Skip to main content
OpenTrials
Completed

NCT Number: NCT04547361

A Study to Assess the Safety and Tolerability of E2511 in Healthy Participants

The primary objective of this study is to evaluate the safety, tolerability, and pharmacokinetic (PK) of E2511 following single ascending oral doses in healthy adult and elderly participants.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Healthy Volunteers

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Worldwide Clinical Trials

San Antonio, Texas, 78217, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Non-smoking, age greater than or equal to (>=) 18 years and less than (<) 55 years old adult male or female (Cohorts 1 - 6) or age >=65 years and less than or equal to (<=) 85 years old elderly male or female (Cohort 7) at the time of informed consent
  • Weight of at least 50 kilogram (kg) and body mass index >=18 and <30 kilogram per square meter (kg/m^2) at Screening

Exclusion criteria

  • Males who have not had a successful vasectomy (confirmed azoospermia) or they and their female partners do not meet the criteria (that is, not of childbearing potential or practicing highly effective contraception throughout the study period plus 90 days after study drug discontinuation). No sperm donation is allowed during the study period plus 90 days after discharge from the study.
  • Females who are breastfeeding or pregnant at Screening or Baseline
  • Females of childbearing potential who:
  • Within 28 days before study entry, did not use a highly effective method of contraception,
  • Do not agree to use a highly effective method of contraception (as described above) throughout the entire study period and for 28 days after study drug discontinuation.
  • Clinically significant illness that requires medical treatment within 8 weeks or a clinically significant infection that requires medical treatment within 4 weeks of dosing
  • Evidence of disease that may influence the outcome of the study within 4 weeks before dosing
  • Evidence of disease related to chronic headaches, migraines, joint pain or other disorders or disease resulting in chronic or intermittent pain within 4 weeks before dosing
  • Any personal or family history of seizures (including febrile seizures) or diagnosis of epilepsy or episode of unexplained loss of consciousness
  • Any history of neurological or other medical conditions which in the opinion of the investigator has the potential to reduce seizure threshold
  • Any epileptiform discharges in EEG at Screening
  • A prolonged QT/ QT interval corrected for heart rate (QTc) interval >450 millisecond [ms]) A history of risk factors for torsade de pointes
  • History of prolonged QT/QTc interval
  • Left bundle branch block
  • History of myocardial infarction or active ischemic heart disease
  • History of clinically significant arrhythmia or uncontrolled arrhythmia
  • Any lifetime history of suicidal ideation or any lifetime history of suicidal behavior as indicated by the C-SSRS
  • Any lifetime history of psychiatric disease

Treatment and study plan

E2511

Drug

E2511 tablets.

E2511 Matched Placebo

Drug

Placebo tablets matching E2511 tablets.

Primary outcomes

  1. Cohorts 1, 2, 3, 4, 5, 6, 7: Number of Participants Reporting one or More Treatment-emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs)

    Time frame: From screening up to 28 days after last dose of study drug (up to 63 days)

  2. Cohorts 1, 2, 3, 4, 5, 6, 7: Number of Participants With Markedly Abnormal Laboratory Values

    Time frame: From screening up to 28 days after last dose of study drug (up to 63 days)

  3. Cohorts 1, 2, 3, 4, 5, 6, 7: Number of Participants With Clinically Significant Change From Screening in Vital Signs Values

    Time frame: From screening up to 28 days after last dose of study drug (up to 63 days)

  4. Cohorts 1, 2, 3, 4, 5, 6, 7: Number of Participants With Clinically Significant Change From Screening in Electrocardiograms (ECGs) Findings

    Time frame: From screening up to 28 days after last dose of study drug (up to 63 days)

  5. Cohorts 1, 2, 3, 4, 5, 6, 7: Number of Participants With Treatment-emergent Suicidal Ideation or Suicidal Behavior as Measured Using Columbia-Suicide Severity Rating Scale (C-SSRS)

    Time frame: From screening up to 28 days after last dose of study drug (up to 63 days)

    The C-SSRS (mapped to Columbia Classification Algorithm of Suicide Assessment [C-CASA]) is an interview-based rating scale to systematically assess any suicidality, suicidal behavior, or suicidal ideation. Any suicidality is emergence of any suicidal ideation or suicidal behavior. Any suicidal behavior is indicated when response is "yes" for any these questions- actual attempt to suicide, engaged in non-suicidal self-injurious behavior, interrupted attempt, aborted attempt, preparatory acts. Any suicidal ideation is indicated when response is "yes" for any of these questions- wish to be dead, non-specific active suicidal thoughts, active suicidal ideation with methods without intent to act or some intent to act, without specific plan or with specific plan and intent to suicide.

