Safety, Tolerability and Efficacy of ICV AX 250 Treatment in MPS IIIB -OLE

Allievex

Status and phase: Invitation-only; Phase 4

Conditions: MPS III B

Treatments: Drug: AX 250

Study type: Interventional

Funder types: Industry

Identifiers

NCT05492799

250-401

Details and patient eligibility

About

This is a Phase 3B/4, multicenter, multinational, open label study to further evaluate intracerebroventricular (ICV) delivered AX 250 treatment in MPS IIIB subjects that complete Study 250-202 for up to an additional 3 years (144 weeks) of treatment with AX 250 administered by ICV infusion every other week. Subjects will be evaluated for neurocognitive function, communication, adaptive behavior, quality of life, imaging characteristics and biochemical markers of disease burden. Safety will be assessed by adverse events, clinical labs, and physical exams.

Enrollment: 15 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Must have completed 240 weeks of Study 250-202 and enter 250-401 within 8 weeks of dosing completion.
2. Provides written informed consent from parent or legal guardian and assent from subject, if required
3. Has the ability to comply with protocol requirements in the opinion of the investigator
4. If female with childbearing potential, must have a negative pregnancy test at the Screening visit and be willing to have additional pregnancy tests during the study

Exclusion criteria

1. Has (1) a cognitive age equivalent (AEq ) score ≤ 18 months, (2) a development quotient (DQ) score ≤ 20, and (3) no evidence of improvement during the 250-202 study in secondary or exploratory efficacy endpoints
2. Would not benefit from enrolling in the study in the opinion of the investigator
3. Has received stem cell, gene therapy or enzyme replacement therapy (other than AX 250) for MPS IIIB
4. Has a history of poorly controlled seizure disorder
5. Is prone to complications from ICV drug administration including patients with hydrocephalus or ventricular shunts
6. Has received any investigational medication within 30 days prior to the Baseline visit or is scheduled to receive any investigational drug during the course of the study
7. Has a medical condition or extenuating circumstance that, in the opinion of the investigator, might compromise the subject's ability to comply with protocol requirements, the subject's well-being or safety, or the interpretability of the subject's clinical data

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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15 participants in 1 patient group

single arm

Experimental group

Description:

AX 250 300 mg - open label

Treatment:

Drug: AX 250