A Study of Etripamil in Healthy Subjects

A Single Center, Randomized, Double-Blind, Placebo-Controlled Phase 1 Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of Etripamil in Healthy Chinese Subjects

The objectives of the study are as below:

Primary:

·To evaluate the pharmacokinetics (PK) of Etripamil in healthy adult Chinese subjects

Secondary:

• To evaluate the pharmacodynamics (PD) of Etripamil in healthy adult Chinese subjects
• To evaluate the safety and tolerability of Etripamil in healthy adult Chinese subjects

Exploratory:

·To evaluate the PK exposure-PD response relationship of etripamil in healthy adult Chinese subjects

Study Overview

• Status: Completed
• Conditions: Healthy Chinese Subjects
• Intervention / Treatment: Drug: Placebo; Drug: Etripamil Nasal Spray 70mg

Detailed Description

This is a randomized, double-blind, placebo-controlled phase 1 study in healthy adult Chinese subjects to evaluate the PK, PD, safety and tolerability of single dose of etripamil, 70 mg nasal spray (NS). After signing the informed consent form (ICF), potential subjects will undergo screening procedures within 28 days prior to dosing. Eligible subjects will be admitted to the clinical unit on Day -1 and screening procedures will be repeated to confirm eligibility. Subjects will fast overnight for at least 10 hours prior to dosing. 12 healthy adult Chinese subjects will be randomized to receive etripamil 70 mg single dose (n=10) or placebo (n=2).

Blood and urine samples will be collected for PK assessments of etripamil and the inactive main metabolite MSP-2030.

AEs, 12-lead ECGs, clinical laboratory tests, vital signs, physical examinations, and concomitant medications will be collected and evaluated over the course of study.

Subjects will remain in clinic until discharged on Day 2. There will be a follow-up telephone call on Day 11 (±1 day) of dosing. Total duration for each subject will be approximately 1.5 months.

• Study Type: Interventional
• Enrollment (Actual): 12
• Phase: Phase 1

Contacts and Locations

Study Locations

• China
  • Shanghai
    • Shanghai, Shanghai, China
      • Huashan Hospital Affiliated to Fudan University

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 45 years (Adult)
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

• Subjects who meet all the following criteria at screening may be included in the study:

  1. Ethnically Chinese men or women, 18 to 45 years of age (inclusive).
  2. Body weight: male ≥50 kg, female ≥45 kg; body mass index (BMI) within 18 to 26 kg/m2 (inclusive).
  3. Healthy subject as determined by medical evaluation including medical history, physical examination, clinical laboratory tests, vital signs.
  4. Able to comprehend and willing to sign the ICF which includes compliance with the inclusion and exclusion criteria listed in the ICF and in the protocol.
  5. Non-smoker or ex-smoker for >6 months.
  6. From the time they sign the informed consent to 90 days (male subject within 30 days) after dosing, subjects have no plans to have children and voluntarily use effective contraception

Exclusion Criteria:

• Any of the following will exclude subjects from the study:

