Study to Assess the Effects of PTC857 Treatment in Participants With Amyotrophic Lateral Sclerosis ALS

Phase
Recruitment status
Participants
Lead sponsor
PTC Therapeutics
Start date
Number of sites

Summary
This study will assess the efficacy and safety of PTC857 treatment in participants diagnosed with ALS.
Acronym
Short title
Study to Assess the Effects of PTC857 Treatment in Participants With Amyotrophic Lateral Sclerosis ALS
Official title
A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Parallel Study to Assess the Efficacy, Safety, Tolerability, PK, and Biomarker Effects of PTC857 in Adult Subjects With Amyotrophic Lateral Sclerosis (CARDINALS)

Control arm
Active comparator
Registry reports results
Listing at source
Recruitment status
Phase
Study type
Interventional
Reason stopped
Company decision

Completion date
First posted
Registry last updated
Primary completion date
Start date

Actual participants
Participants
Participant count basis
Protocol amendments
Number of sites

Data monitoring committee
Registry sponsor category
Lead sponsor
PTC Therapeutics
Source registry
ClinicalTrials.gov

Registry ID
ClinicalTrials.gov ID
Registry record
Open registry record

Allocation
Randomised
Model
Parallel groups
Purpose
Treatment
Masking
Quadruple masking
Masked roles
Participants, Care providers, Investigators, Outcome assessors
Sources for study design

  1. Combined Assessment of Function (ALS Functional Rating Scale-Revised [ALSFRS-R]) and Survival (CAFS) Rank After 24 Weeks of Treatment (Intention-to-Treat [ITT] 1 Analysis Population)

    Timeframe: Week 24

    The CAFS is a composite endpoint based on time to earlier occurrence of death and change from baseline in ALSFRS-R score. ALSFRS-R is a rating scale where 12 functions were rated on 5-point scales (from 0 to 4) with a maximum score of 48 (sum of all 12 items), with a higher score indicating better function. Each participant's outcome was compared to every other participant's outcome in a pairwise fashion by time to death and change on ALSFRS-R, assigned a score which was sum of comparisons (+1 \[better\], 0 \[tie\], -1 \[worse\]), and summed scores were ranked, from 1 to 306 (ITT1 Analysis Set) lowest rank corresponds to participant who died first and highest rank to the participant with best ALSFRS-R outcome among those who survived. Multiple imputation was used to impute participants with missing ALSFRS-R score at Week 24. A higher rank was considered a better outcome. Least square (LS) means and standard error (SE) were calculated using analysis of covariance (ANCOVA) model.

  1. Combined Assessment of Function (ALSFRS-R) and Survival (CAFS) Rank After 24 Weeks of Treatment (ITT2 Analysis Population)

    Timeframe: Week 24

    The CAFS is a composite endpoint based on time to earlier occurrence of death and change from baseline in ALSFRS-R score. ALSFRS-R is a rating scale where 12 functions were rated on 5-point scales (from 0 to 4) with a maximum score of 48 (sum of all 12 items), with a higher score indicating better function. Each participant's outcome was compared to every other participant's outcome in a pairwise fashion by time to death and change on ALSFRS-R, assigned a score which was sum of comparisons (+1 \[better\], 0 \[tie\], -1 \[worse\]), and summed scores were ranked, from 1 to 334 (ITT2 Analysis Set) lowest rank corresponds to participant who died first and highest rank to the participant with best ALSFRS-R outcome among those who survived. A higher rank was considered a better outcome. LS mean and SE were calculated using ANCOVA model.

  2. Change From Baseline in ALSFRS-R Score at Week 24 (ITT1 Analysis Population)

    Timeframe: Baseline, Week 24

    The ALSFRS-R is a quickly administered (5-minute) ordinal rating scale that assesses the participant's capability and independence in 12 functional activities across 4 subdomains of bodily function (bulbar, gross motor, fine motor, and respiratory) relevant in ALS. Each activity was recorded to the closest approximation from a list of 5 choices, scored 0 (total loss of function) to 4 (no loss of function), with the total score ranging from 0 to 48 and higher scores indicating less functional impairment. LS mean and SE were calculated using mixed model repeated measures (MMRM).

