Essential Tremor
Conditions
Keywords
Movement Disorder, Benign Essential Tremor, Familial Tremor, Hereditary Essential Tremor, Movement Disorder Agents, Calcium Channels, T-type
Brief summary
This is a 2-part clinical trial to evaluate the efficacy, safety, and tolerability of 40 and 120 mg oral PRAX-944 compared to placebo in the treatment of adults with essential tremor. Part A is designed to study the dose titration from 20 to 40 mg every morning (QAM) (ie, 2 weeks with 7 days at each dose level). Part B is designed to study the dose titration from 20 to up to 120 mg QAM with at least 14 days of dosing at the highest tolerated dose for each participant. Blood levels of PRAX-944 will also be measured throughout the trial and pharmacokinetics will be evaluated.
Interventions
Once daily oral treatment
Once daily oral treatment with titration
Once daily oral treatment with titration followed by placebo
Sponsors
Study design
Masking description
Part A: Open label Part B: Open label titration followed by quadruple-blind, randomized withdrawal
Intervention model description
Part A: Single group Part B: Parallel group, randomized withdrawal
Eligibility
Inclusion criteria
1. Clinical diagnosis of ET consistent with Movement Disorders Society Criteria, a duration of ET of at least 3 years and with onset before the age of 65 2. TETRAS upper limb score (ie, sum of bilateral upper limb items 4a, 4b, and 4c) of ≥10 as rated by the Investigator at Screening and Baseline OR A score of ≥2 on 2 or more of the following TETRAS activities of daily living (ADL) subscale items: (2) Feeding with a spoon, (3) Drinking from a glass, (5) Dressing, (6) Pouring, (9) Writing OR A score of ≥2 on 1 of the following TETRAS ADL subscale items: (2) Feeding with a spoon, (3) Drinking from a glass, (5) Dressing, (6) Pouring, or (9) Writing AND a score of ≥2 on both of the following TETRAS ADL subscale items: (10) Working and (12) Social Impact 3. If currently receiving any medication for ET, is on a stable dose of any of these medications for ET for 28 days prior to Screening and is willing to maintain stable doses throughout the trial. If receiving primidone for ET, is willing and able to discontinue 14 days prior to Day 1. 4. Body mass index (BMI) between 18 and 40 kg/m2 (inclusive).
Exclusion criteria
1. Sporadically using a benzodiazepine, sleep medication, or anxiolytic that would confound the assessment of tremor. 2. Trauma to the nervous system within 3 months preceding the onset of tremor. 3. History of other medical, neurological or psychiatric condition that may explain or cause tremor, including but not limited to Parkinson's disease, dystonia, cerebellar disease, family history of Fragile X syndrome, traumatic brain injury, alcohol abuse or withdrawal, benzodiazepine abuse or withdrawal, multiple sclerosis, polyneuropathy, and endocrine states such as hyperthyroidism. 4. Prior magnetic resonance-guided focused ultrasound or surgical intervention for ET such as deep brain stimulation or thalamotomy. 5. Botulinum toxin injection for ET in the 6 months prior to Screening. 6. Unwilling or unable to refrain from alcohol 24 hours before and during clinical trial visits. 7. History of substance use disorder
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Part A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score | Baseline (Day 0), Days 7 and 14 | The TETRAS upper limb score is calculated as the sum of the 6 separate upper-limb maneuvers assessed by the clinician: forward-outstretched postural tremor \[right\], forward outstretched postural tremor \[left\], lateral wing-beating postural tremor \[right\], lateral wing-beating postural tremor \[left\], kinetic tremor \[right\], kinetic tremor \[left\], each on a 0 (no tremor) to 4 (maximum tremor) severity scale in 0.5-point increments. TETRAS Part 4 score for both upper limbs ranged from 0 to 24, higher scores indicated more severe tremor. A negative change from baseline indicated less tremor. Baseline is defined as the last non-missing value collected prior to receiving first dose of study drug. Change from baseline will be defined as assessment value minus baseline value. |
| Part B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Up to Day 70 | An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of a study intervention, whether or not considered related to the study intervention. Incidence and Severity of Adverse Events have been reported. |
| Part B: Number of Participants With Clinically Significant Abnormalities in Vital Signs, Laboratory Values and Electrocardiogram Parameters | Up to Day 70 | Vital signs parameters included body temperature, pulse rate, respiratory rate, blood pressure (systolic and diastolic), clinical laboratory measures (chemistry, hematology, urinalysis, and coagulation), electrocardiogram parameters (heart rate, PR, QRS, QT, and corrected QT intervals). Any change in vital sign abnormalities that was clinically significant in the medical and scientific judgment of the investigator and not related to an underlying disease was reported as an unsolicited adverse event (AE). Any clinically significant abnormality associated with underlying disease does not require reporting as an (S)AE unless judged by the investigator to be more severe than expected for the participant's condition. |
