A Study About Antibody Levels and Biomarkers in the Blood in People With Late-onset Pompe Disease

NCT06150820 — Not applicable, Active not recruiting, 119 participants, Astellas Gene Therapies

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A Study to Evaluate Seroprevalence of Antibodies to AAV8 and Assessment of Biomarkers in Patients With Late-Onset Pompe Disease

RegistryNCT06150820
StatusActive not recruiting
PhaseNot applicable
Study typeInterventional; na, single group, masking: none, other
Enrollment119 (Actual)
SponsorAstellas Gene Therapies (Industry)
ConditionsPompe Disease (Late-onset)
InterventionsNo Intervention (Other)
Datesstart 2024-02-01, primary completion 2027-06-30 (estimated), completion 2027-06-30 (estimated), first posted 2023-11-29, last updated 2026-10-08
Locations53 sites in United States, Australia, Brazil, Canada, France, Germany, Italy, Japan and 3 more countries

Related Papers Related Patents Related Grants Related Experts
All trials for Pompe Disease (Late-onset) All trials of No Intervention

-Summary

Pompe disease is a genetic condition which causes muscle weakness over time. People with Pompe disease have a faulty gene that makes an enzyme called acid alpha-glucosidase (or GAA). This enzyme breaks down a type of sugar called glycogen. Without this enzyme, there is a build-up of glycogen in the cells of the body. This causes muscle weakness and other symptoms. Pompe disease can happen at any age, but in late-onset Pompe disease, symptoms generally start from 12 months old onwards.

The standard treatment for people with Pompe disease is to receive regular infusions of the GAA enzyme. This is known as enzyme replacement therapy. However, people can build up antibodies against the GAA enzyme over time.

Gene therapy is used to treat conditions caused by a faulty gene. It works by replacing the faulty gene with a working gene inside the cells of the body. The working gene is delivered into the cells using certain viruses as carriers (vectors). Viruses are often used as carriers as they can easily get inside cells. The genetic material of the original virus is replaced with the working gene, so only the working gene gets inside the cells. A common virus used as a carrier in gene therapy is the adeno-associated virus (or AAV). This is like an adenovirus, which causes the common cold.

The original type of AAV does not cause any harm to humans. However, people that have previously been infected with the original type of AAV may have built up antibodies against AAV. These antibodies may stop the AAV carrier with the working gene getting inside the cells.

Researchers want to learn more about antibody levels against AAV and the GAA enzyme in people with late-onset Pompe disease. They also want to learn about other substances in the blood that provide more information about late-onset Pompe disease. These are known as biomarkers.

In this study, older teenagers and adults with late-onset Pompe disease will take part. They will not have had gene therapy using AAV. There will be 2 groups - those who have never had enzyme replacement therapy, and those who have had enzyme replacement therapy for 6 months or more. No study treatment will be given during the study, but blood and urine samples will be taken for testing.

The main aims of the study are to check antibody levels against AAV8 (a type of AAV) in people with late-onset Pompe disease who had not received any treatment using AAV, to check antibody levels against the GAA enzyme in people previously treated with GAA as part of enzyme replacement therapy, to check levels of biomarkers for Pompe disease, and to check for medical problems.

In the study, people will visit the study clinic several times. Some visits may be in the person's home. The first visit is to check if they can take part. Those who can take part will have a medical examination, and have their vital signs checked. Vital signs include blood pressure, heart rate, breathing rate and temperature. Blood samples will be taken to check antibody levels against the GAA enzyme and against AAV8. Blood and urine samples will also be taken to check for biomarkers for Pompe disease. Blood and urine samples will be taken about every 4 months for up to 2 years.

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+Detailed description

No investigational drug will be administered to participants in this study. Blood and urine will be collected as part of the study. The duration of the study is approximately 2 years, participants may withdraw at any time.

+Arms and interventions

ArmTypeInterventionsDescription
Participants with Late-Onset Pompe DiseaseOtherOther: No InterventionAdolescent or adult participants with LOPD.
  • No Intervention (Other): No investigational drug will be administered to participants in this study.

+Outcome measures

Primary outcomes

  • Occurrence of total antibodies to AAV8 [Up to 2 years]: Antibodies to AAV8 will be recorded from serum blood samples collected.
  • Occurrence of neutralizing antibodies to AAV8 [Up to 2 years]: Antibodies to AAV8 will be recorded from serum blood samples collected.

