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Clinical Trial Summary

The main objective of this prospective, observational, long-term follow-up (LTFU) study is to evaluate the long-term safety profile of the gene therapy products evaluated by Krystal Biotech, Inc. which have a shared backbone of HSV-1, in participants who received at least one dose of investigational product (IP).


Clinical Trial Description

Due to the guidelines for gene therapy for vectors which may undergo latency/ reactivation, Krystal Biotech, Inc. has established a Long-Term Follow-up Protocol which will identify and mitigate the long-term risks to the participants receiving their gene therapy products and capture delayed adverse events in participants, annually, for 5-years following the last study visit. Additionally, it will allow the Sponsor to further understand the persistence of the gene therapy products used in their parent treatment protocols. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04917887
Study type Observational
Source Krystal Biotech, Inc.
Contact Brittani Agostini
Phone 4125865830
Email bagostini@krystalbio.com
Status Recruiting
Phase
Start date May 25, 2021
Completion date May 25, 2028

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