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A Clinical Trial for AMN: Validation of Biomarkers of Oxidative Stress, Efficacy and Safety of a Mixture of Antioxidants

Primary Purpose

Adrenomyeloneuropathy

Status
Completed
Phase
Phase 2
Locations
Spain
Study Type
Interventional
Intervention
N-acetylcysteine
lipoic acid
vitamin E
Sponsored by
Onofre, Aurora Pujol, M.D.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Adrenomyeloneuropathy focused on measuring XALD, AMN

Eligibility Criteria

18 Years - 64 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Symptomatic AMN patients,
  • 18-64 years old,
  • male and female,
  • clinically and biochemically diagnosed;
  • females must be obligated heterozygotes or must have gene mutation identified.

Exclusion Criteria:

  • Pregnant and lactation in females,
  • Cerebral inflammatory disease with cognitive disorder, and/or
  • need the help of two walking sticks,
  • epilepsy,
  • hypersensibility to cysteine related compounds,
  • transaminases 2 fold up normal values.

Sites / Locations

  • Hospital Universitari de Bellvitge

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

N-acetylcysteine, lipoic acid and vitamin E

Arm Description

Two Dose titration design

Outcomes

Primary Outcome Measures

oxidative lesion biomarkers
oxidative lesion biomarkers: protein, DNA and peroxidation biomarkers

Secondary Outcome Measures

clinical parameters
spasticity, disability,electroneurograms and evocated potentials. Cranial and spinal NMR will be done at the beginning and the end of the trial.

Full Information

First Posted
November 28, 2011
Last Updated
March 7, 2019
Sponsor
Onofre, Aurora Pujol, M.D.
Collaborators
Ministerio de Sanidad, Servicios Sociales e Igualdad, Fundacion Hesperia
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1. Study Identification

Unique Protocol Identification Number
NCT01495260
Brief Title
A Clinical Trial for AMN: Validation of Biomarkers of Oxidative Stress, Efficacy and Safety of a Mixture of Antioxidants
Official Title
A Clinical Trial for Adrenomyeloneuropathy (AMN): Validation of Biomarkers of Oxidative Stress, and Efficacy, Tolerance and Safety of a Mixture of the Antioxidants N-acetylcysteine, Lipoic Acid and Vitamin E
Study Type
Interventional

2. Study Status

Record Verification Date
September 2016
Overall Recruitment Status
Completed
Study Start Date
September 2011 (undefined)
Primary Completion Date
November 2013 (Actual)
Study Completion Date
November 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Onofre, Aurora Pujol, M.D.
Collaborators
Ministerio de Sanidad, Servicios Sociales e Igualdad, Fundacion Hesperia

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
X-linked adrenoleukodystrophy is a rare, demyelinating and neurodegenerative disorder, due to a loss of function of a fatty acid transporter, the peroxisomal ABCD1protein. Its more frequent phenotype, the adrenomyeloneuropathy in adults, is characterized by axonal degeneration in spinal cord, spastic paraparesis and a disabling peripheral neuropathy. Actually, there is no efficient treatment for the disease. Our work in the last twelve years dissecting the physiopathological basis of the disorder has uncovered an involvement of the oxidative stress early in the neurodegenerative cascade. In a preclinical trial we have identified an antioxidant cocktail that efficiently reverse the clinical symptoms and the axonal degeneration in the mouse model for the disease. We propose the translation of the results to an open trial to test the tolerance and effectiveness of these drugs in the correction of the previously identified oxidative lesion biomarkers, as a first step to a randomized versus placebo, multicentric and international trial. You will be clinically explored and assessed in the Hospital Universitari of Bellvitge (HUB) using clinical scales for spasticity, disability, electroneurogram and cranial and spinal Nuclear Magnetic resonance (NMR). The information will be collected in a data base that will be of great value to improve the present attention and the future follow-up to facilitate your inclusion in therapeutic randomized, double blind, against placebo clinical trials.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adrenomyeloneuropathy
Keywords
XALD, AMN

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
13 (Actual)

