A Phase 3 Study of Fenfluramine Hydrochloride in Rett Syndrome

ConditionRett Syndrome
Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age5-35
SponsorUCB BIOSCIENCES, Inc.

About this trial

The purpose of this study is to investigate the efficacy of fenfluramine hydrochloride (HCl) versus placebo in study participants with Rett syndrome (RTT).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Participant has typical or classic Rett Syndrome (RTT) according to the RettSearch Consortium 2010 revised criteria

Participant has a documented disease-causing mutation or deletion in the methyl-CpG-binding protein 2 (MECP2) gene

No loss or degradation of ambulation (including gait, coordination, or independence of walking/standing);

No loss or degradation of hand function; no loss or degradation of speech (including babbling, words, or previously developed communicative vocalizations);

Disqualifiers

Participant has a history of lymphoma, leukemia, or any malignancy within the past 5 years except for basal cell or squamous epithelial carcinomas of the skin that have been resected with no evidence of metastatic disease for 3 years.

Participant has clinically significant abnormality in vital signs according to the Investigator

Greater than trace aortic valve regurgitation.

Greater than mild mitral valve regurgitation.

Trial design

Design model

Parallel

Treatments tested in this trial

  • fenfluramine hydrochloride

    Drug

    Oral solution

  • Placebo

    Other intervention

    Oral solution

Treatment groups

200 Participants
are divided into 2 treatment groups
Group A: fenfluramine hydrochlorideExperimental treatment 1 intervention
Group B: PlaceboPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Change from Baseline to Week 14 in Rett Syndrome Behaviour Questionnaire (RSBQ) Total Score

The RSBQ is a caregiver-completed, instrument assessing behavioral and emotional features in RTT. The RSBQ consists of 45 items, including 8 subscales: General mood (8 items); Breathing problems (5 items); Hand behavior (6 items); Face movements (4 items); Body rocking and expressionless face (6 items); Nighttime behaviors (3 items); Fear/anxiety (4 items); and Walking/standing (2 items). Caregivers are asked to evaluate each RTT feature based on the current status of the patients on a 3-point scale as 0 ("not true"), 1 ("somewhat or sometimes true"), or 2 ("often true"), with the total score ranging from 0 to 90. Higher scores indicate increased disease severity. Seven items that do not belong under any of the subscales are classed as "uncategorized" but contribute to the overall total score.

Time frame
From Baseline (Day 1) to Week 14
2

Clinical Global Impression of Change (CGIC) Score at Week 14

The CGIC is a clinician-rated single item evaluating the degree of improvement or worsening of a participant's condition from Baseline following treatment or intervention. The CGIC uses a 7-point response scale, with the following ratings: "1: Very Much improved", "2: Much improved", "3: Minimally improved", "4: No change", "5: Minimally worse", "6: Much worse", "7: Very Much Worse".

Time frame
At Week 14

Secondary outcomes

1

Change from Baseline to Week 14 in Patient-Reported Outcomes Measurement Information System-Sleep Disturbance (PROMIS-SD) score

Sleep disturbances will be assessed by the PROMIS-SD parent proxy 8a version. Caregivers are asked to rate 8 items over the past 7 days on a 5-point scale: "1: Never", "2: Almost never", "3: Sometimes", "4: Almost always", and "5: Always", with higher scores indicating more severe sleep disturbances.

Time frame
From Baseline (Day 1) to Week 14
2

Change from Baseline to Week 14 in Observer-Reported Communication Ability (ORCA) score

The ORCA is an 84-item, observer-reported measure of communication ability over the past 30 days. The majority of the items included in the ORCA measure have 3 response options: "No or only once," "Sometimes," and "Yes, almost all the time", which enable derivation of an overall communication score and scores for each form of communication (expressive, receptive, and pragmatic), with higher scores indicating greater communication ability.

Time frame
From Baseline (Day 1) to Week 14
3

Caregiver Global Impression of Change - Seizure (CaGIC-Seizure) score at Week 14

The CaGIC-Seizure is a caregiver-reported item assessing the change from Baseline in the participant's seizure status. The CaGIC-Seizure uses a 7-point response scale, with the following ratings: "1: Very Much improved", "2: Much improved", "3: Minimally improved", "4: No change", "5: Minimally worse", "6: Much worse", "7: Very Much Worse".

Time frame
At Week 14
4

Incidence of treatment-emergent adverse events (TEAEs) during the double-blind intervention period

An AE is any untoward medical occurrence in a clinical study participant temporally associated with the use of study intervention, whether or not considered related to the study intervention. Treatment emergent adverse events (TEAEs) are adverse events that are not present prior to the pharmaceutical product administration or an already present event that worsens either in intensity or frequency.

Time frame
From Baseline (Day 1) up to Week 14

Other outcomes

Sponsors and contacts

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