Myasthenia Gravis (MG)AXISNCT07761026
AXIS MG Patient Registry
An observational study of Myasthenia Gravis (MG) and Myasthenia Gravis, Generalized, run by Autoimmune Neurology Alliance at 1 site in United States.
Trial summary
The goal of the AXIS Autoimmune Neurology Registry is to learn about the experiences of adults living with autoimmune neurological disorders, starting with myasthenia gravis (MG), over time. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Myasthenia Gravis (MG), Myasthenia Gravis, Generalized, Myasthenia Gravis, Ocular
- How many people
- 1,000 participants
- Where
- 1 siteUnited States
- Study dates
- 19 Mar 2026to Mar 2036
- How long will I take part?
- 10 Years
- 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: Adults in the United States with a healthcare provider diagnosis of myasthenia gravis will be recruited from the community. Participants may be identified through healthcare providers, patient advocacy and research organizations, existing patient communities or registries, digital and social media outreach, and direct communications. The registry is decentralized, so participants may enroll and complete study activities remotely from locations across the United States.
Who may be able to join
- Physician-confirmed diagnosis of myasthenia gravis (MG)
- Willing and legally able to provide consent
- Lives in the United States
Who cannot join
- Unwilling or unable to provide consent or comprehend and complete questionnaires
- Cognitively impaired adults/unable to comprehend or understand the consent or overall study information
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
President, Board of Directors, Autoimmune Neurology Alliance contact
United States1 site, 1 recruiting
- Recruiting
Alira Health - Virtual/Remote Site - Can Be Completed 100% Online - All US Residents Accepted
Framingham, Massachusetts, 01702
AXIS Patient Registry Team - US, 765-632-2517, support@axispatientregistry.com
President, Board of Directors, Autoimmune Neurology Alliance, info@ainalliance.org
About this study
Official title: AXIS Autoimmune Neurology Registry
The goal of the AXIS Autoimmune Neurology Registry is to learn about the experiences of adults living with autoimmune neurological disorders, starting with myasthenia gravis (MG), over time.
The main questions the registry aims to answer are:
Read more
- How do symptoms, daily functioning, and quality of life change over time?
- What treatments do participants use, and how are these treatments related to their symptoms and health?
- What challenges do participants experience with treatment, including side effects, treatment burden, missed doses, and access to care?
Participants will:
- Join the registry and complete an enrollment survey (online or through a mobile app)
- Complete a brief online survey about their MG approximately once a month
- Provide information that can help confirm their MG diagnosis
- Optionally, share their medical records with the research team
This is an observational study. The registry will not assign treatments or ask participants to change their medical care. Information collected through the registry may help researchers better understand MG and improve future research and care.
Read the detailed description
The AXIS Autoimmune Neurology Registry is a prospective, longitudinal, observational registry of adults in the United States with autoimmune neurological disorders. The registry is beginning with myasthenia gravis (MG), and participants with MG are currently being enrolled. The registry may expand to include other autoimmune neurological disorders in the future.
The registry is decentralized. Participants complete study activities remotely through a secure website or mobile application. The registry does not assign treatments and does not ask participants to change their usual medical care.
The registry collects information directly from participants to support research on the natural history and real-world management of MG. At enrollment, participants provide information about their MG diagnosis, whether they have ocular or generalized MG, age at diagnosis, demographic characteristics, education, employment, other medical conditions, prior testing, and treatments they have used.
Participants are also asked about MG-related antibody testing, including acetylcholine receptor (AChR), muscle-specific kinase (MuSK), low-density lipoprotein receptor-related protein 4 (LRP4), agrin, and other antibody tests. The registry collects participant-reported information about chest imaging, thymus findings, and thymectomy when applicable.
Participants identify MG treatments they have used and treatments taken during the prior month. These may include symptomatic therapies, corticosteroids, other immunosuppressive therapies, biologic or targeted therapies, intravenous or subcutaneous immunoglobulin, and plasma exchange. Additional questions may collect information about current and prior prednisone doses.
At enrollment and during monthly follow-up, participants complete standardized measures of MG symptoms, functioning, and quality of life. These include:
- The Myasthenia Gravis Activities of Daily Living profile (MG-ADL), which asks about talking, chewing, swallowing, breathing, brushing teeth or combing hair, rising from a chair, double vision, and eyelid droop during the previous week
- The revised 15-item Myasthenia Gravis Quality of Life questionnaire (MG-QOL15r), which asks about the effect of MG on areas such as social activities, work, family responsibilities, mobility, driving, personal care, emotional well-being, and enjoyment of activities during the previous four weeks
Participants are also asked to describe the severity of their MG symptoms at their worst during the prior month as a patient-reported proxy of MGFA Clinical Classification. Monthly questionnaires collect information about MG exacerbations and healthcare use, including emergency department visits, intensive care unit stays, and the use of mechanical ventilation. Questions may change or use branching logic based on a participant's earlier responses.