  3. Change From Baseline in ALSFRS-R Score at Week 24 (ITT2 Analysis Population)

    Timeframe: Baseline, Week 24

    The ALSFRS-R is a quickly administered (5-minute) ordinal rating scale that assesses the participant's capability and independence in 12 functional activities across 4 subdomains of bodily function (bulbar, gross motor, fine motor, and respiratory) relevant in ALS. Each activity was recorded to the closest approximation from a list of 5 choices, scored 0 (total loss of function) to 4 (no loss of function), with the total score ranging from 0 to 48 and higher scores indicating less functional impairment. LS mean and SE were calculated using MMRM.

  4. Number of Participants With Treatment-emergent Adverse Events (TEAEs)

    Timeframe: Day 1 through Week 24

    An adverse event (AE) was any untoward medical occurrence in a participant who received study drug without regard to possibility of causal relationship. Serious adverse event (SAE) was an AE resulting in any of the following outcomes or deemed significant for any other reason: death; initial or prolonged inpatient hospitalization; life-threatening experience (immediate risk of dying); persistent or significant disability/incapacity; congenital anomaly. AEs included both SAEs and non-serious AEs. A TEAE was defined as an AE that began after the first administration of study drug or any existing AEs that worsened after the first dose of study drug. A summary of other non-serious AEs and all SAEs, regardless of causality is located in the 'Reported AE section'.

  5. Change From Baseline in Percent Predicted Slow Vital Capacity (SVC) at Week 24

    Timeframe: Baseline, Week 24

    The SVC is a measure of breathing function. SVC measures the volume that can be exhaled from a full inhalation after exhaling to a maximum as slowly as possible. The percent of predicted SVC is reported. LS mean and SE were calculated using MMRM.

  6. Change From Baseline in Modified Norris Scale Total Score at Week 24

    Timeframe: Baseline, Week 24

    Modified Norris scale is used to assess the motor/limb and bulbar function. The Modified Norris Scale is a rating scale for ALS that consists of 2 parts: the Limb Norris Scale and the Norris Bulbar Scale. The Limb Norris Scale has 21 items to evaluate extremity function, and the Norris Bulbar Scale has 13 items to evaluate bulbar function. Each item was rated in 4 ordinal categories, corresponding to the following values and ratings or functional scores: normal (3 points), somewhat impaired (2 points), inadequate (1 point), and "cannot do at all" (0 points). The total score was calculated by summing all the scales, ranging from 0 (worst) to 102 (best) where higher scores indicated better functional abilities. LS mean and SE were calculated using MMRM.

  7. Overall Survival Rate

    Timeframe: Baseline to Week 24

    Overall survival rate was defined as percentage of participants who were alive at given timepoint. Overall survival was defined as the time in months from the date of first dose to the date of death from any cause or date last known alive for those who did not die.

  8. Overall Survival

    Timeframe: Baseline to Week 24

    Overall survival was defined as the time in months from the date of first dose to the date of death from any cause or date last known alive for those who did not die.

  9. Change From Baseline in ALS Assessment Questionnaire (ALSAQ-40) Total Score at Week 24

    Timeframe: Baseline, Week 24

    The ALSAQ-40 is a disease-specific measure of health-related quality of life (QOL) for ALS. The ALSAQ-40 is comprised of 40 questions measuring 5 discrete dimensions of health status that are affected by the disease: physical mobility (10 items); activities of daily living and independence (10 items); eating and drinking (3 items); communication (7 items); emotional reactions (10 items). Participants were asked to indicate the frequency of each event by selecting one of 5 options (Likert scale: 0-4): never/rarely/sometimes/often/ always or cannot do at all. The total score ranging from 0 (no impairment) to 160 (severe impairment) was calculated by adding the 5 domain scores. A lower score indicates a better health state. LS mean and SE were calculated using MMRM.

  10. Change From Baseline in Neurofilament Light Chain (NfL) Activity at Week 24

    Timeframe: Baseline, Week 24

    The NfL is a marker of axonal degeneration and is robustly elevated in the blood of many neurological and neurodegenerative conditions.

