Phase 2
N=30
A Study of AT2101 (Afegostat Tartrate) in Adult Patients With Type 1 Gaucher Disease Currently Receiving Enzyme Replacement Therapy
Gaucher Disease, Type 1 · Type 1 Gaucher Disease · Gaucher Disease
Bottom Line
View on ClinicalTrials.gov: NCT00433147 ↗Enrolled (actual)
30
Serious AEs
0.0%
Results posted
Aug 2018
Primary outcome: Primary: Number Of Participants Who Experienced Severe Treatment-emergent Adverse Events (TEAEs) — 0; 0; 0; 0 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- Afegostat tartrate (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Amicus Therapeutics
- Primary completion
- Feb 2008
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number Of Participants Who Experienced Severe Treatment-emergent Adverse Events (TEAEs) |
0; 0; 0; 0 | — |
| SECONDARY Change From Baseline To End Of Treatment In Beta-glucocerebrosidase (GCase) Levels In White Blood Cells (WBC) |
8.732; 8.543; 9.371; 12.035; 19.148; 23.557 | — |
Summary
This study was conducted to test the safety and tolerability of afegostat tartrate in participants with type 1 Gaucher disease already receiving enzyme replacement therapy.
Eligibility Criteria
Inclusion Criteria
- Had a confirmed diagnosis of type 1 Gaucher disease with a known documented missense gene mutation in at least 1 of the 2 gene-encoding β-glucosidase alleles
- Clinically stable
- Male or female participants, 18 to 74 years old inclusive
- All participants of childbearing potential used adequate birth control
- Provided written informed consent to participate in the study
Exclusion Criteria
- Clinically significant disease, severe complications from Gaucher disease, or serious illness that precluded participation in the study in the opinion of the Investigator that compromised the safety of the participant or precluded the participant from completing the study
- During the screening period, any clinically significant findings, as deemed by the Investigator
- Partial or total splenectomy (removal of spleen) within the 2 years prior to study entry
- History of pulmonary hypertension or Gaucher related lung disease
- History of allergy or sensitivity to the study drug or any excipients, including any prior serious adverse reaction to iminosugars (for example, N-butyldeoxynojirimycin or miglustat)
- Pregnant or breast-feeding
- Current/recent drug or alcohol abuse
- Treatment with any investigational product in the 90 days before study entry
- Treatment in the previous 90 days with any drug known to have a well-defined potential for toxicity to a major organ
- Presence or symptoms of gastrointestinal, liver or kidney disease, or other conditions known to interfere with the absorption, distribution, metabolism, or excretion of drugs
Data sourced from ClinicalTrials.gov (NCT00433147). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.