Study to Assess Safety, Tolerability and Pharmacokinetics of XC7 (Which is Planned Use in the Treatment of COVID-19) in Healthy Volunteers

Double Blind, Randomized, Placebo-controlled Study of Safety, Tolerability, and Pharmacokinetics of Ascending Doses of XC7 After Single and Multiple Oral Administration in Healthy Volunteers

A double-blind, randomized, placebo-controlled, Phase I clinical study of the safety, tolerability and pharmacokinetics (PK) of ascending doses of XC7 after single and multiple oral administration in healthy volunteers. It's planned to include sequentially 2 cohorts of 4 volunteers who will receive a single dose of XC7 (100 mg and 200 mg) or placebo (cohort ratio 3:1) and 1 cohort of 8 volunteers who will receive multiple doses of the XC7 (200 mg) or placebo during 14 days (cohort ratio 6:2).

Study Overview

• Status: Completed
• Conditions: Covid19; Healthy Volunteers
• Intervention / Treatment: Drug: XC7 100 mg single; Drug: XC7 200 mg single; Drug: Placebo single; Drug: XC7 200 mg multiple; Drug: Placebo multiple

Detailed Description

The study will be conducted in 1 centre. The study will consist of 3 periods: screening (7 days), treatment (1 or 14 days) and follow-up (7 or 28 days).

The volunteers of single dosing cohorts will receive the investigated drug (ID) ХС7 or placebo once and stay at the study center for at least 24 hours after the ID administration to monitor the safety parameters and for sampling for PK analysis. The Follow-up will last 7 days, during which safety parameters and PK in volunteers will be studied. Based on all safety data from the XC7 100 mg cohort, the Data Safety Monitoring Committee (DSMC) will consider dose increase and entry of the 200 mg cohort. If the single dose of ХС7 200 mg is considered to be safe, the third multiple dosing cohort of 200 mg will be included in the study.

The volunteers from multiple dosing cohort will receive the ID (ХС7 or placebo) once a day during 14 days and will stay at the hospital (study center) during the first five days after administration of the ID. The Follow-up will last 14 days, during which they will study safety parameters and PK in volunteers.

• Study Type: Interventional
• Enrollment (Actual): 16
• Phase: Phase 1

Contacts and Locations

Study Locations

• Russian Federation
  • Moscow, Russian Federation, 119991
    • Federal State Autonomous Educational Institution of Higher Education "The First Moscow State Medical University named after I.M. Sechenov" of the Ministry of Health of the Russian Federation

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 45 years (Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: Male

Description

Inclusion Criteria:

1. Non-smoking men (nonsmokers at least within the last year before the screening) at the ages from 18 through 45;
2. Verified diagnosis "healthy" according to standard clinical, laboratory and instrumental methods of examination;
3. Body mass index from 18.5 to 30.0 kg/m2 with body weight of more than 45 kg and no more than 110 kg;
4. Negative result for alcohol vapor content in the exhaled air, narcotic substances in the urine;
5. Agreement to use adequate contraception methods during the study and 3 months after its completion: condoms with spermicide (foam, gel, cream, suppository);
6. Signed patient explanation sheet and informed consent for participation in the study.

Exclusion Criteria:

1. Chronic diseases of the cardiovascular, bronchopulmonary, nervous, endocrine, musculoskeletal system, as well as the gastrointestinal tract, liver, kidneys, blood, mental illness, epilepsy or convulsive seizures;
2. Abnormal results of standard laboratory tests and investigations at the screening visit;
3. Gastrointestinal surgery (except for appendectomy) in the past medical history;
4. Systolic blood pressure of less than 90 mm Hg or above 139 mm Hg, diastolic blood pressure of less than 60 mm Hg or above 90 mm Hg, heart rate of less than 60 bpm or above 90 bpm - at screening;
5. Regular administration of drugs within 2 weeks prior to screening (including herbal agents and dietary supplements);
6. Use of drugs with significant effect on hemodynamics, hepatic function, etc. (e.g. barbiturates, omeprazole, cimetidine, etc.) within 30 days prior to screening;
7. Antibodies to HIV and hepatitis C, hepatitis B surface antigen, positive test for syphilis;
8. Unstable sleep architecture (e.g. night work, sleep disorders, insomnia, recently returned from another time zone, etc.), extreme physical activity (e.g. weight lifting);
9. Special diet (for example, vegetarian, vegan, low calorie (less than 1000 kcal/day));
10. Signs of alcohol abuse (intake of more than 10 units of alcohol per week) or 50 ml of hard alcohol; drinking alcohol within 4 days prior to screening;
11. Signs of drug abuse; taking narcotic and psychotropic drugs (opiates/morphine, methamphetamine, amphetamine, cannabinoids/marijuana, cocaine, methadone, ecstasy, tricyclic antidepressants, barbiturates) at the moment and in the history;
12. burdened past allergic history;
13. Hypersensitivity to the components of the investigated drugs;
14. Blood/plasma donation (from 450 ml blood or plasma) within 2 months prior to screening;
15. Participation in other clinical studies within 3 months prior to screening;
16. Acute infectious diseases within 4 weeks prior to screening;
17. Inability to read or write; unwillingness to understand and follow the procedures of the study protocol; noncompliance with the drugs administration or procedures schedule, which according to the researchers may affect the study results or the volunteer safety and prevent the further participation of the volunteer in the study; any other associated medical or serious mental conditions that make the volunteer inadequate for participation in the clinical study and restrict the validity of informed consent or may affect the volunteer's ability to participate in the study.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Sequential Assignment
• Masking: Double

