Myasthenia Gravis
Conditions
Brief summary
This was a multicenter, randomized, double-blind, placebo-controlled, Phase 3 study to evaluate the efficacy and safety of tolebrutinib compared with placebo in adult participants aged 18 to 85 years old with moderate-to-severe generalized myasthenia gravis (gMG), who received Standard of Care (SoC). The double-blind (DB) treatment period of 26 weeks comprised of 7 site visits followed by a 2-year open label extension (OLE) period with quarterly visits. The efficacy of tolebrutinib versus placebo during the DB period was assessed by clinical evaluations, including scales based on physician examination or direct participant feedback i.e., patient reported outcomes (PROs). These evaluations continued during the OLE to measure long term efficacy and safety.
Detailed description
The duration of the DB period was 26 weeks. The OLE was planned up to 104 weeks. The duration of the whole study DB+OLE was planned up to130 weeks.
Interventions
DRUGTolebrutininb
Pharmaceutical form: Film-coated tablet Route of administration: Oral
DRUGPlacebo
Pharmaceutical form: Film-coated tablet Route of administration: Oral
Sponsors
Sanofi
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No
Inclusion criteria
* Participants were 18 years of age to 85 years of age inclusive, at the time of signing the informed consent. * Participants with a diagnosis of gMG at screening with generalized muscle weakness meeting the clinical criteria for diagnosis of MG, as defined by the myasthenia gravis foundation of America (MGFA) Clinical Classification Class II, III, or IV, and likely not in need of a respirator for the duration of the study, as judged by the Investigator. * Positive serologic testing for anti-acetylcholine receptor (anti-AChR) or anti-muscle-specific kinase (anti-MuSK) autoantibody at screening OR * Seronegative for both anti-AChR and anti-MuSK autoantibodies and with prior diagnosis supported by greater than or equal to (\>=) 1 of the following 3 tests: 1. History of abnormal neuromuscular transmission demonstrated by single-fiber electromyography or repetitive nerve stimulation. 2. History of positive edrophonium chloride test. 3. Participant had demonstrated improvement in gMG signs on oral acetylcholinesterase inhibitors as assessed by the treating physician. * The participant had a total score \>=6 on myasthenia gravis-activities of daily living scale at screening and Day 1 with greater than half of the score attributed to non-ocular items.
Exclusion criteria
* MGFA Class I (ocular MG) or Class V. * Participants had undergone thymectomy within 6 months of screening or having a planned thymectomy during the trial period. * The participant had a history of infection or might be at risk for infection: A history of active or latent tuberculosis (TB); Participants at risk of developing or having reactivation of hepatitis; Persistent chronic or active recurring infection required treatment with antibiotics, antivirals, or antifungals; Fever within 4 weeks of the Screening Visit (\>=38 degree Celsius; however, if due to brief and mild ear, nose, throat viral infection participant might be included based on the Investigator's judgment); A history of infection with human immunodeficiency virus (HIV); A history of T-lymphocyte or T-lymphocyte-receptor vaccination, transplantation (including solid organ, stem cell, and bone marrow transplantation) and/or antirejection therapy. * Any malignancy within the past 5 years prior Screening Visit (except for effectively treated carcinoma in situ of the cervix, adequately treated non-metastatic squamous or basal cell carcinoma of the skin and malignant thymoma that had been resected or were considered as cured by any treatment with no evidence of metastatic disease for \>=3 years) will be exclusionary. * Conditions that might predispose the participant to excessive bleeding. * Clinically significant laboratory abnormalities (including evidence of liver injury) or electrocardiogram abnormalities at Screening. The above information was not intended to contain all considerations relevant to a participant's potential participation in a clinical trial.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| DB Period: Change From Baseline in Myasthenia Gravis-activities of Daily Living (MG-ADL) Total Score at Week 26 | Baseline (Day 1), Week 26 | The MG-ADL is an 8-item patient-reported categorical scale that assesses MG symptoms and their effects on daily activities. The MG-ADL targeted symptoms and disability across ocular (2 items), bulbar (3 items), respiratory (1 items), and gross motor or limb impairment (2 items) symptoms. It evaluates a participant's capacity to perform different activities in their daily life. Each item is scored on a 4-point scale ranged from 0 (normal) to 3 (severe), where higher score represents the more severe symptoms or impaired performance. MG-ADL total score is the sum of each item score which ranged from 0 (normal) to 24 (severe). Higher score represents severe disability due to MG. DB period Baseline value was defined as last available value prior to the first dose of the study medication in the DB period. |
| OLE Period: Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events Leading to Permanent Study Intervention Discontinuation and Adverse Events of Special Interests (AESIs) | From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61) | An AE was defined as any untoward medical occurrence in a participant who received study drug and did not necessarily have to have a causal relationship with the treatment. A SAE was any untoward medical occurrence that at any dose: resulted in death, was life-threatening, required inpatient hospitalization or prolongation of existing hospitalization, resulted in persistent or significant disability/incapacity, was a congenital anomaly/birth defect, or was a medically important event. An AESI was defined as one of scientific & medical concern specific to the Sponsor's product or program, for which ongoing monitoring and immediate notification by the Investigator to the Sponsor was considered appropriate. Relatedness to study vaccine was based on Investigator's discretion. |
| OLE Period: Number of Participants With Hematological Abnormalities | From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61) | Hematological parameters assessed were: platelet count, red blood cell count, hemoglobin, hematocrit, white blood cell, neutrophils, lymphocytes, monocytes, eosinophils, and basophils. Only those categories in which at least 1 participant had data were reported. |
| OLE Period: Number of Participants With Clinical Chemistry Parameter Abnormalities | From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61) | Clinical chemistry parameters assessed were blood urea nitrogen, creatinine, glucose, total and direct bilirubin, potassium, sodium, chloride, bicarbonate, calcium, albumin, creatine phosphokinase, alkaline phosphatase, aspartate aminotransferase/serum glutamic-oxaloacetic transaminase, alanine aminotransferase/serum glutamic-pyruvic transaminase, lipase, and total protein. Only the category (Alkaline phosphatase) in which at least 1 participant had data were reported. |
| OLE Period: Number of Participants With Electrocardiogram (ECG) Abnormalities | From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61) | ECG parameters assessed were heart rate, pulse rate, QRS interval, QT interval and QT interval corrected using Fridericia's formula \[QTcF\]). |
