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Intellia Therapeutics

NTLAGene Editing
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Analyst Summary
✓ VERIFIED2026-04-11

Intellia Therapeutics (NTLA) is the lead sponsor of 6 active clinical trials listed on ClinicalTrials.gov[4], including 3 Phase 3[1], 1 Phase 2[2], 1 Phase 1[3].

Trial NCT06634420[5] evaluates NTLA-2002 in Hereditary Angioedema with a target enrollment of 60 participants. Trial NCT06672237[6] evaluates nexiguran ziclumeran in Neuromuscular Disease with a target enrollment of 50 participants. Trial NCT06128629[7] evaluates NTLA-2001 in Transthyretin Amyloidosis (ATTR) With Cardiomyopathy with a target enrollment of 1200 participants.

No Form 4 insider filings for NTLA were recorded at the SEC in the past 30 days[8].

Sources

  1. ClinicalTrials.gov (2026-04-11)
  2. ClinicalTrials.gov (2026-04-11)
  3. ClinicalTrials.gov (2026-04-11)
  4. ClinicalTrials.gov (2026-04-11)
  5. ClinicalTrials.gov · NCT06634420 (2025-12-18)
  6. ClinicalTrials.gov · NCT06672237 (2025-11-26)
  7. ClinicalTrials.gov · NCT06128629 (2026-03-27)
  8. SEC EDGAR · 0001652130 (2026-04-11)
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Upcoming Catalysts
NTLA-2001 — ATTR cardiomyopathy
2026-08-10
in 67d
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Clinical Trials
6
NCT05120830Hereditary Angioedema
Source ↗
clinicaltrials_gov · Retrieved 2026-04-11
NCT05697861Transthyretin-Related (ATTR) Familial Amyloid Polyneuropathy, Transthyretin-Related (ATTR) Familial Amyloid Cardiomyopathy, Wild-Type Transthyretin Cardiac Amyloidosis
Source ↗
clinicaltrials_gov · Retrieved 2026-04-11
NCT06128629Transthyretin Amyloidosis (ATTR) With Cardiomyopathy
Source ↗
clinicaltrials_gov · Retrieved 2026-04-11
NCT06262399Hereditary Angioedema
Source ↗
clinicaltrials_gov · Retrieved 2026-04-11
NCT06634420Hereditary Angioedema
Source ↗
clinicaltrials_gov · Retrieved 2026-04-11
NCT06672237Neuromuscular Disease, Neuromuscular Diseases (NMD), Neurodegenerative Disease, Neurodegenerative Disease, Hereditary, Neurodegenerative Diseases, Neuromuscular Diseases, Nerve Disorders, Nervous System Disease, Nervous System Diseases, Genetic Disease, Inborn, Amyloidosis, Familial, Amyloidosis, Hereditary, Amyloidosis, Polyneuropathies, Amyloid Neuropathies, Amyloid Neuropathies, Familial, Peripheral Nervous System Disease, Peripheral Nervous System Diseases, Metabolism, Inborn Errors, Metabolic Diseases
Source ↗
clinicaltrials_gov · Retrieved 2026-04-11
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Insider Activity
1
0 filings
Source ↗
sec_edgar · Retrieved 2026-04-11
Not financial advice. BiotechSigns profiles are AI-generated from verified public sources (ClinicalTrials.gov, SEC EDGAR) and are for informational purposes only. Always do your own due diligence before making investment decisions.
Score Breakdown
Score Trend
2026-04-132026-06-02
Signal Summary
PDUFA Dates1
Insider Filings1
Clinical Trials1
Data Provenance
cik1 verified
clinical trial6 verified
insider buy1 verified
trial count4 verified
Every claim backed by source URL from ClinicalTrials.gov or SEC EDGAR