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NCT04747431CompletedPhase 1/2

Phase 1b Study to Assess the Safety, Tolerability and Pharmacodynamics of PBFT02 in Adult Participants with Frontotemporal Dementia (FTD) and GRN or C9orf72 Mutations

Source: EU CTIS (euclinicaltrials.eu) · Last updated 15 May 2026

Status (registry)
Completed
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
4 (actual)
First submitted
31 Aug 2023
Start date
1 Feb 2024
Lead sponsor
Passage Bio Inc.
NCT number
NCT04747431
EU CT number
2023-507724-23-00
EudraCT number
2020-004499-17

What you commit to

  • Study type: Interventional · Phase 1/2
  • Participants enrolled: 4
  • 3 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study, not your situation.

Sites (3)

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

SiteCityCountrySite status
Hospital Universitario Central De Asturias
Coordinator of this site? Confirm its status
OviedoSpainCompleted
University Hospital Virgen Del Rocio S.L.
Coordinator of this site? Confirm its status
SevillaSpainCompleted
Unidade Local de Saúde de Coimbra, E.P.E.
Coordinator of this site? Confirm its status
CoimbraPortugalCompleted

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