| OLE Period: Number of Participants With Vital Signs Abnormalities | From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61) | Vital signs assessed were heart rate, systolic blood pressure, diastolic blood pressure, weight and temperature. Only those category (Weight \>=5% decrease from Baseline) in which at least 1 participant had data were reported. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| DB Period: Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events Leading to Permanent Study Intervention Discontinuation and Adverse Events of Special Interests (AESIs) | From Day 1 up to Week 26 | An AE was defined as any untoward medical occurrence in a participant who received study drug and did not necessarily have to have a causal relationship with the treatment. A SAEs was any untoward medical occurrence that at any dose: resulted in death, was life-threatening, required inpatient hospitalization or prolongation of existing hospitalization, resulted in persistent or significant disability/incapacity, was a congenital anomaly/birth defect, was a medically important event. AESI was defined as one of scientific & medical concern specific to the Sponsor's product or program, for which ongoing monitoring and immediate notification by the Investigator to the Sponsor was considered appropriate. Relatedness to study vaccine was based on Investigator's discretion. |
| DB Period: Number of Participants With Hematological Abnormalities | From Day 1 up to Week 26 | Hematological parameters assessed were: platelet count, red blood cell count, hemoglobin, hematocrit, white blood cell, neutrophils, lymphocytes, monocytes, eosinophils, and basophils. Only those categories in which at least 1 participant had data were reported. |
| DB Period: Number of Participants With Clinical Chemistry Parameter Abnormalities | From Day 1 up to Week 26 | Clinical chemistry parameters assessed were blood urea nitrogen, creatinine, glucose, total and direct bilirubin, potassium, sodium, chloride, bicarbonate, calcium, albumin, creatine phosphokinase, alkaline phosphatase, aspartate aminotransferase/serum glutamic-oxaloacetic transaminase, alanine aminotransferase/serum glutamic-pyruvic transaminase, lipase, and total protein. Only those categories in which at least 1 participant had data were reported. |
| DB Period: Number of Participants With Electrocardiogram Abnormalities | From Day 1 up to Week 26 | ECG parameters assessed were heart rate, pulse rate, QRS interval, QT interval and QTcF. |
| DB Period: Number of Participants With Vital Signs Abnormalities | From Day 1 up to Week 26 | Vital signs assessed were heart rate, systolic blood pressure, diastolic blood pressure, weight and temperature. Only those category (Weight \>=5% increase from Baseline) in which at least 1 participant had data were reported. |
| OLE Period: Change From Baseline in Myasthenia Gravis-activities of Daily Living Total Score | From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61) | The MG-ADL is an 8-item patient-reported categorical scale that assesses MG symptoms and their effects on daily activities. The MG-ADL targeted symptoms and disability across ocular (2 items), bulbar (3 items), respiratory (1 items), and gross motor or limb impairment (2 items) symptoms. It evaluates a participant's capacity to perform different activities in their daily life. Each item is scored on a 4-point scale ranged from 0 (normal) to 3 (severe), where higher score represents the more severe symptoms or impaired performance. MG-ADL total score is the sum of each item score which ranged from 0 (normal) to 24 (severe). Higher score represents severe disability due to MG. OLE period Baseline value was defined as last available value prior to the first dose of the study medication in the OLE period. |
| DB Period: Change From Baseline in Quantitative Myasthenia Gravis (QMG) Total Score at Week 26 | Baseline (Day 1), Week 26 | The QMG is a clinician-reported outcome to assess muscle weakness in participants with MG. The QMG test consists of 13 items: ocular (2 items), facial (1 item), bulbar (2 items), gross motor (6 items), axial (1 item), and respiratory (1 item). Each item is scored on 3-point scale ranged from 0 (none) to 3 (severe), where higher score represents most severe muscle weakness. The QMG total score is the sum of each individual item score which ranged from 0 (normal) to 39 (severe). Higher score represents greater disease activity. DB period Baseline value was defined as last available value prior to the first dose of the study medication in the DB period. |
| OLE Period: Change From Baseline in Myasthenia Gravis Impairment Index Total Score | From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61) | MGII: measure of MG severity, with demonstrated fatigability, reliability and construct validity. It consists of 22-item patient-reported questionnaire & 6 clinician-assessment items. MGII can be divided into 2 sub-scale-scores: ocular (8 items) & generalized (20 items) impairments. Ocular sub-score: calculated by summing 1 to 6 items from patient questionnaire and items 1 & 2 of clinician-assessment. Generalized score: calculated by adding items 7 to 22 from patient questionnaire & items 3 to 6 from the clinician-assessment. Each item is scored on 4-point scale: from 0 (none) to 3 (severe), where higher score=more disease severity. MGII total score: sum of each item of patient questionnaire (total score:0 \[normal\] to 23 \[severe\]) & clinician assessment items (total score:0 \[normal\] to 61 \[severe\]); ranged from 0 (normal) to 84 (severe). Higher scores=greater disease severity. OLE period Baseline:defined as last available value prior to 1st dose of study medication in the OLE period. |
| OLE Period: Change From Baseline in Myasthenia Gravis-quality of Life 15-item Scale Total Score | From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61) | The MG-QOL15 is a 15-item, participant self-reported QoL instrument for participants with MG. The instrument is developed and validated to evaluate general QoL of participants with MG by a clinician in the practice setting. The domains covered by the questionnaire are mobility (9 items), symptoms (3 items), general contentment (1 item) and emotional well-being (2 items). Each item is scored on a scale of 0 (not at all) to 4 (very much), where higher score indicates severe QoL impairment. The MG-QOL15 total score is the sum of each individual item score and ranged from 0 (none) to 60 (severe). Higher scores indicate greater extent and dissatisfaction with MG-related dysfunction. |
| OLE Period: Percentage of Participants With >=2-point Improvement (Reduction) in Myasthenia Gravis-activities of Daily Living Total Score | From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61) | The MG-ADL is an 8-item patient-reported categorical scale that assesses MG symptoms and their effects on daily activities. The MG-ADL targeted symptoms and disability across ocular (2 items), bulbar (3 items), respiratory (1 items), and gross motor or limb impairment (2 items) symptoms. It evaluates a participant's capacity to perform different activities in their daily life. Each item is scored on a 4-point scale ranged from 0 (normal) to 3 (severe), where higher score represents the more severe symptoms or impaired performance. MG-ADL total score is the sum of each item score which ranged from 0 (normal) to 24 (severe). Higher score represents severe disability due to MG. OLE period Baseline value was defined as last available value prior to the first dose of the study medication in the OLE period. |
