Safety, Tolerance and Pharmacokinetics Study of Compound Edaravone Injection

NCT04219865 | Completed Phase 1

• 1 other identifier: NJYK-CPEDRV-I
• Study Type: interventional
• Target: 40
• Locations: 1 country
• Sites: 1

Brief Summary

Study on the Safety, Tolerance and Pharmacokinetics of Single-dose, Increasing and Loading Dose and Maintenance Dose Sequential Intravenous Infusion of Compound Edaravone Injection in Chinese Healthy Volunteers

Conditions

Pharmacokinetics

Keywords

Edaravone; Compound edaravone injection

Outcome Measures

Primary Outcomes (4)

• Area under curve (AUC) of edaravone and 2-aminoethanesulfonic Acid in single dose groups of compound edaravone injection

  24 hours

• Area under curve (AUC) of edaravone and 2-aminoethanesulfonic Acid in multiple doses group after multiple intravenous infusion of compound edaravone injection

  7 Days

• Cmax of edaravone and 2-aminoethanesulfonic Acid in single dose groups of compound edaravone injection

  24 hours

• Cmax of edaravone and 2-aminoethanesulfonic Acid in multiple doses group after multiple intravenous infusion of compound edaravone injection

  7 Days

Secondary Outcomes (1)

• Incidence of adverse events of compound edaravone injection

  7 Days

Study Arms (2)

Compound Edaravone

ACTIVE COMPARATOR

10 mL per vial (containing edaravone 10 mg and 2-aminoethanesulfonic acid 200 mg)

Drug: Group 1: Compound Edaravone/Placebo Injection; Drug: Group 2: Compound Edaravone/Placebo Injection; Drug: Group 3: Compound Edaravone/Placebo Injection; Drug: Group 4: Compound Edaravone/Placebo Injection; Drug: Group 5: Compound Edaravone/Placebo Injection

Placebo

PLACEBO COMPARATOR

10 mL per vial

Drug: Group 1: Compound Edaravone/Placebo Injection; Drug: Group 2: Compound Edaravone/Placebo Injection; Drug: Group 3: Compound Edaravone/Placebo Injection; Drug: Group 4: Compound Edaravone/Placebo Injection; Drug: Group 5: Compound Edaravone/Placebo Injection

Interventions

Group 1: Compound Edaravone/Placebo Injection DRUG

Compound Edaravone 30mg-600mg (containing edaravone 30 mg and 2-aminoethanesulfonic acid 600 mg) / placebo single intravenous infusion for 30min

Compound Edaravone; Placebo

Group 2: Compound Edaravone/Placebo Injection DRUG

Compound Edaravone 60mg-1200mg (containing edaravone 60 mg and 2-aminoethanesulfonic acid 1200 mg) / placebo single intravenous infusion for 30min

Compound Edaravone; Placebo

Group 3: Compound Edaravone/Placebo Injection DRUG

Compound Edaravone 90mg-1800mg (containing edaravone 90 mg and 2-aminoethanesulfonic acid 1800 mg) / placebo single intravenous infusion for 30min

Compound Edaravone; Placebo

Group 4: Compound Edaravone/Placebo Injection DRUG

Compound Edaravone 120mg-2400mg (containing edaravone 120 mg and 2-aminoethanesulfonic acid 2400 mg) / placebo single intravenous infusion for 30min

Compound Edaravone; Placebo

Group 5: Compound Edaravone/Placebo Injection DRUG

Maximum tolerated dose of drug / placebo for a single intravenous infusion for 30 minutes three times a day at an interval of 8 h until the last dose on the morning of Day 3, after which the sequential test drug 30 mg-600 mg / placebo will be administered daily from Day 3 night Intravenous infusion, 30 minutes at 12-hour intervals until morning on Day 7

Compound Edaravone; Placebo

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Age: 18-65 years old (including upper and lower limits);
• Weight ≥50 kg, body mass index (BMI) between 18-28 kg / m2 (including upper and lower limits);
• Understand and sign the informed consent voluntarily, and volunteer to participate in this research.

You may not qualify if:

• A history of diseases of the heart, liver, lung, kidney, digestive tract, blood, or neuropsychiatric system judged by the investigator as clinically significant;
• A comprehensive physical examination, neurological examination, laboratory examination, ECG examination, or cognitive assessment indicates that the subject has an abnormality that the researcher has determined to be clinically significant;
• Have taken any drug within two weeks before the study administration, and the researcher believes that this situation may affect the evaluation results of this study;
• There is a history of food or drug allergy or allergies that the researcher judges to be clinically significant;
• Those with positive results of serological examination (HBsAg, anti-HCV, anti-HIV, TP-Ab);
• A history of alcohol or drug abuse that the investigator believes may affect the evaluation results of this study within one year before the study administration;
• Cannot quit smoking or drinking during the study period or the carbon monoxide breath test\> 7 ppm during the screening period CO breath test, so if the subject's CO breath is\> 7ppm, but the urine cotinine test is negative, it means that the CO breath test result may be false positive, the subject can be enrolled;
• As a subject who has participated in any drug clinical trial within 3 months before the first administration of the study;
• Those who donated blood or blood products ≥400 mL or 2 units within three months of the study;
• Do not agree to avoid the use of tobacco, alcohol or caffeinated beverages, or vigorous exercise, or other factors that affect drug absorption, distribution, metabolism, excretion, etc. during the 24 hours before and during the test;
• Pregnant or lactating women, or those who tested positive for serum HCG before the test administration, or those who were unable or unwilling to take researcher-approved contraception during the study according to the researcher's instructions;
• Subjects with poor compliance or unable to comply with the relevant provisions of the research protocol due to personal reasons, the investigator judges that the subjects are not suitable to participate in this clinical study.

Sponsors & Collaborators

• Nanjing Yoko Biomedical Co., Ltd.: lead

Study Sites (1)

Beijing Tiantan Hospital, Capital Medical University

Beijing, Beijing Municipality, 100050, China

Location

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: TRIPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR
• Purpose: BASIC SCIENCE
• Intervention Model: FACTORIAL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Model Details: Factorial Assignment

Study Record Dates

• First Submitted: December 18, 2019
• First Posted: January 7, 2020
• Study Start: June 5, 2019
• Primary Completion: August 16, 2019
• Study Completion: August 16, 2019
• Last Updated: March 22, 2021

Record last verified: 2021-03

Locations

CN (1)