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CompletedNCT03441815Updated Feb 22, 2018

XC8 Safety, Tolerability and Pharmacokinetics in Healthy Volunteers

A Phase 1 interventional study of XC8 and Placebo in Asthma, sponsored by PHARMENTERPRISES LLC. Completed at 1 site in Russian Federation. Open to male participants aged 18 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2018-02-22.

Sponsored by PHARMENTERPRISES LLC · Phase 1, Interventional, and Treatment

Phase
Phase 1
Study type
Interventional
Enrollment
28
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
Male
01

Study summary

A double-blind, randomized, placebo-controlled, Phase I clinical study of the safety and tolerability of increasing doses of XC8 after single and repeated oral administration in healthy volunteers. The volunteers received the study drug once, and then continued daily intake for 14 days after a 6-day break.

The primary objective of the study was to evaluate the safety and tolerability profile for XC8 after single and multiple administration based on the frequency and severity of adverse events and changes in vital signs, laboratory results, electrocardiography and results of the physical examination.

The secondary objective of the study was to assess pharmacokinetics of XC8.

Read the detailed description

One Russian center was approved for participation in this study. One center was initiated. Healthy volunteers were enrolled in 1 center. The study consisted of 4 periods: screening, single administration, multiple administration and follow-up.

All eligible subjects were randomized into the study in appropriate cohort groups sequentially.

Cohort 1 - XC8 or Placebo 2 mg once and then daily 14 days after a 6-day break; Cohort 2 - XC8 or Placebo 10 mg once and then daily during 14 days after a 6-day break; Cohort 3 - XC8 or Placebo 50 mg once and then daily during 14 days after a 6-day break; Cohort 4 - XC8 or Placebo 200 mg once and then daily during 14 days after a 6-day break.

The decision regarding increasing of the study drug dose for a subsequent cohort was made by the Data Safety Monitoring Committee on the basis of preliminary safety results assessment.

A total of 20 volunteers received XC8 (2 mg, 10 mg, 50 mg or 200 mg) and a total of 8 volunteers received the placebo during the study participation. The follow-up period lasted for 4 weeks.

02

Conditions studied

  • Asthma

Keywords

  • Healthy volunteers
  • Phase I
  • Histamine glutarimide
  • PHARMENTERPRISES
03

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Inclusion criteria

  1. Non-smoking men aged 18 to 50 years (inclusive);
  2. Verified diagnosis "healthy" according to standard clinical, laboratory and instrumental methods of examination;
  3. Body mass index of 19 to 30 kg/m2 (inclusive);
  4. Consent to use reliable methods of contraception during the study and 3 months after its completion (condoms with spermicide);
  5. Signed patient information sheet and informed consent form for participation in the study.

Exclusion criteria

Exclusion Criteria:

  1. Hepatic disorder or renal disease; any other disease that, in the opinion investigator, may affect the results of the study, or may lead to the health aggravation during the study;
  2. Laboratory abnormalities at screening;
  3. Course intake of medicinal products (including herbs and biologically active additives) for preventive or curative purposes within 1 month prior to screening;
  4. Antibodies to HIV and hepatitis C virus, the presence of the hepatitis B surface antigen, a positive syphilis test;
  5. The presence of a sleep disorder (for example, night work, sleep disturbances, insomnia, recent return from another time zone, etc.);
  6. Signs of alcohol or drug abuse; taking alcohol or drugs during 4 days before screening;
  7. History of allergies (including medicines and food products);
  8. Symptomatic rhinitis in anamnesis during 2 years prior to screening (allergic rhinitis, non-allergic rhinitis or pollinosis);
  9. Blood donation / plasma, surgical intervention (in a hospital environment) during 12 weeks before screening;
  10. Participation in other clinical trials or taking the study drug during 3 months before screening;
  11. Impossibility to understand or follow protocol instructions;
  12. Smoking 3 months before screening;
  13. Lactase deficiency, lactose intolerance, glucose-galactose malabsorption;
  14. Acute infectious diseases less than 4 weeks before the start of the study.
04

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Sequential assignment
Masking
Double (Participant, Investigator)
Enrollment
28 participants (actual)

Study arms

  • Experimental
    XC8 2 mg

    Cohort 1: 6 subjects were randomized in a 2:1 ratio to be treated either with 2 mg XC8 (4 subjects) or placebo (2 subjects, see placebo arm).

    Drug: XC8

  • Experimental
    XC8 10 mg

    Cohort 2: 6 subjects were randomized in a 2:1 ratio to be treated either with 10 mg XC8 (4 subjects) or placebo (2 subjects, see placebo arm).

    Drug: XC8

  • Experimental
    XC8 50 mg

    Cohort 3: 6 subjects were randomized in a 2:1 ratio to be treated either with 50 mg XC8 (4 subjects) or placebo (2 subjects, see placebo arm).

