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

NP Therapeutics

Status and phase: Completed; Phase 1

Conditions: Healthy Volunteers; Covid19

Treatments: Drug: XC7 200 mg single; Drug: Placebo single; Drug: Placebo multiple; Drug: XC7 200 mg multiple; Drug: XC7 100 mg single

Study type: Interventional

Funder types: Other

Identifiers

NCT04679493

COVID-XC7-01

Details and patient eligibility

About

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).

Full 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.

Enrollment: 16 patients

Sex: Male

Ages: 18 to 45 years old

Volunteers: Accepts Healthy Volunteers

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.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Sequential Assignment

Masking: Double Blind

---

16 participants in 5 patient groups, including a placebo group

XC7 100 mg single

Experimental group

Description:

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)

Treatment:

Drug: XC7 100 mg single

XC7 200 mg single

Experimental group

Description:

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)

Treatment:

Drug: XC7 200 mg single

Placebo single

Placebo Comparator group

Description:

Placebo comparator arm will consist of 2 subjects (1 subject from Сohorts 1 and 2)

Treatment:

Drug: Placebo single

XC7 200 mg multiple

Experimental group

Description:

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)

Treatment:

Drug: XC7 200 mg multiple

Placebo multiple

Placebo Comparator group

Description:

Placebo comparator arm will consist of 2 subjects from cohort 3

Treatment:

Drug: Placebo multiple