  11. Area Under the Concentration-time Curve From 0 to Measurable Timepoint (AUC0-t) of Utreloxastat in Plasma

    Timeframe: Day 1 and Day 29

  12. Maximum Observed Concentration (Cmax) of Utreloxastat in Plasma

    Timeframe: Day 1 and Day 29

  13. Mean Concentration of Utreloxastat in Cerebrospinal Fluid (CSF)

    Timeframe: Day 1 and Day 29

Sources for outcomes

Sex
All
Age groups
Adults, Older adults
Minimum age
18 Years
Maximum age
80 Years
Healthy volunteers
No

Key Inclusion Criteria:

  • ALS with preserved function, defined as:

    1. Onset of the first symptom leading to the diagnosis of ALS ≤24 months at the time of the initial Screening Visit
    2. Revised EL Escorial criteria of either:

    (i) Clinically definite ALS (ii) Clinically probable ALS

  • A total ALSFRS-R score of at least 34 at the start of the Screening Period

  • No significant respiratory compromise as evidenced by slow vital capacity ≥60% at the start of the Screening Period

  • All chronic concomitant medications (both prescription and over the counter), and non-pharmacologic therapy regimens, excluding standard-of-care therapy riluzole, edaravone, or sodium phenylbutyrate/taurursodiol, should be stable and unchanged from 14 days prior to the start of the Screening Period and intend to remain stable and unchanged throughout the course of the study

  • Female participants must have a negative breast cancer imaging screening status (not considered clinically abnormal and/or requiring further evaluation/treatment) within 6 months prior to the Screening Visit, or during the Screening Period.

  • Standard-of-care therapy for the treatment of ALS (riluzole, edaravone, or sodium phenylbutyrate/taurursodiol) should be stable and unchanged from 30 (-3) days prior to the start of the Screening Period and intend to remain stable and unchanged throughout the course of the study.

Key Exclusion Criteria:

  • Females who are pregnant or nursing or plan to become pregnant during the study
  • Participants with clinically significant gastrointestinal, renal, hepatic, neurologic, hematologic, endocrine, oncologic, pulmonary, immunologic, psychiatric, or cardiovascular/ischemic disease or any other condition that, in the opinion of the investigator would jeopardize the safety of the participant or impact the validity of the study results
  • Any clinically significant medical or psychiatric condition or medical history that, in the opinion of the investigator or the medical monitor, would interfere with the participant's ability to participate in the study or increase the risk of participation for that participant
  • Current participation in any other investigational study with an investigational product or participation within 30 days prior to the start of the Screening Period or 5 half-lives of the previously taken investigational drug, whichever is longer
  • Participant has previously received PTC857
  • Participant is receiving a combination of edaravone and sodium phenylbutyrate/taurursodiol treatment, where applicable, within 30 days prior to the start of the Screening Period
  • For female participants, any past medical history of breast cancer, regardless of remission status, or any first degree relative with history of breast cancer
Sources for eligibility

  • UC Irvine Health ALS and Neuromuscular CenterOrange, United States
  • Forbes Norris MDA/ALS Research Center at California Pacific Medical CenterSan Francisco, United States
  • Holy Cross Hospital, Phil Smith Neuroscience InstituteFort Lauderdale, United States
  • University of South Florida - Carol and Frank Morsani Center for Advanced HealthcareTampa, United States
  • Augusta UniversityAugusta, United States
  • University of Kansas Medical Center (KUMC) - Landon Center on AgingKansas City, United States
  • Henry Ford Health System Department of NeurologyDetroit, United States
  • Neurology Associates, P.C. / Somnos Clinical ResearchLincoln, United States
  • University of Nebraska Medical CenterOmaha, United States
  • Providence Brain and Spine InstitutePortland, United States
  • Lewis Katz School of Medicine at Temple UniverstiyPhiladelphia, United States
  • National Neuromuscular Research InstituteAustin, United States
  • Nerve and Muscle Center of TexasHouston, United States
  • Medical College of WisconsinMilwaukee, United States
  • STAT Research S.A.Ciudad Autónoma de Buenos Aires, Argentina
  • Iadin Srl.Buenos Aires, Argentina
  • Hospital Ramos MejíaBuenos Aires, Argentina
  • Royal Brisbane and Women's HospitalBrisbane, Australia
  • Gold Coast HospitalSouthport, Australia
  • Calvary Health Care BethlehemCaulfield South, Australia
  • Austin HealthHeidelberg, Australia
  • AZ Sint-Lucas GentGhent, Belgium
  • UZ LeuvenLeuven, Belgium
  • University hospital Brno, Department of NeurologyBrno, Czechia
  • FORBELI s.r.o.Prague, Czechia

And 30 more, listed on the interactive page.

Sources for sites

  • 2023
  • 2023-510317-26-00
  • 2021-006511-29
Sources for references

Related records

Drugs (1)

Lead sponsors (1)

Conditions (1)