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Generalized Myasthenia GravisPhase 3RELIEVENCT06744920

A Study to Investigate the Efficacy, Safety and Tolerability of Remibrutinib Versus Placebo in Adult Patients With Generalized Myasthenia Gravis

A Phase 3 study testing Remibrutinib (Blinded) and Remibrutinib (Open Label) in people with Generalized Myasthenia Gravis, run by Novartis Pharmaceuticals at 120 sites in 20 countries.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
Search all trials

Trial summary

A study to evaluate the efficacy, safety and tolerability of Remibrutinib versus placebo in adult patients with Generalized Myasthenia Gravis who are on stable, standard-of-care (SOC) treatment. Read more about this study

Who is it for?
Ages 18 to 85 years
Conditions the study is for
Generalized Myasthenia Gravis
What is being tested?
Remibrutinib (Blinded) and Remibrutinib (Open Label)
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
180 participants
Where
120 sitesin 20 countries
Study dates
7 Feb 2025to 26 Feb 2033
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 to 85 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Adult patients with gMG (age 18-85 years)
  • Confirmed diagnosis of Myasthenia Gravis Foundation of America (MGFA) Class II-IV gMG at screening and likely not in need of a respirator for the duration of the study, as judged by the Investigator
  • Documented evidence of positive serologic testing for AChR+ antibody or MuSK+ antibody at screening, OR seronegative for both AChR and MuSK antibodies at screening
  • Baseline MG-ADL score ≥ 6 with ≥ 50% of the total score due to non ocular symptoms
  • Participants who have been receiving a standard-of-care treatment as specified in the protocol
  • Able to safely swallow the study medication according to investigator clinical judgement based on a bedside swallowing test or another formal swallowing test in line with local practice, both at Screening and Baseline

Who cannot join

  • Prior to baseline have been treated with intravenous immunoglobulins or plasma exchange (IVIg/PLEX) in the past month, with rituximab in the past 6 months, eculizumab in the past 2 months, ravulizumab or other complement inhibitors in the past 3 months, efgartigimod or other anti-FcRn therapies in the past 3 months, or had a thymectomy in the past 6 months or a planned thymectomy during the trial period
  • Women of child bearing potential, defined as all women physiologically capable of becoming pregnant, from menarche until becoming post-menopausal, unless they are using highly effective methods of contraception during dosing and for 1 week after stopping of study treatment
  • Other protocol-defined inclusion/exclusion criteria may apply.

Trial locations and contacts

120 sites in 20 countries.