| OLE Period: Percentage of Participants With >=3-point Improvement (Reduction) in Quantitative Myasthenia Gravis Total Score | From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61) | The MG-ADL is an 8-item patient-reported categorical scale that assesses MG symptoms and their effects on daily activities. The MG-ADL targeted symptoms and disability across ocular (2 items), bulbar (3 items), respiratory (1 items), and gross motor or limb impairment (2 items) symptoms. It evaluates a participant's capacity to perform different activities in their daily life, including talking, chewing, swallowing, breathing, brushing their teeth or combing their hair, getting up from a chair, double vision and eyelid droop. Each item is scored on a 4-point scale ranged from 0 (normal) to 3 (severe), where higher score represents the more severe symptoms or impaired performance. MG-ADL total score is the sum of each item score which ranged from 0 to 24, where a higher score represents severe disability due to MG. OLE period Baseline value was defined as last available value prior to the first dose of the study medication in the OLE period. |
| OLE Period: Percentage of Participants Achieving Any Reduction From Baseline of Daily Dose of Oral Corticosteroids (OCS) at Week 61 | Baseline (Day 1), Week 61 | The use of rescue therapy for generalized MG worsening is allowed at any time during both the DB and OLE parts of the study at discretion of the Investigator in case of at least a 2-point increase of individual non-ocular MG-ADL items compared to the Day 1 MG-ADL value or new or worsening of respiratory/ bulbar symptoms. Rescue therapy includes intravenous immunoglobulin, plasma exchange, change in the standard of care OCS dose or any use of new CS. OLE period Baseline value was defined as last available value prior to the first dose of the study medication in the OLE period. |
| OLE Period: Change From Baseline in Quantitative Myasthenia Gravis Total Score | From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61) | The QMG is a clinician-reported outcome to assess muscle weakness in participants with MG. The QMG test consists of 13 items: ocular (2 items), facial (1 item), bulbar (2 items), gross motor (6 items), axial (1 item), and respiratory (1 item). Each item is scored on 3-point scale ranged from 0 (none) to 3 (severe), where higher score represents most severe muscle weakness. The QMG total score is the sum of each individual item score which ranged from 0 (normal) to 39 (severe). Higher score represents greater disease activity. OLE period Baseline value was defined as last available value prior to the first dose of the study medication in the OLE period. |
| DB Period: Change From Baseline in Quantitative Myasthenia Gravis (QMG) Total Score at Week 12 | Baseline (Day 1), Week 12 | The QMG is a clinician-reported outcome to assess muscle weakness in participants with MG. The QMG test consists of 13 items: ocular (2 items), facial (1 item), bulbar (2 items), gross motor (6 items), axial (1 item), and respiratory (1 item). Each item is scored on 3-point scale ranged from 0 (none) to 3 (severe), where higher score represents most severe muscle weakness. The QMG total score is the sum of each individual item score which ranged from 0 (normal) to 39 (severe). Higher score represents greater disease activity. The QMG total score at Week 12 is reported in this outcome measure. DB period Baseline value was defined as last available value prior to the first dose of the study medication in the DB period. |
| DB Period: Change From Baseline in Myasthenia Gravis Impairment Index (MGII) Total Score at Week 26 | Baseline (Day 1), Week 26 | MGII: measure of MG severity, with demonstrated fatigability, reliability and construct validity. It consists of 22-item patient-reported questionnaire and 6 clinician-assessment items. MGII can be divided into 2 sub-scale-scores: ocular (8 items) & generalized (20 items) impairments. Ocular sub-score: calculated by summing 1 to 6 items from patient questionnaire and items 1 & 2 of clinician-assessment. Generalized score: calculated by adding items 7 to 22 from patient questionnaire & items 3 to 6 from the clinician-assessment. Each item is scored on 4-point scale: from 0 (none) to 3 (severe), where higher score=more disease severity. MGII total score: sum of each item of patient questionnaire (total score:0 \[normal\] to 23 \[severe\]) & clinician assessment items (total score:0 \[normal\] to 61 \[severe\]); ranged from 0 (normal) to 84 (severe). Higher scores=greater disease severity. DB period Baseline: defined as last available value prior to 1st dose of study medication in the DB period. |
| DB Period: Change From Baseline in Myasthenia Gravis-quality of Life 15-item Scale (MG-QoL15) Total Score at Week 26 | Baseline (Day 1), Week 26 | The MG-QOL15 is a 15-item, participant self-reported QoL instrument for participants with MG. The instrument is developed and validated to evaluate general QoL of participants with MG by a clinician in the practice setting. The domains covered by the questionnaire are mobility (9 items), symptoms (3 items), general contentment (1 item) and emotional well-being (2 items). Each item is scored on a scale of 0 (not at all) to 4 (very much), where higher score indicates severe QoL impairment. The MG-QOL15 total score is the sum of each individual item score and ranged from 0 (none) to 60 (severe). Higher scores indicates greater extent and dissatisfaction with MG-related dysfunction. DB period Baseline value was defined as last available value prior to the first dose of the study medication in the DB period. |
| DB Period: Percentage of Participants With Greater Than Equal to (>=) 2-point Improvement (Reduction) in Myasthenia Gravis-activities of Daily Living Total Score at Week 26 | Week 26 | The MG-ADL is an 8-item patient-reported categorical scale that assesses MG symptoms and their effects on daily activities. The MG-ADL targeted symptoms and disability across ocular (2 items), bulbar (3 items), respiratory (1 items), and gross motor or limb impairment (2 items) symptoms. It evaluates a participant's capacity to perform different activities in their daily life. Each item is scored on a 4-point scale ranged from 0 (normal) to 3 (severe), where higher score represents the more severe symptoms or impaired performance. MG-ADL total score is the sum of each item score which ranged from 0 (normal) to 24 (severe). Higher score represents severe disability due to MG. |
| DB Period: Percentage of Participants With >=3-point Improvement (Reduction) in Quantitative Myasthenia Gravis Total Score at Week 26 | Week 26 | The MG-ADL is an 8-item patient-reported categorical scale that assesses MG symptoms and their effects on daily activities. The MG-ADL targeted symptoms and disability across ocular (2 items), bulbar (3 items), respiratory (1 items), and gross motor or limb impairment (2 items) symptoms. It evaluates a participant's capacity to perform different activities in their daily life. Each item is scored on a 4-point scale ranged from 0 (normal) to 3 (severe), where higher score represents the more severe symptoms or impaired performance. MG-ADL total score is the sum of each item score which ranged from 0 (normal) to 24 (severe). Higher score represents severe disability due to MG. |
Countries
Canada, China, Hungary, Italy, Japan, Poland, Spain, United Kingdom, United States
Participant flow
Recruitment details
Study was conducted at 22 sites in 9 countries from 03-Dec-2021 to 21-Feb-2023. A total of 6 participants were randomized in a 1:1 ratio to receive treatment with tolebrutinib or placebo.
