person/hand-held assistance, braces, orthoses, over the malleoli insoles or any other type of support) 10 meters in ≤ 30 seconds as measures by the Timed 10-Meter Walk/Run Test \[10MWRT\] at screening Inclusion Criteria for Part 1 Cohort D only: * Participants who are able to sit, defined by: A score of 3 on Item 9 of the MFM32 (sitting without upper limb support while maintaining contact between the two hands for 5 seconds); A score of at least 2 on Item 10 of the MFM32 (while seated, leaning forward to touch a tennis ball and sitting back again, either with or without upper limb support) * Participants who are able to raise a standardized plastic cup with a 200g weight in it to the mouth, using both hands if necessary, defined by a score of 3 on the entry item of the Revised Upper Limb Module (RULM) Exclusion Criteria: * Concomitant or previous participation in any investigational drug or device study within 90 days prior to screening or 5 half-lives of the drug whichever is longer, with the exception of those who have completed a risdiplam study, or participated in a nusinersen or onasemnogene abeparvovec study * Receiving or have received previous administration of anti-myostatin therapies * Any history of cell therapy * Hospitalization for a pulmonary event within the last 2 months or planned hospitalization at the time of screening * Past surgery for scoliosis or hip fixation in the 6 months preceding screening or planned within the next 9 months (Part 1) or 21 months (Part 2) * Unstable gastrointestinal, renal, hepatic, endocrine, or cardiovascular system diseases considered to be clinically significant * Clinically significant ECG abnormalities at screening from average of triplicate measurement, abnormal findings at echocardiography, or cardiovascular disease indicating a safety risk for participants at the time of screening * Any major illness within 1 month before screening * Received any multidrug and toxin extrusion (MATE1/2K) substrates within 2 weeks before screening * Hereditary fructose intolerance * Used any of the following medications within 90 days prior to screening: riluzole, valproic acid, hydroxyurea, sodium phenylbutyrate, butyrate derivatives, creatine, carnitine, growth hormone, anabolic steroids, probenecid, acetyl cholinesterase inhibitors, agents that could potentially increase or decrease muscle strength, and agents with known or presumed histone deacetylase (HDAC) inhibitory effect * Clinically significant abnormalities in laboratory test results at the time of screening * Ascertained or presumptive hypersensitivity to RO7204239 or risdiplam, or to the constituents of its formulations * Clinically relevant history of anaphylactic reaction requiring inotropic support * Any abnormal skin conditions, pigmentation or lesions in the area intended for SC injection (abdomen) and that would prevent visualization of potential injection site reactions to RO7204239 * Immobilization, surgical procedures, fracture, or trauma to the upper or lower limbs within 90 days prior to screening Exclusion Criteria for Part 1 Cohorts A and B only: * Participants with contraindications for MRI scan (including, but not restricted to, claustrophobia, pacemaker, artificial heart valves, cochlear implants, presence of foreign metal objects in heart or body, including spinal rods, intracranial vascular clips, insulin pumps, etc.), difficulties maintaining a prolonged supine position, or any other clinical history or examination finding that would pose a potential hazard in combination with MRI Exclusion Criteria for Part 1 Cohort D only: * Participants who are unable to adopt the correct position to endure adequate quality of DXA scan acquisition, as determined by the DXA scan technologist * Participants who have contractures at screening that would interfere with DXA scan acquisition or functional assessments, as confirmed by the DXA scan technologist and clinical evaluator * For participants able to take steps only: Able to walk unassisted (i.e., without the use of assistive devices such as canes, walking sticks, crutches, walkers, person/hand held assistance, braces, orthoses, over the malleoli insoles or any other type of support) 10 meters in ≤ 30 seconds as measured by the timed 10MWRT at screening * Participants who have severe scoliosis (curvature \> 40°) at screening based on the participant's most recent X-ray as performed per standard of care or scoliosis that would interfere with functional assessments, as confirmed by the clinical evaluator. An X-ray is not required if it is not clinically indicated (e.g., in participants with mild scoliosis) * Participants who require invasive ventilation, tracheostomy, or the use of noninvasive ventilation (e.g., bilevel positive airway pressure) during the daytime

Primary outcome measure(s)

Trial sites (30)

FacilityCityRegionStatus
Boston Childrens Hospital Boston Massachusetts
Columbia University Medical Center New York New York
Sydney Children's Hospital Randwick New South Wales
UZ Gent Ghent Belgium
Chr de La Citadelle Liège Belgium
British Columbia Children's Hospital Vancouver British Columbia
The Hospital for Sick Children Toronto Ontario
McGill University Health Centre - Glen Site Montreal Quebec
Clinical Hospital Centre Zagreb Zagreb Croatia
Policlinico Agostino Gemelli Rome Lazio
IRCCS Istituto Giannina Gaslini Genoa Liguria
Fondazione IRCCS Istituto Neurologico ?Carlo Besta? Milan Lombardy
Asst Grande Ospedale Metropolitano Niguarda Milan Lombardy
Ospedali Riuniti Torrette di Ancona Ancona The Marches
Kobe University Hospital Hyōgo Japan
Kagoshima University Hospital Kagoshima Japan
National Center for Global Health and Medicine Shinjuku-ku Japan
Universitair Medisch Centrum Utrecht Utrecht Netherlands
Instytut Centrum Zdrowia Matki Polki ?ód? Poland
Uniwersyteckie Centrum Kliniczne Gda?sk Poland
Uniwersytecki Szpital Kliniczny w Poznaniu Późna Poland
Klinika Neurologii I Wydzialu Lekarskiego WUM w Warszawie Warsaw Poland
Instytut Pomnik Centrum Zdrowia Dziecka Warsaw Poland
CHULC, E.P.E. - Hospital Dona Estefania Lisbon Portugal
Hospital de Santa Maria Lisbon Portugal
Hospital Sant Joan De Deu Esplugues de Llobregas Barcelona
Hospital Universitario La Paz Madrid Spain
Hospital Universitario la Fe Valencia Spain
Birmingham Heartlands Hospital Birmingham United Kingdom
John Radcliffe Hospital Oxford United Kingdom

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05115110 on ClinicalTrials.gov ↗ ← All trials in the UK