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Clinical Trials/NCT05147337
NCT05147337
Completed
Phase 1

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

Eisai Inc.1 site in 1 country47 target enrollmentDecember 1, 2021
InterventionsE2511Placebo

Overview

Phase
Phase 1
Intervention
E2511
Conditions
Healthy Volunteers
Sponsor
Eisai Inc.
Enrollment
47
Locations
1
Primary Endpoint
Number of Participants With Treatment-emergent Adverse Events (TEAEs)
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

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

Registry
clinicaltrials.gov
Start Date
December 1, 2021
End Date
August 18, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Eisai Inc.
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Non-smoking, male, or female, non-Japanese participants age \>=18 years and \<55 years old (Cohorts 1 to 4) or age \>=55 years and \<=85 years old (Cohort 8); or Japanese participants age \>=20 years and \<55 years old (Cohorts 5 to 7) at the time of informed consent
  • Japanese participants must also satisfy the following requirements:
  • Must have been born in Japan of Japanese parents and Japanese grandparents
  • Must have lived no more than 5 years outside of Japan
  • Must not have changed their lifestyle or habits, including diet, while living outside of Japan
  • Weight of at least 50 kilogram (kg) and body mass index (BMI) \>=18 and \<30 kilogram per square meter (kg/m\^2) (Cohorts 1 to 7) or BMI \>=18 and \<32 kg/m\^2 (Cohort 8) at Screening

Exclusion Criteria

  • 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 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; example, psychiatric disorders and disorders of the gastrointestinal tract, liver, kidney, respiratory system, endocrine system, hematological system, neurological system, or cardiovascular system, or participants who have a congenital abnormality in metabolism
  • Evidence of disease within 4 weeks before dosing related to chronic headaches, migraines, joint pain, or other disorders or disease resulting in chronic or intermittent pain
  • 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 history of gastrointestinal surgery that may affect PK profiles of E2511, example, hepatectomy, nephrectomy, digestive organ resection at Screening

Arms & Interventions

Cohort 1: E2511 10 mg or Placebo

Non-Japanese adult (greater than or equal to \[\>=\] 18 years and less than \[\<\] 55 years old) participants will receive 10 milligram (mg) E2511 or E2511 matched placebo, tablets, orally, once daily from Day 1 to Day 14.

Intervention: E2511

Cohort 1: E2511 10 mg or Placebo

Non-Japanese adult (greater than or equal to \[\>=\] 18 years and less than \[\<\] 55 years old) participants will receive 10 milligram (mg) E2511 or E2511 matched placebo, tablets, orally, once daily from Day 1 to Day 14.

Intervention: Placebo

Cohort 2: E2511 20 mg or Placebo

Non-Japanese adult participants will receive 20 mg E2511 or E2511 matched placebo, tablets, orally, once daily from Day 1 to Day 14.

Intervention: E2511

Cohort 2: E2511 20 mg or Placebo

Non-Japanese adult participants will receive 20 mg E2511 or E2511 matched placebo, tablets, orally, once daily from Day 1 to Day 14.

Intervention: Placebo

Cohort 7: E2511 80 mg or Placebo

Japanese adult participants will receive 80 mg E2511 or E2511 matched placebo, tablets, orally, once daily from Day 1 to Day 14.

Intervention: E2511

Cohort 3: E2511 40 mg or Placebo

Non-Japanese adult participants will receive 40 mg E2511 or E2511 matched placebo, tablets, orally, once daily from Day 1 to Day 14.

Intervention: E2511

Cohort 3: E2511 40 mg or Placebo

Non-Japanese adult participants will receive 40 mg E2511 or E2511 matched placebo, tablets, orally, once daily from Day 1 to Day 14.

Intervention: Placebo

Cohort 4: E2511 80 mg or Placebo

Non-Japanese adult participants will receive 80 mg E2511 or E2511 matched placebo, tablets, orally, once daily from Day 1 to Day 14.

Intervention: E2511

Cohort 4: E2511 80 mg or Placebo

Non-Japanese adult participants will receive 80 mg E2511 or E2511 matched placebo, tablets, orally, once daily from Day 1 to Day 14.

Intervention: Placebo

Cohort 5: E2511 20 mg or Placebo

Japanese adult (\>=20 years and \<55 years old) participants will receive 20 mg E2511 or E2511 matched placebo, tablets, orally, once daily from Day 1 to Day 14.