  6. Cohorts 1, 2, 3, 4, 5, 6, 7: Number of Participants With Clinically Significant Change From Screening in Physical Examination Findings

    Time frame: From screening up to 28 days after last dose of study drug (up to 63 days)

  7. Cohorts 1, 2, 3, 4, 5, 6, 7: Number of Participants With Clinically Significant Change From Screening in Neurological Exam Findings

    Time frame: Cohorts 1, 2, 4, 5, 6, 7: Screening up to Day 1 (approximately 28 days); Cohort 3: Screening up to Day 7 (approximately 35 days)

  8. Cohorts 1, 2, 3, 4, 5, 6, 7: Number of Participants With Clinically Significant Change From Screening in Psychiatric Assessment

    Time frame: From screening up to 28 days after last dose of study drug (up to 63 days)

    Number of participants with clinically significant change in psychiatric assessment will be evaluated by a psychiatrist as a measure of mental health assessment.

  9. Cohorts 1, 2, 3, 4, 5, 6, 7: Number of Participants With Clinically Significant Change From Screening in Electroencephalogram (EEG) Measurements

    Time frame: From screening up to Day 2 (approximately 30 days)

  10. Cohorts 1, 2, 3, 4, 5, 6, 7: Maximum Observed Plasma Concentration (Cmax) for E2511 on Day 1

    Time frame: Day 1: pre-dose up to a potential maximum of 120 hours post-dose

  11. Cohort 3: Maximum Observed Plasma Concentration (Cmax) for E2511 on Day 7

    Time frame: Day 7: pre-dose up to a potential maximum of 120 hours post-dose

  12. Cohorts 1, 2, 3, 4, 5, 6, 7: Time to Reach Cmax (tmax) for E2511 on Day 1

    Time frame: Day 1: pre-dose up to a potential maximum of 120 hours post-dose

  13. Cohort 3: Time to Reach Cmax (tmax) for E2511 on Day 7

    Time frame: Day 7: pre-dose up to a potential maximum of 120 hours post-dose

  14. Cohorts 1, 2, 3, 4, 5, 6, 7: Area Under the Plasma Concentration-time Curve (AUC(0-t)) From Time Zero to the Last Quantifiable Plasma Concentration for E2511 on Day 1

    Time frame: Day 1: pre-dose up to a potential maximum of 120 hours post-dose

  15. Cohort 3: Area Under the Plasma Concentration-time Curve (AUC(0-t)) From Time Zero to the Last Quantifiable Plasma Concentration for E2511 on Day 7

    Time frame: Day 7: pre-dose up to a potential maximum of 120 hours post-dose

  16. Cohorts 1, 2, 3, 4, 5, 6, 7: Area Under the Plasma Concentration-time Curve (AUC(0-inf)) From Time Zero to Infinity for E2511 on Day 1

    Time frame: Day 1: pre-dose up to a potential maximum of 120 hours post-dose

  17. Cohort 3: Area Under the Plasma Concentration-time Curve (AUC(0-inf)) From Time Zero to Infinity for E2511 on Day 7

    Time frame: Day 7: pre-dose up to a potential maximum of 120 hours post-dose

  18. Cohorts 1, 2, 3, 4, 5, 6, 7: Area Under the Plasma Concentration-time Curve (AUC(0-24)) From Time Zero to 24 Hours Postdose for E2511 on Day 1

    Time frame: Day 1: pre-dose up to a potential maximum of 24 hours post-dose

  19. Cohort 3: Area Under the Plasma Concentration-time Curve (AUC(0-24)) From Time Zero to 24 Hours Postdose for E2511 on Day 7

