Long-Term Follow-Up of Subjects Treated With NTLA-2002
Research type
Research Study
Full title
Long-Term Follow-Up of Subjects Treated With NTLA-2002
IRAS ID
1008843
Contact name
Peggy Sung
Contact email
Sponsor organisation
Intellia Therapeutics, Inc.
Eudract number
2022-003778-22
Research summary
This Study aims to Evaluate the long term effects of NTLA-2002 in adults with Hereditary Angioedema (HAE). The purposes of this study are to evaluate the long-term safety of NTLA-2002 in previously treated subjects and evaluate the long-term efficacy of NTLA-2002 in previously treated subjects.
When subjects complete or prematurely discontinue a previous Intellia study with NTLA-2002, they will be asked to consent and participate in this long-term follow-up study, in order to better define the benefit-risk profile of treatment with NTLA-2002. No investigational drugs will be administered during this study.REC name
London - West London & GTAC Research Ethics Committee
REC reference
23/LO/0904
Date of REC Opinion
4 Jan 2024
REC opinion
Further Information Favourable Opinion