| Part B: Number of Participants With Suicidal Ideation or Behavior Assessed Using Columbia Suicide Severity Rating Scale (C-SSRS) | Up to Day 70 | The C-SSRS is described as a scale developed at Columbia University that has 2-6 questions each in categories of Suicidal Ideation, Intensity of Ideation, Suicidal Behavior, and Actual Attempts. Four constructs were measured. Severity of Suicidal ideation is rated on a 5-point ordinal scale. Intensity of ideation is comprised of 5 items (frequency, duration, controllability, deterrents, and reason for ideation), each rated on a 5-point ordinal scale. Suicidal behavior is rated on a nominal scale that includes actual, aborted, and interrupted attempts; preparatory behavior; and non-suicidal self-injurious behavior. Lethality, assesses actual attempts; actual lethality is rated on a 6-point ordinal scale, and if actual lethality is 0, potential lethality of attempts is rated on a 3-point ordinal scale.The higher the C-SSRS score, the higher the suicide risk (ie. worse outcome). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Part A: Number of Participants With Clinically Significant Abnormalities in Vital Signs, Laboratory Values and Electrocardiogram Parameters | Up to Day 21 | Vital signs parameters included body temperature, pulse rate, respiratory rate, blood pressure (systolic and diastolic), clinical laboratory measures (chemistry, hematology, urinalysis, and coagulation), electrocardiogram parameters (heart rate, PR, QRS, QT, and corrected QT intervals). Any change in vital sign abnormalities that was clinically significant in the medical and scientific judgment of the investigator and not related to an underlying disease was reported as an unsolicited adverse event (AE). Any clinically significant abnormality associated with underlying disease does not require reporting as an (S)AE unless judged by the investigator to be more severe than expected for the participant's condition. |
| Part A: Number of Participants With Suicidal Ideation or Behavior Assessed Using Columbia Suicide Severity Rating Scale (C-SSRS) | Up to Day 21 | The C-SSRS is described as a scale developed at Columbia University that has 2-6 questions each in categories of Suicidal Ideation, Intensity of Ideation, Suicidal Behavior, and Actual Attempts. Four constructs were measured. Severity of Suicidal ideation is rated on a 5-point ordinal scale. Intensity of ideation is comprised of 5 items (frequency, duration, controllability, deterrents, and reason for ideation), each rated on a 5-point ordinal scale. Suicidal behavior is rated on a nominal scale that includes actual, aborted, and interrupted attempts; preparatory behavior; and non-suicidal self-injurious behavior. Lethality, assesses actual attempts; actual lethality is rated on a 6-point ordinal scale, and if actual lethality is 0, potential lethality of attempts is rated on a 3-point ordinal scale.The higher the C-SSRS score, the higher the suicide risk (ie. worse outcome). |
| Part B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score During OLT Phase | Baseline (Day 0) and Day 42 | The TETRAS upper limb score is calculated as the sum of the 6 separate upper-limb maneuvers assessed by the clinician: forward-outstretched postural tremor \[right\], forward outstretched postural tremor \[left\], lateral wing-beating postural tremor \[right\], lateral wing-beating postural tremor \[left\], kinetic tremor \[right\], kinetic tremor \[left\], each on a 0 (no tremor) to 4 (maximum tremor) severity scale in 0.5-point increments. TETRAS Part 4 score for both upper limbs ranged from 0 to 24, higher scores indicated more severe tremor. A negative change from baseline indicated less tremor. Baseline is defined as the last non-missing value collected prior to receiving first dose of study drug. Change from baseline will be defined as assessment value minus baseline value. |
| Part B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Subscale During OLT Phase | Baseline (Day 0) and Days 7, 21 and 42 | TETRAS Performance Subscale was used to assess essential tremor as scored by the independent video raters. The performance subscale consists of 9 items, i.e. item 1 (head), item 2 (face), item 3 (voice), each of the 6 sub-items for item 4 (upper limb), the maximum of the 4 sub-items for item 5 (lower limb), 2 sub-items (right and left side) for item 6 (Archimedes spirals), item 7 (handwriting), 2 sub-items (right and left side) for item 8 (dot approximation), and item 9 (standing) for a total score ranging from 0 to 64 from 16 sub-items. Each item is rated on a scale of 0 to 4, including 0.5 increments. A lower score is indicative of improvement. The total score has been presented. Baseline is defined as the last non-missing value collected prior to receiving first dose of study drug. Change from baseline will be defined as assessment value minus baseline value. |
| Part A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Subscale | Baseline (Day 0), Days 7 and 14 | The TETRAS is an essential tremor and activities of daily living rating scale. The full scale has 2 sections, the Performance subscale (PS) and the ADL subscale. The PS consists of 9 items covering different body regions. These 9 items are rated on a 5-point scale (ranging from 0 to 4). One item, Item 4, consists of ratings for 3 tasks rated separately for upper limbs on both sides of the body for a total of 6 ratings. The total score of the 9 items (14 ratings) ranges from 0 to 70 with higher scores indicating greater tremor severity. The total score and individual item ratings will be evaluated as outcomes in this trial. Baseline is defined as the last non-missing value collected prior to receiving first dose of study drug. |
| Part B: Change From Baseline in TETRAS Performance Subscale Individual Items # 6 (Spiral Drawing) and Items #7 (Handwriting) | Baseline (Day 0), Days 7, 21 and 42 | TETRAS Performance Subscale was used to assess essential tremor as scored by the independent video raters. The performance subscale consists of 9 items, i.e. item 1 (head), item 2 (face), item 3 (voice), each of the 6 sub-items for item 4 (upper limb), the maximum of the 4 sub-items for item 5 (lower limb), 2 sub-items (right and left side) for item 6 (Archimedes spirals), item 7 (handwriting), 2 sub-items (right and left side) for item 8 (dot approximation), and item 9 (standing) for a total score ranging from 0 to 64 from 16 sub-items. Each item is rated on a scale of 0 to 4, including 0.5 increments. A lower score is indicative of improvement. Baseline is defined as the last non-missing value collected prior to receiving first dose of study drug. Change from baseline will be defined as assessment value minus baseline value. |