    Time frame: Day 7: pre-dose up to a potential maximum of 24 hours post-dose

  20. Cohorts 1, 2, 3, 4, 5, 6, 7: Terminal Elimination Phase Half-Life (t1/2) for E2511 on Day 1

    Time frame: Day 1: pre-dose up to a potential maximum of 120 hours post-dose

  21. Cohort 3: Terminal Elimination Phase Half-Life (t1/2) for E2511 on Day 7

    Time frame: Day 7: pre-dose up to a potential maximum of 120 hours post-dose

  22. Cohorts 1, 2, 3, 4, 5, 6, 7: Apparent Total Clearance (CL/F) for E2511 on Day 1

    Time frame: Day 1: pre-dose up to a potential maximum of 120 hours post-dose

  23. Cohort 3: Apparent Total Clearance (CL/F) for E2511 on Day 7

    Time frame: Day 7: pre-dose up to a potential maximum of 120 hours post-dose

  24. Cohorts 1, 2, 3, 4, 5, 6, 7: Apparent Volume of Distribution at Terminal Phase (Vz/F) for E2511 on Day 1

    Time frame: Day 1: pre-dose up to a potential maximum of 120 hours post-dose

  25. Cohort 3: Apparent Volume of Distribution at Terminal Phase (Vz/F) for E2511 on Day 7

    Time frame: Day 7: pre-dose up to a potential maximum of 120 hours post-dose

Secondary outcomes

  1. Cohort 3: Geometric Mean Ratio of Cmax Between the Fasted and Fed State for E2511 20 mg

    Time frame: Days 1 and 7: pre-dose up to a potential maximum of 120 hours post-dose

  2. Cohort 3: Geometric Mean Ratio of AUC(0-t) Between the Fasted and fed State for E2511 20 mg

    Time frame: Days 1 and 7: pre-dose up to a potential maximum of 120 hours post-dose

  3. Cohort 3: Geometric Mean Ratio of AUC(0-inf) Between the Fasted and fed State for E2511 20 mg

    Time frame: Days 1 and 7: pre-dose up to a potential maximum of 120 hours post-dose

  4. Cohort 3 and Cohort 7: Geometric Mean Ratio of Cmax Between the Healthy Elderly and Adult Participants for E2511 20 mg

    Time frame: Cohort 3: Days 1 and 7: pre-dose up to a potential maximum of 120 hours post-dose; Cohort 7: Day 1: pre-dose up to a potential maximum of 120 hours post-dose

  5. Cohort 3 and Cohort 7: Geometric Mean Ratio of AUC(0-t) Between the Healthy Elderly and Adult Participants for E2511 20 mg

    Time frame: Cohort 3: Days 1 and 7: pre-dose up to a potential maximum of 120 hours post-dose; Cohort 7: Day 1: pre-dose up to a potential maximum of 120 hours post-dose

  6. Cohort 3 and Cohort 7: Geometric Mean Ratio of AUC(0-inf) Between the Healthy Elderly and Adult Participants for E2511 20 mg

    Time frame: Cohort 3: Days 1 and 7: pre-dose up to a potential maximum of 120 hours post-dose; Cohort 7: Day 1: pre-dose up to a potential maximum of 120 hours post-dose

  7. Cohorts 1, 2, 3, 4, 5, 6, 7: Correlation Between QTc and E2511 Plasma Concentrations

    Time frame: Day 1: Pre-dose through 24 hours post dose

    To explore the correlation between changes in QTc interval (msec) and E2511 plasma concentrations, appropriate correction method for QTc interval calculation such as QTcF will used for analysis. Holter monitors will be used to collect continuous 12-lead ECG data, from which high precision ECG recordings will be extracted from the Holter monitor data prior to the PK blood samples collected.

Sponsors and collaborators

Lead sponsor

Eisai Inc.

Industry

Registry information

Official study title

A Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Study to Assess the Safety, Tolerability, and Pharmacokinetics of E2511 in Healthy Subjects

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Sep 14, 2020
Registry last updated
Jul 12, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.