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A Clinical Trial of PRAX-944 in Participants With Essential Tremor

A Phase 2 Clinical Trial Evaluating the Efficacy, Safety, Tolerability, and Pharmacokinetics of PRAX-944 in Adults With Essential Tremor

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05021978
Enrollment
24
Registered
2021-08-26
Start date
2020-03-03
Completion date
2022-03-24
Last updated
2024-03-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Essential Tremor

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

DRUGPart A: 20 and 40 mg PRAX-944

Once daily oral treatment

DRUGPart B: 120 mg PRAX-944

Once daily oral treatment with titration

DRUGPart B: 120 mg PRAX-944 and Placebo

Once daily oral treatment with titration followed by placebo

Sponsors

Praxis Precision Medicines
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

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

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

MeasureTime frameDescription
Part A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb ScoreBaseline (Day 0), Days 7 and 14The 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 DiscontinuationUp to Day 70An 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 ParametersUp to Day 70Vital 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 70The 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

MeasureTime frameDescription
Part A: Number of Participants With Clinically Significant Abnormalities in Vital Signs, Laboratory Values and Electrocardiogram ParametersUp to Day 21Vital 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 21The 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 PhaseBaseline (Day 0) and Day 42The 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 PhaseBaseline (Day 0) and Days 7, 21 and 42TETRAS 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 SubscaleBaseline (Day 0), Days 7 and 14The 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 42TETRAS 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) ScoreBaseline (Day 0), Days 7, 21 and 42The 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 42Quality 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 PhaseBaseline (Day 0), and Days 7, 21 and 42Accelerometer 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 AccelerometryBaseline (Day 0), Days 7 and 14Accelerometer 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 14The 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 DiscontinuationUp to Day 21An 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

ArmCount
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
Total24

Withdrawals & dropouts

PeriodReasonFG000FG001FG002FG003
PART A OLT Phase (Day 1 to Day 21)Adverse Event1000
PART B OLT Phase (Day 1 to Day 42)Adverse Event0600

Baseline characteristics

CharacteristicPart A: PRAX-944 20mg to 40mg OLTPart B: PRAX-944 20mg to 120mg OLTTotal
Age, Continuous67.7 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 Participants0 Participants0 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
7 Participants17 Participants24 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race/Ethnicity, Customized
Aborigines
1 Participants1 Participants2 Participants
Race/Ethnicity, Customized
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race/Ethnicity, Customized
Asian
0 Participants0 Participants0 Participants
Race/Ethnicity, Customized
Black or African American
0 Participants0 Participants0 Participants
Race/Ethnicity, Customized
More than one race
0 Participants0 Participants0 Participants
Race/Ethnicity, Customized
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race/Ethnicity, Customized
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race/Ethnicity, Customized
White
6 Participants16 Participants22 Participants
Sex: Female, Male
Female
2 Participants3 Participants5 Participants
Sex: Female, Male
Male
5 Participants14 Participants19 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
EG003
affected / at risk
deaths
Total, all-cause mortality
0 / 70 / 170 / 60 / 5
other
Total, other adverse events
6 / 715 / 171 / 61 / 5
serious
Total, serious adverse events
0 / 71 / 170 / 60 / 5

Outcome results

Primary

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.

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Part A: PRAX-944 20mg to 40mg OLTPart A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb ScoreChange from baseline to Day 7-1.427 Scores on a scale
Part A: PRAX-944 20mg to 40mg OLTPart A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb ScoreChange from baseline to Day 14-2.912 Scores on a scale
Comparison: Sample size is a convenience sample determined according to feasibility to provide sufficient and safety data to inform the development of future controlled studies with PRAX-944. In the open-label phase of the trial (Part A ), at least 10 participants would provide an 80% probability of observing at least 1 AE with an underlying incidence of 15% or greater and provide approximately 80% power to detect an effect size of 1.0 on the primary endpoint change from baseline in TETRAS Upper Limb score.p-value: 0.1048Mixed Models Analysis
p-value: 0.0028Mixed Models Analysis
Primary

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.