| Part B: Change From Baseline in TETRAS Activities of Daily Living (ADL) Score | Baseline (Day 0), Days 7, 21 and 42 | The TETRAS ADL subscale is a 12-item assessment of typical daily activities that are impacted by tremor. Activities are assessed in the following functional domains: speaking, feeding, drinking, personal hygiene, dressing, writing, and social activity. The impact to each function is rated on a 5-point Likert scale from 0 to 4. The ADL subscale score is calculated as the sum of all 12 items and ranges from 0 to 48 with higher scores reflecting higher impact. Baseline is defined as the last non-missing value collected prior to receiving first dose of study drug. Change from baseline will be defined as assessment value minus baseline value. |
| Part B: Change From Baseline in Quality of Life in Essential Tremor Questionnaire (QUEST) Total Scores. | Baseline (Day 0), Days 7, 21 and 42 | Quality of Life in Essential Tremor Questionnaire (QUEST) is a patient-reported ET-specific 30-item, specific quality of life scale. Items contribute to five dimensions. Physical/ADL (9 items ), Psychosocial (9 items), Communication (3 items), Hobbies/Leisure (3 items), and Work/Finances (6 items). The QUEST total and subscale scores are calculated as the sum of all applicable items divided by the number of applicable items times 100. Higher score indicates greater dissatisfaction with that domain of QOL. Maximal score 100: worse quality of life. Minimal Score 0: best quality of life. Baseline is defined as the last non-missing value collected prior to receiving first dose of study drug. Change from baseline will be defined as assessment value minus baseline value. |
| Part B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score Measured by Accelerometry During OLT Phase | Baseline (Day 0), and Days 7, 21 and 42 | Accelerometer was used to evaluate record coordinates and accelerations in the 3D space over time. The 3 maneuvers in the upper limb item will be completed for both arms, first for the right arm and then for the left. Each upper limb sub-item is scored on a scale from 0 to 4 including to 0.1 increments. The accelerometer upper limb total score, ranges from 0 to 24. A decrease in score is indicative of improvement. Baseline is defined as the last non-missing value collected prior to receiving first dose of study drug. Change from baseline will be defined as assessment value minus baseline value. |
| Part A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score Measured by Accelerometry | Baseline (Day 0), Days 7 and 14 | Accelerometer was used to evaluate record coordinates and accelerations in the 3D space over time. The 3 maneuvers in the upper limb item will be completed for both arms, first for the right arm and then for the left. Each upper limb sub-item is scored on a scale from 0 to 4 including to 0.1 increments. The accelerometer upper limb total score, ranges from 0 to 24. A decrease in score is indicative of improvement. Baseline is defined as the last non-missing value collected prior to receiving first dose of study drug. Change from baseline will be defined as assessment value minus baseline value. |
| Part A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Subscale Individual Items # 6 (Spiral Drawing) and Items #7 (Handwriting) | Baseline (Day 0), Days 7 and 14 | The TETRAS ADL subscale is a 12-item assessment of typical daily activities that are impacted by tremor. Activities are assessed in the following functional domains: speaking, feeding, drinking, personal hygiene, dressing, writing, and social activity. The impact to each function is rated on a 5-point Likert scale from 0 to 4. The ADL subscale score is calculated as the sum of all 12 items and ranges from 0 to 48 with higher scores reflecting higher impact. Baseline is defined as the last non-missing value collected prior to receiving first dose of study drug. Change from baseline will be defined as assessment value minus baseline value. |
| Part A: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Up to Day 21 | An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of a study intervention, whether or not considered related to the study intervention. Incidence and Severity of Adverse Events have been reported. |
Countries
Australia, New Zealand, United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Part A: PRAX-944 20mg to 40mg OLT Participants in open-label titration phase were administered once daily oral dose of PRAX-944 titrated from 20 mg (7 days) to 40 mg (7 days). | 7 |
| Part B: PRAX-944 20mg to 120mg OLT Participants in open-label titration phase were administered once daily oral dose of PRAX-944 titrated from 20 mg to up to 120 mg for 6-weeks | 17 |
| Total | 24 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 | FG002 | FG003 |
|---|---|---|---|---|---|
| PART A OLT Phase (Day 1 to Day 21) | Adverse Event | 1 | 0 | 0 | 0 |
| PART B OLT Phase (Day 1 to Day 42) | Adverse Event | 0 | 6 | 0 | 0 |
Baseline characteristics
| Characteristic | Part A: PRAX-944 20mg to 40mg OLT | Part B: PRAX-944 20mg to 120mg OLT | Total |
|---|---|---|---|
| Age, Continuous | 67.7 years STANDARD_DEVIATION 6.6 | 59.3 years STANDARD_DEVIATION 13.81 | 61.8 years STANDARD_DEVIATION 12.62 |
| Ethnicity (NIH/OMB) Hispanic or Latino | 0 Participants | 0 Participants | 0 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 7 Participants | 17 Participants | 24 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Race/Ethnicity, Customized Aborigines | 1 Participants | 1 Participants | 2 Participants |