  1. Have a history of, or current clinically significant medical illness including but not limited to, cardiac arrhythmias or other cardiac disease; hematologic disease; coagulation disorders (including any abnormal bleeding or blood dyscrasias); significant pulmonary disease, including bronchospastic respiratory disease; diabetes mellitus; hepatic or renal disease; thyroid disease; neurologic or psychiatric disease; or any other illness that the investigator considers should exclude the subject or that could interfere with the interpretation of the study results.
  2. A history of atrioventricular (AV) block, (1st, 2nd or 3rd degree), myocardial infarction (MI) or angina, non-sustained or sustained ventricular tachycardia (VT), torsade de pointes, family history of sudden death or prolonged QT interval, vaso-vagal syncope, sick sinus syndrome, supraventricular tachycardia, atrial flutter, atrial fibrillation (AFib), stroke, transient ischemic attack (TIA), unexplained syncope, congestive heart failure (CHF).
  3. Acute upper respiratory tract infection within 14 days prior to dosing.
  4. Any abnormality of the nasal passage.
  5. Unable to tolerate IN administration.
  6. Known sensitivity to verapamil or other drugs or foods.
  7. Clinically significant abnormal values for clinical laboratory tests at screening as deemed appropriate by the investigator.
  8. Serum potassium <3.5mmol/L or serum magnesium <0.75mmol/L or serum calcium <2.11mmol/L.
  9. Systolic blood pressure (SBP) <100 or >140 mmHg, diastolic blood pressure (DBP) <55 or >90 mmHg, HR <65 or >95 bpm.
  10. QTcF >440 msec, flat or biphasic T waves, QRS >105 ms, evidence of a prior MI, pathologic U waves or U waves that interfere with the QT measurement, AV block or left anterior hemiblock (LAHB) or left posterior hemiblock (LPHB) or right bundle branch block (RBBB) or left bundle branch block (LBBB), pre-excitation syndrome.
  11. Clinically significant abnormal physical examination, vital signs or 12-lead ECG at screening as deemed appropriate by the Investigator.
  12. Have a history of human immunodeficiency virus (HIV) antibody positive, or tests positive for HIV; have a history of treponema pallidum antibody positive, or tests positive for treponema pallidum; have a history of hepatitis B virus surface antigen (HBsAg) or hepatitis C virus antibody (HCVAb) positive, or other clinically active liver disease, or tested positive for HBsAg or HCVAb at screening.
  13. History of drug or alcohol abuse in the last 2 years..
  14. Positive test result(s) for alcohol and/or drugs of abuse at screening or admission (Day-1).
  15. Received an investigational drug or used an invasive investigational medical device within 1 month or within a period less than 10 times the drug's half-life, whichever is longer, before dosing.
  16. Use of any prescription or non-prescription medication within 14 days or 5 half-lives (whichever is longer), or complementary and alternative medicine within 28 days before dosing (excluding aspirin, ibuprofen, and acetaminophen).
  17. Any blood donation within 60 days prior to dosing, or any plasma donation within 30 days prior to dosing, or receipt of blood products within 60 days prior to dosing.
  18. Vaccinated within 30 days prior to dosing or planned to be vaccinated during this study.
  19. Have preplanned surgery or procedures that will interfere with the conduct of the study.
  20. Sponsor staff and/or staff at the study site.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Basic Science
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Double

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Etripamil Nasal Spray 70mg; Etripamil Nasal Spray 70mg single dose	Drug: Etripamil Nasal Spray 70mg; Etripamil NS 70 mg will be administered via the Aptar Pharma Nasal Spray Bidose System, supplied as prefilled devices packaged into child-resistant boxes with instructions for use provided in the study drug box.
Placebo Comparator: Etripamil Placebo Nasal Spray 70mg; Etripamil Placebo Nasal Spray 70mg single dose	Drug: Placebo; Placebo will be administered via the Aptar Pharma Nasal Spray Bidose System, supplied as prefilled devices packaged into child-resistant boxes with instructions for use provided in the study drug box.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Cmax of Etripamil after single dosing	To measure Cmax of Etripamil after single dosing	Day -1 to Day 11
Cmax of MSP-2030 after single dosing	To measure Cmax of MSP-2030 after single dosing	Day -1 to Day 11

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
PR interval after single dosing	To measure PR interval by electrocardiogram after single dosing	Day -1 to Day 11
Blood pressure after single dosing	To measure systolic and diastolic blood pressure after single dosing	Day -1 to Day 11
Heart rate after single dosing	To measure heart rate after single dosing	Day -1 to Day 11
Subject incidence of Adverse Event (AE)	To record subject incidence of Adverse Event (AE)	Day -1 to Day 11
Subject electrocardiogram outcomes	To record number of participants with abnormal electrocardiogram readings	Day -1 to Day 11
Subject clinical laboratory tests outcomes	To record number of participants with abnormal laboratory test results	Day -1 to Day 11
Concomitant medications that subjects take	To record subject clinical laboratory tests outcomes	Day -1 to Day 11

Collaborators and Investigators

• Sponsor: Ji Xing Pharmaceuticals (Shanghai) Co., Ltd.
• Collaborators: Milestone Pharmaceuticals Inc.

Study record dates

Study Major Dates

• Study Start (Actual): March 7, 2023
• Primary Completion (Actual): March 26, 2023
• Study Completion (Actual): March 26, 2023

Study Registration Dates

• First Submitted: August 7, 2022
• First Submitted That Met QC Criteria: August 22, 2022
• First Posted (Actual): August 23, 2022

Study Record Updates

• Last Update Posted (Actual): April 10, 2023
• Last Update Submitted That Met QC Criteria: April 7, 2023
• Last Verified: March 1, 2023

More Information

Terms related to this study

• Keywords: Tachycardia; Paroxysmal supraventricular tachycardia; Tachycardia, Supraventricular; Etripamil
• Additional Relevant MeSH Terms: Physiological Effects of Drugs; Molecular Mechanisms of Pharmacological Action; Membrane Transport Modulators; Calcium-Regulating Hormones and Agents; Calcium Channel Blockers; Etripamil
• Other Study ID Numbers: JX02001

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: Yes