Ireland
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Priya Life Science Compound trial record
Compound · clinical trials

N-Acetyl-L-Leucine clinical trials

Also listed in trial records as IB1001, Levacetylleucine
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 3 trials in our UK, USA, Germany, Switzerland, Italy, Austria, Spain, Netherlands, Czechia and Australia registers that name N-Acetyl-L-Leucine as an intervention. Synced 10 Nov 2026
3Current trials
1Recruiting now
1Lead sponsor
10Country registers
At a glance

N-Acetyl-L-Leucine is named as an intervention in 3 current clinical trials in our UK, USA, Germany, Switzerland, Italy, Austria, Spain, Netherlands, Czechia and Australia registers. 1 is recruiting patients now. All registered phases are Phase 3. The lead sponsor is IntraBio Inc. The most-studied condition is CACNA1A.

Where N-Acetyl-L-Leucine is approved

All regulators →

Of the three regulators tracked here, the first to approve N-Acetyl-L-Leucine was the US, on 24 Sep 2024.

USUnited States (FDA)
24 Sep 2024
Aqneursa
NDA219132 on Drugs@FDA
First original NDA/BLA approval
EUEuropean Union (EMA)
No centralised EU authorisation (it may be authorised nationally)
First centralised authorisation
CACanada (Health Canada)
No new-drug Notice of Compliance since 1994
First new-drug NOC

From the regulators' own registers: FDA Drugs@FDA, the EMA medicines list and Health Canada's Notice of Compliance database. Dates are the first listed approval of a product containing only this substance; combination products and nationally authorised EU medicines are not counted.

N-Acetyl-L-Leucine patents and exclusivity

Expiry tracker →

Protections still running for marketed products containing N-Acetyl-L-Leucine, as listed by the regulators. Expired patents and exclusivities, and discontinued products, are not shown.

US FDA Orange Book Aqneursa
  • 4 listed patents; the last listed expires 19 Apr 2037 (US 11400067).
  • Exclusivity ODE-498: Orphan drug exclusivity: treatment of neurological manifestations of niemann-pick disease type c (npc) in adults and pediatric patients wei…, until 24 Sep 2031.
  • Exclusivity NCE: New chemical entity, until 24 Sep 2029.
See the Orange Book listing for NDA 219132

Reproduced from the FDA Orange Book and Purple Book (checked 8 Nov 2026) and the European Commission's Union Register of medicinal products (CC BY 4.0; the EU expiry date is calculated exactly as the Commission's register displays it). Listed patents and dates are as submitted to or published by the regulator and may not reflect litigation, invalidation, settlements, lapsed fees or later extensions. This is not legal advice or a freedom-to-operate opinion, and it does not say when a generic or biosimilar will launch.

What health systems spend on N-Acetyl-L-Leucine

All medicines →
ENNHS England
Not dispensed in the community in England in the last 12 months under this name
Net ingredient cost, community prescriptions
USUS Medicaid
$18.7m
463 prescriptions in 2025 · Aqneursa
Amount Medicaid reimbursed, before rebates

From NHSBSA Prescription Cost Analysis (Open Government Licence v3.0) and CMS State Drug Utilization Data. Both are gross amounts: neither system publishes its discounts or rebates per drug. Products combining several substances are not counted here.

Patient leaflets for N-Acetyl-L-Leucine

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-approved labels, including patient and medication guides.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Trials by status

  • Recruiting133%
  • Active, closed267%

Trials by phase

  • Phase 33100%
01

Clinical trials of N-Acetyl-L-Leucine

3 trials
StudyPhaseStatusLead sponsorRegisters
A Pivotal Study of N-Acetyl-L-Leucine on Niemann-Pick Disease Type C
NCT05163288 · Niemann-Pick Disease, Type C
Phase 3 Recruiting IntraBio Inc UK, USA, Germany, Netherlands, Switzerland, Czechia, Australia
A Pivotal Study of N-Acetyl-L-Leucine on Ataxia-Telangiectasia (A-T)
NCT06673056 · Ataxia-Telangiectasia, Ataxia-Telangiectasia (A-T)
Phase 3 Active, closed IntraBio Inc UK, USA, Germany, Spain, Switzerland
Pivotal Study of N-acetyl-L-leucine for CACNA1A
NCT07221292 · CACNA1A, Spinocerebellar Ataxia Type 6, Episodic Ataxia Type 2
Phase 3 Active, closed IntraBio Inc UK, USA, Germany, Italy, Switzerland, Austria

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied with N-Acetyl-L-Leucine

7 conditions
CACNA1A1Spinocerebellar Ataxia Type 61Episodic Ataxia Type 21Familial Hemiplegic Migraine-11Ataxia-Telangiectasia1Ataxia-Telangiectasia (A-T)1Niemann-Pick Disease, Type C1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
IntraBio Inc3
04

By country register

RegisterTrialsRecruiting
Clinical trials in UK31
Clinical trials in USA31
Clinical trials in Germany31
Clinical trials in Switzerland31
Clinical trials in Italy10
Clinical trials in Austria10
Clinical trials in Spain10
Clinical trials in Netherlands11
Clinical trials in Czechia11
Clinical trials in Australia11

A trial with sites in more than one country appears in each of those registers.

05

Questions about N-Acetyl-L-Leucine trials

How many clinical trials are testing N-Acetyl-L-Leucine?

3 current trials in our UK, USA, Germany, Switzerland, Italy, Austria, Spain, Netherlands, Czechia and Australia registers name N-Acetyl-L-Leucine (also registered as IB1001) as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.

Are N-Acetyl-L-Leucine trials recruiting patients?

Yes. 1 of the 3 trials is recruiting: 1 with sites in UK, 1 with sites in USA, 1 with sites in Germany, 1 with sites in Switzerland, 1 with sites in Netherlands, 1 with sites in Czechia and 1 with sites in Australia. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors N-Acetyl-L-Leucine clinical trials?

The lead sponsor is IntraBio Inc. The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how N-Acetyl-L-Leucine works or whether it is effective, and it is not medical advice.

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How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how N-Acetyl-L-Leucine works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists N-Acetyl-L-Leucine (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 10 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.