TrialSignal
Clinical trial intelligence report
MAGNITUDE: A Phase 3, Multinational, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of NTLA-2001 in Participants With Transthyretin Amyloidosis With Cardiomyopathy (ATTR-CM)
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 17, 2026
NCT ID
NCT06128629
Status
RECRUITING
Phase
Phase 3
Sponsor
Intellia Therapeutics
Executive brief
Investment-Ready Snapshot
Intellia Therapeutics is advancing NTLA-2001, a CRISPR/Cas9-based therapeutic targeting transthyretin amyloidosis with cardiomyopathy (ATTR-CM). This Phase 3 trial, MAGNITUDE, aims to establish NTLA-2001's efficacy and safety compared to placebo in approximately 1,200 participants. The ATTR-CM market is growing, driven by increasing diagnosis rates and the need for effective therapies. Competitive landscape includes existing treatments like tafamidis and patisiran, but NTLA-2001's novel mechanism may provide a significant advantage if proven effective. Successful trial outcomes could position Intellia as a leader in the ATTR-CM space, enhancing its market valuation and attracting potential partnerships or acquisitions.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT06128629
Indication
Transthyretin Amyloidosis (ATTR) With Cardiomyopathy
Modality
protein therapy
Target
Transthyretin (TTR) protein
Intervention
NTLA-2001, Placebo
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.