8. Arms, Groups, and Interventions

Arm Title
N-acetylcysteine, lipoic acid and vitamin E
Arm Type
Experimental
Arm Description
Two Dose titration design
Intervention Type
Drug
Intervention Name(s)
N-acetylcysteine
Intervention Description
N-acetylcysteine, 800-2400 mg daily for 2 months
Intervention Type
Drug
Intervention Name(s)
lipoic acid
Intervention Description
lipoic acid, 300-600 mg daily for 2 months
Intervention Type
Drug
Intervention Name(s)
vitamin E
Intervention Description
vitamin E, 150-300 mg daily for 2 months
Primary Outcome Measure Information:
Title
oxidative lesion biomarkers
Description
oxidative lesion biomarkers: protein, DNA and peroxidation biomarkers
Time Frame
12 months
Secondary Outcome Measure Information:
Title
clinical parameters
Description
spasticity, disability,electroneurograms and evocated potentials. Cranial and spinal NMR will be done at the beginning and the end of the trial.
Time Frame
2, 6 and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
64 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Symptomatic AMN patients, 18-64 years old, male and female, clinically and biochemically diagnosed; females must be obligated heterozygotes or must have gene mutation identified. Exclusion Criteria: Pregnant and lactation in females, Cerebral inflammatory disease with cognitive disorder, and/or need the help of two walking sticks, epilepsy, hypersensibility to cysteine related compounds, transaminases 2 fold up normal values.
Facility Information:
Facility Name
Hospital Universitari de Bellvitge
City
L'Hospitalet de LLobregat
State/Province
Barcelona
ZIP/Postal Code
08907
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
21786300
Citation
Lopez-Erauskin J, Fourcade S, Galino J, Ruiz M, Schluter A, Naudi A, Jove M, Portero-Otin M, Pamplona R, Ferrer I, Pujol A. Antioxidants halt axonal degeneration in a mouse model of X-adrenoleukodystrophy. Ann Neurol. 2011 Jul;70(1):84-92. doi: 10.1002/ana.22363.
Results Reference
background
PubMed Identifier
21453200
Citation
Galino J, Ruiz M, Fourcade S, Schluter A, Lopez-Erauskin J, Guilera C, Jove M, Naudi A, Garcia-Arumi E, Andreu AL, Starkov AA, Pamplona R, Ferrer I, Portero-Otin M, Pujol A. Oxidative damage compromises energy metabolism in the axonal degeneration mouse model of X-adrenoleukodystrophy. Antioxid Redox Signal. 2011 Oct 15;15(8):2095-107. doi: 10.1089/ars.2010.3877. Epub 2011 Jun 8.
Results Reference
background
PubMed Identifier
35778568
Citation
Parameswaran J, Goicoechea L, Planas-Serra L, Pastor A, Ruiz M, Calingasan NY, Guilera C, Aso E, Boada J, Pamplona R, Portero-Otin M, de la Torre R, Ferrer I, Casasnovas C, Pujol A, Fourcade S. Activating cannabinoid receptor 2 preserves axonal health through GSK-3beta/NRF2 axis in adrenoleukodystrophy. Acta Neuropathol. 2022 Aug;144(2):241-258. doi: 10.1007/s00401-022-02451-2. Epub 2022 Jul 1.
Results Reference
derived
PubMed Identifier
31077039
Citation
Casasnovas C, Ruiz M, Schluter A, Naudi A, Fourcade S, Veciana M, Castaner S, Alberti A, Bargallo N, Johnson M, Raymond GV, Fatemi A, Moser AB, Villarroya F, Portero-Otin M, Artuch R, Pamplona R, Pujol A. Biomarker Identification, Safety, and Efficacy of High-Dose Antioxidants for Adrenomyeloneuropathy: a Phase II Pilot Study. Neurotherapeutics. 2019 Oct;16(4):1167-1182. doi: 10.1007/s13311-019-00735-2.
Results Reference
derived
Links:
URL
http://www.neurometabolic-lab.org/
Description
The Neurometabolic Diseases Lab, led by ICREA Research Professor Aurora Pujol, is integrated in the Neurosciences Area of IDIBELL.
URL
http://www.idibell.cat/
Description
Related Info
URL
http://www.bellvitgehospital.cat/
Description
Related Info

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A Clinical Trial for AMN: Validation of Biomarkers of Oxidative Stress, Efficacy and Safety of a Mixture of Antioxidants

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