RecruitingPhase 1Phase 2NCT07282847

A Study to Evaluate Safety, Tolerability, and Efficacy of AB-1009 Gene Therapy (GAA Gene) in Adult Participants With Late Onset Pompe Disease (PROGRESS-GT LOPD)

A Single-Arm, Open-Label, Dose-Escalation Study to Evaluate the Safety, Tolerability and Efficacy of a Single Intravenous Infusion of AB-1009 in Adult Participants With Late Onset Pompe Disease (LOPD)


Sponsor

AskBio Inc

Enrollment

12 participants

Start Date

Feb 10, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This is a single-arm, open-label, dose-escalation study to evaluate the safety, tolerability and efficacy of a single intravenous infusion of AB-1009 in adult participants with late-onset Pompe disease (LOPD).


Eligibility

Min Age: 18 Years

Inclusion Criteria7

  • Participant must be ≥18 years of age at the time of signing the informed consent form.
  • Confirmed GAA enzyme deficiency from any tissue source and/or confirmed biallelic GAA gene mutations.
  • Undergone enzyme replacement treatment (ERT) (either alglucosidase alfa (Lumizyme®) or avalglucosidase alfa-ngpt (Nexviazyme®)), for at least 6 months (at least 10 infusions) before signing the initial informed consent form. During the screening process, participants need to remain on their current ERT until close to dosing;
  • FVC in the upright position ≥30% and ≤80% of predicted;
  • Capable of walking at least 100 meters in the 6MWT (use of a cane, quad cane, or standard walker is permitted);
  • Contraceptive/barrier use by men and women requirements as per protocol.
  • Capable of giving informed consent and able to understand and comply with all study procedures.

Exclusion Criteria10

  • Severe cardiomyopathy, defined as left ventricular ejection fraction (LVEF) <40% or New York Heart Association (NYHA) functional class 3 or above;
  • Require invasive mechanical ventilation, or rely on noninvasive ventilation during the day;
  • Intolerance to ERT or investigator-assessed intolerance to ERT, prior experience of serious ERT-related infusion-associated reactions (IARs);
  • Have known intrinsic liver diseases, including hepatitis, HIV-related liver disease, prior diagnosis of portal hypertension, splenomegaly, hepatic encephalopathy, severe fatty liver, cirrhosis or liver fibrosis ≥stage 2, ultrasound-identified liver neoplasms, or laboratory tests suggesting elevated alpha-fetoprotein. Patients with liver function tests including ALT or AST >3× upper limit of normal (ULN) or any total bilirubin above ULN during screening will also be excluded;
  • Prior or ongoing medical condition(s), physical finding(s), assessment findings, or laboratory abnormality that, in the investigator's opinion, would impact participant's safety and compliance with the study procedures.
  • Have received gene therapy prior to screening;
  • Have received any systemic immunosuppressants (except inhalation or topical use) other than glucocorticoids or investigator-recommended immunosuppressants 30 days prior to screening through completion of screening, and/or known intolerance to immunosuppressants such as glucocorticoids;
  • Use of investigational drugs or drugs that could affect this study as evaluated by the investigator within 30 days prior to screening through completion of Week 52 or within 5 half-lives of the investigational drug (whichever is longer);
  • Have received any vaccine within 30 days prior to dosing;
  • Other conditions that make the participant not eligible for the study according to the investigator.

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Interventions

GENETICAB-1009 (GAA Gene)

A single intravenous infusion of AB-1009


Locations(10)

Barrow Neurological Institute

Phoenix, Arizona, United States

University of California, Irvine (UCI)

Irvine, California, United States

Stanford Neuroscience Health Center

Palo Alto, California, United States

NYU Langone

New York, New York, United States

Duke University

Durham, North Carolina, United States

Oregon Health and Science University (OHSU)

Portland, Oregon, United States

University of Pennsylvania

Philadelphia, Pennsylvania, United States

University of Pittsburgh Medical Center (UPMC)

Pittsburgh, Pennsylvania, United States

University of Texas Southwest Medical Center

Dallas, Texas, United States

Virginia Commonwealth University (VCU)

Richmond, Virginia, United States

View Full Details on ClinicalTrials.gov

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NCT07282847


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