Clinical Trial to Evaluate Pharmacokinetic Characteristics of MIT-001 After SC Administration in Healthy Subjects

Heathly Subjects Clinical Trial

Official title:

Clinical Trial to Evaluate Safety, Tolerability and Pharmacokinetic Characteristics of MIT-001 After Subcutaneous and Intravenous Administration in Healthy Subjects

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05389696
• Other study ID #: MIT001-FD-SC01
• Status: Completed
• Phase: Phase 1
• Start date: May 13, 2022
• Est. completion date: April 28, 2023

Study information

• Verified date: August 2023
• Source: MitoImmune Therapeutics
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

1. Part 1 Randimization, Double blinded, Placebo controlled, Dose escalation(10mg, 20mg, 40mg) of MIT-001 SC or IV single administration to evaluate safety, tolerability and PK in healthy adult.

2. Part2 Randimization, Double blinded, Placebo controlled, MIT-001 SC multiple administration for 7days (20mg & 40mg) to evaluate safety, tolerability and PK in healthy adult.

Description:

This is a Phase 1, randomized, double-blind, placebo-controlled, single and multiple dose, dose escalation clinical trial in 40 healthy subjects. This study consists of part 1(single dose for group 1, 2, 3) and part 2(multiple dose for 7 days to group 1 and 2). Subjects will be assigned in 6:2 allocation to receive active or placebo treatments. The purpose of this clinical trial is to evaluate the safety, tolerability and pharmacokinetic properties of MIT-001 after single and multiple subcutaneous administration in healthy adults and to compare IV administration.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 40
• Est. completion date: April 28, 2023
• Est. primary completion date: February 13, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 19 Years to 45 Years

Eligibility

Inclusion Criteria:

1. A healthy adult between 19 and 45 at the time of screening

2. A person who weigh 55.0 kg or more and 90.0 kg or less at the time of screening and have a body mass index (BMI) of 18.0 or more and 27.0 or less

? BMI (kg/m2) = Weight (kg) / {Height (m)}2

3. A person who voluntarily decides to participate after hearing and fully understanding the detailed explanation of this clinical trial and consents in writing before the screening procedure

4. A person suitable as a test subject for this study when judged by the investigator through physical examination, clinical laboratory examination, questionnaire, etc.

Exclusion Criteria:

1. Clinically significant liver, kidney, nervous system, immune system, respiratory system, endocrine system disease, blood/tumor disease, cardiovascular disease, mental disease (mood disorder, obsessive-compulsive disorder, etc.) or a history of above diseases

2. A person with a history of hypersensitivity or clinically significant hypersensitivity to clinical investigational drugs, drugs containing the same class of ingredients, and other drugs (aspirin, antibiotics, etc.)

3. At screening, QTc > 450 ms on ECG or other clinically significant findings

4. A person with AST and ALT exceeding 1.5 times the upper limit of the normal range during screening

5. A person with eGFR of less than 60 mL/min/1.73m2 measured using the CKD EPI formula in clinical laboratory tests at screening

6. At screening, systolic blood pressure > 160 mmHg or < 90 mmHg, or diastolic blood pressure > 100 mmHg or < 50 mmHg

7. A person with a history of drug abuse or who have tested positive for drugs of abuse in urine drug screening tests

8. A person who has taken any prescription drugs or herbal medicines within 2 weeks before the first scheduled administration date, or have taken any over-the-counter (OTC), health functional food, or vitamin preparations within 1 week In cases where it is reasonable, they can participate in the clinical trial) or those who are expected to take it

9. A person who has taken drugs that induce or inhibit drug metabolizing enzymes, such as barbiturates, within 1 month before the first scheduled administration date

10. A person who has participated in other clinical trials or bioequivalence studies within 6 months prior to the scheduled first administration date and received the investigational drug or bioequivalence study drug

11. A person who has donated whole blood within 2 months before the first scheduled dose or donated component blood within 1 month, or received blood transfusion within 1 month before the first scheduled dose

12. A person who continuously drinks alcohol (more than 21 units/week, 1 unit = 10 g of pure alcohol (? 1 glass of soju or 250 mL of beer)) or cannot abstain from alcohol during the clinical trial period

13. Smokers (However, if you quit smoking 3 months before the first scheduled dose, you can be selected as a test subject)

14. A person who has consumed caffeine-containing foods (coffee, tea (black tea, green tea, etc.), carbonated drinks, coffee milk, nourishing drinks, etc.) within 24 hours of hospitalization for clinical trials and those who cannot refrain from consuming them during hospitalization

15. A person who does not use the following medically acceptable contraceptive methods for 1 month from participation in the clinical trial to the last administration of the investigational drug A. Use of an intrauterine device (copper loop, hormone-containing intrauterine system) with a proven rate of pregnancy failure in the spouse (or partner) B. Concomitant use of either a spermicide or a parenteral hormonal contraceptive with a barrier contraceptive method (male or female) C. Surgery of you or your partner (vasectomy, fallopectomy/ligation, hysterectomy, etc.) D. Use of a cervical cap or contraceptive diaphragm with a male condom