| Race/Ethnicity, Customized American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants |
| Race/Ethnicity, Customized Asian | 0 Participants | 0 Participants | 0 Participants |
| Race/Ethnicity, Customized Black or African American | 0 Participants | 0 Participants | 0 Participants |
| Race/Ethnicity, Customized More than one race | 0 Participants | 0 Participants | 0 Participants |
| Race/Ethnicity, Customized Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants |
| Race/Ethnicity, Customized Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Race/Ethnicity, Customized White | 6 Participants | 16 Participants | 22 Participants |
| Sex: Female, Male Female | 2 Participants | 3 Participants | 5 Participants |
| Sex: Female, Male Male | 5 Participants | 14 Participants | 19 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk | EG003 affected / at risk |
|---|---|---|---|---|
| deaths Total, all-cause mortality | 0 / 7 | 0 / 17 | 0 / 6 | 0 / 5 |
| other Total, other adverse events | 6 / 7 | 15 / 17 | 1 / 6 | 1 / 5 |
| serious Total, serious adverse events | 0 / 7 | 1 / 17 | 0 / 6 | 0 / 5 |
Outcome results
Part A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score
The TETRAS upper limb score is calculated as the sum of the 6 separate upper-limb maneuvers assessed by the clinician: forward-outstretched postural tremor \[right\], forward outstretched postural tremor \[left\], lateral wing-beating postural tremor \[right\], lateral wing-beating postural tremor \[left\], kinetic tremor \[right\], kinetic tremor \[left\], each on a 0 (no tremor) to 4 (maximum tremor) severity scale in 0.5-point increments. TETRAS Part 4 score for both upper limbs ranged from 0 to 24, higher scores indicated more severe tremor. A negative change from baseline indicated less tremor. Baseline is defined as the last non-missing value collected prior to receiving first dose of study drug. Change from baseline will be defined as assessment value minus baseline value.
Time frame: Baseline (Day 0), Days 7 and 14
Population: Full Analysis Set (FAS): all participants who took at least 1 dose of study drug and had a valid baseline TETRAS assessment and at least 1 valid post-baseline TETRAS assessment. Only those participants with data available at indicated timepoints have been presented.
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Part A: PRAX-944 20mg to 40mg OLT | Part A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score | Change from baseline to Day 7 | -1.427 Scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score | Change from baseline to Day 14 | -2.912 Scores on a scale |
Part B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation
An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of a study intervention, whether or not considered related to the study intervention. Incidence and Severity of Adverse Events have been reported.
Time frame: Up to Day 70
Population: Safety Analysis Set included all participants who received at least 1 dose of study drug.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Any AE | 15 participants |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Related AE | 12 participants |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Severe AE | 0 participants |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | AE Leading to Treatment Discontinuation | 6 participants |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Mild AE | 13 participants |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Moderate AE | 7 participants |
| Part B: PRAX-944 120mg RWD | Part B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Mild AE | 1 participants |
| Part B: PRAX-944 120mg RWD | Part B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Moderate AE | 1 participants |
| Part B: PRAX-944 120mg RWD | Part B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | AE Leading to Treatment Discontinuation | 0 participants |
| Part B: PRAX-944 120mg RWD | Part B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Any AE | 1 participants |
| Part B: PRAX-944 120mg RWD | Part B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Severe AE | 0 participants |
| Part B: PRAX-944 120mg RWD | Part B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Related AE | 0 participants |
| Part B: Placebo RWD | Part B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Severe AE | 1 participants |
| Part B: Placebo RWD | Part B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Any AE | 1 participants |
| Part B: Placebo RWD | Part B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | AE Leading to Treatment Discontinuation | 0 participants |
| Part B: Placebo RWD | Part B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Mild AE | 1 participants |
| Part B: Placebo RWD | Part B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Moderate AE | 0 participants |
| Part B: Placebo RWD | Part B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Related AE | 1 participants |
Part B: Number of Participants With Clinically Significant Abnormalities in Vital Signs, Laboratory Values and Electrocardiogram Parameters
Vital signs parameters included body temperature, pulse rate, respiratory rate, blood pressure (systolic and diastolic), clinical laboratory measures (chemistry, hematology, urinalysis, and coagulation), electrocardiogram parameters (heart rate, PR, QRS, QT, and corrected QT intervals). Any change in vital sign abnormalities that was clinically significant in the medical and scientific judgment of the investigator and not related to an underlying disease was reported as an unsolicited adverse event (AE). Any clinically significant abnormality associated with underlying disease does not require reporting as an (S)AE unless judged by the investigator to be more severe than expected for the participant's condition.
