Business
Intellia Therapeutics Announces Upcoming Investor Event to Present Interim Clinical Data from Ongoing First-in-Human Studies of NTLA-2002 and NTLA-2001 on September 16, 2022
Review of first clinical data from ongoing Phase 1/2 Study of NTLA-2002 for the treatment of hereditary angioedema (HAE) presented at the 2022 Bradykinin
About this update from Intellia Therapeutics, Inc.
[{"type":"text","content":"Review of first clinical data from ongoing Phase 1/2 Study of NTLA-2002 for the treatment of hereditary angioedema (HAE) presented at the 2022 Bradykinin Symposium Event to include interim safety and serum TTR reduction data from the cardiomyopathy arm of the Phase 1 study of NTLA-2001 for the treatment of transthyretin (ATTR) amyloidosis CAMBRIDGE, Mass., Sept. 08, 2022 (GLOBE NEWSWIRE) -- Intellia Therapeutics, Inc. (NASDAQ:NTLA), a leading clinical-stage genome editing company focused on developing potentially curative therapeutics leveraging CRISPR-based technologies, today announced that it will host a virtual investor event to present interim data from the first-in-human clinical studies of NTLA-2002 and NTLA-2001 on September 16, 2022, at 8:00 a.m. ET. NTLA-2002 First Interim Clinical Data Review Intellia will review the interim clinical data from the Phase 1/2 study of NTLA-2002 for the treatment of hereditary angioedema (HAE), which is scheduled to be presented at the 2022 Bradykinin Symposium on September 16 in Berlin, Germany. The presentation will focus on the initial safety, kallikrein protein reduction and HAE attack rate data from the dose-escalation portion of the study. NTLA-2002 is Intellia’s wholly owned, second systemically administered in vivo CRISPR candidate. NTLA-2001 Interim Clinical Data Update from the Cardiomyopathy ArmIntellia will present interim clinical data from the ongoing Phase 1 study of NTLA-2001 for the treatment of transthyretin (ATTR) amyloidosis. The study update will focus on the dose-escalation portion of the cardiomyopathy arm of the study. The event will include a presentation by Julian Gillmore, M.D., Ph.D., FRCP, FRCPath, Professor of Medicine, National Amyloidosis Centre, UCL Division of Medicine, Royal Free Hospital, U.K., the trial’s national coordinating investigator. NTLA-2001, which is being developed as part of a multi-target collaboration with Regeneron, is being evaluated in patients with either ATTR amyloidosis with polyneuropathy (ATTRv-PN) or ATTR amyloidosis with cardiomyopathy (ATTR-CM). To join the webcast on September 16, 2022, at 8:00 a.m. ET, please visit this link, or the Events and Presentations page of the Investors & Media section on Intellia’s website at www.intelliatx.com. A replay of the events will be available through the Events and Presentations page of t...