A Study to Investigate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Efficacy of RO7034067 in Type 2 and 3 Spinal Muscular Atrophy (SMA) Participants (SUNFISH)

  • Muscle And Peripheral Nerve Disease
  • Spinal Muscular Atrophy (SMA)
Please note that the recruitment status of the trial at your site may differ from the overall study status because some study sites may recruit earlier than others.
Trial Status:


This trial runs in
  • Ankara
  • Barcelona
  • bei-jing-shi
  • Beograd
  • Bron
  • Calgary
  • Esplugues de Llobregat
  • Freiburg im Breisgau
  • Fukuoka
  • Gdańsk
  • Genova
  • Gent
  • Hiroshima
  • İstanbul
  • Kodaira
  • Leuven
  • Lille
  • Liège
  • London
  • Madrid
  • Milano
  • Minamikyūshū
  • Montréal
  • Moriyama
  • Moscow
  • Nantes
  • New York
  • Nishinomiya
  • Oxford
  • Paris
  • Poznań
  • Rio de Janeiro
  • Roma
  • Sendai
  • Sevilla
  • shang-hai-shi
  • Shimotsuke
  • Shinjuku City
  • Shizuoka
  • Stanford
  • Warszawa
  • Zagreb
Trial Identifier:

NCT02908685 2016-000750-35 BP39055

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      The source of the below information is public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc.. It has been summarised and edited into simpler language. For more information about this clinical trial see the For Expert tab on the specific ForPatients page or follow these links to https://clinicaltrials.gov and/or https://euclinicaltrials.eu and/or https://www.isrctn.com.

      The below information is taken directly from public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc., and has not been edited.

      Results Disclaimer

      Trial Summary

      Multi-center, randomized, double-blind, placebo-controlled study to assess the safety, tolerability, pharmacokinetics, pharmacodynamics, and efficacy of Risdiplam in adult and pediatric participants with Type 2 and Type 3 SMA. The study consists of two parts, an exploratory dose finding part (Part 1) of Risdiplam for 12 weeks and a confirmatory part (Part 2) of Risdiplam for 24 months.

      Hoffmann-La Roche Sponsor
      Phase 2 Phase
      NCT02908685,BP39055,2016-000750-35 Trial Identifier
      Placebo, RO7034067 Treatments
      Muscular Atrophy, Spinal Condition
      Official Title

      A Two Part Seamless, Multi-Center Randomized, Placebo-Controlled, Double-Blind Study to Investigate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Efficacy of Risdiplam (RO7034067) in Type 2 and 3 Spinal Muscular Atrophy Patients

      Eligibility Criteria

      All Gender
      ≥ 2 Years & ≤ 25 Years Age
      No Healthy Volunteers
      Inclusion Criteria
      • Confirmed diagnosis of 5q-autosomal recessive SMA
      • Negative blood pregnancy test at screening and agreement to comply with measures to prevent pregnancy and restrictions on sperm donation
      • For Part 1: Type 2 or 3 SMA ambulant or non-ambulant
      • For Part 2: 1) Type 2 or 3 SMA non-ambulant; 2) RULM entry item A greater than or equal to 2; 3) ability to sit independently as assessed by item 9 of the MFM
      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
      • Concomitant or previous administration of a SMN2-targeting antisense oligonucleotide, SMN2 splicing modifier or gene therapy either in a clinical study or as part of medical care
      • Any history of cell therapy
      • Hospitalization for a pulmonary event within the last 2 months or planned at time of screening
      • Surgery for scoliosis or hip fixation in the one year preceding screening or planned within the next 18 months
      • Unstable gastrointestinal, renal, hepatic, endocrine, or cardiovascular system diseases as considered to be clinically significant by the Investigator
      • Presence of clinically significant electrocardiogram abnormalities before study drug administration from average of triplicate measurement or cardiovascular disease indicating a safety risk for participants as determined by the Investigator
      • Any major illness within one month before the screening examination or any febrile illness within one week prior to screening and up to first dose administration
      • Recently initiated treatment (within less than [<] 6 months prior to randomization) with oral salbutamol or another beta 2-adrenergic agonist taken orally
      • Any prior use of chloroquine, hydroxychloroquine, retigabin, vigabatrin or thioridazine, is not allowed
      • Ascertained or presumptive hypersensitivity (e.g., anaphylactic reaction) to Risdiplam or to the constituents of its formulation
      • Recent history (less than one year) of ophthalmological diseases
      • Participants requiring invasive ventilation or tracheostomy

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