120 sites in 20 countries

United States23 sites
  • Mid Atlantic Epilepsy and Sleep Ctr

    Bethesda, Maryland, 20817-1807

  • SFM Clinical Research LLC

    Boca Raton, Florida, 33487

  • Massachusetts General Hospital

    Boston, Massachusetts, 02114

  • Dent Neurological Institute

    Buffalo, New York, 14209

  • University of Chicago Medical Centr

    Chicago, Illinois, 60637

  • Cleveland Clinic Foundation

    Cleveland, Ohio, 44195

  • Michigan State University-Department of Neurology

    East Lansing, Michigan, 48824

  • Fullerton Neuro and Headache Ctr

    Fullerton, California, 92835

  • Center for Neurological Disorders G

    Greenfield, Wisconsin, 53228-1321

  • Homestead Assoc In Research Inc

    Homestead, Florida, 33033

  • Houston Methodist Hospital

    Houston, Texas, 77030

  • UT Health Science Center

    Houston, Texas, 77030

  • University Of Southern California

    Los Angeles, California, 90033

  • Neurology Associates PA

    Maitland, Florida, 32751

  • AdventHealth

    Orlando, Florida, 32804

  • Neurological Services of Orlando PA

    Orlando, Florida, 32806

  • Neuromuscular Research Center

    Phoenix, Arizona, 85013

  • University of Pittsburgh Medical Center

    Pittsburgh, Pennsylvania, 15213

  • California Pacific Medical Center

    Sacramento, California, 94115

  • University of Texas Health Science Center at San Antonio

    San Antonio, Texas, 78229-3900

  • Honor Health Research Institute

    Scottsdale, Arizona, 85258

  • University of WA Division of Cardio

    Seattle, Washington, 98195

  • Medstar Washington Hospital Center

    Washington D.C., District of Columbia, 20010-2975

Other trials in United States

Japan14 sites
  • Novartis Investigative Site

    Chiba, 2608677

  • Novartis Investigative Site

    Fukuoka, 8128582

  • Novartis Investigative Site

    Fukushima, 9601295

  • Novartis Investigative Site

    Hanamaki, Iwate, 0250082

  • Novartis Investigative Site

    Higashi-Matsuyama, Saitama, 3550005

  • Novartis Investigative Site

    Hiroshima, 7348551

  • Novartis Investigative Site

    Koshigaya, Saitama, 3438555

  • Novartis Investigative Site

    Nishinomiya, Hyōgo, 6638501

  • Novartis Investigative Site

    Sapporo, Hokkaido, 0608543

  • Novartis Investigative Site

    Sapporo, Hokkaido, 0630005

  • Novartis Investigative Site

    Sendai, Miyagi, 9838520

  • Novartis Investigative Site

    Shinjuku Ku, Tokyo, 1600023

  • Novartis Investigative Site

    Shinjuku-ku, Tokyo, 1608582

  • Novartis Investigative Site

    Suita, Osaka, 5650871

Other trials in Japan

China12 sites
  • Novartis Investigative Site

    Beijing, 100034

  • Novartis Investigative Site

    Beijing, 100730

  • Novartis Investigative Site

    Changchun, Jilin, 130021

  • Novartis Investigative Site

    Guangzhou, Guangdong, 510080

  • Novartis Investigative Site

    Hefei, Anhui, 230001

  • Novartis Investigative Site

    Qingdao, 266000

  • Novartis Investigative Site

    Shanghai, 200040

  • Novartis Investigative Site

    Shanghai, 200080

  • Novartis Investigative Site

    Shijiazhuang, Hebei, 050030

  • Novartis Investigative Site

    Wuhan, Hubei, 430030

  • Novartis Investigative Site

    Wuxi, Jiangsu, 214023

  • Novartis Investigative Site

    Zhengzhou, Henan, 450003

Other trials in China

Poland12 sites
  • Novartis Investigative Site

    Bydgoszcz, 85-065

  • Novartis Investigative Site

    Katowice, 40-689

  • Novartis Investigative Site

    Krakow, POL, 31-505

  • Novartis Investigative Site

    Lodz, 93-113

  • Novartis Investigative Site

    Lublin, Lublin Voivodeship, 20-064

  • Novartis Investigative Site

    Lublin, Lublin Voivodeship, 20-080

  • Novartis Investigative Site

    Lublin, 20-410

  • Novartis Investigative Site

    Lublin, 20-701

  • Novartis Investigative Site

    Poznan, 61-731

  • Novartis Investigative Site

    Skorzewo, 60-185

  • Novartis Investigative Site

    Warsaw, 01-684

  • Novartis Investigative Site

    Warsaw, 02-172

Other trials in Poland

India8 sites
  • Novartis Investigative Site

    Gurugram, Haryana, 122011

  • Novartis Investigative Site

    Hyderabad, Telangana, 500082

  • Novartis Investigative Site

    Lucknow, Uttar Pradesh, 226007

  • Novartis Investigative Site

