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Ocular Myasthenia GravisPhase 3IMCOMGNCT06342544

Immediate Corticosteroid Therapy and Rituximab to Prevent Generalization in Ocular Myasthenia: a PROBE Multicenter Open-label Randomized Controlled Trial.

A Phase 3 study testing immediate treatment with corticosteroids and addition of rituximab if recurrence in people with Ocular Myasthenia Gravis, run by Fondation Ophtalmologique Adolphe de Rothschild at 11 sites in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Myasthenia is an autoimmune disease causing dysfunction of the neuromuscular junction, resulting in fluctuating and variable muscle weakness. In the initial phase of the disease, 70% of patients present with ocular onset myasthenia (OMG), i.e. weakness limited to the oculomotor muscles. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Ocular Myasthenia Gravis
What is being tested?
immediate treatment with corticosteroids and addition of rituximab if recurrence
Could I receive a placebo?
No, everyone receives an active treatment
How many people
128 participants
Where
11 sitesFrance
Study dates
29 Apr 2025to Jun 2029
Phase
Phase 3
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patients over 18 years of age
  • Diagnosis of ocular myasthenia within the last 6 months, defined :
  • either by a typical clinical examination objectified by an expert clinician: ptosis and/or binocular diplopia, with a variable and fluctuating character (either spontaneous or provoked by effort or rest)
  • or by positive anti-AChR antibodies or the presence of decrement on repetitive nerve stimulation or a positive edrophonium test
  • Ocular symptoms lasting at least one month and limited to extra-ocular muscles (weakness in one or both orbicularis oculi)
  • No non-ocular symptoms on MMS, MGC and MG-ADL.
  • Naïve to immunosuppressive therapy for ocular myasthenia gravis.

Who cannot join

  • Thymoma
  • Pupillary anomaly other than that resulting from previous local disease or surgery.
  • Signs of restrictive abduction or supraduction myopathy due to dysthyroid ophthalmopathy.
  • Graves' ophthalmopathy
  • Onset of ocular symptoms more than one year before screening date
  • Hypersensitivity to rituximab, murine proteins, prednisone, methylprednisone, aziathioprine or 6-mercaptopurine, paracetamol, dexchlorpheniramine.
Show all 17Show fewer
  • Any infectious condition
  • Patients with severe immune deficiency
  • Severe heart failure (New York Heart Association (NYHA) Class IV) or severe uncontrolled heart disease
  • Severe hepatic insufficiency
  • Psychotic states not yet controlled by treatment
  • Hyperuricemia on xanthine oxidase inhibitors (allopurinol and febuxostat)
  • Risk of angle-closure glaucoma
  • Risk of urinary retention due to urethro-prostatic disorders
  • Vaccination with live attenuated vaccine required during study and up to 6 months after rituximab discontinuation
  • Women of childbearing age who do not wish to use effective contraception during their participation and at least 12 months after
  • Pregnant or breast-feeding women

Trial locations and contacts

11 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Antoine Gueguen contact

+33148036852

agueguen@for.paris

11 sites in 1 country

France11 sites, 8 recruiting
  • Centre Hospitalier Universitaire De Bordeaux

    Bordeaux, 33000

    Dr Guilhem Sole, +33557821380, guilhem.sole@chu-bordeaux.fr

    Dr Guilhem Sole

    Recruiting
  • Hôpital Raymond Pointcarre

    Garches, 92380

    Dr Edouard Berling, +33147107900, edouard.berling@aphp.fr

    Dr Edouard Berling

    Not yet recruiting
  • Centre Hospitalier Universitaire De Lille

    Lille, 59037

    Dr Céline Tard, +33320444145, celine.tard@chru-lille.fr

    Dr Céline Tard

    Recruiting
  • Hospices Civils De Lyon

    Lyon, 69500

    Pr Caroline Froment, +33472118012, caroline.froment01@chu-lyon.fr

    Pr Caroline Froment

    Recruiting
  • Centre Hospitalier Universitaire De Nice

    Nice, 06000

    Dr Saskia Bresch, +33492038173, bresch.s@chu-nice.fr

    Dr Saskia Bresch

    Recruiting
  • CHNO

    Paris, 75012

    Active, not recruiting
  • Hôpital de la Pitié-Salpêtrière

    Paris, 75013

    Dr Sophie Demeret, +33142161831, sophie.demeret@aphp.fr

    Dr Sophie Demeret

    Not yet recruiting
  • Centre Hospitalier Sainte Anne

    Paris, 75014

    Active, not recruiting
  • Fondation Adolphe de Rothschild

    Paris, 75019

    Dr Antoine Gueguen, +33148036755, agueguen@for.paris

    Dr Antoine Gueguen

    Recruiting
  • Les Hopitaux Universitaires De Strasbourg

    Strasbourg, 67098

    Dr Aleksandra Nadaj-Pakleza, +33388128556, Aleksandra.Nadaj-Pakleza@chru-strasbourg.fr

