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NCT05629559RecruitingPhase 1/2

4D-310 in Adults With Fabry Disease and Cardiac Involvement

An Open-Label, Phase 1/2a Trial of Gene Therapy 4D-310 in Adults With Fabry Disease and Cardiac Involvement

Source: ClinicalTrials.gov · Last updated 21 Feb 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This is a prospective multicenter, open-label, dose-escalation trial to assess the safety, tolerability, and pharmacodynamics of 4D-310 following a single IV administration. The study population is comprised of adult males and females with Fabry Disease and cardiac involvement

Status (registry)
Recruiting
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
18 (estimated)
First submitted
4 Nov 2022
Start date
16 Oct 2022
Primary completion date
Jun 2026
Lead sponsor
4D Molecular Therapeutics
NCT number
NCT05629559

What you commit to

  • Study type: Interventional · Phase 1/2
  • Planned participants: 18
  • From 16 Oct 2022 to the primary completion date, Jun 2026
  • 4 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Presence of pre-existing antibodies to 4D-310 capsid or to AGA
  • Undergone kidney transplantation or currently on hemodialysis or peritoneal dialysis
  • Contraindication to systemic corticosteroid therapy or immunosuppressive therapy
  • Chronic steroid use, defined as ≥ 3 months of oral corticosteroid use within the last 12 months.
  • Currently receiving investigational drug, device or therapy or having ever received gene therapy

Other illness

  • HIV, active or chronic hepatitis B or C,
  • Evidence of liver disease, severe pulmonary disease or diabetes with poor glycemic control
  • History of stroke or transient ischemic attack within the last 12 months, or other significant thromboembolic disease history (e.g. pulmonary embolism)
  • Moderately severe to severe cardiovascular disease or uncontrolled hypertension
  • History of infusion related response to ERT or any adverse reaction leading to ERT discontinuation
  • History of cancer within 2 years (exceptions include non-melanoma skin cancer, localized prostate cancer treated with curative intent)

Lab values

  • eGFR \<65 mL/min/1.73 m2
  • Left ventricular ejection fraction of \<45% on echocardiogram (ECHO)

Other

  • Pregnant or breast-feeding
    • Note: Other inclusion and exclusion criteria apply

Who the study is looking for

  • Male or female ≥ 18 to ≤65 years of age
  • Pathogenic GLA mutation consistent with Fabry Disease
  • Confirmed diagnosis of classic or late-onset Fabry disease with cardiac involvement
  • Intolerant of ERT, unable or unwilling to receive ERT, or progressive disease despite ERT or migalastat
  • Individuals receiving ERT, must be on a stable dose for at least 6 months
  • Agree to use highly effective contraception

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Royal Melbourne Hospital
Coordinator of this site? Confirm its status
MelbourneAustraliaActive, not recruiting
Royal Perth Hospital
Coordinator of this site? Confirm its status
PerthAustraliaActive, not recruiting
Westmead Hospital
Coordinator of this site? Confirm its status
WestmeadAustraliaNot yet recruiting
Taipei Veterans General Hospital
Coordinator of this site? Confirm its status
TaipeiTaiwanRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.