    Ludhiana, Punjab, 141001

  • Novartis Investigative Site

    Mangalore, Karnataka, 575002

  • Novartis Investigative Site

    Nashik, Maharashtra, 422005

  • Novartis Investigative Site

    New Delhi, National Capital Territory of Delhi, 110029

  • Novartis Investigative Site

    Vellore, Tamil Nadu, 632004

Other trials in India

France6 sites
  • Novartis Investigative Site

    Bordeaux, 33076

  • Novartis Investigative Site

    Nice, 06000

  • Novartis Investigative Site

    Paris, 75013

  • Novartis Investigative Site

    Paris, 75940

  • Novartis Investigative Site

    Strasbourg, 67081

  • Novartis Investigative Site

    Toulouse, 31059

Other trials in France

Argentina5 sites
  • Novartis Investigative Site

    Buenos Aires, C1012AAR

  • Novartis Investigative Site

    Caba, C1055AAF

  • Novartis Investigative Site

    Capital Federal, C1023AAB

  • Novartis Investigative Site

    Rosario, Santa Fe Province, 2000

  • Novartis Investigative Site

    San Miguel de Tucumán, T4000AXL

Other trials in Argentina

Brazil5 sites
  • Novartis Investigative Site

    Brasília, Federal District, 70200-730

  • Novartis Investigative Site

    Caxias do Sul, Rio Grande do Sul, 95070-560

  • Novartis Investigative Site

    Porto Alegre, Rio Grande do Sul, 90480-110

  • Novartis Investigative Site

    Salvador, Estado de Bahia, 40050-410

  • Novartis Investigative Site

    São Paulo, 05403-000

Other trials in Brazil

Spain5 sites
  • Novartis Investigative Site

    Barcelona, 08035

  • Novartis Investigative Site

    Lleida, 25198

  • Novartis Investigative Site

    Madrid, 28034

  • Novartis Investigative Site

    Málaga, 29010

  • Novartis Investigative Site

    Valencia, 46026

Other trials in Spain

Taiwan5 sites
  • Novartis Investigative Site

    Kaohsiung City, 833

  • Novartis Investigative Site

    Tainan, 704302

  • Novartis Investigative Site

    Taipei, 10002

  • Novartis Investigative Site

    Taipei, 111045

  • Novartis Investigative Site

    Taoyuan, 33305

Other trials in Taiwan

Germany4 sites
  • Novartis Investigative Site

    Frankfurt am Main, Hesse, 60590

  • Novartis Investigative Site

    Gummersbach, 51643

  • Novartis Investigative Site

    Hamburg, 20246

  • Novartis Investigative Site

    Münster, 48149

Other trials in Germany

South Korea4 sites
  • Novartis Investigative Site

    Busan, 49241

  • Novartis Investigative Site

    Seoul, 03080

  • Novartis Investigative Site

    Seoul, 03722

  • Novartis Investigative Site

    Seoul, 05278

Other trials in South Korea

Canada3 sites
  • Novartis Investigative Site

    London, Ontario, N6A 5W9

  • Novartis Investigative Site

    Ottawa, Ontario, K1H 8L6

  • Novartis Investigative Site

    Québec, Quebec, G1J 1Z4

Other trials in Canada

Georgia3 sites
  • Novartis Investigative Site

    Kutaisi, 4600

  • Novartis Investigative Site

    Tbilisi, 0114

  • Novartis Investigative Site

    Tbilisi, 0144

Other trials in Georgia

Romania3 sites
  • Novartis Investigative Site

    Brasov, 500283

  • Novartis Investigative Site

    Bucharest, 040215

  • Novartis Investigative Site

    Sibiu, 550245

Other trials in Romania

Serbia3 sites
  • Novartis Investigative Site

    Belgrade, 11000

  • Novartis Investigative Site

    Niš, 18108

  • Novartis Investigative Site

    Novi Sad, 21000

Other trials in Serbia

Italy2 sites
  • Novartis Investigative Site

    Bergamo, BG, 24127

  • Novartis Investigative Site

    Orbassano, TO, 10043

Other trials in Italy

Australia1 site
  • Novartis Investigative Site

    Fitzroy, Victoria, 3065

Other trials in Australia

Netherlands1 site
  • Novartis Investigative Site

    Amsterdam, North Holland, 1105 AZ

Other trials in Netherlands

United Kingdom1 site
  • Novartis Investigative Site

    London, SW17 0QT

Other trials in United Kingdom

About this study

Official title: A Randomized, Double-blind, Placebo-controlled Phase III Study to Evaluate the Efficacy, Safety, and Tolerability of Remibrutinib in Patients With Generalized Myasthenia Gravis, Followed by an Open-label Extension Phase

A study to evaluate the efficacy, safety and tolerability of Remibrutinib versus placebo in adult patients with Generalized Myasthenia Gravis who are on stable, standard-of-care (SOC) treatment.