Time frame: Up to Day 70
Population: Safety Analysis Set
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Number of Participants With Clinically Significant Abnormalities in Vital Signs, Laboratory Values and Electrocardiogram Parameters | 0 participants |
| Part B: PRAX-944 120mg RWD | Part B: Number of Participants With Clinically Significant Abnormalities in Vital Signs, Laboratory Values and Electrocardiogram Parameters | 0 participants |
| Part B: Placebo RWD | Part B: Number of Participants With Clinically Significant Abnormalities in Vital Signs, Laboratory Values and Electrocardiogram Parameters | 0 participants |
Part B: Number of Participants With Suicidal Ideation or Behavior Assessed Using Columbia Suicide Severity Rating Scale (C-SSRS)
The C-SSRS is described as a scale developed at Columbia University that has 2-6 questions each in categories of Suicidal Ideation, Intensity of Ideation, Suicidal Behavior, and Actual Attempts. Four constructs were measured. Severity of Suicidal ideation is rated on a 5-point ordinal scale. Intensity of ideation is comprised of 5 items (frequency, duration, controllability, deterrents, and reason for ideation), each rated on a 5-point ordinal scale. Suicidal behavior is rated on a nominal scale that includes actual, aborted, and interrupted attempts; preparatory behavior; and non-suicidal self-injurious behavior. Lethality, assesses actual attempts; actual lethality is rated on a 6-point ordinal scale, and if actual lethality is 0, potential lethality of attempts is rated on a 3-point ordinal scale.The higher the C-SSRS score, the higher the suicide risk (ie. worse outcome).
Time frame: Up to Day 70
Population: FAS population
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Number of Participants With Suicidal Ideation or Behavior Assessed Using Columbia Suicide Severity Rating Scale (C-SSRS) | 0 Participants |
| Part B: PRAX-944 120mg RWD | Part B: Number of Participants With Suicidal Ideation or Behavior Assessed Using Columbia Suicide Severity Rating Scale (C-SSRS) | 0 Participants |
| Part B: Placebo RWD | Part B: Number of Participants With Suicidal Ideation or Behavior Assessed Using Columbia Suicide Severity Rating Scale (C-SSRS) | 0 Participants |
Part A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Subscale
The TETRAS is an essential tremor and activities of daily living rating scale. The full scale has 2 sections, the Performance subscale (PS) and the ADL subscale. The PS consists of 9 items covering different body regions. These 9 items are rated on a 5-point scale (ranging from 0 to 4). One item, Item 4, consists of ratings for 3 tasks rated separately for upper limbs on both sides of the body for a total of 6 ratings. The total score of the 9 items (14 ratings) ranges from 0 to 70 with higher scores indicating greater tremor severity. The total score and individual item ratings will be evaluated as outcomes in this trial. Baseline is defined as the last non-missing value collected prior to receiving first dose of study drug.
Time frame: Baseline (Day 0), Days 7 and 14
Population: FAS population. Only those participants with data available at indicated timepoints have been presented.
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Part A: PRAX-944 20mg to 40mg OLT | Part A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Subscale | Change from baseline to Day 7 | -1.990 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Subscale | Change from baseline to Day 14 | -5.163 scores on a scale |
Part A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Subscale Individual Items # 6 (Spiral Drawing) and Items #7 (Handwriting)
The TETRAS ADL subscale is a 12-item assessment of typical daily activities that are impacted by tremor. Activities are assessed in the following functional domains: speaking, feeding, drinking, personal hygiene, dressing, writing, and social activity. The impact to each function is rated on a 5-point Likert scale from 0 to 4. The ADL subscale score is calculated as the sum of all 12 items and ranges from 0 to 48 with higher scores reflecting higher impact. Baseline is defined as the last non-missing value collected prior to receiving first dose of study drug. Change from baseline will be defined as assessment value minus baseline value.
Time frame: Baseline (Day 0), Days 7 and 14
Population: FAS population. Only those participants with data available at indicated timepoints have been presented.