Pre-assignment details
Randomization was stratified by Myasthenia Gravis Foundation of America (MGFA) class (II, IIIa/IVa, or IIIb/IVb) and region (United States \[US\], non-US). Due to early termination of the study by sponsor, several planned efficacy analysis were not performed for the study.
Participants by arm
| Arm | Count |
|---|---|
| Overall Participants Participants with moderate-to-severe gMG received tolebrutinib 60 mg tablet or matched placebo tablet orally once daily as an add-on therapy to their SoC for 26 weeks in the DB treatment period. Participants who received treatment with tolebrutinib 60 mg orally daily in the DB period entered the OLE period and continued the same treatment in the OLE period. Participants who received matched placebo in the DB period received tolebrutinib 60 mg orally daily along with SoC starting from Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61). | 6 |
| Total | 6 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 |
|---|---|---|---|
| DB Period: 26 Weeks | Study terminated by sponsor | 1 | 1 |
| DB Period: 26 Weeks | Withdrawal by Subject | 0 | 1 |
| OLE: Week 27 Till Termination (Week 61) | Study terminated by sponsor | 2 | 1 |
Baseline characteristics
| Characteristic | Overall Participants |
|---|---|
| Age, Continuous | 56.0 years STANDARD_DEVIATION 12.4 |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants |
| Race (NIH/OMB) Asian | 4 Participants |
| Race (NIH/OMB) Black or African American | 0 Participants |
| Race (NIH/OMB) More than one race | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants |
| Race (NIH/OMB) White | 2 Participants |
| Sex: Female, Male Female | 3 Participants |
| Sex: Female, Male Male | 3 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 0 / 3 | 1 / 5 |
| other Total, other adverse events | 2 / 3 | 3 / 5 |
| serious Total, serious adverse events | 1 / 3 | 1 / 5 |
Outcome results
Primary
DB Period: Change From Baseline in Myasthenia Gravis-activities of Daily Living (MG-ADL) Total Score at Week 26
The MG-ADL is an 8-item patient-reported categorical scale that assesses MG symptoms and their effects on daily activities. The MG-ADL targeted symptoms and disability across ocular (2 items), bulbar (3 items), respiratory (1 items), and gross motor or limb impairment (2 items) symptoms. It evaluates a participant's capacity to perform different activities in their daily life. Each item is scored on a 4-point scale ranged from 0 (normal) to 3 (severe), where higher score represents the more severe symptoms or impaired performance. MG-ADL total score is the sum of each item score which ranged from 0 (normal) to 24 (severe). Higher score represents severe disability due to MG. DB period Baseline value was defined as last available value prior to the first dose of the study medication in the DB period.
Time frame: Baseline (Day 1), Week 26
Population: Evaluable data was collected for 3 participants only; and thus, was not presented to protect participant confidentiality.
Primary
OLE Period: Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events Leading to Permanent Study Intervention Discontinuation and Adverse Events of Special Interests (AESIs)
An AE was defined as any untoward medical occurrence in a participant who received study drug and did not necessarily have to have a causal relationship with the treatment. A SAE was any untoward medical occurrence that at any dose: resulted in death, was life-threatening, required inpatient hospitalization or prolongation of existing hospitalization, resulted in persistent or significant disability/incapacity, was a congenital anomaly/birth defect, or was a medically important event. An AESI was defined as one of scientific & medical concern specific to the Sponsor's product or program, for which ongoing monitoring and immediate notification by the Investigator to the Sponsor was considered appropriate. Relatedness to study vaccine was based on Investigator's discretion.
Time frame: From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61)
Population: Analysis was performed on the safety population which included all randomized participants who took at least 1 dose of study intervention and were analyzed according to the intervention they actually received.