Read the detailed description

This study is a randomized, double-blind, placebo-controlled, multicenter, Phase III study, to evaluate the efficacy, safety and tolerability of remibrutinib in gMG patients who are on stable SOC treatment. Approximately 180 eligible participants will be randomized in a ratio of 1:1, to receive either remibrutinib or matching placebo.

The study consists of a Core Part (6-months double-blind treatment) and an Extension Part (up to 60-month open-label treatment).

Being tested
Remibrutinib (Blinded), Placebo, Remibrutinib (Open Label)
Keywords
Myasthenia Gravis, gMG, Generalized Myasthenia Gravis, LOU064, Remibrutinib, placebo-controlled, double-blind, phase III
Medical subject headings
Myasthenia Gravis

What participants receive

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

  • Remibrutinib (Blinded)Drug

    Also called LOU64

    Remibrutinib (Blinded) active treatment

  • PlaceboOther

    Placebo

  • Remibrutinib (Open Label)Drug

    Also called LOU064

    Remibrutinib (Open Label) active treatment

Study groups in NCT06744920
Study groupRoleWhat they receive
Remibrutinib armExperimentalCore Part: Remibrutinib tablet taken orally [Extension Part: Open-label remibrutinib tablet taken orally]
Receives: Drug: Remibrutinib (Blinded); Drug: Remibrutinib (Open Label)
Placebo armPlacebo comparatorCore Part: Placebo tablet taken orally [Extension Part: Open-label remibrutinib tablet taken orally]
Receives: Other: Placebo; Drug: Remibrutinib (Open Label)

What is being measured

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

  1. Change from baseline to Month 6 in Myasthenia Gravis Activity of Daily Living (MG-ADL) total score

    The MG-ADL is a categorical scale that assesses MG symptoms and their effects on daily activities. MG-ADL is composed of items related to patient's assessment of functional disability secondary to ocular (2 items), bulbar (3 items), respiratory (1 item), and gross motor or limb (2 items) impairment related to effects from MG.

    Each item is assessed on a 4-points scale where a score 0 represents normal function and a score 3 represents loss of ability to perform that function (total score 0 to 24).

    Measured: Baseline to Month 6

Secondary outcomes (16)
  1. Change from baseline to Month 6 in Quantitative Myasthenia Gravis (QMG) total score

    The Quantitative Myasthenia Gravis (QMG) Score is a 13-item direct physician assessment scoring system that quantifies disease severity, based on impairments of body functions and structures. The total QMG score ranges from 0 to 39, where higher scores indicated greater disease severity. The QMG score is composed of the following items: ocular (2 items), facial (1 item), bulbar (2 items), gross motor (6 items), axial (1 item) and respiratory (1 item).

    Measured: Baseline to Month 6

  2. Proportion of participants with ≥ 5 points reduction from baseline to Month 6 of QMG total score without rescue medication and/or strongly confounding prohibited medication

    The Quantitative Myasthenia Gravis (QMG) Score is a 13-item direct physician assessment scoring system that quantifies disease severity, based on impairments of body functions and structures. The total QMG score ranges from 0 to 39, where higher scores indicated greater disease severity. The QMG score is composed of the following items: ocular (2 items), facial (1 item), bulbar (2 items), gross motor (6 items), axial (1 item) and respiratory (1 item).

    Measured: Baseline to Month 6

  3. Proportion of participants with ≥ 3 points reduction from baseline to Month 6 of Myasthenia Gravis Activity of Daily Living (MG-ADL) scale total score without rescue medication and/or strongly confounding prohibited medication

    The MG-ADL is a categorical scale that assesses MG symptoms and their effects on daily activities. MG-ADL is composed of items related to patient's assessment of functional disability secondary to ocular (2 items), bulbar (3 items), respiratory (1 item), and gross motor or limb (2 items) impairment related to effects from MG.

    Each item is assessed on a 4-points scale where a score 0 represents normal function and a score 3 represents loss of ability to perform that function (total score 0 to 24).