    Dr Aleksandra Nadaj-Pakleza

    Recruiting
  • Centre Hospitalier Universitaire De Toulouse

    Toulouse, 31300

    Active, not recruiting

Other trials in France

About this study

Myasthenia is an autoimmune disease causing dysfunction of the neuromuscular junction, resulting in fluctuating and variable muscle weakness.

In the initial phase of the disease, 70% of patients present with ocular onset myasthenia (OMG), i.e. weakness limited to the oculomotor muscles. Generalization to skeletal, bulbar and axial muscles occurs in 20-40% of cases, with a higher frequency in the first and second years, respectively 46% and 60% of generalizations. This reflects the maturation of the autoimmune response in the early years of the disease, and represents a therapeutic window of opportunity to modify the course of the disease.

Read more

Generalization is a critical event, putting the patient at risk of admission to an intensive care unit and necessitating the use of long-term immunosuppressants.

There is currently no validated strategy for preventing generalization. On the one hand, a preventive role for corticosteroid therapy in ocular-onset myasthenia has been observed in some studies, but not confirmed by others. These contradictory results may be explained by the bias of retrospective observational studies and the use of different corticosteroid administration regimens.

On the other hand, recent data on the use of low-dose Rituximab in the early phase of the disease shows greater efficacy than later use, enabling prolonged remission of the disease with a very good tolerability profile.

We propose to compare in a randomized controlled trial the usual practice with a proactive strategy with a standardized corticosteroid regimen immediate at diagnosis.

Patients with ocular myasthenia are usually treated symptomatically with acetylcholinesterase inhibitors. The introduction of corticosteroids is delayed and limited to patients with persistent disabling diplopia or ptosis with occlusion. When corticosteroids are tapered off, ocular symptoms may recur. This level of corticosteroid dependence observed in patients treated for ocular myasthenia has not been specifically studied. In order to reduce the levels of corticosteroids administered and avoid recurrence of ocular symptoms and their delayed generalization, it is usually proposed to introduce another immunosuppressant.

The aim of this study is to evaluate the efficacy of a standardized proactive prevention strategy on the generalization of ocular onset myasthenias during the first 2 years. It will combine immediate treatment with corticosteroids at the time of diagnosis, with the addition of rituximab in the event of recurrence of ocular symptoms as corticosteroids are tapered off.

Being tested
immediate treatment with corticosteroids, addition of rituximab if recurrence
Medical subject headings
Myasthenia Gravis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • immediate treatment with corticosteroidsDrug

    Immediate standardized treatment with corticosteroids. Standardized treatment in the experimental arm will start at 0.5mg/kg/d prednisone.

  • addition of rituximab if recurrenceDrug

    rituximab added if ocular symptoms reappear as corticosteroids are tapered off. Rituximab will be given at a dose of 500mg/6months for 12 months.

Study groups in NCT06342544
Study groupRoleWhat they receive
immediate treatment with corticosteroids addition of rituximab if recurrenceExperimentalNot described
Receives: Drug: immediate treatment with corticosteroids; Drug: addition of rituximab if recurrence
based on standard practiceNo interventionNot described

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. proportion of patients who progressed to generalized myasthenia within 2 years of follow-up

    Generalization is defined by a loss of 5 points or more on any Myasthenic Muscle Score (MMS) item, excluding "eyelid occlusion" and "extrinsic ocular musculature".

    Progress towards generalization will be assessed by an expert physician, blinded to the intervention arm.

    Measured: Day0 to month24

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Apr 2024
  2. Study start29 Apr 2025
  3. Primary completionJun 2028 (estimated)
  4. Study completionJun 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
128 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06342544
Sponsor's protocol ID
AGN_2023_14
Acronym
IMCOMG
Status last verified
Jan 2026
First submitted
22 Mar 2024
Last updated
21 Jan 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing immediate treatment with corticosteroids and addition of rituximab if recurrence in people with Ocular Myasthenia Gravis, run by Fondation Ophtalmologique Adolphe de Rothschild at 11 sites in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 17 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 21 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 11 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Antoine Gueguen (+33148036852, agueguen@for.paris), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

proportion of patients who progressed to generalized myasthenia within 2 years of follow-up (time frame: Day0 to month24). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Jan 2026.

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