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Part A: PRAX-944 20mg to 40mg OLT | Part A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Subscale Individual Items # 6 (Spiral Drawing) and Items #7 (Handwriting) | Item 6 Archimedes Spiral (Right) Change from baseline to Day 7 | -0.091 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Subscale Individual Items # 6 (Spiral Drawing) and Items #7 (Handwriting) | Item 6 Archimedes Spiral (Left) Change from baseline to Day 7 | -0.213 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Subscale Individual Items # 6 (Spiral Drawing) and Items #7 (Handwriting) | Item 7 Handwriting Change from baseline to Day 7 | -0.012 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Subscale Individual Items # 6 (Spiral Drawing) and Items #7 (Handwriting) | Item 7 Handwriting Change from baseline to Day 14 | -0.348 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Subscale Individual Items # 6 (Spiral Drawing) and Items #7 (Handwriting) | Item 6 Archimedes Spiral (Right) Change from baseline to Day 14 | -0.346 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Subscale Individual Items # 6 (Spiral Drawing) and Items #7 (Handwriting) | Item 6 Archimedes Spiral (Left) Change from baseline to Day 14 | -0.468 scores on a scale |
Part A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score Measured by Accelerometry
Accelerometer was used to evaluate record coordinates and accelerations in the 3D space over time. The 3 maneuvers in the upper limb item will be completed for both arms, first for the right arm and then for the left. Each upper limb sub-item is scored on a scale from 0 to 4 including to 0.1 increments. The accelerometer upper limb total score, ranges from 0 to 24. A decrease in score is indicative of improvement. Baseline is defined as the last non-missing value collected prior to receiving first dose of study drug. Change from baseline will be defined as assessment value minus baseline value.
Time frame: Baseline (Day 0), Days 7 and 14
Population: FAS Population. Only those participants with data available at indicated timepoints have been presented.
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Part A: PRAX-944 20mg to 40mg OLT | Part A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score Measured by Accelerometry | Change from baseline to Day 7 | -1.100 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score Measured by Accelerometry | Change from baseline to Day 14 | -1.300 scores on a scale |
Part A: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation
An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of a study intervention, whether or not considered related to the study intervention. Incidence and Severity of Adverse Events have been reported.
Time frame: Up to Day 21
Population: Safety Analysis Set
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Part A: PRAX-944 20mg to 40mg OLT | Part A: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Any AE | 6 participants |
| Part A: PRAX-944 20mg to 40mg OLT | Part A: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Related AE | 4 participants |
| Part A: PRAX-944 20mg to 40mg OLT | Part A: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | AE Leading to Treatment Discontinuation | 1 participants |
| Part A: PRAX-944 20mg to 40mg OLT | Part A: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Mild AE | 6 participants |
| Part A: PRAX-944 20mg to 40mg OLT | Part A: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Moderate AE | 1 participants |
| Part A: PRAX-944 20mg to 40mg OLT | Part A: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment Discontinuation | Severe AE | 0 participants |
Part A: Number of Participants With Clinically Significant Abnormalities in Vital Signs, Laboratory Values and Electrocardiogram Parameters
Vital signs parameters included body temperature, pulse rate, respiratory rate, blood pressure (systolic and diastolic), clinical laboratory measures (chemistry, hematology, urinalysis, and coagulation), electrocardiogram parameters (heart rate, PR, QRS, QT, and corrected QT intervals). Any change in vital sign abnormalities that was clinically significant in the medical and scientific judgment of the investigator and not related to an underlying disease was reported as an unsolicited adverse event (AE). Any clinically significant abnormality associated with underlying disease does not require reporting as an (S)AE unless judged by the investigator to be more severe than expected for the participant's condition.
Time frame: Up to Day 21
Population: Safety Analysis Set
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Part A: PRAX-944 20mg to 40mg OLT | Part A: Number of Participants With Clinically Significant Abnormalities in Vital Signs, Laboratory Values and Electrocardiogram Parameters | 0 Participants |
Part A: Number of Participants With Suicidal Ideation or Behavior Assessed Using Columbia Suicide Severity Rating Scale (C-SSRS)
The C-SSRS is described as a scale developed at Columbia University that has 2-6 questions each in categories of Suicidal Ideation, Intensity of Ideation, Suicidal Behavior, and Actual Attempts. Four constructs were measured. Severity of Suicidal ideation is rated on a 5-point ordinal scale. Intensity of ideation is comprised of 5 items (frequency, duration, controllability, deterrents, and reason for ideation), each rated on a 5-point ordinal scale. Suicidal behavior is rated on a nominal scale that includes actual, aborted, and interrupted attempts; preparatory behavior; and non-suicidal self-injurious behavior. Lethality, assesses actual attempts; actual lethality is rated on a 6-point ordinal scale, and if actual lethality is 0, potential lethality of attempts is rated on a 3-point ordinal scale.The higher the C-SSRS score, the higher the suicide risk (ie. worse outcome).