    Measured: Baseline to Month 6

  4. Proportion of participants achieving Minimal Symptom Expression (MSE) at Month 6, defined as MG-ADL score of 0 or 1 at Month 6 without rescue therapy and/or strongly confounding prohibited medication

    The MG-ADL is a categorical scale that assesses MG symptoms and their effects on daily activities. MG-ADL is composed of items related to patient's assessment of functional disability secondary to ocular (2 items), bulbar (3 items), respiratory (1 item), and gross motor or limb (2 items) impairment related to effects from MG.

    Each item is assessed on a 4-points scale where a score 0 represents normal function and a score 3 represents loss of ability to perform that function (total score 0 to 24).

    Measured: Month 6

  5. Change from baseline to Month 6 in Myasthenia Gravis Composite score (MGC) total score

    The MGC is a 10-item instrument that measures the symptoms and signs of MG based on physician examination and patient history. Items relate to ptosis, double vision, eye closure, talking, chewing, swallowing, breathing, neck flexion, shoulder abduction, and hip flexion. Each item is scored on an ordinal scale with 4 possible categories and weighted. The total score ranges from 0 to 50, where higher scores indicating more severe impairments.

    Measured: Baseline to Month 6

  6. Change from baseline to Month 6 in revised Myasthenia Gravis Quality of Life Questionnaire (MG-QOL15r) survey score

    The revised MG-QoL15 is a 15-item health related quality of life questionnaire completed by participants, designed to measure quality of life in gMG. Items on the MG-QoL15 relate to physical, social, and psychological components and are scored from 0 (not at all) to 2 (very much). The cumulative scores range from 0 to 30, with higher scores representing worse quality of life and dissatisfaction with MG-related dysfunction.

    Measured: Baseline to Month 6

  7. Incidence of adverse events

    Incidence of adverse events including changes in clinical laboratory values, vital signs, electrocardiograms and suicidality results qualifying and reported as AEs.

    Measured: Baseline to Month 6

  8. Proportion of time during which participants showed a reduction of ≥ 2 points in MG-ADL total score, that was maintained up to Month 6

    The MG-ADL is a categorical scale that assesses MG symptoms and their effects on daily activities. MG-ADL is composed of items related to patient's assessment of functional disability secondary to ocular (2 items), bulbar (3 items), respiratory (1 item), and gross motor or limb (2 items) impairment related to effects from MG. Each item is assessed on a 4-points scale where a score 0 represents normal function and a score 3 represents loss of ability to perform that function (total score 0 to 24).

    Measured: Baseline to Month 6

  9. Proportion of early MG-ADL responders during treatment (early responders with first MG-ADL improvement from baseline of ≥ 2 points occurring by week 4)

    The MG-ADL is a categorical scale that assesses MG symptoms and their effects on daily activities. MG-ADL is composed of items related to patient's assessment of functional disability secondary to ocular (2 items), bulbar (3 items), respiratory (1 item), and gross motor or limb (2 items) impairment related to effects from MG. Each item is assessed on a 4-points scale where a score 0 represents normal function and a score 3 represents loss of ability to perform that function (total score 0 to 24). Participants with a first MG-ADL improvement from baseline of ≥ 2 points occurring by week 4 are considered early responders.

    Measured: Baseline to week 4

  10. Change from baseline to Month 6 in EuroQol-5 Dimensions-5 Level (EQ-5D-5L)

    The EQ-5D-5L is a widely used questionnaire designed to assess health status in adults. The measure is divided into two distinct sections, the descriptive system and the EQ visual analogue scale (EQ VAS). The first section includes one item addressing each of five dimensions (mobility, self-care, usual activity, pain/discomfort, and anxiety/depression). Participants rate each of these items from 1 of the 5 levels: no problems, slight problems, moderate problems, severe problems, or unable to/extreme. A composite health state is then defined by combining the levels for each dimension into a 5-digit number. The second section includes the EQ visual analogue scale (EQ VAS) that measures self-rated (global) health status utilizing a vertically oriented visual analogue scale where 100 represents the "best imaginable health state" and 0 represents the "worst imaginable health state." Respondents are asked to rate their current health by placing a mark along this continuum.