Intervention: E2511

Cohort 5: E2511 20 mg or Placebo

Japanese adult (\>=20 years and \<55 years old) participants will receive 20 mg E2511 or E2511 matched placebo, tablets, orally, once daily from Day 1 to Day 14.

Intervention: Placebo

Cohort 6: E2511 40 mg or Placebo

Japanese adult participants will receive 40 mg E2511 or E2511 matched placebo, tablets, orally, once daily from Day 1 to Day 14.

Intervention: E2511

Cohort 6: E2511 40 mg or Placebo

Japanese adult participants will receive 40 mg E2511 or E2511 matched placebo, tablets, orally, once daily from Day 1 to Day 14.

Intervention: Placebo

Cohort 7: E2511 80 mg or Placebo

Japanese adult participants will receive 80 mg E2511 or E2511 matched placebo, tablets, orally, once daily from Day 1 to Day 14.

Intervention: Placebo

Cohort 8: E2511 40 mg or Placebo

Non-Japanese older (\>=55 years and less than or equal to \[\<=\] 85 years old) participants will receive 40 mg E2511 or E2511 matched placebo, tablets, orally, once daily from Day 1 to Day 14.

Intervention: E2511

Cohort 8: E2511 40 mg or Placebo

Non-Japanese older (\>=55 years and less than or equal to \[\<=\] 85 years old) participants will receive 40 mg E2511 or E2511 matched placebo, tablets, orally, once daily from Day 1 to Day 14.

Intervention: Placebo

Outcomes

Primary Outcomes

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

Time Frame: From Screening up to 14 days after the last dose of study drug (up to 56 days)

Number of Participants With Serious Adverse Events (SAEs)

Time Frame: From Screening up to 14 days after the last dose of study drug (up to 56 days)

Number of Participants With Clinically Significant Abnormal Laboratory Values

Time Frame: From Screening up to 14 days after the last dose of study drug (up to 56 days)

Number of Participants With Clinically Significant Abnormal Vital Signs Values

Time Frame: From Screening up to 14 days after the last dose of study drug (up to 56 days)

Number of Participants With Clinically Significant Abnormal Electrocardiograms (ECGs) Findings

Time Frame: From Screening up to 14 days after the last dose of study drug (up to 56 days)

Number of Participants With Clinically Significant Abnormal Ambulatory Blood Pressure

Time Frame: From Screening up to 14 days after the last dose of study drug (up to 56 days)

Number of Participants With Suicidal Ideation or Suicidal Behavior as Measured Using Columbia-suicide Severity Rating Scale (C-SSRS)

Time Frame: From Screening up to 14 days after the last dose of study drug (up to 56 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.

Number of Participants With Clinically Significant Abnormal Physical Examination Findings

Time Frame: From Screening up to 14 days after the last dose of study drug (up to 56 days)

Number of Participants With Clinically Significant Abnormal Neurological Examination Findings

Time Frame: From Screening up to 14 days after the last dose of study drug (up to 56 days)

Number of Participants With Clinically Significant Abnormal Electroencephalogram (EEG) Findings

Time Frame: From Screening up to 14 days after the last dose of study drug (up to 56 days)

Cmax: Maximum Observed Plasma Concentration for E2511

Time Frame: Day 1: pre-dose up to 24 hours post-dose

Css,max: Maximum Observed Plasma Concentration at Steady State for E2511

Time Frame: Day 14: pre-dose up to 24 hours post-dose

tmax: Time to Reach Maximum Observed Plasma Concentration (Cmax) for E2511

Time Frame: Day 1: pre-dose up to 24 hours post-dose

tss,max: Time to Reach Maximum Observed Plasma Concentration (Cmax) at Steady State for E2511

Time Frame: Day 14: pre-dose up to 24 hours post-dose

Css,av: Average Steady State Plasma Concentration for E2511

Time Frame: Day 14: pre-dose up to 24 hours post-dose

AUC(0-t): Area Under the Plasma Concentration-time Curve From Time Zero to Time of Last Quantifiable Concentration for E2511

Time Frame: Day 1: pre-dose up to 24 hours post-dose; Day 14: pre-dose up to 24 hours post-dose

AUC(0-inf): Area Under the Plasma Concentration-time Curve From Time Zero to Infinite for E2511

Time Frame: Day 1: pre-dose up to 24 hours post-dose

AUC(0-24h): Area Under the Plasma Concentration-time Curve From Time Zero to 24 hours Post-dose for E2511

