Safety and Efficacy of Olesoxime (TRO19622) in 3-25 Years SMA Patients.

• Status: Completed
• Trial end date: 2013-10-01
• Target enrollment: 0
• Participant gender: All

Summary

Assess the efficacy and the safety of olesoxime in SMA type 2 or type 3 non ambulant patients aged 3-25 years

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Hoffmann-La Roche
• Collaborator: Association Française contre les Myopathies (AFM), Paris

Criteria

Inclusion Criteria:

• Weakness and hypotonia consistent with a clinical diagnosis of spinal muscular atrophy (SMA) type II or III

• Laboratory documentation of homozygous absence of SMNI exon 7 and/or deletion and mutation on other allele

• MFM relative score (percentage of the maximum sum of both dimensions) >= 15% (D1 + D2 score)

• HFMS score at baseline >= 3

• Non ambulant patients defined as patients with HFMS score =< 38

• Must be 3 years of age or older, but younger than 26 years of age, at time of enrolment

• Age of onset of symptoms =< 3 years of age

• Signed informed consent of patient and/or parents/guardian

• Laboratory results drawn within 31 days prior to start of study entry demonstrating no clinically significant abnormalities

• Ability to take the study treatment (tested at screening after informed consent)

Exclusion Criteria:

• Evidence of renal dysfunction, blood dysplasia, hepatic insufficiency, symptomatic pancreatitis, congenital heart defect, known history of metabolic acidosis, hypertension,significant central nervous system impairment, or neurodegenerative or neuromuscular disease other than SMA

• Any clinically significant ECG abnormality

• Any acute co-morbid condition interfering with the well-being of the subject within 7 days of enrolment including bacterial infection, viral infectious processes, food poisoning, temperature > 37.0 °C, the need for acute treatment or observation due to any other reason, as judged by the investigator; patient can be included after resolution of the acute event

• Use of medications intended for the treatment of SMA including riluzole, valproic acid, hydroxyurea, sodium phenylbutyrate, butyrate derivatives, creatine, carnitine, growth hormone, anabolic steroids, probenecid, oral or parenteral use of corticosteroids at entry, agents anticipated to increase or decrease muscle strength or agents with known or presumed histone deacetylase (HDAC) inhibition, within 30 days prior to study entry. Subjects who use a nebulizer or require an inhaler to steroids will be allowed in the study; however oral use of steroids is prohibited. The oral use of salbutamol is permitted with the following restrictions: patients should have been on salbutamol for at least 6 months before inclusion in the trial, with good tolerance. The dose of salbutamol should remain constant for the duration of the trial. The use of inhaled beta-agonists (for the treatment of asthma crisis for example) is allowed.

• Spinal rod or fixation for scoliosis within the past 6 months or anticipated need of rod or fixation within 6 months of enrolment.

• Inability to meet study visit requirements or cooperate reliably with functional testing

• Coexisting medical conditions that contraindicate travel, testing or study medications

• Olesoxime is contraindicated in subjects/patients who develop drug hypersensitivity to it or one of the formulation excipients including hypersensitivity to sesame oil.

• Patients with hemostasis disorders

• Patients with known biliary tract obstruction

• Current or planned pregnancy or nursing period

• For Women: Failure to use one of the following safe methods of contraception:

1. Female condoms, diaphragm or coil, each used in combination with spermicides

2. Intra-uterine device

3. Hormonal contraception in combination with a mechanical method of contraception

• Participation in any other investigational drug or therapy study within the previous 3 months.