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Myasthenia GravisEARLY-MGNCT07411963

Evaluation of the Condition of Patients Receiving EARLY Ravulizumab and Admitted in ICU for gMG Crisis

An observational study of Myasthenia Gravis, run by Centre Hospitalier Universitaire de Nice at 8 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 Gravis (MG) is a rare autoimmune disease that causes muscle weakness and fatigue. It occurs when the immune system produces antibodies that block communication between nerves and muscles. In some patients, the disease can suddenly worsen and cause severe breathing problems. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Myasthenia Gravis
What is being tested?
early use of Ravulizumab
How many people
30 participants
Where
8 sitesFrance
Study dates
26 Nov 2025to 1 Jun 2027
Phase
Observational
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

Study population: Patients with myasthenia gravis

Who may be able to join

  • Male or female aged ≥18 years.
  • Diagnosed with gMG with confirmed documentation and supported by a physical exam and confirmed seropositivity for AChR-Abs.
  • Patients having received more than 1 cycle of PLEX or IVIg 1-2 g/kg (max 50g/day), according to clinical practice.
  • Meets the clinical criteria as defined by the Myasthenia Gravis Foundation of America (MFGA) for generalized MG class V - IV, at ICU admission.
  • Patients treated with at least one standard MG-targeted therapy.
  • Patients receiving Ravulizumab following PLEX of IVIg during their stay in the ICU, as per local label and reimbursement conditions. The prescription must be validated by experts from the French Health Care Network for rare neuromuscular diseases FILNEMUS.
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  • Patients capable of understanding written informed consent and providing signed, dated, and witnessed written informed consent. If unable to sign the consent due to muscular weakness, a dedicated informed consent can be signed by a trusted witness.
  • Patients willing and able to comply with scheduled visits, treatment plan, study restrictions and other study procedures.
  • Patients affiliated to a European social security system.
  • Patients agree to comply with the prevention of meningococcal infections by vaccination and/or antibiotic prophylaxis in accordance with the current local vaccination/antibiotic prophylaxis recommendations.
  • Patients with no contraindication to anti-C5 treatment.
  • Patients with no contraindication to antibiotic therapy.

Who cannot join

  • Active infection or other disorders causing weakness, known immunoglobulin A deficiency, active renal or hepatic disease, clinically significant cardiac disease, known hyperviscosity, or hypercoagulable state.
  • Any active malignancy.
  • Presence of antibodies other than anti-AChR-Ab+ (anti-titin-Ab+ were permitted as these are considered complementary markers to anti-AChR-Ab+).
  • Patient with a diagnosed thymoma.
  • Patient with a pathology judged by the investigator to interfere with the proper conduct of the study.
  • Positive pregnancy test. A urine pregnancy test will be carried out for women of childbearing age.
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  • Any current mental condition (psychiatric disorder, senility, or dementia) that, in the opinion of the investigator, may affect study compliance or prevent understanding of the aims, investigational procedures, or possible consequences of the study.
  • Vaccination with live or live-attenuated vaccines within the 6 weeks.
  • Refusal of the subject to participate in the study.
  • Patient protected by law, under guardianship or curator ship, or not able to participate in a clinical study according to the article L.1121-16 of the French Public Health Code.
  • Known hypersensitivity to the active substance or to any of the excipients.