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| DB Period: Placebo | OLE Period: Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events Leading to Permanent Study Intervention Discontinuation and Adverse Events of Special Interests (AESIs) | AEs | 2 Participants |
| DB Period: Placebo | OLE Period: Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events Leading to Permanent Study Intervention Discontinuation and Adverse Events of Special Interests (AESIs) | SAEs | 0 Participants |
| DB Period: Placebo | OLE Period: Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events Leading to Permanent Study Intervention Discontinuation and Adverse Events of Special Interests (AESIs) | AEs leading to permanent study intervention discontinuation | 0 Participants |
| DB Period: Placebo | OLE Period: Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events Leading to Permanent Study Intervention Discontinuation and Adverse Events of Special Interests (AESIs) | AESIs | 0 Participants |
| DB Period: Tolebrutinib | OLE Period: Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events Leading to Permanent Study Intervention Discontinuation and Adverse Events of Special Interests (AESIs) | AESIs | 0 Participants |
| DB Period: Tolebrutinib | OLE Period: Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events Leading to Permanent Study Intervention Discontinuation and Adverse Events of Special Interests (AESIs) | AEs | 0 Participants |
| DB Period: Tolebrutinib | OLE Period: Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events Leading to Permanent Study Intervention Discontinuation and Adverse Events of Special Interests (AESIs) | AEs leading to permanent study intervention discontinuation | 0 Participants |
| DB Period: Tolebrutinib | OLE Period: Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events Leading to Permanent Study Intervention Discontinuation and Adverse Events of Special Interests (AESIs) | SAEs | 0 Participants |
Primary
OLE Period: Number of Participants With Clinical Chemistry Parameter Abnormalities
Clinical chemistry parameters assessed were blood urea nitrogen, creatinine, glucose, total and direct bilirubin, potassium, sodium, chloride, bicarbonate, calcium, albumin, creatine phosphokinase, alkaline phosphatase, aspartate aminotransferase/serum glutamic-oxaloacetic transaminase, alanine aminotransferase/serum glutamic-pyruvic transaminase, lipase, and total protein. Only the category (Alkaline phosphatase) in which at least 1 participant had data were reported.
Time frame: From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61)
Population: Analysis was performed on the safety population.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| DB Period: Placebo | OLE Period: Number of Participants With Clinical Chemistry Parameter Abnormalities | 0 Participants |
| DB Period: Tolebrutinib | OLE Period: Number of Participants With Clinical Chemistry Parameter Abnormalities | 1 Participants |
Primary
OLE Period: Number of Participants With Electrocardiogram (ECG) Abnormalities
ECG parameters assessed were heart rate, pulse rate, QRS interval, QT interval and QT interval corrected using Fridericia's formula \[QTcF\]).
Time frame: From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61)
Population: Analysis was performed on the safety population.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| DB Period: Placebo | OLE Period: Number of Participants With Electrocardiogram (ECG) Abnormalities | 0 Participants |
| DB Period: Tolebrutinib | OLE Period: Number of Participants With Electrocardiogram (ECG) Abnormalities | 0 Participants |
Primary
OLE Period: Number of Participants With Hematological Abnormalities
Hematological parameters assessed were: platelet count, red blood cell count, hemoglobin, hematocrit, white blood cell, neutrophils, lymphocytes, monocytes, eosinophils, and basophils. Only those categories in which at least 1 participant had data were reported.
Time frame: From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61)
Population: Analysis was performed on safety population.
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| DB Period: Placebo | OLE Period: Number of Participants With Hematological Abnormalities | Hematocrit | 1 Participants |
| DB Period: Placebo | OLE Period: Number of Participants With Hematological Abnormalities | Hemoglobin | 1 Participants |
| DB Period: Placebo | OLE Period: Number of Participants With Hematological Abnormalities | White blood cells | 1 Participants |
| DB Period: Placebo | OLE Period: Number of Participants With Hematological Abnormalities | Monocytes | 2 Participants |
| DB Period: Tolebrutinib | OLE Period: Number of Participants With Hematological Abnormalities | Monocytes | 0 Participants |
| DB Period: Tolebrutinib | OLE Period: Number of Participants With Hematological Abnormalities | Hematocrit | 0 Participants |
| DB Period: Tolebrutinib | OLE Period: Number of Participants With Hematological Abnormalities | White blood cells | 0 Participants |
| DB Period: Tolebrutinib | OLE Period: Number of Participants With Hematological Abnormalities | Hemoglobin | 0 Participants |
Primary
OLE Period: Number of Participants With Vital Signs Abnormalities
Vital signs assessed were heart rate, systolic blood pressure, diastolic blood pressure, weight and temperature. Only those category (Weight \>=5% decrease from Baseline) in which at least 1 participant had data were reported.
Time frame: From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61)
Population: Analysis was performed on the safety population.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| DB Period: Placebo | OLE Period: Number of Participants With Vital Signs Abnormalities | 1 Participants |
| DB Period: Tolebrutinib | OLE Period: Number of Participants With Vital Signs Abnormalities | 0 Participants |
Secondary
DB Period: Change From Baseline in Myasthenia Gravis Impairment Index (MGII) Total Score at Week 26
MGII: measure of MG severity, with demonstrated fatigability, reliability and construct validity. It consists of 22-item patient-reported questionnaire and 6 clinician-assessment items. MGII can be divided into 2 sub-scale-scores: ocular (8 items) & generalized (20 items) impairments. Ocular sub-score: calculated by summing 1 to 6 items from patient questionnaire and items 1 & 2 of clinician-assessment. Generalized score: calculated by adding items 7 to 22 from patient questionnaire & items 3 to 6 from the clinician-assessment. Each item is scored on 4-point scale: from 0 (none) to 3 (severe), where higher score=more disease severity. MGII total score: sum of each item of patient questionnaire (total score:0 \[normal\] to 23 \[severe\]) & clinician assessment items (total score:0 \[normal\] to 61 \[severe\]); ranged from 0 (normal) to 84 (severe). Higher scores=greater disease severity. DB period Baseline: defined as last available value prior to 1st dose of study medication in the DB period.
Time frame: Baseline (Day 1), Week 26
Population: Evaluable data was collected for 3 participants only; and thus, was not presented to protect participant confidentiality.
Secondary
DB Period: Change From Baseline in Myasthenia Gravis-quality of Life 15-item Scale (MG-QoL15) Total Score at Week 26
The MG-QOL15 is a 15-item, participant self-reported QoL instrument for participants with MG. The instrument is developed and validated to evaluate general QoL of participants with MG by a clinician in the practice setting. The domains covered by the questionnaire are mobility (9 items), symptoms (3 items), general contentment (1 item) and emotional well-being (2 items). Each item is scored on a scale of 0 (not at all) to 4 (very much), where higher score indicates severe QoL impairment. The MG-QOL15 total score is the sum of each individual item score and ranged from 0 (none) to 60 (severe). Higher scores indicates greater extent and dissatisfaction with MG-related dysfunction. DB period Baseline value was defined as last available value prior to the first dose of the study medication in the DB period.
