Clinical Study for Treatment-naïve IOPD Babies to Evaluate Efficacy and Safety of ERT With Avalglucosidase Alfa
Investigating an Investigational Medication for Infantile-Onset Pompe Disease (a rare genetic disorder causing muscle weakness and heart problems)
Study Overview
This is a single group, treatment, Phase 3, open-label study to assess efficacy, safety, pharmacokinetic (PK), pharmacodynamics (PD) of avalglucosidase alfa in treatment-naïve male and female participants with IOPD.
Study details include:
- Study duration: Screening - up to 4 weeks;
- Primary Analysis Period (PAP) - 52 weeks;
- Extended Treatment Period (ETP) - 52 weeks;
- Extended Long term Treatment Period (ELTP) - 104 weeks; 4-week follow-up period for a total study duration - up to 4.08 years.
- Treatment duration: Up to 4 years
- Visit frequency: every other week and potentially every week
Study Details
Study duration may be variable by country, including at least completion of the PAP and ETP, and up to 4.08 years.
Eligibility Criteria
You may be eligible for this study if you meet the following criteria:
- Conditions: Glycogen Storage Disease Type II
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Age: 12 months or below
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Gender: All
Inclusion Criteria:
- Participants must have confirmed diagnosis of infantile-onset Pompe disease defined as: the presence of 2 lysosomal acid α-glucosidase (GAA) pathogenic variants and a documented GAA deficiency from blood, skin, or muscle tissue; or the presence of 1 GAA pathogenic variant and a documented GAA deficiency from blood, skin and muscle tissue in 2 separate samples (from either 2 different tissues or from the same tissue but at 2 different sampling dates).
- Participants must have established cross-reactive immunological material (CRIM) status available prior to enrollment.
- Participants must have cardiomyopathy at the time of diagnosis: ie, left ventricular
mass index (LVMI) equivalent to mean age specific LVMI
- +1 standard deviation for participants diagnosed by newborn screening or sibling screening;
- +2 standard deviation for participants diagnosed by clinical evaluation.
- Parents or legally authorized representative(s) must be capable of giving signed
informed consent.
Exclusion Criteria:
- Participants with symptoms of respiratory insufficiency, including any ventilation use (invasive or noninvasive) at the time of enrollment.
- Participants with major congenital abnormality.
- Participants with clinically significant organic disease (with the exception of symptoms relating to Pompe disease).
- Participant received any Pompe disease specific treatment, eg enzyme-replacement gene therapy (ERT).
- Participant who has previously been treated in any clinical trial of avalglucosidase alfa.
- Participant not suitable for participation, whatever the reason, as judged by the Investigator, including medical or clinical conditions, or participants potentially at risk of noncompliance to study procedures.
The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
This study investigates the effects of an investigational medication on individuals with infantile-onset Pompe disease (IOPD). IOPD is a rare genetic disorder caused by the buildup of glycogen in the body's cells, leading to muscle weakness and heart problems. The study aims to understand how the investigational medication works in the body and its safety and effectiveness.
Participants in the study will receive the investigational medication and undergo various procedures to monitor their health. These procedures include regular assessments of heart function and muscle strength. The study will also involve collecting blood samples to analyze how the medication is processed in the body.
- Who can participate: Individuals diagnosed with infantile-onset Pompe disease can join. Participants must be able to provide informed consent through a parent or legal representative.
- Study Details: Participants will receive the investigational medication regularly. The study includes frequent health assessments to monitor the effects of the medication.
- Study Timelines: The study will last up to 4.08 years.
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