    Measured: Baseline to Month 6

  11. Proportion of participants achieving a reduction from baseline of ≥ 3 points in MGC total score at Month 6

    The MGC is a 10-item instrument that measures the symptoms and signs of MG based on physician examination and patient history. Items relate to ptosis, double vision, eye closure, talking, chewing, swallowing, breathing, neck flexion, shoulder abduction, and hip flexion. Each item is scored on an ordinal scale with 4 possible categories and weighted. The total score ranges from 0 to 50, where higher scores indicating more severe impairments.

    Measured: Baseline to Month 6

  12. Change from baseline in MG-ADL total score

    The MG-ADL is a categorical scale that assesses MG symptoms and their effects on daily activities. MG-ADL is composed of items related to patient's assessment of functional disability secondary to ocular (2 items), bulbar (3 items), respiratory (1 item), and gross motor or limb (2 items) impairment related to effects from MG. Each item is assessed on a 4-points scale where a score 0 represents normal function and a score 3 represents loss of ability to perform that function (total score 0 to 24).

    Measured: Baseline to Month 66

  13. Change from baseline in QMG total score

    The Quantitative Myasthenia Gravis (QMG) Score is a 13-item direct physician assessment scoring system that quantifies disease severity, based on impairments of body functions and structures. The total QMG score ranges from 0 to 39, where higher scores indicated greater disease severity. The QMG score is composed of the following items: ocular (2 items), facial (1 item), bulbar (2 items), gross motor (6 items), axial (1 item) and respiratory (1 item).

    Measured: Baseline to Month 66

  14. Change from baseline in MGC total score

    The MGC is a 10-item instrument that measures the symptoms and signs of MG based on physician examination and patient history. Items relate to ptosis, double vision, eye closure, talking, chewing, swallowing, breathing, neck flexion, shoulder abduction, and hip flexion. Each item is scored on an ordinal scale with 4 possible categories and weighted. The total score ranges from 0 to 50, where higher scores indicating more severe impairments.

    Measured: Baseline to Month 66

  15. Proportion of participants achieving a reduction from core part in oral corticosteroids (OCS) dose till the end of extension part

    Participants receiving oral corticosteroids are required to be on a stable dose for at least 4 weeks prior to baseline. The dose can be reduced or discontinued during the open label extension period at investigator discretion. Oral corticosteroids use will be recorded.

    Measured: Baseline to month 66

  16. Incidence of adverse events

    Incidence of adverse events including changes in clinical laboratory values, vital signs, electrocardiograms and suicidality results qualifying and reported as AEs.

    Measured: Month 7 to month 66

Timeline

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

  1. First posted20 Dec 2024
  2. Study start7 Feb 2025
  3. Primary completion25 Feb 2028 (estimated)
  4. Study completion26 Feb 2033 (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
Double blind
Who is masked
Participant, Investigator
Enrolment
180 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06744920
Sponsor's protocol ID
CLOU064O12301
Other IDs
2023-510026-32, 2023
Acronym
RELIEVE
Status last verified
Sep 2026
First submitted
17 Dec 2024
Last updated
28 Sep 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Yes: Novartis is committed to sharing with qualified external researchers, access to patient-level data and supporting clinical documents from eligible studies. These requests are reviewed and approved by an independent review panel on the basis of scientific merit. All data provided is anonymized to respect the privacy of patients who have participated in the trial in line with applicable laws and regulations. This trial data availability is according to the criteria and process described on www.clinicalstudydatarequest.com.

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Remibrutinib (Blinded) and Remibrutinib (Open Label) in people with Generalized Myasthenia Gravis, run by Novartis Pharmaceuticals at 120 sites in 20 countries.

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 6 inclusion and 3 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: under way, not looking for participants, as of the sponsor's last update on 28 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 120 sites in United States, Japan, China, Poland, India and 15 more countries. 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. Some participants in this study may receive a placebo. 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?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change from baseline to Month 6 in Myasthenia Gravis Activity of Daily Living (MG-ADL) total score (time frame: Baseline to Month 6). 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 28 Sep 2026; AzTrials last refreshed its copy on 7 Nov 2026.

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