Time frame: Baseline (Day 1), Week 26
Population: Evaluable data was collected for 3 participants only; and thus, was not presented to protect participant confidentiality.
Secondary
DB Period: Change From Baseline in Quantitative Myasthenia Gravis (QMG) Total Score at Week 12
The QMG is a clinician-reported outcome to assess muscle weakness in participants with MG. The QMG test consists of 13 items: ocular (2 items), facial (1 item), bulbar (2 items), gross motor (6 items), axial (1 item), and respiratory (1 item). Each item is scored on 3-point scale ranged from 0 (none) to 3 (severe), where higher score represents most severe muscle weakness. The QMG total score is the sum of each individual item score which ranged from 0 (normal) to 39 (severe). Higher score represents greater disease activity. The QMG total score at Week 12 is reported in this outcome measure. DB period Baseline value was defined as last available value prior to the first dose of the study medication in the DB period.
Time frame: Baseline (Day 1), Week 12
Population: Analysis was performed on modified intention-to-treat (mITT) population which included all randomized and treated participants with a Baseline value and at least 1 post-baseline value for any efficacy assessment. Data for this outcome measure was not collected and analyzed for OLE period of the study.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| DB Period: Placebo | DB Period: Change From Baseline in Quantitative Myasthenia Gravis (QMG) Total Score at Week 12 | -2.0 score on a scale | Standard Deviation 7.9 |
| DB Period: Tolebrutinib | DB Period: Change From Baseline in Quantitative Myasthenia Gravis (QMG) Total Score at Week 12 | -1.7 score on a scale | Standard Deviation 2.9 |
Secondary
DB Period: Change From Baseline in Quantitative Myasthenia Gravis (QMG) Total Score at Week 26
The QMG is a clinician-reported outcome to assess muscle weakness in participants with MG. The QMG test consists of 13 items: ocular (2 items), facial (1 item), bulbar (2 items), gross motor (6 items), axial (1 item), and respiratory (1 item). Each item is scored on 3-point scale ranged from 0 (none) to 3 (severe), where higher score represents most severe muscle weakness. The QMG total score is the sum of each individual item score which ranged from 0 (normal) to 39 (severe). Higher score represents greater disease activity. DB period Baseline value was defined as last available value prior to the first dose of the study medication in the DB period.
Time frame: Baseline (Day 1), Week 26
Population: Evaluable data was collected for 3 participants only; and thus, was not presented to protect participant confidentiality.
Secondary
DB Period: Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events Leading to Permanent Study Intervention Discontinuation and Adverse Events of Special Interests (AESIs)
An AE was defined as any untoward medical occurrence in a participant who received study drug and did not necessarily have to have a causal relationship with the treatment. A SAEs was any untoward medical occurrence that at any dose: resulted in death, was life-threatening, required inpatient hospitalization or prolongation of existing hospitalization, resulted in persistent or significant disability/incapacity, was a congenital anomaly/birth defect, was a medically important event. AESI was defined as one of scientific & medical concern specific to the Sponsor's product or program, for which ongoing monitoring and immediate notification by the Investigator to the Sponsor was considered appropriate. Relatedness to study vaccine was based on Investigator's discretion.
Time frame: From Day 1 up to Week 26
Population: Analysis was performed on safety population.
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| DB Period: Placebo | DB Period: Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events Leading to Permanent Study Intervention Discontinuation and Adverse Events of Special Interests (AESIs) | AEs | 1 Participants |
| DB Period: Placebo | DB Period: Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events Leading to Permanent Study Intervention Discontinuation and Adverse Events of Special Interests (AESIs) | SAEs | 1 Participants |
| DB Period: Placebo | DB Period: Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events Leading to Permanent Study Intervention Discontinuation and Adverse Events of Special Interests (AESIs) | AEs leading to permanent study intervention discontinuation | 0 Participants |
| DB Period: Placebo | DB Period: Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events Leading to Permanent Study Intervention Discontinuation and Adverse Events of Special Interests (AESIs) | AESIs | 1 Participants |
| DB Period: Tolebrutinib | DB Period: Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events Leading to Permanent Study Intervention Discontinuation and Adverse Events of Special Interests (AESIs) | AESIs | 1 Participants |
| DB Period: Tolebrutinib | DB Period: Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events Leading to Permanent Study Intervention Discontinuation and Adverse Events of Special Interests (AESIs) | AEs | 2 Participants |
| DB Period: Tolebrutinib | DB Period: Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events Leading to Permanent Study Intervention Discontinuation and Adverse Events of Special Interests (AESIs) | AEs leading to permanent study intervention discontinuation | 0 Participants |
| DB Period: Tolebrutinib | DB Period: Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events Leading to Permanent Study Intervention Discontinuation and Adverse Events of Special Interests (AESIs) | SAEs | 1 Participants |
Secondary
DB Period: Number of Participants With Clinical Chemistry Parameter Abnormalities
Clinical chemistry parameters assessed were blood urea nitrogen, creatinine, glucose, total and direct bilirubin, potassium, sodium, chloride, bicarbonate, calcium, albumin, creatine phosphokinase, alkaline phosphatase, aspartate aminotransferase/serum glutamic-oxaloacetic transaminase, alanine aminotransferase/serum glutamic-pyruvic transaminase, lipase, and total protein. Only those categories in which at least 1 participant had data were reported.
Time frame: From Day 1 up to Week 26
Population: Analysis was performed on safety population.
