Status:
ACTIVE_NOT_RECRUITING
Phase 1/2 Clinical Trial of PR001 in Infants With Type 2 Gaucher Disease (PROVIDE)
Lead Sponsor:
Prevail Therapeutics
Collaborating Sponsors:
Eli Lilly and Company
Conditions:
Gaucher Disease, Type 2
Eligibility:
All Genders
Up to 24 years
Phase:
PHASE1
PHASE2
Brief Summary
J3Z-MC-OJAB is an open-label, Phase 1/2, multicenter study to evaluate the safety and efficacy of single-dose LY3884961 (formerly PR001) in infants diagnosed with Type 2 Gaucher disease (GD2). For eac...
Eligibility Criteria
Inclusion
- Bi-allelic GBA1 mutations consistent with a diagnosis of GD2 confirmed by the central laboratory.
- Clinical diagnosis of GD2
- Parent/legal guardian is capable of providing signed informed consent; including compliance with the requirements and restrictions listed in the informed consent form (ICF) in this protocol.
- Patient has a parent/legal guardian able to participate in the study as a source of information on the patient's health status and cognitive and functional abilities (including providing input into the rating scales).
Exclusion
- Significant CNS disease other than GD2 that may be a cause for the patient's symptoms or interfere with study objectives.
- Achieved independent gait.
- Severe peripheral symptoms of GD which, in the opinion of the Investigator, would pose an unacceptable risk to the patient or interfere with the patient's ability to comply with study procedures or interfere with the conduct of the study.
- Concomitant disease, condition, or treatment which, in the opinion of the Investigator, would pose an unacceptable risk to the patient or interfere with the patient's ability to comply with study procedures or interfere with the conduct of the study.
- Use of any substrate reduction therapy (SRT) for GD treatment.
- Use of prohibited medications, herbals, or over-the-counter agents as listed in the protocol.
- Any type of prior gene or cell therapy.
- Use of systemic immunosuppressant or corticosteroid therapy other than protocol-specified immunosuppression.
- Participation in another investigational drug or device study within the past 3 months.
- Brain MRI (magnetic resonance imaging) and MRA (magnetic resonance angiography) showing clinically significant abnormality deemed a contraindication to intracisternal injection.
- Clinically significant laboratory test result abnormalities assessed at screening.
- Contraindications or intolerance to radiographic visualization methods (e.g. MRI, MRA, CT), and intolerance to contrast agents used for MRI or CT scans.
- Contraindications to general anesthesia or sedation.
- Other protocol-defined inclusion/exclusion criteria may apply.
Key Trial Info
Start Date :
June 29 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2028
Estimated Enrollment :
7 Patients enrolled
Trial Details
Trial ID
NCT04411654
Start Date
June 29 2021
End Date
May 1 2028
Last Update
December 15 2025
Active Locations (5)
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1
UCSF Benioff Children's Hospital, 5700 Martin Luther King Jr Way
Oakland, California, United States, 94609
2
University of Minnesota Masonic Children's Hospital, 2450 Riverside Avenue
Minneapolis, Minnesota, United States, 55454
3
Children's Hospital of Pittsburgh, 4401 Penn Avenue
Pittsburgh, Pennsylvania, United States, 15224
4
Lysosomal & Rare Disorders Research and Treatment Center
Fairfax, Virginia, United States, 22030