Home infusions may help patients stick to treatment
NCT ID NCT07494058
First seen Jun 27, 2026 · Last updated Sep 11, 2026 · Updated 1 time
Summary
This study looks at whether people with Fabry, Gaucher, or Hunter disease are more likely to continue their IV treatment when it's given at home versus at a hospital. Researchers will review existing data from 222 patients in Mexico. No new treatments are given; the goal is to understand what helps patients stay on track with their infusions.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could show that home infusions help patients stick to their treatment better than hospital visits.
- What could go wrong
- This is an observational study reviewing existing data, not a controlled trial. Results may not apply to other countries or settings.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
232 people
The number who actually took part.
- Started
-
Dec 2025
- Finished
-
Jul 2026
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Pediatric and adult participants of all ages diagnosed with lysosomal diseases (Fabry disease, Gaucher disease, or Hunter syndrome) who are enrolled in the PSP and have consented to the use of their anonymized data for research purposes will be included in this study, regardless of whether they receive modular or hospital-based infusions.
- Ages
-
Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria * Participants who met the inclusion criteria of the "Modular infusion" program * Confirmed diagnosis of Fabry disease, Gaucher disease, or Hunter syndrome * Confirmatory diagnostic test * Referral to the PSP from the treating physician * Original PSP informed consent and * Privacy notice signed * Participants who met the inclusion criteria of the "Hospital infusion" program * Confirmed diagnosis of Fabry disease, Gaucher disease, or Hunter syndrome * Confirmatory diagnostic test * Referral to the PSP from the treating physician * Original PSP informed consent and * Privacy notice signed * Agreement that their anonymized information will be used for research purposes Exclusion Criteria * Participants who do not agree or withdraw his/her explicit consent for research purposes may have the right to withdraw; however, once their data has been integrated into the database, it is no longer identifiable by any participant in the research team. * Discontinuation of Participants
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Fabry disease are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Takeda Site
Mexico City, 05348, Mexico
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a One-Time gene therapy fix fabry disease for years?
- Can brain scans and typing tests reveal early Parkinson's signs?
- Can a new pill stop fatty buildup in fabry disease?
- Gene Therapy's lasting promise: can one infusion safely control fabry disease for years?
- Can early enzyme therapy save kidneys in fabry disease?
- Can continued lucerastat access help fabry patients?