Participants complete an enrollment questionnaire and an initial monthly questionnaire when they join. After enrollment, they are asked to complete a follow-up questionnaire approximately once per month. Participants may pause a questionnaire, save their progress, and return later.
Participants provide information indicating that a healthcare provider has diagnosed them with MG. They are also asked to provide information that can help the research team confirm the diagnosis. Participants may confirm their diagnosis through one or more of the following methods:
- Uploading a laboratory report showing a positive MG-related antibody test
- Uploading another medical document supporting the MG diagnosis
- Authorizing the registry to contact their healthcare provider
- Authorizing the registry to request relevant medical records
- Connecting electronic medical records through an available secure process
Sharing medical records is optional. Participants may continue in the registry if their diagnosis has not yet been confirmed, although diagnosis confirmation may be required for certain participant incentives. Authorized registry staff review submitted documentation or information received from healthcare providers to determine whether the diagnosis has been confirmed.
The registry uses structured electronic questionnaires and data-quality procedures to support accurate and consistent data collection. Required fields, response options, date and age validations, branching rules, and other predefined checks are built into the questionnaires. Responses may also be reviewed for completeness, ambiguity, values outside expected ranges, and inconsistencies with other information in the registry. Participants may be contacted when clarification is needed.
Source data verification may be conducted by comparing participant-reported information with uploaded diagnostic documents, laboratory reports, healthcare-provider confirmation, connected electronic health information, or medical records authorized by the participant. Because medical-record sharing is optional, the amount of externally verified information may differ among participants.
Study data are associated with a unique participant code. Information that directly identifies participants is stored separately, and access is limited to authorized personnel who need the information for registry operations, participant support, diagnosis verification, monitoring, or other approved purposes. Data used for research analyses are de-identified.
The Principal Investigator and the Scientific Committee are responsible for monitoring the quality and integrity of the registry. The registry may also be reviewed, audited, or inspected by the institutional review board, regulatory authorities, sponsor representatives, and authorized quality or compliance personnel. The electronic system maintains records of informed consent and participant activity that can be provided for monitoring, audit, or inspection.
Registry procedures are governed by the study protocol and supporting study documents. These procedures address informed consent, participant recruitment, questionnaire administration, diagnosis confirmation, medical-record authorization, participant communications and reminders, data management, confidentiality, data sharing, withdrawal, monitoring, and changes to registry procedures. Questionnaire specifications document the questions, response options, required fields, and branching logic used for data collection.
There is no fixed maximum sample size. Broad recruitment is planned to support analyses of the overall MG population and clinically relevant subgroups, including groups based on MG type, symptom severity, antibody status, treatment use, age, and other participant characteristics.
Statistical methods will depend on the research question and may include descriptive statistics, comparisons among participant subgroups, regression modeling, longitudinal analyses, and survival analyses. Analyses may evaluate changes in symptoms, functioning, quality of life, treatment use, and healthcare use over time.
Missing data are expected in this long-term observational registry. Electronic and email reminders are used to encourage participants to complete enrollment, diagnosis-confirmation, and monthly questionnaires. Other follow-up methods may include telephone calls or mail when appropriate. Data-quality reviews will identify missing or inconsistent responses. The methods used to address missing data in an analysis will depend on the research question, the variables involved, and the amount and pattern of missingness.
The registry is designed to continue over many years. Research questions, questionnaires, variables, and analyses may be updated as clinical practice changes, additional treatments become available, other autoimmune neurological disorders are added, and new research needs emerge. Any material changes to the protocol or participant-facing study materials will undergo required review and approval before implementation.
- Conditions
- Myasthenia Gravis (MG), Myasthenia Gravis, Generalized, Myasthenia Gravis, Ocular, Myasthenia Gravis Crisis, Myasthenia Gravis Associated With Thymoma, Myasthenia Gravis Exacerbations
- Keywords
- myasthenia gravis, autoimmune diseases of the nervous system, neuromuscular junction diseases, patient registries, natural history, longitudinal studies, observational study, patient-reported outcome measures, quality of life, activities of daily living, treatment patterns, medication adherence, treatment burden, healthcare utilization, disease progression, real-world data
- Medical subject headings
- Myasthenia Gravis, Autoimmune Diseases of the Nervous System, Neuromuscular Junction Diseases, Medication Adherence, Disease Progression
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Myasthenia Gravis (MG) | Adults with confirmed diagnosis of MG |
What is being measured
The primary outcome is the main question the study is designed to answer.
