Open Label, Adaptive, Parallel Group PET Study Using RO7017773 And [11C] RO15-4513

  • Neurodevelopmental Disorder
  • Autism Spectrum Disorder
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
  • United Kingdom
Trial Identifier:

NCT03507569 BP40257

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      Trial Summary

      This is a single dose (SD), non-randomized, open-label, adaptive, parallel group study with the purpose of investigating the occupancy of alpha5-containing GABAA receptors by RO7017773 in healthy participants.

      Hoffmann-La Roche Sponsor
      Phase 1 Phase
      NCT03507569,BP40257 Trial Identifier
      RO7017773, [11C] Ro15-4513 Treatments
      Autism Spectrum Disorder Condition
      Official Title

      A Non-Randomized Open Label, Adaptive, Parallel Group, Human Positron Emission Tomography (PET) Study to Assess Occupancy of Brain alpha5-Containing GABAA Receptors of Ro7017773 Using [11C] Ro15-4513 Following Single Oral Doses in Healthy Participants

      Eligibility Criteria

      All Gender
      ≥ 23 Years & ≤ 55 Years Age
      Accepts Healthy Volunteers Healthy Volunteers
      Inclusion Criteria
      • Healthy (absence of evidence of any active or chronic disease following a detailed medical and surgical history, a complete physical examination including vital signs, 12-lead ECG, hematology, blood chemisty, serology, and urinalysis), as judged by the Investigator.
      • Males and women of non-childbearing potential (WONCBP)
      Exclusion Criteria
      • History of convulsions (other than benign febrile convulsions of childhood) including epilepsy, or personal history of significant cerebral trauma or CNS infections
      • Clinically significant abnormal finding from the MRI performed after the initial screening examination
      • Abnormal blood pressure, i.e, systolic blood pressure (SBP) greater than 140 or less than 90 mm Hg, and diastolic blood pressure (DBP) greater than 90 or less than 50 mm Hg
      • Abnormal pulse rate, resting pulse rate greater than 100 or less than 40 bpm
      • History or presence of clinically significant ECG abnormalities before study drug administration or cardiovascular disease
      • Show evidence of human immunodeficiency virus (HIV) infection and/or positive human HIV antibodies
      • Positive result on hepatitis B (HBV) or hepatitis C (HCV), presence of hepatitis B surface antigen (HBsAg) or positive hepatitis C antibody test result at screening or within 3 months prior to starting study treatment

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