Secondary outcomes

  • Seroconversion of antibodies to AAV8 over time [Up to 2 years]: Seroconversion of antibodies to AAV8 will be recorded from serum blood samples collected.
  • Creatine kinase [CK] levels [Up to 2 years]: CK levels will be recorded from blood plasma samples collected.
  • Urine glucose tetrasaccharide [Glc4]/hexose tetrasaccharide [Hex4] over time [Up to 2 years]: Glc4/Hex4 will be recorded from urine samples collected.
  • Occurrence of anti-GAA antibodies in participants on ERT [Up to 2 years]: Anti-GAA antibodies will be recorded from serum blood samples collected.

+Eligibility

Sex: All, ages: 16 Years to 69 Years

Inclusion Criteria:

* Participant has a documented clinical diagnosis of LOPD.
* Participant is enzyme replacement therapy ERT-naïve (ERT-N) or if the participant is currently taking an approved ERT treatment or is participating in an ERT-interventional study, the ERT must have been received for at least 6 months or more (ERT-experienced \[ERT-E\]).
* Participant is willing and able to comply with study visits and procedures.
* Participant agrees to not start participating in any other clinical study involving an investigational study treatment, including ERT, while participating in this study.

Exclusion Criteria:

* Participant previously received an AAV-related product (any serotype).
* Participant is currently participating in a Pompe-related interventional study (other than ERT-interventional studies) or has received gene or cell therapy.
* Participant requires any invasive or noninvasive ventilation support while awake and upright (non-invasive support while sleeping with either continuous positive airway pressure (CPAP) or bilevel positive airway pressure (BiPAP) is acceptable for eligibility).
* Participant is unable to ambulate (assistive devices \[e.g., cane or walker\] are acceptable for eligibility).
* Participants who have received any ERT for less than 6 months as of the Baseline visit are not eligible.

+Locations (53)

FacilityCityCountryStatus
Emory ClinicAtlanta, GeorgiaUnited States
University of Kansas Medical CenterKansas City, KansasUnited States
University of MichiganAnn Arbor, MichiganUnited States
Children's Hospitals and Clinics of MinnesotaMinneapolis, MinnesotaUnited States
Hackensack University Medical CenterHackensack, New JerseyUnited States
University of CincinnatiCincinnati, OhioUnited States
University of PennsylvaniaPhiladelphia, PennsylvaniaUnited States
University of Pittsburgh Medical CenterPittsburgh, PennsylvaniaUnited States
University of UTAH - PPDSSalt Lake City, UtahUnited States
Lysosomal and Rare Diseases Research and Treatment Center, Inc.Fairfax, VirginiaUnited States
AU61003AdelaideAustralia
AU61001HerstonAustralia
BR55003FlamengoBrazil
BR55002Porto AlegreBrazil
BR55001São PauloBrazil
CN15003EdmontonCanada
CA15001MontrealCanada
FR33006AngersFrance
FR33009GarchesFrance
FR33005LilleFrance
FR33007LimogesFrance
FR33002MarseilleFrance
FR33003NantesFrance
FR33004NiceFrance
FR33001StrasbourgFrance
DT49005BonnGermany
DT49004EssenGermany
DT49003HöchheimGermany
DT49006MünsterGermany
IT39002FlorenceItaly
IT39005GussagoItaly
IT39012MessinaItaly
IT39009MilanItaly
IT39011MilanItaly
IT39008PaviaItaly
IT39006PisaItaly
IT39004RomaItaly
IT39003UdineItaly
National Center of Neurology and PsychiatryKodaira-ShiJapan
Tokyo Women's Medical University HospitalShinjuku-KuJapan
ES34003AlbaceteSpain
ES34004BarcelonaSpain
ES34009Donostia / San SebastianSpain
ES34007L'Hospitalet de LlobregatSpain
ES34001MadridSpain
ES34005MadridSpain
ES34002ValenciaSpain
TW88601TaipeiTaiwan
TW88602TaipeiTaiwan
TW88603Taoyuan CityTaiwan
UK44003CambridgeUnited Kingdom
UK44001Newcastle upon TyneUnited Kingdom
UK44004SalfordUnited Kingdom

+Investigators

  • Medical Director, Study director, Astellas Gene Therapies