ArmMeasureGroupValue (NUMBER)
Part A: PRAX-944 20mg to 40mg OLTPart B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationAny AE15 participants
Part A: PRAX-944 20mg to 40mg OLTPart B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationRelated AE12 participants
Part A: PRAX-944 20mg to 40mg OLTPart B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationSevere AE0 participants
Part A: PRAX-944 20mg to 40mg OLTPart B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationAE Leading to Treatment Discontinuation6 participants
Part A: PRAX-944 20mg to 40mg OLTPart B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationMild AE13 participants
Part A: PRAX-944 20mg to 40mg OLTPart B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationModerate AE7 participants
Part B: PRAX-944 120mg RWDPart B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationMild AE1 participants
Part B: PRAX-944 120mg RWDPart B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationModerate AE1 participants
Part B: PRAX-944 120mg RWDPart B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationAE Leading to Treatment Discontinuation0 participants
Part B: PRAX-944 120mg RWDPart B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationAny AE1 participants
Part B: PRAX-944 120mg RWDPart B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationSevere AE0 participants
Part B: PRAX-944 120mg RWDPart B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationRelated AE0 participants
Part B: Placebo RWDPart B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationSevere AE1 participants
Part B: Placebo RWDPart B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationAny AE1 participants
Part B: Placebo RWDPart B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationAE Leading to Treatment Discontinuation0 participants
Part B: Placebo RWDPart B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationMild AE1 participants
Part B: Placebo RWDPart B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationModerate AE0 participants
Part B: Placebo RWDPart B: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationRelated AE1 participants
Primary

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

ArmMeasureValue (NUMBER)
Part A: PRAX-944 20mg to 40mg OLTPart B: Number of Participants With Clinically Significant Abnormalities in Vital Signs, Laboratory Values and Electrocardiogram Parameters0 participants
Part B: PRAX-944 120mg RWDPart B: Number of Participants With Clinically Significant Abnormalities in Vital Signs, Laboratory Values and Electrocardiogram Parameters0 participants
Part B: Placebo RWDPart B: Number of Participants With Clinically Significant Abnormalities in Vital Signs, Laboratory Values and Electrocardiogram Parameters0 participants
Primary

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

ArmMeasureValue (NUMBER)
Part A: PRAX-944 20mg to 40mg OLTPart 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 RWDPart B: Number of Participants With Suicidal Ideation or Behavior Assessed Using Columbia Suicide Severity Rating Scale (C-SSRS)0 Participants
Part B: Placebo RWDPart B: Number of Participants With Suicidal Ideation or Behavior Assessed Using Columbia Suicide Severity Rating Scale (C-SSRS)0 Participants
Secondary

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.

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Part A: PRAX-944 20mg to 40mg OLTPart A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance SubscaleChange from baseline to Day 7-1.990 scores on a scale
Part A: PRAX-944 20mg to 40mg OLTPart A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance SubscaleChange from baseline to Day 14-5.163 scores on a scale
p-value: 0.4025Mixed Models Analysis
p-value: 0.0766Mixed Models Analysis
Secondary

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.

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Part A: PRAX-944 20mg to 40mg OLTPart 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 OLTPart 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 OLTPart 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 OLTPart 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 OLTPart 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 OLTPart 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
p-value: 0.4722Mixed Models Analysis
p-value: 0.6215Mixed Models Analysis
p-value: 0.9648Mixed Models Analysis
p-value: 0.2855Mixed Models Analysis
p-value: 0.205Mixed Models Analysis
p-value: 0.2364Mixed Models Analysis
Secondary

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.

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Part A: PRAX-944 20mg to 40mg OLTPart A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score Measured by AccelerometryChange from baseline to Day 7-1.100 scores on a scale
Part A: PRAX-944 20mg to 40mg OLTPart A: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score Measured by AccelerometryChange from baseline to Day 14-1.300 scores on a scale
p-value: 0.2501Mixed Models Analysis
p-value: 0.1874Mixed Models Analysis
Secondary

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

ArmMeasureGroupValue (NUMBER)
Part A: PRAX-944 20mg to 40mg OLTPart A: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationAny AE6 participants
Part A: PRAX-944 20mg to 40mg OLTPart A: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationRelated AE4 participants
Part A: PRAX-944 20mg to 40mg OLTPart A: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationAE Leading to Treatment Discontinuation1 participants
Part A: PRAX-944 20mg to 40mg OLTPart A: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationMild AE6 participants
Part A: PRAX-944 20mg to 40mg OLTPart A: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationModerate AE1 participants
Part A: PRAX-944 20mg to 40mg OLTPart A: Number of Participants With Adverse Events (AE), Related AE, and AE Leading to Treatment DiscontinuationSevere AE0 participants
Secondary

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

ArmMeasureValue (NUMBER)
Part A: PRAX-944 20mg to 40mg OLTPart A: Number of Participants With Clinically Significant Abnormalities in Vital Signs, Laboratory Values and Electrocardiogram Parameters0 Participants
Secondary

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

ArmMeasureValue (NUMBER)
Part A: PRAX-944 20mg to 40mg OLTPart A: Number of Participants With Suicidal Ideation or Behavior Assessed Using Columbia Suicide Severity Rating Scale (C-SSRS)0 Participants
Secondary

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.

