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Clinical Trials/NCT04049578
NCT04049578
Terminated
Phase 1

A Phase Ib, Multicenter, Open-Label, 6-Week Study With a 48-Week Extension to Investigate the Pharmacokinetics, Safety, and Tolerability of Balovaptan in Children Ages 2-4 Years With Autism Spectrum Disorder

Hoffmann-La Roche5 sites in 1 country2 target enrollmentDecember 19, 2019

Overview

Phase
Phase 1
Intervention
Balovaptan
Conditions
Autism Spectrum Disorder
Sponsor
Hoffmann-La Roche
Enrollment
2
Locations
5
Primary Endpoint
Plasma Concentration of Balovaptan
Status
Terminated
Last Updated
5 years ago

Overview

Brief Summary

This was a Phase Ib, multicenter, open-label study in children 2-4 years old with autism spectrum disorder (ASD) to investigate the pharmacokinetics, safety, and tolerability of an oral dose of balovaptan once a day (QD). The study was to consists of a 6-week treatment period to evaluate the pharmacokinetics of balovaptan in 2 to 4 year old children followed by an optional extension period of 48 weeks.

Registry
clinicaltrials.gov
Start Date
December 19, 2019
End Date
May 6, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of ASD according to Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) criteria for ASD. Diagnostics will be performed by a team of autism experts and confirmed by Autism Diagnostic Observation ScheduleTM, Second Edition (ADOS-2) criteria. The DSM-5 criteria for diagnosis of autism must be met with the highest confidence in the opinion of the investigator. Children with ambiguous diagnostic results cannot be enrolled in the study. If the ADOS-2 assessment has been performed by a certified rater and documented within 12 months of the screening visit, it is not mandatory to repeat it unless the subject was assessed below an age of 2 years.
  • Hearing and vision compatible with the study assessments, as judged by the investigator
  • Ability for subject and the caregiver to comply with the study protocol, in the investigator's judgment
  • Availability of a parent or other reliable caregiver who is fluent in language of the site and has frequent and sufficient contact with the subject.

Exclusion Criteria

  • Clinically significant psychiatric and/or neurologic comorbidity that may interfere with the safety or efficacy endpoints in the view of the investigator
  • Clinically significant regression of any acquired language and motor function skills in the opinion of the investigator throughout the subject's development
  • History of seizures with the exception of a single, non-complicated febrile seizure \>= 6 months before screening
  • Clinical diagnosis of peripheral neuropathy or signs and symptoms indicative of peripheral neuropathy
  • Any clinically relevant cardiovascular disease
  • Confirmed elevation in cardiac troponin I (cTn I), high-sensitive cardiac troponin T (hs cTn T), N-terminal pro-B-type natriuretic peptide (NT-proBNP) or, if conducted, clinically relevant abnormality in Doppler echocardiogram
  • Confirmed clinically significant abnormality on ECG at screening, including, but not limited to, a QT interval corrected through use of Fridericia's formula (QTcF) of \>= 450 ms, absence of dominating sinus rhythm, or second- or third-degree atrioventricular block
  • Confirmed systolic or diastolic blood pressure above the 95th percentile or below the 5th percentile according to the Centers for Disease Control and Prevention (CDC) norm tables referring to stature (height)-for-age percentiles
  • Confirmed heart rate: \>150 bpm in 2-year old children, \>135 bpm in 3-year old children, or \>120 bpm in 4-year old children.
  • Concomitant disease or condition that could interfere with, or treatment of which might interfere with, the conduct of the study; or discontinuation of prohibited medication that might pose unacceptable risks to the subject in the opinion of the investigator

Arms & Interventions

Balovaptan

Intervention: Balovaptan

Outcomes

Primary Outcomes

Plasma Concentration of Balovaptan

Time Frame: Predose, 2, 4, 6 hours postdose at Week 2; predose at Week 6; predose at Week 12; predose at Week 24, predose at Week 54

Plasma Concentation of M3 Metabolite

Time Frame: Predose, 2, 4, 6 hours postdose at Week 2; predose at Week 6; predose at Week 12; predose at Week 24, predose at Week 54

Plasma Concentration Ratio of M2 to Balovaptan, as Applicable

Time Frame: Predose, 2, 4, 6 hours postdose at Week 2; predose at Week 6; predose at Week 12; predose at Week 24, predose at Week 54

Plasma Concentration of M2 Metabolite, as Applicable

Time Frame: Predose, 2, 4, 6 hours postdose at Week 2; predose at Week 6; predose at Week 12; predose at Week 24, predose at Week 54

Area Under the Curve at Steady State (AUCss) of Balovaptan

Time Frame: Predose, 2, 4, 6 hours postdose at Week 2; predose at Week 6; predose at Week 12; predose at Week 24, predose at Week 54

Plasma Concentration Ratio of M3 to Balovaptan

Time Frame: Predose, 2, 4, 6 hours postdose at Week 2; predose at Week 6; predose at Week 12; predose at Week 24, predose at Week 54

Secondary Outcomes

  • Number of Participants With Adverse Events(Up to approximately week 20)

Study Sites (5)

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