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A Phase 3, Randomized, Double-Blinded Study to Evaluate the Safety and Efficacy of Salanersen (BIIB115) After Onasemnogene Abeparvovec Treatment in Infants with Genetically Diagnosed Spinal Muscular Atrophy

Status
Not yet recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-523857-32-00
Enrollment
2
Registered
2026-08-31
Start date
Unknown
Completion date
Unknown
Last updated
2026-09-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spinal Muscular Atrophy

Brief summary

Parts A: Number of Participants with Adverse Events (AEs) and Serious Adverse Events (SAEs) [Time Frame: Part A: Up to Day 365]

Detailed description

1. Part B: Number of Participants with Adverse Events (AEs) and Serious Adverse Events (SAEs) [Time Frame: Part B: Up to Day 1825], 2. Parts A and B: Change From Baseline in Plasma Levels of Neurofilament Light Chain (NfL) Blood will be collected to characterize changes in plasma NfL following treatment with salanersen. NfL is a protein released from damaged neurons and is a biomarker of neurodegeneration. [Time Frame: Part A: At Days 180 and 365; Part B: Up to Day 1825], 3. Parts A and B: Change from Baseline in Compound Muscle Action Potential (CMAP) Amplitudes CMAP is a well-validated method for tracking disease progression in neuromuscular disorders such as SMA and amyotrophic lateral sclerosis and has been proposed as a potential biomarker of a therapeutic effect in SMA., 3continued...CMAPs will be performed for the following nerve-muscle pairs: ulnar-abductor digiti minimi and peroneal-tibialis anterior. [Time Frame: Part A: At Day 365 and Part B: Up to Day 1825], 4.Parts A and B: Percentage of Participants Attaining World Health Organization (WHO) Motor Milestones. The WHO motor milestones will include six key developmental milestones: sitting without support, standing with assistance, hands-and-knees crawling, walking with assistance, standing alone, and walking alone. [Time Frame: Part A: At Day 365 and Part B: Up to Day 1825], 5.Parts A and B: Percentage of Participants Attaining Hammersmith Infant Neurological Examination Section 2 (HINE-2) Motor Milestones Section 2 of the HINE is used to assess motor milestones and includes 8 motor milestone categories: voluntary grasp (0 to 3), ability to kick in supine position (0 to 4), head control (0 to 2), rolling (0 to 3), sitting (0 to 4), crawling (0 to 4), standing (0 to 3), and walking (0 to 3)., 5continued...Total HINE-2 score is the sum of points from each item and can range from 0 to 26, with higher scores depicting a better level of ability. [Time Frame: Part A: At Day 365 and Part B: Up to Day 1825], 6.Parts A and B: Change From Baseline in Children's Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOP INTEND) Motor Function Scale The CHOP INTEND test is designed to evaluate the motor skills of participants with significant motor weakness., 6continued...It includes 16 items (capturing neck, trunk, and proximal and distal limb strength) structured to move from easiest to hardest with the grading including gravity eliminated (lower scores) to antigravity movements (higher scores). All item scores range from 0-4., 6continued...The total score ranges from 0-64, with higher scores depicting better motor function. [Time Frame: Part A: At Day 365 and Part B: Up to Day 1825], 7.Parts A and B: Percentage of Participants who Remain Free of Clinically Manifested Spinal Muscular Atrophy (SMA) [Time Frame: Part A: At Day 365 and Part B: At Day 545], 8.Part B: Percentage of Participants who Develop Spinal Muscular Atrophy (SMA) Subtypes (Non-Sitters, Sitters and Walkers) as Assessed by the Investigator [Time Frame: Part B: Up to Day 1825], 9.Part B: Hammersmith Functional Motor Scale Expanded (HFMSE) Total Score The HFMSE is a tool used to assess motor function in individuals with SMA. Participants will be asked to complete a specific movement and are then graded on the quality and execution of that movement. Higher scores indicate higher levels of motor ability., 9Continued...The overall score is the sum of the scores for all 33 items, with a maximum score of 66, with higher scores depicting better ability to perform activities. [Time Frame: Part B: Up to Day 1825], 10.Part B: Revised Upper Limb Module (RULM) Total Score The RULM is developed to assess upper limb functional abilities of participants with SMA. This test consists of a total of 20 upper limb performance items that are reflective of activities of daily living. The RULM is scored from 0 to 37 points, with higher scores indicating better function. [Time Frame: Part B: Up to Day 1825], 11.Parts A and B: Time to Death (Overall Survival) [Time Frame: Part A: Up to Day 365 and Part B: Up to Day 1825], 12.Parts A and B: Time to Death or Permanent Ventilation Permanent ventilation is defined as tracheostomy or ≥16 hours ventilation/day continuously for >21 days in the absence of an acute reversible event. [Time Frame: Part A: Up to Day 365 and Part B: Up to Day 1825], 13.Parts A and B: Concentration of Salanersen in Cerebrospinal Fluid (CSF) [Time Frame: Part A: Up to Day 365 and Part B: Up to Day 1460], 14.Parts A and B: Concentration of Salanersen in Serum [Time Frame: Part A: Up to Day 365 and Part B: Up to Day 1825]

Interventions

Sponsors

Biogen Idec Research Limited
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
0 Years to 17 Years

Design outcomes

Primary

MeasureTime frame
Parts A: Number of Participants with Adverse Events (AEs) and Serious Adverse Events (SAEs) [Time Frame: Part A: Up to Day 365]

Secondary

MeasureTime frame
1. Part B: Number of Participants with Adverse Events (AEs) and Serious Adverse Events (SAEs) [Time Frame: Part B: Up to Day 1825], 2. Parts A and B: Change From Baseline in Plasma Levels of Neurofilament Light Chain (NfL) Blood will be collected to characterize changes in plasma NfL following treatment with salanersen. NfL is a protein released from damaged neurons and is a biomarker of neurodegeneration. [Time Frame: Part A: At Days 180 and 365; Part B: Up to Day 1825], 3. Parts A and B: Change from Baseline in Compound Muscle Action Potential (CMAP) Amplitudes CMAP is a well-validated method for tracking disease progression in neuromuscular disorders such as SMA and amyotrophic lateral sclerosis and has been proposed as a potential biomarker of a therapeutic effect in SMA., 3continued...CMAPs will be performed for the following nerve-muscle pairs: ulnar-abductor digiti minimi and peroneal-tibialis anterior. [Time Frame: Part A: At Day 365 and Part B: Up to Day 1825], 4.Parts A and

Outcome results

None listed

Source: EU CTIS · Data processed: Sep 2, 2026