16. Pregnant or lactating women

17. A person who judged the investigator to be inappropriate to participate in the clinical trial due to other reasons

Related Conditions & MeSH terms

• Heathly Subjects

Intervention

Drug:
• Single subcutaneous administration and Blood collection
Single subcutaneous administration and Blood collection
• Single subcutaneous administration and then IV injection.
Single subcutaneous administration and then single intravenous administration after 2 weeks. In addition Blood collection is conducted as scheduled.
• MIT-001 20mg and 40mg_Multiple administration
Multiple subcutaneous administration for 7 days and then blood collection

Locations

Country	Name	City	State
Korea, Republic of	Seoul National University	Seoul

Sponsors (1)

Lead Sponsor	Collaborator
MitoImmune Therapeutics

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	PK_Cmax_Part1 Group 1&2	Part 1, Group 1,2: Cmax	Part1. Group 1&2: Before SC administration(Day0, 0hour) to 144hour after administration 16 points.
Primary	PK_Cmax_Part1 Group 3	Part 1, Group 3: Cmax	Part1. Group 3_Before SC administration(Day0, 0hour) to 144hour 16 points and then Before IV administration on 15th day(0hour) to 144hour after IV administration 17points.
Primary	PK_AUClast_Part1 Group 1&2	Part1, Group 1&2: AUClast	Part1. Group 1&2_Before SC administration(Day0, 0hour) to 144hour after administration 16 points.
Primary	PK_AUClast_Part1 Group 3	Part 1, Group 3: AUClast	Part1. Group 3_Before SC administration(Day0, 0hour) to 144hour 16 points and then Before IV administration on 15th day(0hour) to 144hour after IV administration 17points.
Primary	PK_AUCinf_Part 1, Group 1&2	Part 1, Group 1&2: AUCinf	Part1. Group 1&2_Before SC administration(Day0, 0hour) to 144hour after administration 16 points.
Primary	PK_AUCinf_Part 1, Group 3	Part 1, Group 3: AUCinf	Part1. Group 3_Before SC administration(Day0, 0hour) to 144hour 16 points and then Before IV administration on 15th day(0hour) to 144hour after IV administration 17points.
Primary	PK_Tmax_Part 1, Group 1&2	Part 1, Group 1&2: Tmax	Part1. Group 1&2_Before SC administration(Day0, 0hour) to 144hour after administration 16 points.
Primary	PK_Tmax_Part 1, Group 3	Part 1, Group 3: Tmax	Part1. Group 3_Before SC administration(Day0, 0hour) to 144hour 16 points and then Before IV administration on 15th day(0hour) to 144hour after IV administration 17points.
Primary	PK_t1/2_Part 1, Group 1&2	Part 1, Group 1&2: t1/2	Part1. Group 1&2_Before SC administration(Day0, 0hour) to 144hour after administration 16 points.
Primary	PK_t1/2_Part 1, Group 3	Part 1, Group 3: t1/2	Part1. Group 3_Before SC administration(Day0, 0hour) to 144hour 16 points and then Before IV administration on 15th day(0hour) to 144hour after IV administration 17points.
Primary	PK_Vd/F_Part 1, Group 1&2	Part 1, Group 1&2: Vd/F	Part1. Group 1&2_Before SC administration(Day0, 0hour) to 144hour after administration 16 points.
Primary	PK_Vd/F_Part 1, Group 3	Part 1, Group 3: Vd/F	Part1. Group 3_Before SC administration(Day0, 0hour) to 144hour 16 points and then Before IV administration on 15th day(0hour) to 144hour after IV administration 17points.
Primary	PK_CL/F_Part 1, Group 1,2	Part 1, Group 1,2: CL/F	Part1. Group 1&2_Before SC administration(Day0, 0hour) to 144hour after administration 16 points.
Primary	PK_CL/F_Part 1, Group 3	Part 1, Group 3: CL/F	Part1. Group 3_Before SC administration(Day0, 0hour) to 144hour 16 points and then Before IV administration on 15th day(0hour) to 144hour after IV administration 17points.
Primary	PK_MRT_Part 1, Group 1&2	Part 1, Group 1,2: MRT	Part1. Group 1&2_Before SC administration(Day0, 0hour) to 144hour after administration 16 points.
Primary	PK_MRT_Part 1, Group 3	Part 1, Group 3: MRT	Part1. Group 3_Before SC administration(Day0, 0hour) to 144hour 16 points and then Before IV administration on 15th day(0hour) to 144hour after IV administration 17points.
