Evaluation of the Efficacy, Safety, and Tolerability of Sarizotan in Rett Syndrome With Respiratory Symptoms



Status:Active, not recruiting
Conditions:Other Indications, Neurology
Therapuetic Areas:Neurology, Other
Healthy:No
Age Range:4 - Any
Updated:2/6/2019
Start Date:August 2016
End Date:April 2019

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A Randomised, Double-Blind, Placebo-Controlled 6-month Study to Evaluate the Efficacy, Safety, and Tolerability of Sarizotan in Patients With Rett Syndrome With Respiratory Symptoms

This study evaluates the safety, tolerability and efficacy of Sarizotan in reducing
respiratory abnormalities in Rett Syndrome.

This is a randomized, double-blind, placebo-controlled study designed to evaluate the safety,
tolerability, and efficacy of multiple doses of sarizotan in patients with Rett syndrome with
respiratory abnormalities. The study participants will be randomized to either sarizotan
between 2 and 10 mg bid or placebo bid, based on age and weight criteria.

Inclusion Criteria:

- Body weight ≥ 10 kg

- Age ≥ 4 years

- Diagnosis of Rett syndrome based on consensus clinical criteria and patients with
MECP2 duplications will not be eligible.

- Has at least 10 episodes of breathing dysrhythmia, defined by episodes ≥10 seconds of
breath holding (apnea), per hour during cardiorespiratory monitoring

- Ability to take study medication provided either as capsules or combined with
food/drink.

- Patient is cooperative, willing to complete all aspects of the study, and capable of
doing so with assistance of a caregiver.

Exclusion Criteria:

- Meets any of the diagnostic exclusion criteria for Rett syndrome, Typical (Neul et al,
2010);

- Patient is participating in a clinical trial with another investigational drug

- Hypersensitivity to sarizotan or other 5-HT1a agonists;

- Current clinically significant (as determined by Investigator) cardiovascular,
respiratory (e.g. severe asthma), gastrointestinal, renal, hepatic, hematologic or
other medical disorders, in addition to those directly related to the patient's Rett
syndrome;

- QTcF interval on the ECG is greater than 450 msec.

- Surgery planned during the study (except for insertion of gastrostomy tube);

- Severe diabetes mellitus or fatty acid oxidation disorder.

- Ophthalmologic history including any of the following conditions: albino patients,
family history of hereditary retinal disease, retinitis pigmentosa, any active
retinopathy or severe diabetic retinopathy.

- Females who are pregnant, breastfeeding, or of childbearing potential and not using a
hormonal contraceptive.
We found this trial at
6
sites
14 Barry Marshall Parade
Murdoch, Western Australia 6150
Principal Investigator: Janine Spencer, MBBS
Phone: .+61 8 9489 7774
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1200 Moursund Street
Houston, Texas 77030
(713) 798-4951
Principal Investigator: Daniel Glaze, MD
Phone: 832-822-1258
Baylor College of Medicine Baylor College of Medicine in Houston, the only private medical school...
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Houston, TX
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Birmingham, Alabama 35294
Principal Investigator: Alan Percy, MD
Phone: 205-934-1130
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Birmingham, AL
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1653 W. Congress Parkway
Chicago, Illinois 60612
(312) 942-5000
Principal Investigator: Peter Heydemann, MD
Phone: 312-942-0079
Rush University Medical Center Rush University Medical Center encompasses a 664-bed hospital serving adults and...
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Chicago, IL
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Saint Paul, Minnesota 55101
Principal Investigator: Arthur Beisang, MD
Phone: 651-229-1768
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Saint Paul, MN
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San Diego, California 92103
Principal Investigator: Richard Haas, MD
Phone: 858-246-2288
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San Diego, CA
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