Time frame: Up to Day 21
Population: Safety Analysis Set
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Part A: PRAX-944 20mg to 40mg OLT | Part A: Number of Participants With Suicidal Ideation or Behavior Assessed Using Columbia Suicide Severity Rating Scale (C-SSRS) | 0 Participants |
Part B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Subscale During OLT Phase
TETRAS Performance Subscale was used to assess essential tremor as scored by the independent video raters. The performance subscale consists of 9 items, i.e. item 1 (head), item 2 (face), item 3 (voice), each of the 6 sub-items for item 4 (upper limb), the maximum of the 4 sub-items for item 5 (lower limb), 2 sub-items (right and left side) for item 6 (Archimedes spirals), item 7 (handwriting), 2 sub-items (right and left side) for item 8 (dot approximation), and item 9 (standing) for a total score ranging from 0 to 64 from 16 sub-items. Each item is rated on a scale of 0 to 4, including 0.5 increments. A lower score is indicative of improvement. The total score has been presented. Baseline is defined as the last non-missing value collected prior to receiving first dose of study drug. Change from baseline will be defined as assessment value minus baseline value.
Time frame: Baseline (Day 0) and Days 7, 21 and 42
Population: FAS population. Only those participants with data available at indicated timepoints have been presented.
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Subscale During OLT Phase | Change from baseline to Day 7 | -1.253 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Subscale During OLT Phase | Change from baseline to Day 21 | -1.449 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Subscale During OLT Phase | Change from baseline to Day 42 | -2.771 scores on a scale |
Part B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score During OLT Phase
The TETRAS upper limb score is calculated as the sum of the 6 separate upper-limb maneuvers assessed by the clinician: forward-outstretched postural tremor \[right\], forward outstretched postural tremor \[left\], lateral wing-beating postural tremor \[right\], lateral wing-beating postural tremor \[left\], kinetic tremor \[right\], kinetic tremor \[left\], each on a 0 (no tremor) to 4 (maximum tremor) severity scale in 0.5-point increments. TETRAS Part 4 score for both upper limbs ranged from 0 to 24, higher scores indicated more severe tremor. A negative change from baseline indicated less tremor. Baseline is defined as the last non-missing value collected prior to receiving first dose of study drug. Change from baseline will be defined as assessment value minus baseline value.
Time frame: Baseline (Day 0) and Day 42
Population: FAS Population. Only those participants with data available at indicated timepoints have been presented.
| Arm | Measure | Value (LEAST_SQUARES_MEAN) |
|---|---|---|
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score During OLT Phase | -2.090 scores on a scale |
Part B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score During OLT Phase
The TETRAS upper limb score is calculated as the sum of the 6 separate upper-limb maneuvers assessed by the clinician: forward-outstretched postural tremor \[right\], forward outstretched postural tremor \[left\], lateral wing-beating postural tremor \[right\], lateral wing-beating postural tremor \[left\], kinetic tremor \[right\], kinetic tremor \[left\], each on a 0 (no tremor) to 4 (maximum tremor) severity scale in 0.5-point increments. TETRAS Part 4 score for both upper limbs ranged from 0 to 24, higher scores indicated more severe tremor. A negative change from baseline indicated less tremor. Baseline is defined as the last non-missing value collected prior to receiving first dose of study drug. Change from baseline will be defined as assessment value minus baseline value.
Time frame: Baseline (Day 0), Days 7 and 21
Population: FAS. Only those participants with data available at indicated timepoints have been presented.
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score During OLT Phase | Change from baseline to Day 7 | -0.967 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score During OLT Phase | Change from baseline to Day 21 | -1.143 scores on a scale |
Part B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score Measured by Accelerometry During OLT Phase
Accelerometer was used to evaluate record coordinates and accelerations in the 3D space over time. The 3 maneuvers in the upper limb item will be completed for both arms, first for the right arm and then for the left. Each upper limb sub-item is scored on a scale from 0 to 4 including to 0.1 increments. The accelerometer upper limb total score, ranges from 0 to 24. A decrease in score is indicative of improvement. Baseline is defined as the last non-missing value collected prior to receiving first dose of study drug. Change from baseline will be defined as assessment value minus baseline value.
Time frame: Baseline (Day 0), and Days 7, 21 and 42
Population: FAS population. Only those participants with data available at indicated timepoints have been presented.
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score Measured by Accelerometry During OLT Phase | Change from baseline to Day 7 | -1.235 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score Measured by Accelerometry During OLT Phase | Change from baseline to Day 21 | -1.835 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score Measured by Accelerometry During OLT Phase | Change from baseline to Day 42 | -1.766 scores on a scale |
Part B: Change From Baseline in Quality of Life in Essential Tremor Questionnaire (QUEST) Total Scores.
Quality of Life in Essential Tremor Questionnaire (QUEST) is a patient-reported ET-specific 30-item, specific quality of life scale. Items contribute to five dimensions. Physical/ADL (9 items ), Psychosocial (9 items), Communication (3 items), Hobbies/Leisure (3 items), and Work/Finances (6 items). The QUEST total and subscale scores are calculated as the sum of all applicable items divided by the number of applicable items times 100. Higher score indicates greater dissatisfaction with that domain of QOL. Maximal score 100: worse quality of life. Minimal Score 0: best quality of life. Baseline is defined as the last non-missing value collected prior to receiving first dose of study drug. Change from baseline will be defined as assessment value minus baseline value.