Primary	PK_F_Part1, Group1,2	Part 1, Group 1,2: F	Part1. Group 1&2_Before SC administration(Day0, 0hour) to 144hour after administration 16 points.
Primary	PK_F_Part1, Group3	Part 1, Group 3: F	Part1. Group 3_Before SC administration(Day0, 0hour) to 144hour 16 points and then Before IV administration on 15th day(0hour) to 144hour after IV administration 17points.
Primary	PK_Part2_Cmax	Part 2: Cmax	Part2: Before SC administration(Day0, 0hour) to 24hour 13points, Day5 0hour, Day6 0hour and then Day7 0hour to 216hour after SC administration 17points
Primary	PK_Part2_Cmin	Part 2: Cmin, Cavg, AUCtau, Tmax, t1/2, Vd/F, CL/F, Cmax,ss, Cmin,ss, Cavg,ss, AUCtau,ss, Tmax,ss, t1/2,ss, Vdss/F, CLss/F, PTF, Rac	Part2: Before SC administration(Day0, 0hour) to 24hour 13points, Day5 0hour, Day6 0hour and then Day7 0hour to 216hour after SC administration 17points
Primary	PK_Part2_Cavg	Part 2: Cavg	Par2_Before SC administration(Day0, 0hour) to 24hour 13points, Day5 0hour, Day6 0hour and then Day7 0hour to 216hour after SC administration 17points
Primary	PK_Part2_AUCtau	Part 2: AUCtau	Part2: Before SC administration(Day0, 0hour) to 24hour 13points, Day5 0hour, Day6 0hour and then Day7 0hour to 216hour after SC administration 17points
Primary	PK_Part2_Tmax	Part 2: Tmax	Part2: Before SC administration(Day0, 0hour) to 24hour 13points, Day5 0hour, Day6 0hour and then Day7 0hour to 216hour after SC administration 17points
Primary	PK_Part2_t1/2	Part 2: t1/2	Part2: Before SC administration(Day0, 0hour) to 24hour 13points, Day5 0hour, Day6 0hour and then Day7 0hour to 216hour after SC administration 17points
Primary	PK_Part2_Vd/F	Part 2: Vd/F	Part2: Before SC administration(Day0, 0hour) to 24hour 13points, Day5 0hour, Day6 0hour and then Day7 0hour to 216hour after SC administration 17points
Primary	PK_Part2_CL/F	Part 2: CL/F	Part2: Before SC administration(Day0, 0hour) to 24hour 13points, Day5 0hour, Day6 0hour and then Day7 0hour to 216hour after SC administration 17points
Primary	PK_Part2_Cmax,ss	Part 2: Cmax,ss	Part2: Before SC administration(Day0, 0hour) to 24hour 13points, Day5 0hour, Day6 0hour and then Day7 0hour to 216hour after SC administration 17points
Primary	PK_Part2_Cmin,ss	Part 2: Cmin,ss	Part2: Before SC administration(Day0, 0hour) to 24hour 13points, Day5 0hour, Day6 0hour and then Day7 0hour to 216hour after SC administration 17points
Primary	PK_Part2_Cavg,ss	Part 2: Cavg,ss	Part2: Before SC administration(Day0, 0hour) to 24hour 13points, Day5 0hour, Day6 0hour and then Day7 0hour to 216hour after SC administration 17points
Primary	PK_Part2_AUCtau,ss	Part 2: AUCtau,ss	Part2: Before SC administration(Day0, 0hour) to 24hour 13points, Day5 0hour, Day6 0hour and then Day7 0hour to 216hour after SC administration 17points
Primary	PK_Part2_Tmax,ss	Part 2: Tmax,ss	Part2: Before SC administration(Day0, 0hour) to 24hour 13points, Day5 0hour, Day6 0hour and then Day7 0hour to 216hour after SC administration 17points
Primary	PK_Part2_t1/2,ss	Part 2: _t1/2,ss	Part2: Before SC administration(Day0, 0hour) to 24hour 13points, Day5 0hour, Day6 0hour and then Day7 0hour to 216hour after SC administration 17points
Primary	PK_Part2_Vdss/F	Part 2: _Vdss/F	Part2: Before SC administration(Day0, 0hour) to 24hour 13points, Day5 0hour, Day6 0hour and then Day7 0hour to 216hour after SC administration 17points
Primary	PK_Part2_CLss/F	Part 2: _VCLss/F	Part2: Before SC administration(Day0, 0hour) to 24hour 13points, Day5 0hour, Day6 0hour and then Day7 0hour to 216hour after SC administration 17points
Primary	PK_Part2_PTF	Part 2: _PTF	Part2: Before SC administration(Day0, 0hour) to 24hour 13points, Day5 0hour, Day6 0hour and then Day7 0hour to 216hour after SC administration 17points
Primary	PK_Part2_Rac	Part 2: _Rac	Part2: Before SC administration(Day0, 0hour) to 24hour 13points, Day5 0hour, Day6 0hour and then Day7 0hour to 216hour after SC administration 17points