MG-ADL
The Myasthenia Gravis Activities of Daily Living (MG-ADL) profile assesses the severity of myasthenia gravis symptoms during the previous week. Participants rate 8 activities: talking, chewing, swallowing, breathing, brushing teeth or combing hair, rising from a chair, double vision, and eyelid droop. Each item is scored from 0 to 3. Item scores are summed for a total score ranging from 0 to 24. A score of 0 indicates no reported impairment, and higher scores indicate greater symptom severity and functional impairment.
Measured: through study completion, up to 10 years
Secondary outcomes (2)
MG-QOL15r
The revised 15-item Myasthenia Gravis Quality of Life (MG-QOL15r) questionnaire assesses how myasthenia gravis affected the participant's life during the previous 4 weeks. Participants rate 15 items covering physical functioning, social activities, work, family responsibilities, mobility, personal care, emotional well-being, and enjoyment of activities. Each item is scored from 0 to 2. Item scores are summed for a total score ranging from 0 to 30. A score of 0 indicates no reported effect on quality of life, and higher scores indicate a greater negative effect of myasthenia gravis on quality of life.
Measured: through study completion, up to 10 years
MGFA Clinical Classification (patient-reported proxy)
A patient-reported proxy for the Myasthenia Gravis Foundation of America Clinical Classification, based on the participant's MG symptoms at their worst during the past month. Participants select 1 of 5 ordered categories: Class I, weakness limited to the eye or eyelid muscles; Class II, mild weakness affecting other muscles; Class III, moderate weakness affecting other muscles; Class IV, severe weakness affecting other muscles; or Class V, use of a breathing tube, except when planned for surgery. Eye or eyelid weakness may also occur in Classes II-IV. Higher classes indicate more severe MG. This proxy is not a clinician-assessed classification.
Measured: through study completion, up to 10 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 Aug 2026
- Study start19 Mar 2026
- Primary completionMar 2036 (estimated)
- Study completionMar 2036 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Myasthenia Gravis (MG)Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- 1,000 participants (estimated)
- Target duration
- 10 Years
Sponsor and investigators
- Lead sponsor
- Autoimmune Neurology Alliance
- Sponsor type
- University, hospital or other
- Collaborators
- Alira Health
- Responsible party
- Sponsor
- Investigators
- Richard J Nowak, MD, MS, Study chair, Yale UniversityGary R Cutter, PhD, Study director, University of Alabama at BirminghamNeelam Goyal, MD, Study director, Stanford UniversitySrikanth Muppidi, MD, Study director, Stanford UniversityJared R Adams, MD, PhD, Principal investigator, Alira Health
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07761026
- Sponsor's protocol ID
- AXIS
- Acronym
- AXIS
- Status last verified
- Aug 2026
- First submitted
- 4 Aug 2026
- Last updated
- 17 Aug 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: De-identified individual participant data may be made available to qualified researchers for approved research projects. Requests will be reviewed by the AXIS Registry Scientific Committee and/or other applicable scientific or governance bodies. Access will be subject to an approved research proposal, applicable data-use agreements, participant consent, privacy protections, and any legal, ethical, or contractual requirements. A data dictionary describing the shared variables will be provided with approved datasets. Direct identifiers will not be shared.
Study at a glance
From the registry record, last updated by the sponsor on 17 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- AXIS Autoimmune Neurology Registry
- ClinicalTrials.gov ID
- NCT07761026
- Acronym / sponsor ID
- AXIS / AXIS
- Conditions
- Myasthenia Gravis (MG), Myasthenia Gravis, Generalized, Myasthenia Gravis, Ocular, Myasthenia Gravis Crisis, Myasthenia Gravis Associated With Thymoma, Myasthenia Gravis Exacerbations
- Keywords
- myasthenia gravis, autoimmune diseases of the nervous system, neuromuscular junction diseases, patient registries, natural history, longitudinal studies, observational study, patient-reported outcome measures
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 1,000 participants (estimated)
- Lead sponsor
- Autoimmune Neurology AllianceUniversity, hospital or other
- Collaborators
- Alira Health
- Study start
- 19 Mar 2026 (actual)
- Primary completion
- Mar 2036 (estimated)
- Study completion
- Mar 2036 (estimated)
- First posted
- 12 Aug 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of the AXIS Autoimmune Neurology Registry is to learn about the experiences of adults living with autoimmune neurological disorders, starting with myasthenia gravis (MG), over time.