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| DB Period: Placebo | DB Period: Number of Participants With Clinical Chemistry Parameter Abnormalities | Alanine aminotransferase | 1 Participants |
| DB Period: Placebo | DB Period: Number of Participants With Clinical Chemistry Parameter Abnormalities | Alkaline phosphatase | 0 Participants |
| DB Period: Placebo | DB Period: Number of Participants With Clinical Chemistry Parameter Abnormalities | Aspartate aminotransferase | 1 Participants |
| DB Period: Placebo | DB Period: Number of Participants With Clinical Chemistry Parameter Abnormalities | Total bilirubin | 0 Participants |
| DB Period: Placebo | DB Period: Number of Participants With Clinical Chemistry Parameter Abnormalities | Protein | 1 Participants |
| DB Period: Tolebrutinib | DB Period: Number of Participants With Clinical Chemistry Parameter Abnormalities | Total bilirubin | 1 Participants |
| DB Period: Tolebrutinib | DB Period: Number of Participants With Clinical Chemistry Parameter Abnormalities | Protein | 1 Participants |
| DB Period: Tolebrutinib | DB Period: Number of Participants With Clinical Chemistry Parameter Abnormalities | Alanine aminotransferase | 0 Participants |
| DB Period: Tolebrutinib | DB Period: Number of Participants With Clinical Chemistry Parameter Abnormalities | Aspartate aminotransferase | 0 Participants |
| DB Period: Tolebrutinib | DB Period: Number of Participants With Clinical Chemistry Parameter Abnormalities | Alkaline phosphatase | 1 Participants |
Secondary
DB Period: Number of Participants With Electrocardiogram Abnormalities
ECG parameters assessed were heart rate, pulse rate, QRS interval, QT interval and QTcF.
Time frame: From Day 1 up to Week 26
Population: Analysis was performed on safety population.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| DB Period: Placebo | DB Period: Number of Participants With Electrocardiogram Abnormalities | 0 Participants |
| DB Period: Tolebrutinib | DB Period: Number of Participants With Electrocardiogram Abnormalities | 0 Participants |
Secondary
DB Period: Number of Participants With Hematological Abnormalities
Hematological parameters assessed were: platelet count, red blood cell count, hemoglobin, hematocrit, white blood cell, neutrophils, lymphocytes, monocytes, eosinophils, and basophils. Only those categories in which at least 1 participant had data were reported.
Time frame: From Day 1 up to Week 26
Population: Analysis was performed on safety population.
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| DB Period: Placebo | DB Period: Number of Participants With Hematological Abnormalities | Eosinophils | 1 Participants |
| DB Period: Placebo | DB Period: Number of Participants With Hematological Abnormalities | Hemoglobin | 1 Participants |
| DB Period: Placebo | DB Period: Number of Participants With Hematological Abnormalities | Hematocrit | 1 Participants |
| DB Period: Placebo | DB Period: Number of Participants With Hematological Abnormalities | Monocytes | 1 Participants |
| DB Period: Tolebrutinib | DB Period: Number of Participants With Hematological Abnormalities | Monocytes | 0 Participants |
| DB Period: Tolebrutinib | DB Period: Number of Participants With Hematological Abnormalities | Hematocrit | 1 Participants |
| DB Period: Tolebrutinib | DB Period: Number of Participants With Hematological Abnormalities | Hemoglobin | 0 Participants |
| DB Period: Tolebrutinib | DB Period: Number of Participants With Hematological Abnormalities | Eosinophils | 0 Participants |
Secondary
DB Period: Number of Participants With Vital Signs Abnormalities
Vital signs assessed were heart rate, systolic blood pressure, diastolic blood pressure, weight and temperature. Only those category (Weight \>=5% increase from Baseline) in which at least 1 participant had data were reported.
Time frame: From Day 1 up to Week 26
Population: Analysis was performed on safety population.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| DB Period: Placebo | DB Period: Number of Participants With Vital Signs Abnormalities | 1 Participants |
| DB Period: Tolebrutinib | DB Period: Number of Participants With Vital Signs Abnormalities | 0 Participants |
Secondary
DB Period: Percentage of Participants With >=3-point Improvement (Reduction) in Quantitative Myasthenia Gravis Total Score at Week 26
The MG-ADL is an 8-item patient-reported categorical scale that assesses MG symptoms and their effects on daily activities. The MG-ADL targeted symptoms and disability across ocular (2 items), bulbar (3 items), respiratory (1 items), and gross motor or limb impairment (2 items) symptoms. It evaluates a participant's capacity to perform different activities in their daily life. Each item is scored on a 4-point scale ranged from 0 (normal) to 3 (severe), where higher score represents the more severe symptoms or impaired performance. MG-ADL total score is the sum of each item score which ranged from 0 (normal) to 24 (severe). Higher score represents severe disability due to MG.
Time frame: Week 26
Population: Evaluable data was collected for 3 participants only; and thus, was not presented to protect participant confidentiality.
Secondary
DB Period: Percentage of Participants With Greater Than Equal to (>=) 2-point Improvement (Reduction) in Myasthenia Gravis-activities of Daily Living Total Score at Week 26
The MG-ADL is an 8-item patient-reported categorical scale that assesses MG symptoms and their effects on daily activities. The MG-ADL targeted symptoms and disability across ocular (2 items), bulbar (3 items), respiratory (1 items), and gross motor or limb impairment (2 items) symptoms. It evaluates a participant's capacity to perform different activities in their daily life. Each item is scored on a 4-point scale ranged from 0 (normal) to 3 (severe), where higher score represents the more severe symptoms or impaired performance. MG-ADL total score is the sum of each item score which ranged from 0 (normal) to 24 (severe). Higher score represents severe disability due to MG.
Time frame: Week 26
Population: Evaluable data was collected for 3 participants only; and thus, was not presented to protect participant confidentiality.
Secondary
OLE Period: Change From Baseline in Myasthenia Gravis-activities of Daily Living Total Score
The MG-ADL is an 8-item patient-reported categorical scale that assesses MG symptoms and their effects on daily activities. The MG-ADL targeted symptoms and disability across ocular (2 items), bulbar (3 items), respiratory (1 items), and gross motor or limb impairment (2 items) symptoms. It evaluates a participant's capacity to perform different activities in their daily life. Each item is scored on a 4-point scale ranged from 0 (normal) to 3 (severe), where higher score represents the more severe symptoms or impaired performance. MG-ADL total score is the sum of each item score which ranged from 0 (normal) to 24 (severe). Higher score represents severe disability due to MG. OLE period Baseline value was defined as last available value prior to the first dose of the study medication in the OLE period.