Time Frame: Day 1: pre-dose up to 24 hours post-dose; Day 14: pre-dose up to 24 hours post-dose

t1/2: Terminal Elimination Phase Half-life for E2511

Time Frame: Day 1: pre-dose up to 24 hours post-dose; Day 14: pre-dose up to 24 hours post-dose

PTF: Peak-trough Fluctuation for E2511

Time Frame: Day 14: pre-dose up to 24 hours post-dose

CL/F: Apparent Total Clearance for E2511

Time Frame: Day 1: pre-dose up to 24 hours post-dose

CLss/F: Apparent Total Clearance at Steady State for E2511

Time Frame: Day 14: pre-dose up to 24 hours post-dose

Vz/F: Apparent Volume of Distribution at Terminal Phase for E2511

Time Frame: Day 1: pre-dose up to 24 hours post-dose; Day 14: pre-dose up to 24 hours post-dose

Rac: Accumulation Ratio for E2511 Based on Cmax and AUC

Time Frame: Day 14: pre-dose up to 24 hours post-dose

Rss: Accumulation Ratio for E2511 Based on Time and Concentration

Time Frame: Day 14: pre-dose up to 24 hours post-dose

Secondary Outcomes

  • Change From Baseline in the Concentration of Acetylcholine (ACh) in Cerebrospinal Fluid (CSF)(Baseline, Day 13)
  • Change From Baseline in Heart Rate (HR)(Baseline up to Day 15)
  • Change From Baseline in PR Interval of the ECG (PR), QRS Interval of the ECG (QRS), and QT Interval Corrected for Heart Rate (QTc) of the ECG(Baseline up to Day 15)
  • Placebo Corrected Change From Baseline in HR(Baseline up to Day 15)
  • Placebo Corrected Change From Baseline in PR, QRS, and QTc Interval(Baseline up to Day 15)
  • Number of Participants With Categorical Outliers for HR, PR, QRS and QTc Interval(Baseline up to Day 15)
  • Number of Participants With Treatment-emergent T-wave and U-wave abnormalities(Baseline up to Day 15)
  • Mean Change From Baseline in 24-hours Systolic Blood Pressure (SBP) and Diastolic Blood Pressure (DBP) up to Day 15(Up to Day 15)
  • Mean Change From Baseline in Day-time, Night-time, and Hourly SBP and DBP(Baseline up to Day 15)
  • Mean Change From Baseline in Day-time, Night-time, and Hourly HR(Baseline up to Day 15)
  • Mean Change From Baseline in Day-time, Night-time, and Hourly Mean Arterial Pressure (MAP) and Pulse Pressure (PP)(Baseline up to Day 15)
  • Placebo Corrected Mean Change From Baseline in 24-hours SBP and DBP up to Day 15(Up to Day 15)
  • Placebo Corrected Mean Change From Baseline in Day-time, Night-time, and Hourly SBP and DBP(Baseline up to Day 15)
  • Placebo Corrected Mean Change From Baseline in Day-time, Night-time, and Hourly HR(Baseline up to Day 15)
  • Placebo Corrected Mean Change From Baseline in Day-time, Night-time, and Hourly MAP and PP(Baseline up to Day 15)
  • Geometric Mean Ratio Between the Non-japanese (>=18 and <55 years) and Elderly Non-japanese (>=65 to <=85 years) Participants for E2511(Day 1: pre-dose up to 24 hours post-dose; Day 14: pre-dose up to 24 hours post-dose)
  • Number of Participants With Categorical Outliers for SBP and DBP(Baseline up to Day 15)
  • Geometric Mean Ratio of Cmax Between the Healthy Japanese and Non-japanese Participants for E2511(Day 1: pre-dose up to 24 hours post-dose; Day 14: pre-dose up to 24 hours post-dose)
  • Geometric Mean Ratio of AUC Between the Healthy Japanese and Non-japanese Participants for E2511(Day 1: pre-dose up to 24 hours post-dose; Day 14: pre-dose up to 24 hours post-dose)
  • Geometric Mean Ratio of Cmax Between the Younger Non-japanese (>=18 and <55 years) and older Non-japanese (>=55 to <=85 years) Participants for E2511(Day 1: pre-dose up to 24 hours post-dose; Day 14: pre-dose up to 24 hours post-dose)
  • Geometric Mean Ratio of AUC Between the Younger Non-japanese (>=18 and <55 years) and older Non-japanese (>=55 to <=85 years) Participants for E2511(Day 1: pre-dose up to 24 hours post-dose; Day 14: pre-dose up to 24 hours post-dose)

Study Sites (1)

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