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A randomized, placebo-controlled trial to assess the efficacy, tolerability, and pharmacokinetics of clemastine in children and adults with Pitt-Hopkins syndrome

Status
Not yet recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-524195-29-00
Enrollment
40
Registered
2026-04-13
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-13

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

Conditions

Pitt-Hopkins syndrome

Brief summary

Caretaker Global Impression rating scale (CaGI)

Detailed description

Clinical Global Impression rating scale (CGI), PROMIS Custom Short Form – Fatigue; Numeric Rating Scale (NRS) – Fatigue, Aberrant Behavior Checklist; EuroQol-5D-Y-5L; PROMIS Early Childhood Parent Report v1.0 – Child-Caregiver Interactions; PROMIS Early Childhood Parent Report v1.0 – Anxiety; PROMIS Early Childhood Parent Report v1.0 – Depressive Symptoms, PROMIS Early Childhood Parent Report v1.0 - Sleep disturbance; Numeric Rating Scale (NRS) – Sleep; Pediatric Quality of Life Inventory (PedsQL) Gastrointestinal Symptoms questionnaire, ‘stomach pain and hurt’, ‘heart burn and reflux’, ‘gas and bloating’, and ‘constipation’ scales; Rett-syndrome Behavior Questionnaire, Breathing Problems (RSBQ-BP), adapted for PTHS ;Number and type of epileptic seizures during past 30 days, Gross Motor Function Measure (GMFM-88); Two minute walking test, Resting-state electroencephalography (EEG) recording: power spectrum, long term temporal correlations and network level excitation-inhibition dynamics, Pharmacokinetic parameters such as maximum concentration (Cmax), area under the concentration-time curve (AUC), half-life and predicted trough concentration (Ctrough) at steady state, using nonlinear mixed effects modelling (NONMEM)., IMTA Medical Consumption Questionnaire (iMCQ); IMTA Productivity Cost Questionnaire (iPCQ), Semi-structured, qualitative interviews, The relationship between clemastine PK and safety/efficacy-related biomarkers

Interventions

DRUGmicrocrystalline cellulose
DRUGTavegyl 1 mg
DRUGtabletten

Sponsors

Amsterdam UMC Stichting
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
0 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Caretaker Global Impression rating scale (CaGI)

Secondary

MeasureTime frame
Clinical Global Impression rating scale (CGI), PROMIS Custom Short Form – Fatigue; Numeric Rating Scale (NRS) – Fatigue, Aberrant Behavior Checklist; EuroQol-5D-Y-5L; PROMIS Early Childhood Parent Report v1.0 – Child-Caregiver Interactions; PROMIS Early Childhood Parent Report v1.0 – Anxiety; PROMIS Early Childhood Parent Report v1.0 – Depressive Symptoms, PROMIS Early Childhood Parent Report v1.0 - Sleep disturbance; Numeric Rating Scale (NRS) – Sleep; Pediatric Quality of Life Inventory (PedsQL) Gastrointestinal Symptoms questionnaire, ‘stomach pain and hurt’, ‘heart burn and reflux’, ‘gas and bloating’, and ‘constipation’ scales; Rett-syndrome Behavior Questionnaire, Breathing Problems (RSBQ-BP), adapted for PTHS ;Number and type of epileptic seizures during past 30 days, Gross Motor Function Measure (GMFM-88); Two minute walking test, Resting-state electroencephalography (EEG) recording: power spectrum, long term temporal correlations and network level excitation-inhibition dynami

Outcome results

None listed

Source: EU CTIS · Data processed: Apr 14, 2026