Drug-Drug Interaction Study Between AT1001 (Migalastat Hydrochloride) and Agalsidase in Participants With Fabry Disease
Status and phase
Conditions
Treatments
Details and patient eligibility
About
The objective was to determine the effects of a single dose of migalastat hydrochloride (HCl) (migalastat) 150 and 450 milligrams (mg) on the safety and plasma pharmacokinetics (PK) of agalsidase and the effects of agalsidase on the safety and PK of migalastat 150 mg.
Full description
This open-label study was conducted in 2 stages (Stage 1, Stage 2). Stage 1 included migalastat 150 mg; Stage 2 included migalastat 450 mg. Each dose of migalastat was selected to evaluate interaction with each of 3 doses of recombinant agalsidase: 0.5 mg/kilogram (kg) agalsidase beta; 1.0 mg/kg agalsidase beta; 0.2 mg/kg agalsidase alfa.
Migalastat was administered orally. Agalsidase alfa was administered as a 40-minute intravenous (IV) infusion and agalsidase beta was administered as a 2-hour (hr) IV infusion.
Stage 1 consisted of 3 treatment periods with 14 days intervening between each period.
Period 1, Day 1: agalsidase was administered alone.
Period 2, Day 1: migalastat was administered, followed 2 hrs later by agalsidase.
Period 3, Day 7: migalastat was administered alone.
Stage 2 consisted of two 14-day treatment periods in which the plasma exposure of migalastat was characterized when migalastat was administered with agalsidase solely to confirm the attainment of adequate migalastat plasma concentrations.
Period 1, Day 1: agalsidase was administered as an IV infusion using a calibrated infusion pump.
Period 2, Day 1: migalastat was administered, followed 2 hrs later by agalsidase.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- Male diagnosed with Fabry disease and between 18 and 65 years of age, inclusive
- Body mass index between 18-35 kg per meter squared
- Had initiated treatment with agalsidase at least 1 month prior to screening, and had received at least 2 infusions before screening
- Had stable dose level, dosing regimen, and form of agalsidase for at least 1 month before screening
- Had an estimated creatinine clearance greater than or equal to 50 milliliters (mL)/minute at screening
- Agreed to use medically accepted methods of contraception during the study and for 30 days after study completion
- Were willing and able to provide written informed consent
Exclusion criteria
- Had a documented transient ischemic attack, ischemic stroke, unstable angina, or myocardial infarction within the 3 months before screening
- Had clinically significant unstable cardiac disease (for example, cardiac disease requiring active management, such as symptomatic arrhythmia, unstable angina, or New York Heart Association class III or IV congestive heart failure)
- History of allergy or sensitivity to study drug (including excipients) or other iminosugars (such as miglustat, miglitol)
- Required a concomitant medication prohibited by the protocol: Glyset® (miglitol), or Zavesca® (miglustat)
- Any investigational/experimental drug or device within 30 days of screening, except for use of investigational enzyme replacement therapy for Fabry disease
- Had any intercurrent illness or condition that might have precluded the participant from fulfilling the protocol requirements or suggested to the investigator that the potential participant might have had an unacceptable risk by participating in this study
Trial design
Primary purpose
Allocation
Interventional model
Masking
20 participants in 6 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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