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Part A: PRAX-944 20mg to 40mg OLTPart B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Subscale During OLT PhaseChange from baseline to Day 7-1.253 scores on a scale
Part A: PRAX-944 20mg to 40mg OLTPart B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Subscale During OLT PhaseChange from baseline to Day 21-1.449 scores on a scale
Part A: PRAX-944 20mg to 40mg OLTPart B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Subscale During OLT PhaseChange from baseline to Day 42-2.771 scores on a scale
p-value: 0.2971Mixed Models Analysis
p-value: 0.2034Mixed Models Analysis
p-value: 0.1105Mixed Models Analysis
Secondary

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.

ArmMeasureValue (LEAST_SQUARES_MEAN)
Part A: PRAX-944 20mg to 40mg OLTPart B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score During OLT Phase-2.090 scores on a scale
p-value: 0.0216Mixed Models Analysis
Secondary

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.

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Part A: PRAX-944 20mg to 40mg OLTPart B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score During OLT PhaseChange from baseline to Day 7-0.967 scores on a scale
Part A: PRAX-944 20mg to 40mg OLTPart B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score During OLT PhaseChange from baseline to Day 21-1.143 scores on a scale
p-value: 0.1042Mixed Models Analysis
p-value: 0.0257Mixed Models Analysis
Secondary

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.

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Part A: PRAX-944 20mg to 40mg OLTPart B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score Measured by Accelerometry During OLT PhaseChange from baseline to Day 7-1.235 scores on a scale
Part A: PRAX-944 20mg to 40mg OLTPart B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score Measured by Accelerometry During OLT PhaseChange from baseline to Day 21-1.835 scores on a scale
Part A: PRAX-944 20mg to 40mg OLTPart B: Change From Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Upper Limb Score Measured by Accelerometry During OLT PhaseChange from baseline to Day 42-1.766 scores on a scale
p-value: 0.005Mixed Models Analysis
p-value: 0.0018Mixed Models Analysis
p-value: 0.0061Mixed Models Analysis
Secondary

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.

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Part A: PRAX-944 20mg to 40mg OLTPart 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 OLTPart 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 OLTPart 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
p-value: 0.8638Mixed Models Analysis
p-value: 0.0605Mixed Models Analysis
p-value: 0.0871Mixed Models Analysis
Secondary

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.

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Part A: PRAX-944 20mg to 40mg OLTPart B: Change From Baseline in TETRAS Activities of Daily Living (ADL) ScoreChange from baseline to Day 7-1.986 scores on a scale
Part A: PRAX-944 20mg to 40mg OLTPart B: Change From Baseline in TETRAS Activities of Daily Living (ADL) ScoreChange from baseline to Day 21-3.475 scores on a scale
Part A: PRAX-944 20mg to 40mg OLTPart B: Change From Baseline in TETRAS Activities of Daily Living (ADL) ScoreChange from baseline to Day 42-8.207 scores on a scale
p-value: 0.1505Mixed Models Analysis
p-value: 0.0543Mixed Models Analysis
p-value: 0.0015Mixed Models Analysis
Secondary

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.

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Part A: PRAX-944 20mg to 40mg OLTPart 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 70.006 scores on a scale
Part A: PRAX-944 20mg to 40mg OLTPart 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 70.221 scores on a scale
Part A: PRAX-944 20mg to 40mg OLTPart 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 OLTPart 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 OLTPart 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 OLTPart 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 210.107 scores on a scale
Part A: PRAX-944 20mg to 40mg OLTPart 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 OLTPart 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 OLTPart 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
p-value: 0.9776Mixed Models Analysis
p-value: 0.1962Mixed Models Analysis
p-value: 0.9419Mixed Models Analysis
p-value: 0.0668Mixed Models Analysis
p-value: 0.9191Mixed Models Analysis
p-value: 0.6075Mixed Models Analysis
p-value: 0.246Mixed Models Analysis
p-value: 0.6736Mixed Models Analysis
p-value: 0.8511Mixed Models Analysis

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026