    Drug: XC8

  • Experimental
    XC8 200 mg

    Cohort 4: 10 subjects were randomized in a 4:1 ratio to be treated either with 200 mg XC8 (8 subjects) or placebo (2 subjects, see placebo arm).

    Drug: XC8

  • Placebo comparator
    Placebo

    Placebo comparator arm consists of 8 subjects (2 subjects in each cohort).

    Drug: Placebo

Interventions

  • DrugXC8

    Also known as: Histamine glutarimide

  • DrugPlacebo
05

What researchers measure

Primary outcomes

  1. Number of Adverse events per treatment arm

    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. For each preferred term, frequency counts and percentages will be calculated by cohort.The nature, severity, seriousness, and relationship to study medication will be summarized for all study subjects

    Time frame: Change from pre-dose to Day 50

  2. Physical examination

    Physical examination results will be listed for following: general appearance, skin, head, eyes, ears, nose, throat, neck (including thyroid), lymph nodes, chest, heart, abdomen (including liver examination), extremities, and nervous system.

    Time frame: Day 1 till Day 36

  3. 12-lead ECG

    12-lead ECG results will be analyzed descriptively

    Time frame: Change from pre-dose till Day 36

Secondary outcomes

  1. Pharmacokinetics of XC8 by assessing AUC0-inf

    Area under the curve "concentration of the drug-time" from the time of administration of the drug till infinity

    Time frame: Day 1 and 21 (Pre dose, and 20 min, 40 min, 1, 2, 4, 6 and 10 hours post dose), Day 2 and Day 22 (24 hours ±10 minutes post dose), Day 3 (48 hours ±10 minutes post dose), Day 4 (72 hours ±10 minutes post dose), Day 8 to 12 and 15 (Pre dose)

  2. Pharmacokinetics of XC8 by assessing Cmax

    Maximum plasma concentration

    Time frame: Day 1 and 21 (Pre dose, and 20 min, 40 min, 1, 2, 4, 6 and 10 hours post dose), Day 2 and Day 22 (24 hours ±10 minutes post dose), Day 3 (48 hours ±10 minutes post dose), Day 4 (72 hours ±10 minutes post dose), Day 8 to 12 and 15 (Pre dose)

  3. Pharmacokinetics of XC8 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

    Time frame: Day 1 and 21 (Pre dose, and 20 min, 40 min, 1, 2, 4, 6 and 10 hours post dose), Day 2 and Day 22 (24 hours ±10 minutes post dose), Day 3 (48 hours ±10 minutes post dose), Day 4 (72 hours ±10 minutes post dose), Day 8 to 12 and 15 (Pre dose)

  4. Pharmacokinetics of XC8 by assessing Tmax

    Time to maximum drug concentration in the blood plasma administration

    Time frame: Day 1 and 21 (Pre dose, and 20 min, 40 min, 1, 2, 4, 6 and 10 hours post dose), Day 2 and Day 22 (24 hours ±10 minutes post dose), Day 3 (48 hours ±10 minutes post dose), Day 4 (72 hours ±10 minutes post dose), Day 8 to 12 and 15 (Pre dose)

  5. Pharmacokinetics of XC8 by assessing T1/2

    Terminal elimination half-life

    Time frame: Day 1 and 21 (Pre dose, and 20 min, 40 min, 1, 2, 4, 6 and 10 hours post dose), Day 2 and Day 22 (24 hours ±10 minutes post dose), Day 3 (48 hours ±10 minutes post dose), Day 4 (72 hours ±10 minutes post dose), Day 8 to 12 and 15 (Pre dose)

  6. Pharmacokinetics of XC8 by assessing kel

    Elimination rate constant

    Time frame: Day 1 and 21 (Pre dose, and 20 min, 40 min, 1, 2, 4, 6 and 10 hours post dose), Day 2 and Day 22 (24 hours ±10 minutes post dose), Day 3 (48 hours ±10 minutes post dose), Day 4 (72 hours ±10 minutes post dose), Day 8 to 12 and 15 (Pre dose)

  7. Pharmacokinetics of XC8 by assessing Cav

    Average concentration over one dosing interval

    Time frame: Day 8 to 12 and 15 (Pre dose); Day 21 (Pre dose, and 20 min, 40 min, 1, 2, 4, 6 and 10 hours post dose), Day 22 (24 hours ±10 minutes post dose

06

Study locations

1 site
  • SBEI HPE The First Moscow State Medical University n.a. Sechenov of Ministry of Health of Russian Federation, University Hospital #2, Department of Development of New Medicines
    Moscow, 119435, Russian Federation
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT03441815
Lead sponsor
PHARMENTERPRISES LLC
Responsible party
Sponsor
First posted
Feb 22, 2018
Start date
Feb 14, 2015
Primary completion
Jul 7, 2015
Completion
Jul 7, 2015
Last update
Feb 22, 2018

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
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