Number of Arms

5

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: XC7 100 mg single; Cohort 1 - 4 subjects will be randomized in a 3:1 ratio to be treated either XC7 100 mg (3 subjects) or placebo (1 subject, see placebo single arm)	Drug: XC7 100 mg single; The volunteers will receive a single dose of the ID (1 capsule once, 100 mg)
Experimental: XC7 200 mg single; Cohort 2 - 4 subjects will be randomized in a 3:1 ratio to be treated either XC7 200 mg (3 subjects) or placebo (1 subject, see placebo single arm)	Drug: XC7 200 mg single; The volunteers will receive a single dose of the ID (2 capsules once, 100 mg each)
Placebo Comparator: Placebo single; Placebo comparator arm will consist of 2 subjects (1 subject from Сohorts 1 and 2)	Drug: Placebo single; The volunteers will receive a single dose of the ID (1 or 2 capsules once)
Experimental: XC7 200 mg multiple; Cohort 3 - 6 subjects will be randomized in a 6:2 ratio to be treated either XC7 200 mg (6 subjects) or placebo (1 subject, see placebo multiple arm)	Drug: XC7 200 mg multiple; The volunteers will receive multiple doses of the ID during 14 days (2 capsules daily, 100 mg each)
Placebo Comparator: Placebo multiple; Placebo comparator arm will consist of 2 subjects from cohort 3	Drug: Placebo multiple; The volunteers will receive multiple doses of the ID during 14 days (2 capsules daily)

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of Adverse events (AEs) per treatment arm	Adverse events will be classified according to CTCAE ver 4.03. Adverse events will be summarized descriptively by treatment arm. Verbatim terms will be mapped to preferred terms and organ systems using the current Medical Dictionary for Regulatory Activities version.	Day -7 (7 days before first dose) - Day 58

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Pharmacokinetics of XC7 by assessing AUC0-inf	Area under the curve "concentration of the drug-time" from the time of administration of the drug till infinity.	Day 1 - Day 4
Pharmacokinetics of XC7 by assessing Cmax	Maximum plasma concentration	Day 1 - Day 4
Pharmacokinetics of XC7 by assessing AUC0-t	Area under the curve "concentration of the drug-time" from the time of administration of the drug till the time (t) the last blood sampling	Day 1 - Day 4
Pharmacokinetics of XC7 by assessing Tmax	Time to maximum drug concentration in the blood plasma administration	Day 1 - Day 4
Pharmacokinetics of XC7 by assessing T1/2	Terminal elimination half-life	Day 1 - Day 4

Collaborators and Investigators

• Sponsor: NP Therapeutics

Study record dates

Study Major Dates

• Study Start (Actual): December 17, 2020
• Primary Completion (Actual): April 9, 2021
• Study Completion (Actual): April 9, 2021

Study Registration Dates

• First Submitted: December 18, 2020
• First Submitted That Met QC Criteria: December 21, 2020
• First Posted (Actual): December 22, 2020

Study Record Updates

• Last Update Posted (Actual): September 22, 2021
• Last Update Submitted That Met QC Criteria: September 21, 2021
• Last Verified: September 1, 2021

More Information

Terms related to this study

• Keywords: Coronavirus; Phase I
• Additional Relevant MeSH Terms: Coronavirus Infections; Coronaviridae Infections; Nidovirales Infections; RNA Virus Infections; Virus Diseases; Infections; Respiratory Tract Infections; Respiratory Tract Diseases; Pneumonia, Viral; Pneumonia; Lung Diseases; COVID-19
• Other Study ID Numbers: COVID-XC7-01

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No