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Clinical Trials/CTIS2023-504909-37-00
CTIS2023-504909-37-00
Active, not recruiting
Phase 1

A clinical trial to evaluate the long-term safety and durability of efficacy of BI 3720931, an inhaled lentiviral vector gene therapy, after single dose administration in a previous clinical trial in people with cystic fibrosis rolled-over from a previous clinical trial with BI 3720931 (LenticlairTM-ON). - 1504-0003

Boehringer Ingelheim International GmbH0 sites27 target enrollmentJanuary 31, 2024

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Cystic fibrosis
Sponsor
Boehringer Ingelheim International GmbH
Enrollment
27
Status
Active, not recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 31, 2024
End Date
TBD
Last Updated
last year
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • All trial participants who participated in a previous BI sponsored trial with BI 3720931 and have received at least one dose of BI 3720931, or matching placebo, are eligible for participation in extension trial 1504\-0003 and should be enrolled., Signed and dated written informed consent in accordance with International Council for Harmonisation (ICH)\-Good Clinical Practice (GCP) and local legislation prior to admission to the trial.

Exclusion Criteria

  • There are no exclusion criteria for enrolment into the trial.

Outcomes

Primary Outcomes

Not specified

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