Trial locations and contacts

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

Sabrina SACCONI contact

0492035757

sacconi.s@chu-nice.fr

8 sites in 1 country

France8 sites, 8 recruiting
  • Hospices Civils de Lyon

    Bron, 69500

    Juliette SVAHN, PH, +33472116608, juliette.svahn@chu-lyon.fr

    Not yet recruiting
  • Hôpital Raymond Pointcarré

    Garches, 92380

    Diane FRIEDMAN, PH, +33147107785, friedman.diane@aphp.fr

    Not yet recruiting
  • APHP

    Le Kremlin-Bicêtre, 94275

    Céline Labeyrie, PH, +33145213159, celine.labeyrie@aphp.fr

    Recruiting
  • CHU de Lille

    Lille, 59037

    Céline TARD, PH, +33320444145, celine.tard@chu-lille.fr

    Recruiting
  • CHu de la Timone

    Marseille, 13385

    Shahram ATTARIAN, PU-PH, shahram.attarian@ap-hm.fr

    Recruiting
  • CHU de NICE

    Nice, Alpes-maritimes, 06000

    Sabrina SACCONI, 0492035757, sacconi.s@chu-nice.fr

    Recruiting
  • Hôpitaux universitaires de Strasbourg

    Strasbourg, 67200

    Aleksandra NADAJ-PALEKZA, PH, +33388128559, aleksandra.nadaj-pakleza@chru-strasbourg.fr

    Recruiting
  • CHU Pierre Paul Riquet

    Toulouse, 31059

    Blandine ACKET, PH, +33561779989, acket.b@chu-toulouse.fr

    Not yet recruiting

Other trials in France

About this study

Official title: Evaluation of the Condition of Patients Receiving EARLY Treatment With Ravulizumab and Admitted in ICU for Generalized Myasthenia Gravis (gMG) Crisis : an Observational Prospective Multicentric Study in France

Myasthenia Gravis (MG) is a rare autoimmune disease that causes muscle weakness and fatigue. It occurs when the immune system produces antibodies that block communication between nerves and muscles. In some patients, the disease can suddenly worsen and cause severe breathing problems. This life-threatening situation is called a myasthenic crisis and requires immediate treatment in an intensive care unit (ICU). During such crises, patients may need to receive respiratory assistance through a ventilator. These episodes are often long and can lead to complications such as infections or heart problems.

To manage a myasthenic crisis, doctors usually use treatments that remove or neutralize the harmful antibodies: plasma exchange (PLEX) or intravenous immunoglobulin (IVIg). Although both are effective, recovery can be slow, and many patients remain in the ICU for several weeks.

Read more

Ravulizumab (Ultomiris®) is a new medicine that targets a specific part of the immune system called the complement system, which contributes to muscle damage in MG. It is already approved for adults with generalized MG who have anti-acetylcholine receptor (AChR) antibodies. Ravulizumab is given by intravenous infusion every eight weeks. Clinical studies have shown that it can improve symptoms within one week of starting treatment.

Some doctors have started using ravulizumab early, after PLEX or IVIg, for patients hospitalized in the ICU for a myasthenic crisis. Early use of this treatment could help reduce the duration and severity of the crisis, leading to faster recovery and shorter hospital stays. However, there is currently no national study that systematically collects data on this approach.

The EARLY-MG study aims to describe the condition and recovery of patients who receive ravulizumab early during a myasthenic crisis requiring ICU admission. The study will not test an experimental treatment or change medical care. It is an observational study.

The main hypothesis of the study is that early administration of ravulizumab, after PLEX or IVIg, may help patients recover faster, improve muscle strength, and reduce complications and hospital stay.

Around 30 adult patients with generalized MG and anti-AChR antibodies will be enrolled in 10 centers across France.

Each patient will be followed for 26 weeks (about six months). Assessments will be performed at the start of the study and at weeks 2, 4, 10, 18, and 26. Investigators will collect information such as:

  • Duration of stay in the ICU and in the hospital after receiving ravulizumab
  • Duration of mechanical ventilation, if needed
  • Clinical improvement using standard evaluation scales (Myasthenia Gravis Activities of Daily Living, MG Foundation of America classification, and Garches' score)
  • Occurrence of any complications or additional treatments The study will last about 18 months in total, including one year for patient inclusion and six months of follow-up per patient. The results may help guide future recommendations and improve patient care in France and worldwide.
Being tested
early use of Ravulizumab
Medical subject headings
Myasthenia Gravis

