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Tolerance and Efficacy Nicotinamide (Vitamin B3) in Dominant Optic Atrophy OPA1 (NICOPA1-TOL)

Primary Purpose

Nicotinamide Adverse Reaction

Status
Not yet recruiting
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Nicotinamide
Sponsored by
University Hospital, Angers
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nicotinamide Adverse Reaction

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Adult patients Patients with DOA or DOA+ due to a heterozygous pathogenic variant in the OPA1 gene Naïve patients (> 3 months) in terms of taking nicotinamide Patients able to take oral medication and comply with specific study procedures Patients affiliated or beneficiaries of a social security scheme Signature of voluntary, free and informed consent to participate in the study Exclusion Criteria: Asymptomatic patients (= healthy carriers of an OPA1 mutation but not having developed optic neuropathy) Patients with another associated severe ophthalmological pathology (advanced glaucoma, retinal pathology, etc.) Patients treated with Idebenone Patients with a level of transaminase(s) (ASAT and/or ALAT) twice higher than the high normal value. Pregnant, breastfeeding or parturient women Patients with a contraindication to nicotinamide Persons deprived of liberty by administrative or judicial decision Patients subject to a legal protection measure Persons undergoing psychiatric treatment under duress Persons unable to express their consent

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    nicotinamide

    Arm Description

    Outcomes

    Primary Outcome Measures

    Number of patient with neurologic or ophtalmological adverse event
    photopic negative response PhNR, optical coherence tomography

    Secondary Outcome Measures

    Full Information

    First Posted
    July 6, 2023
    Last Updated
    August 29, 2023
    Sponsor
    University Hospital, Angers
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    1. Study Identification

    Unique Protocol Identification Number
    NCT06007391
    Brief Title
    Tolerance and Efficacy Nicotinamide (Vitamin B3) in Dominant Optic Atrophy OPA1
    Acronym
    NICOPA1-TOL
    Official Title
    Pilot Study of Tolerance and Efficacy Nicotinamide (Vitamin B3) in Dominant Optic Atrophy OPA1
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 2023 (Anticipated)
    Primary Completion Date
    March 2025 (Anticipated)
    Study Completion Date
    September 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University Hospital, Angers

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    No

    5. Study Description

    Brief Summary
    Dominant Optic Atrophy (hereafter known as DOA) is a neurodegenerative pathology of the optic nerve inducing progressive loss of central visual field and visual acuity. There is currently no proven treatment for this disease. The metabolomics work of Pascal Reynier's team revealed a specific metabolomic signature of DOA in the plasma of patients. This metabolomic signature revealed a relative deficiency in nicotinamide compared to a control population, a vitamin compound (vitamin B3) known to be neuroprotective for the optic nerve and mitochondria. Note that the investigator have also identified this nicotinamide deficiency in primary open-angle glaucoma and Leber's hereditary optic neuropathy, the other most common cause of hereditary optic neuropathy, these three optic nerve conditions sharing a common pathophysiological mechanism of mitochondrial deficit. In addition, an American team demonstrated the high neuroprotective power on the optic nerve of nicotinamide in a mouse model of glaucoma. These arguments converge towards the potential therapeutic interest of this vitamin in degenerative pathologies of the optic nerve. This is encouraged by the fact that two randomized clinical trials have confirmed a benefit of nicotinamide in glaucoma. The objective of this pilot study is to test the tolerance and efficacy of nicotinamide in DOA and DOA+ patients.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Nicotinamide Adverse Reaction

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2, Phase 3
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    25 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    nicotinamide
    Arm Type
    Experimental
    Intervention Type
    Drug
    Intervention Name(s)
    Nicotinamide
    Intervention Description
    nicotinamide 3g per day
    Primary Outcome Measure Information:
    Title
    Number of patient with neurologic or ophtalmological adverse event
    Description
    photopic negative response PhNR, optical coherence tomography
    Time Frame
    at 6 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Adult patients Patients with DOA or DOA+ due to a heterozygous pathogenic variant in the OPA1 gene Naïve patients (> 3 months) in terms of taking nicotinamide Patients able to take oral medication and comply with specific study procedures Patients affiliated or beneficiaries of a social security scheme Signature of voluntary, free and informed consent to participate in the study Exclusion Criteria: Asymptomatic patients (= healthy carriers of an OPA1 mutation but not having developed optic neuropathy) Patients with another associated severe ophthalmological pathology (advanced glaucoma, retinal pathology, etc.) Patients treated with Idebenone Patients with a level of transaminase(s) (ASAT and/or ALAT) twice higher than the high normal value. Pregnant, breastfeeding or parturient women Patients with a contraindication to nicotinamide Persons deprived of liberty by administrative or judicial decision Patients subject to a legal protection measure Persons undergoing psychiatric treatment under duress Persons unable to express their consent

    12. IPD Sharing Statement

    Learn more about this trial

    Tolerance and Efficacy Nicotinamide (Vitamin B3) in Dominant Optic Atrophy OPA1

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