Time frame: From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61)
Population: Evaluable data was collected for 3 participants only; and thus, was not presented to protect participant confidentiality.
Secondary
OLE Period: Change From Baseline in Myasthenia Gravis Impairment Index Total Score
MGII: measure of MG severity, with demonstrated fatigability, reliability and construct validity. It consists of 22-item patient-reported questionnaire & 6 clinician-assessment items. MGII can be divided into 2 sub-scale-scores: ocular (8 items) & generalized (20 items) impairments. Ocular sub-score: calculated by summing 1 to 6 items from patient questionnaire and items 1 & 2 of clinician-assessment. Generalized score: calculated by adding items 7 to 22 from patient questionnaire & items 3 to 6 from the clinician-assessment. Each item is scored on 4-point scale: from 0 (none) to 3 (severe), where higher score=more disease severity. MGII total score: sum of each item of patient questionnaire (total score:0 \[normal\] to 23 \[severe\]) & clinician assessment items (total score:0 \[normal\] to 61 \[severe\]); ranged from 0 (normal) to 84 (severe). Higher scores=greater disease severity. OLE period Baseline:defined as last available value prior to 1st dose of study medication in the OLE period.
Time frame: From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61)
Population: Evaluable data was collected for 3 participants only; and thus, was not presented to protect participant confidentiality.
Secondary
OLE Period: Change From Baseline in Myasthenia Gravis-quality of Life 15-item Scale Total Score
The MG-QOL15 is a 15-item, participant self-reported QoL instrument for participants with MG. The instrument is developed and validated to evaluate general QoL of participants with MG by a clinician in the practice setting. The domains covered by the questionnaire are mobility (9 items), symptoms (3 items), general contentment (1 item) and emotional well-being (2 items). Each item is scored on a scale of 0 (not at all) to 4 (very much), where higher score indicates severe QoL impairment. The MG-QOL15 total score is the sum of each individual item score and ranged from 0 (none) to 60 (severe). Higher scores indicate greater extent and dissatisfaction with MG-related dysfunction.
Time frame: From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61)
Population: Evaluable data was collected for 3 participants only; and thus, was not presented to protect participant confidentiality.
Secondary
OLE Period: Change From Baseline in Quantitative Myasthenia Gravis Total Score
The QMG is a clinician-reported outcome to assess muscle weakness in participants with MG. The QMG test consists of 13 items: ocular (2 items), facial (1 item), bulbar (2 items), gross motor (6 items), axial (1 item), and respiratory (1 item). Each item is scored on 3-point scale ranged from 0 (none) to 3 (severe), where higher score represents most severe muscle weakness. The QMG total score is the sum of each individual item score which ranged from 0 (normal) to 39 (severe). Higher score represents greater disease activity. OLE period Baseline value was defined as last available value prior to the first dose of the study medication in the OLE period.
Time frame: From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61)
Population: Evaluable data was collected for 3 participants only; and thus, was not presented to protect participant confidentiality.
Secondary
OLE Period: Percentage of Participants Achieving Any Reduction From Baseline of Daily Dose of Oral Corticosteroids (OCS) at Week 61
The use of rescue therapy for generalized MG worsening is allowed at any time during both the DB and OLE parts of the study at discretion of the Investigator in case of at least a 2-point increase of individual non-ocular MG-ADL items compared to the Day 1 MG-ADL value or new or worsening of respiratory/ bulbar symptoms. Rescue therapy includes intravenous immunoglobulin, plasma exchange, change in the standard of care OCS dose or any use of new CS. OLE period Baseline value was defined as last available value prior to the first dose of the study medication in the OLE period.
Time frame: Baseline (Day 1), Week 61
Population: Evaluable data was collected for 3 participants only; and thus, was not presented to protect participant confidentiality.
Secondary
OLE Period: Percentage of Participants With >=2-point Improvement (Reduction) in Myasthenia Gravis-activities of Daily Living Total Score
The MG-ADL is an 8-item patient-reported categorical scale that assesses MG symptoms and their effects on daily activities. The MG-ADL targeted symptoms and disability across ocular (2 items), bulbar (3 items), respiratory (1 items), and gross motor or limb impairment (2 items) symptoms. It evaluates a participant's capacity to perform different activities in their daily life. Each item is scored on a 4-point scale ranged from 0 (normal) to 3 (severe), where higher score represents the more severe symptoms or impaired performance. MG-ADL total score is the sum of each item score which ranged from 0 (normal) to 24 (severe). Higher score represents severe disability due to MG. OLE period Baseline value was defined as last available value prior to the first dose of the study medication in the OLE period.
Time frame: From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61)
Population: Evaluable data was collected for 3 participants only; and thus, was not presented to protect participant confidentiality.
Secondary
OLE Period: Percentage of Participants With >=3-point Improvement (Reduction) in Quantitative Myasthenia Gravis Total Score
The MG-ADL is an 8-item patient-reported categorical scale that assesses MG symptoms and their effects on daily activities. The MG-ADL targeted symptoms and disability across ocular (2 items), bulbar (3 items), respiratory (1 items), and gross motor or limb impairment (2 items) symptoms. It evaluates a participant's capacity to perform different activities in their daily life, including talking, chewing, swallowing, breathing, brushing their teeth or combing their hair, getting up from a chair, double vision and eyelid droop. Each item is scored on a 4-point scale ranged from 0 (normal) to 3 (severe), where higher score represents the more severe symptoms or impaired performance. MG-ADL total score is the sum of each item score which ranged from 0 to 24, where a higher score represents severe disability due to MG. OLE period Baseline value was defined as last available value prior to the first dose of the study medication in the OLE period.
Time frame: From Week 27 up to an additional 35 weeks in the OLE period until the study termination (i.e., up to Week 61)
Population: Evaluable data was collected for 3 participants only; and thus, was not presented to protect participant confidentiality.