ClinicalTrials.gg
Active, not recruitingNCT06672237Updated Nov 5, 2026

A Phase 3 Study of NTLA-2001 in ATTRv-PN

A Phase 3 interventional study of nexiguran ziclumeran and Normal Saline as Placebo in Neuromuscular Disease, Neuromuscular Diseases (NMD) and Neurodegenerative Disease, sponsored by Intellia Therapeutics. Active, not recruiting at 14 sites in 6 countries. Open to participants aged 18 Years to 85 Years. Per ClinicalTrials.gov, last updated 2026-11-05.

Primary conditionPeripheral Nervous System DiseasesRegistry: Neuromuscular DiseasesReclassifiedWhy we changed it
Registry
Neuromuscular Diseases — the first condition term the registry derived for this study.
ClinicalTrials.gg
Peripheral Nervous System Diseases
Why
  1. The study's listed conditions name Peripheral Nervous System Diseases, a narrower term within Neuromuscular Diseases.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Intellia Therapeutics · Phase 3, Interventional, and Treatment

Updated Nov 5, 2026Now Active, not recruitingEnrollment updatedGo to Updates ↓
Phase
Phase 3
Study type
Interventional
Enrollment
67
Allocation
Randomized
Ages
18 Years to 85 Years
Sex
All
01

Study summary

This study will be conducted to evaluate the efficacy and safety of a single dose of nexiguran ziclumeran (NTLA-2001) compared to placebo in participants with ATTRv-PN.

Read the detailed description

This is a multinational, multicenter, double-blind, placebo-controlled study in approximately 60 participants, who will be randomized 1:1 to receive a single infusion of either nexiguran ziclumeran or placebo. To ensure all participants will have the potential to receive nexiguran ziclumeran, participants will have the option to cross over to the opposite study arm at Month 12 or Month 18, depending on study criteria.

02

Conditions studied

  • Neuromuscular 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

Keywords

  • TTR
  • Amyloidosis
  • Polyneuropathy
  • NTLA-2001
  • ATTR
  • ATTR-PN
  • ATTRv-PN
  • Transthyretin
  • TTR-mediated amyloidosis
  • Amyloidosis, hereditary
  • Amyloidosis, hereditary, transthyretin-related amyloidosis
  • Transthretin amyloid polyneuropathy
  • TTR PN
  • TTR polyneuropathy
  • nexiguran ziclumeran
  • nex-z
  • CRISPR
03

In context

Peripheral Nervous System Diseases Reclassified

476 studies on the registry are indexed under Peripheral Nervous System Diseases; 103 are open to participants now.

This study's enrollment of 67 is above the median of 57 across 359 interventional studies indexed under Peripheral Nervous System Diseases.

Browse Peripheral Nervous System Diseases studies →

Lead sponsor

Intellia Therapeutics is the lead sponsor of 9 studies on the registry; 3 are open to participants now.

Compared within Peripheral Nervous System Diseases, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Neuromuscular Diseases. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
18 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Diagnosis of ATTRv-PN
  • Performance Status (KPS) ≥ 60

Exclusion criteria

Exclusion Criteria:

  • Other causes of amyloidosis (amyloidosis caused by non-TTR protein)
  • Other known causes of sensorimotor or autonomic neuropathy
  • Diabetes mellitus
  • Class III or IV heart failure
  • Liver failure
  • , or (HIV) infection
  • Prior receipt of a TTR silencer (Small interfering RNA (siRNA) or Antisense oligonucleotides (ASOs))
  • Estimated \< 30 mL/min/1.73 m2
  • Unable or unwilling to take vitamin A supplementation for the duration of the study
  • History of liver disease
Terms in these criteria, in plain language(6)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Karnofsky performance status (KPS)

A 0–100 scale of how well someone can carry out everyday activities. 100 is no complaints and no signs of illness; 70 is able to look after yourself but not to work or keep up normal activity; 50 is needing considerable help and frequent medical care.

Studies often ask for 60 or 70 and above. Your doctor gives the score.

NYHA class (heart failure)

The New York Heart Association’s four classes of how much heart failure limits physical activity.

I
No limits: ordinary activity causes no undue tiredness or breathlessness.
II
Slight limits: comfortable at rest, ordinary activity causes symptoms.
III
Marked limits: comfortable at rest, less than ordinary activity causes symptoms.
IV
Symptoms even at rest; any activity makes them worse.

Studies set their own limit — many outside heart failure leave out class III–IV, while heart failure studies may ask for a particular class. Check the class this study names.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

GFR and eGFR (kidney filtering)

GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².

Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.

05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
67 participants (actual)

Study arms

  • Experimental
    nexiguran ziclumeran

    nexiguran ziclumeran 55 mg by single IV infusion

    Biological: nexiguran ziclumeran

  • Placebo comparator
    Normal Saline

    Placebo; Normal saline (0.9% NaCl) by single IV infusion

    Drug: Normal Saline as Placebo

Interventions

  • nexiguran ziclumeran 55 mg by single IV infusion

    Also known as: NTLA-2001

  • DrugNormal Saline as Placebo

    Normal saline (0.9% NaCl) by single IV infusion

06

What researchers measure

Primary outcomes

  1. Modified Neuropathy Impairment Score +7 (mNIS+7)

    Time frame: 18 Months

  2. Serum TTR

    Time frame: 29 Days

Secondary outcomes

  1. Norfolk Quality of Life-Diabetic Neuropathy (Norfolk QoL-DN) Questionnaire

    Time frame: 18 Months

  2. Modified Body Mass Index (mBMI)

    Time frame: 18 Months

  3. Serum TTR

    Time frame: 18 Months

07

Study locations

14 sites
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Status
Recruiting→Active, not recruiting
changed Nov 5, 2026
Enrollment
60 (estimated)→67 (actual)
Nov 5, 2026
Show all 1 update
  1. Nov 5, 2026
    Recruiting→Active, not recruiting
    Enrollment 60 (estimated)→67 (actual)
    + 3 other changes: verification date, contact details and site details

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT06672237
Lead sponsor
Intellia Therapeutics
Responsible party
Sponsor
First posted
Nov 4, 2024
Start date
Nov 22, 2024
Primary completion
Jul 2027 (estimated)
Completion
Aug 2028 (estimated)
Last update
Nov 5, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Studies of the drug tested here: NTLA-2001

Start the discussion