The main questions the registry aims to answer are:
- How do symptoms, daily functioning, and quality of life change over time?
- What treatments do participants use, and how are these treatments related to their symptoms and health?
- What challenges do participants experience with treatment, including side effects, treatment burden, missed doses, and access to care?
Participants will:
- Join the registry and complete an enrollment survey (online or through a mobile app)
- Complete a brief online survey about their MG approximately once a month
- Provide information that can help confirm their MG diagnosis
- Optionally, share their medical records with the research team
This is an observational study. The registry will not assign treatments or ask participants to change their medical care. Information collected through the registry may help researchers better understand MG and improve future research and care.
Detailed description
The AXIS Autoimmune Neurology Registry is a prospective, longitudinal, observational registry of adults in the United States with autoimmune neurological disorders. The registry is beginning with myasthenia gravis (MG), and participants with MG are currently being enrolled. The registry may expand to include other autoimmune neurological disorders in the future.
The registry is decentralized. Participants complete study activities remotely through a secure website or mobile application. The registry does not assign treatments and does not ask participants to change their usual medical care.
The registry collects information directly from participants to support research on the natural history and real-world management of MG. At enrollment, participants provide information about their MG diagnosis, whether they have ocular or generalized MG, age at diagnosis, demographic characteristics, education, employment, other medical conditions, prior testing, and treatments they have used.
Participants are also asked about MG-related antibody testing, including acetylcholine receptor (AChR), muscle-specific kinase (MuSK), low-density lipoprotein receptor-related protein 4 (LRP4), agrin, and other antibody tests. The registry collects participant-reported information about chest imaging, thymus findings, and thymectomy when applicable.
Participants identify MG treatments they have used and treatments taken during the prior month. These may include symptomatic therapies, corticosteroids, other immunosuppressive therapies, biologic or targeted therapies, intravenous or subcutaneous immunoglobulin, and plasma exchange. Additional questions may collect information about current and prior prednisone doses.
At enrollment and during monthly follow-up, participants complete standardized measures of MG symptoms, functioning, and quality of life. These include:
- The Myasthenia Gravis Activities of Daily Living profile (MG-ADL), which asks about talking, chewing, swallowing, breathing, brushing teeth or combing hair, rising from a chair, double vision, and eyelid droop during the previous week
- The revised 15-item Myasthenia Gravis Quality of Life questionnaire (MG-QOL15r), which asks about the effect of MG on areas such as social activities, work, family responsibilities, mobility, driving, personal care, emotional well-being, and enjoyment of activities during the previous four weeks
Participants are also asked to describe the severity of their MG symptoms at their worst during the prior month as a patient-reported proxy of MGFA Clinical Classification. Monthly questionnaires collect information about MG exacerbations and healthcare use, including emergency department visits, intensive care unit stays, and the use of mechanical ventilation. Questions may change or use branching logic based on a participant's earlier responses.
Participants complete an enrollment questionnaire and an initial monthly questionnaire when they join. After enrollment, they are asked to complete a follow-up questionnaire approximately once per month. Participants may pause a questionnaire, save their progress, and return later.
Participants provide information indicating that a healthcare provider has diagnosed them with MG. They are also asked to provide information that can help the research team confirm the diagnosis. Participants may confirm their diagnosis through one or more of the following methods:
- Uploading a laboratory report showing a positive MG-related antibody test
- Uploading another medical document supporting the MG diagnosis
- Authorizing the registry to contact their healthcare provider
- Authorizing the registry to request relevant medical records
- Connecting electronic medical records through an available secure process
Sharing medical records is optional. Participants may continue in the registry if their diagnosis has not yet been confirmed, although diagnosis confirmation may be required for certain participant incentives. Authorized registry staff review submitted documentation or information received from healthcare providers to determine whether the diagnosis has been confirmed.
The registry uses structured electronic questionnaires and data-quality procedures to support accurate and consistent data collection. Required fields, response options, date and age validations, branching rules, and other predefined checks are built into the questionnaires. Responses may also be reviewed for completeness, ambiguity, values outside expected ranges, and inconsistencies with other information in the registry. Participants may be contacted when clarification is needed.
Source data verification may be conducted by comparing participant-reported information with uploaded diagnostic documents, laboratory reports, healthcare-provider confirmation, connected electronic health information, or medical records authorized by the participant. Because medical-record sharing is optional, the amount of externally verified information may differ among participants.
Study data are associated with a unique participant code. Information that directly identifies participants is stored separately, and access is limited to authorized personnel who need the information for registry operations, participant support, diagnosis verification, monitoring, or other approved purposes. Data used for research analyses are de-identified.