Time frame: Baseline (Day 0), Days 7, 21 and 42
Population: FAS population. Only those participants with data available at indicated timepoints have been presented.
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in Quality of Life in Essential Tremor Questionnaire (QUEST) Total Scores. | Change from baseline to Day 7 | -0.561 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in Quality of Life in Essential Tremor Questionnaire (QUEST) Total Scores. | Change from baseline to Day 21 | -5.933 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in Quality of Life in Essential Tremor Questionnaire (QUEST) Total Scores. | Change from baseline to Day 42 | -8.203 scores on a scale |
Part B: Change From Baseline in TETRAS Activities of Daily Living (ADL) Score
The TETRAS ADL subscale is a 12-item assessment of typical daily activities that are impacted by tremor. Activities are assessed in the following functional domains: speaking, feeding, drinking, personal hygiene, dressing, writing, and social activity. The impact to each function is rated on a 5-point Likert scale from 0 to 4. The ADL subscale score is calculated as the sum of all 12 items and ranges from 0 to 48 with higher scores reflecting higher impact. Baseline is defined as the last non-missing value collected prior to receiving first dose of study drug. Change from baseline will be defined as assessment value minus baseline value.
Time frame: Baseline (Day 0), Days 7, 21 and 42
Population: FAS population. Only those participants with data available at indicated timepoints have been presented.
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in TETRAS Activities of Daily Living (ADL) Score | Change from baseline to Day 7 | -1.986 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in TETRAS Activities of Daily Living (ADL) Score | Change from baseline to Day 21 | -3.475 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in TETRAS Activities of Daily Living (ADL) Score | Change from baseline to Day 42 | -8.207 scores on a scale |
Part B: Change From Baseline in TETRAS Performance Subscale Individual Items # 6 (Spiral Drawing) and Items #7 (Handwriting)
TETRAS Performance Subscale was used to assess essential tremor as scored by the independent video raters. The performance subscale consists of 9 items, i.e. item 1 (head), item 2 (face), item 3 (voice), each of the 6 sub-items for item 4 (upper limb), the maximum of the 4 sub-items for item 5 (lower limb), 2 sub-items (right and left side) for item 6 (Archimedes spirals), item 7 (handwriting), 2 sub-items (right and left side) for item 8 (dot approximation), and item 9 (standing) for a total score ranging from 0 to 64 from 16 sub-items. Each item is rated on a scale of 0 to 4, including 0.5 increments. A lower score is indicative of improvement. Baseline is defined as the last non-missing value collected prior to receiving first dose of study drug. Change from baseline will be defined as assessment value minus baseline value.
Time frame: Baseline (Day 0), Days 7, 21 and 42
Population: FAS Population. Only those participants with data available at indicated timepoints have been presented.
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in TETRAS Performance Subscale Individual Items # 6 (Spiral Drawing) and Items #7 (Handwriting) | Item#6 Archimedes spirals (right) Change from baseline to Day 7 | 0.006 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in TETRAS Performance Subscale Individual Items # 6 (Spiral Drawing) and Items #7 (Handwriting) | Item#6 Archimedes spirals (left) Change from baseline to Day 7 | 0.221 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in TETRAS Performance Subscale Individual Items # 6 (Spiral Drawing) and Items #7 (Handwriting) | Item#7 Handwriting Change from baseline to Day 7 | -0.019 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in TETRAS Performance Subscale Individual Items # 6 (Spiral Drawing) and Items #7 (Handwriting) | Item#6 Archimedes spirals (right) Change from baseline to Day 21 | -0.240 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in TETRAS Performance Subscale Individual Items # 6 (Spiral Drawing) and Items #7 (Handwriting) | Item#6 Archimedes spirals (left) Change from baseline to Day 21 | -0.012 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in TETRAS Performance Subscale Individual Items # 6 (Spiral Drawing) and Items #7 (Handwriting) | Item#7 Handwriting Change from baseline to Day 21 | 0.107 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in TETRAS Performance Subscale Individual Items # 6 (Spiral Drawing) and Items #7 (Handwriting) | Item#6 Archimedes spirals (right) Change from baseline to Day 42 | -0.239 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in TETRAS Performance Subscale Individual Items # 6 (Spiral Drawing) and Items #7 (Handwriting) | Item#6 Archimedes spirals (left) Change from baseline to Day 42 | -0.072 scores on a scale |
| Part A: PRAX-944 20mg to 40mg OLT | Part B: Change From Baseline in TETRAS Performance Subscale Individual Items # 6 (Spiral Drawing) and Items #7 (Handwriting) | Item#7 Handwriting Change from baseline to Day 42 | -0.054 scores on a scale |