Intracerebral Gene Therapy for Sanfilippo Type A Syndrome

Lysogene

Status and phase: Completed; Phase 2; Phase 1

Conditions: Sanfilippo Disease Type A; Mucopolysaccharidosis Type III A

Treatments: Genetic: SAF-301

Study type: Interventional

Funder types: Industry

Identifiers

NCT01474343

P1-SAF-301

Details and patient eligibility

About

The clinical trial P1-SAF-301 is an open-label, single arm, monocentric, phase I/II clinical study evaluating the tolerance and the safety of intracerebral administration of adeno-associated viral vector serotype 10 carrying the human SGSH and SUMF1 cDNAs for the treatment of Sanfilippo type A syndrome The treatment plan consists on a direct injection of the investigational medicinal product SAF-301 to both sides of the brain through 6 image-guided tracks, with 2 deposits per track, in a single neurosurgical session.

The primary objective is to assess the tolerance and the safety associated to the proposed treatment through a one-year follow up.

The secondary objective is to collect data to define exploratory tests that could become evaluation criteria for further clinical phase III efficacy studies.

Four patients will be included in the clinical trial and will be followed during one year.

The enrollment and the follow-up of the patients will take place at Bicêtre Hospital. The Neurosurgery will be performed at Necker-Enfants Malades Hospital.

Safety will be evaluating on clinical, radiological and biological parameters.

Enrollment: 4 patients

Sex: All

Ages: 18 months to 6 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age: 18 (eighteen) months to end of 6 (six) years
• Onset of clinical manifestations related to MPSIIIA during the first 5 years of life
• SGSH activity in peripheral blood cell and / or cultured fibroblast extracts of less than 10% of controls.
• Patient affiliated to the French social security or assimilated regimens
• Family understanding the procedure and the informed consent
• Signed informed consent
• Vital laboratory parameters within normal range

Exclusion criteria

• Presence of brain atrophy on inclusion MRI judged on a cortico-dural distance of more than 1cm
• No independent walking (Ability to walk without help)
• Any condition that would contraindicate permanently anaesthesia
• Any other permanent medical condition not related to MPSIIIA
• Any vaccination 1 month before investigational drug administration
• Intake of aspirin within one month
• Any medication aiming at modifying the natural course of MPSIIIA given during the 6 months before vector injection
• Any condition that would contraindicate treatment with Prograf®, Modigraf®, Cellcept® and Solupred®

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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4 participants in 1 patient group

SAF-301

Experimental group

Treatment:

Genetic: SAF-301