The Principal Investigator and the Scientific Committee are responsible for monitoring the quality and integrity of the registry. The registry may also be reviewed, audited, or inspected by the institutional review board, regulatory authorities, sponsor representatives, and authorized quality or compliance personnel. The electronic system maintains records of informed consent and participant activity that can be provided for monitoring, audit, or inspection.
Registry procedures are governed by the study protocol and supporting study documents. These procedures address informed consent, participant recruitment, questionnaire administration, diagnosis confirmation, medical-record authorization, participant communications and reminders, data management, confidentiality, data sharing, withdrawal, monitoring, and changes to registry procedures. Questionnaire specifications document the questions, response options, required fields, and branching logic used for data collection.
There is no fixed maximum sample size. Broad recruitment is planned to support analyses of the overall MG population and clinically relevant subgroups, including groups based on MG type, symptom severity, antibody status, treatment use, age, and other participant characteristics.
Statistical methods will depend on the research question and may include descriptive statistics, comparisons among participant subgroups, regression modeling, longitudinal analyses, and survival analyses. Analyses may evaluate changes in symptoms, functioning, quality of life, treatment use, and healthcare use over time.
Missing data are expected in this long-term observational registry. Electronic and email reminders are used to encourage participants to complete enrollment, diagnosis-confirmation, and monthly questionnaires. Other follow-up methods may include telephone calls or mail when appropriate. Data-quality reviews will identify missing or inconsistent responses. The methods used to address missing data in an analysis will depend on the research question, the variables involved, and the amount and pattern of missingness.
The registry is designed to continue over many years. Research questions, questionnaires, variables, and analyses may be updated as clinical practice changes, additional treatments become available, other autoimmune neurological disorders are added, and new research needs emerge. Any material changes to the protocol or participant-facing study materials will undergo required review and approval before implementation.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 10 Years
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Myasthenia Gravis (MG) | – | –Adults with confirmed diagnosis of MG |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Adults in the United States with a healthcare provider diagnosis of myasthenia gravis will be recruited from the community. Participants may be identified through healthcare providers, patient advocacy and research organizations, existing patient communities or registries, digital and social media outreach, and direct communications. The registry is decentralized, so participants may enroll and complete study activities remotely from locations across the United States.
Key inclusion criteria (3 listed)
- Physician-confirmed diagnosis of myasthenia gravis (MG)
- Willing and legally able to provide consent
- Lives in the United States
Key exclusion criteria (2 listed)
- Unwilling or unable to provide consent or comprehend and complete questionnaires
- Cognitively impaired adults/unable to comprehend or understand the consent or overall study information
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
MG-ADL
Time frame: through study completion, up to 10 years
The Myasthenia Gravis Activities of Daily Living (MG-ADL) profile assesses the severity of myasthenia gravis symptoms during the previous week. Participants rate 8 activities: talking, chewing, swallowing, breathing, brushing teeth or combing hair, rising from a chair, double vision, and eyelid droop. Each item is scored from 0 to 3. Item scores are summed for a total score ranging from 0 to 24. A score of 0 indicates no reported impairment, and higher scores indicate greater symptom severity and functional impairment.
2 secondary outcomes
MG-QOL15r
Time frame: through study completion, up to 10 years
MGFA Clinical Classification (patient-reported proxy)
Time frame: through study completion, up to 10 years
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Aug 2026.
- AXIS Autoimmune Neurology Patient Registry WebsiteLink provided by the sponsor.
- Individual participant dataSharing planned: Yes. De-identified individual participant data may be made available to qualified researchers for approved research projects. Requests will be reviewed by the AXIS Registry Scientific Committee and/or other applicable scientific or governance bodies. Access will be subject to an approved research proposal, applicable data-use agreements, participant consent, privacy protections, and any legal, ethical, or contractual requirements. A data dictionary describing the shared variables will be provided with approved datasets. Direct identifiers will not be shared.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
President, Board of Directors, Autoimmune Neurology Alliance contact
Richard J Nowak, MD, MS study chair
Yale University
Gary R Cutter, PhD study director
University of Alabama at Birmingham
Neelam Goyal, MD study director
Stanford University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Myasthenia Gravis (MG) and Myasthenia Gravis, Generalized, run by Autoimmune Neurology Alliance at 1 site in United States.
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 3 inclusion and 2 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 17 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. 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 AXIS Patient Registry Team (765-632-2517, support@axispatientregistry.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
MG-ADL (time frame: through study completion, up to 10 years). 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 17 Aug 2026.