Long-Term Follow-Up (LTFU) of Subjects Dosed With NTLA-2001

Recruiting Observational Study
Transthyretin-Related (ATTR) Familial Amyloid Polyneuropathy Transthyretin-Related (ATTR) Familial Amyloid Cardiomyopathy Wild-Type Transthyretin Cardiac Amyloidosis
No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
72 (estimated)
Sponsor
Intellia Therapeutics · Industry
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About This Trial

This is a follow-up study of subjects who received NTLA-2001 in a previous clinical trial as an observational evaluation of the long-term effects of the investigational therapy.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. A subject has completed or discontinued from an Intellia-sponsored clinical study in which a complete or partial dose of NTLA-2001 was received. 2. A subject has provided informed consent for the LTFU study. Exclusion Criteria: None
Contacts

Trial Manager at Intellia

1-857-285-6200

medicalinformation@intelliatx.com

CONTACT