What participants receive

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

  • early use of RavulizumabOther

    early use of Ravulizumab after PLEX or IVIg for a MG crisis in previously treated anti-AChR antibody-positive (anti-AChR-Ab+) patients with gMG

What is being measured

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

  1. Short-term change in clinical outcomes

    The change from the inclusion to week 2, week 4, and week 10 in the Myasthenia Gravis Activities of Daily Living scale (score from 0 - normal to 3 - worse outcome)

    Measured: Week 0, 2, 4 and 10

  2. Short-term change in clinical outcomes

    The change from the inclusion to week 2, week 4, and week 10 in the Myasthenia Gravis Foundation of America (from class I to class V - worse outcome)

    Measured: Week 0, 2, 4 and 10

  3. Short-term change in clinical outcomes

    The change from the inclusion to week 2, week 4, and week 10 in the Garches' score (from 0 to 100 with lower score indicating a greater disease severity)

    Measured: Week 0, 2, 4 and 10

Secondary outcomes (11)
  1. Long term change in clinical outcomes 1

    change from the inclusion at week 18 and week 26 in the Myasthenia Gravis Activities of Daily Living scale (score from 0 - normal to 3 - worse outcome)

    Measured: Week 18 and 26

  2. Long term change in clinical outcomes 2

    change from the inclusion at week 18 and week 26 in the Myasthenia Gravis Foundation of America scale (from class I to class V - worse outcome)

    Measured: Week 18 and 26

  3. Long term change in clinical outcomes 3

    change from the inclusion at week 18 and week 26 in the Garches' score (from 0 to 100 with lower score indicating a greater disease severity)

    Measured: Week 18 and 26

  4. Time to observe a clinical improvement

    time in days to reach the Myasthenia Gravis Foundation of America III category on the Myasthenia Gravis Foundation of America scale (from class I to class V - worse outcome)

    Measured: From the day the patient begin the study to the first day the patient reach the Myasthenia Gravis Foundation of America III category - in days, up to 180 days

  5. Time in days from Ravulizumab administration to the day of ICU discharge

    Time in days from Ravulizumab administration to the day of ICU discharge

    Measured: From the day the patient begin the Ravulizumab administration to the day the patient leaves ICU - in days, up to 180 days

  6. Total Length Of Stay at the hospital after Ravulizumab administration

    The time in days from Ravulizumab administration to the day of hospital discharge

    Measured: From the day the patient begin the Ravulizumab administration to the day the patient leaves the hospital - in days, up to 180

  7. Duration of ventilation after ravulizumab administration

    if applicable, measured in days, calculated from the beginning to the end of the ventilation.

    Measured: From the day the patient begin the Ravulizumab administration to the day the patient leaves ICU - in days, up to 180 days

  8. Patient's condition

    Evaluated by the type of medical complications.

    Measured: Ongoing from ICF signing to the end of the study

  9. Patient's condition

    Evaluated by the severity of medical complications.

    Measured: Ongoing from ICF signing to the end of the study

  10. Patient's condition

    Evaluated by the frequency of medical complications.

    Measured: Ongoing from ICF signing to the end of the study

  11. Patient's condition

    Evaluated by the seriousness of medical complications.

    Measured: Ongoing from ICF signing to the end of the study

Timeline

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

  1. First posted17 Feb 2026
  2. Study start26 Nov 2025
  3. Primary completion1 Dec 2026 (estimated)
  4. Study completion1 Jun 2027 (estimated)

Resources

More details

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

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07411963
Sponsor's protocol ID
25-PP-09
Acronym
EARLY-MG
Status last verified
Aug 2026
First submitted
4 Dec 2025
Last updated
1 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Myasthenia Gravis, run by Centre Hospitalier Universitaire de Nice at 8 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 12 inclusion and 11 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 1 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 8 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.

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 Sabrina SACCONI (0492035757, sacconi.s@chu-nice.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Short-term change in clinical outcomes (time frame: Week 0, 2, 4 and 10). The study lists 3 primary outcomes in all. 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 1 Sep 2026.

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