Study of Ascending Single Oral Dose of GT-002 in Healthy Volunteers

Safety and Tolerability Clinical Trial

— GAB-001  

Official title:

A Phase I, Randomised, Double-blind, Placebo-controlled Study in Healthy Male Volunteers to Investigate the Safety, Tolerability and Pharmacokinetics of Ascending Single Oral Doses of GT-002

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03817346
• Other study ID #: GAB-001
• Status: Completed
• Phase: Phase 1
• Start date: December 17, 2018
• Est. completion date: May 31, 2019

Study information

• Verified date: February 2020
• Source: Gabather AB
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study does not target any disease or condition in itself, but is evaluating the safety, tolerability and pharmacokinetics of single oral doses of GT-002 in the setting of healthy volunteers.

A longer-term objective is to apply the findings from this study to design and later conduct a clinical development programme of GT-002 as a medication to treat schizophrenia.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 32
• Est. completion date: May 31, 2019
• Est. primary completion date: March 31, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

1. Subject is willing and able to give written informed consent for participation in the study. Sufficient command of the Finnish language will be needed for informed consent and adequate communication with the study personnel.

2. Healthy male subjects from 18 up to 45 years of age.

3. Body mass index (BMI) from 18 kg/m2 up to 28 kg/m2.

4. Body weight from 60 kg up to 120 kg.

5. Clinically normal medical history, physical findings, vital signs, ECG and laboratory values as judged by the investigator at the time of the screening visit. A subject with a clinical abnormality or laboratory parameters outside of the reference range for the population being studied may be included at the investigator´s discretion provided the finding is unlikely to introduce additional risk factors, jeopardize study integrity, or to interfere with the study assessments or procedures.

6. Subjects must be willing to use condom or other contraceptive methods with a failure rate of < 1% and refrain from donating sperm from the date of dosing until one month after last dosing.

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Exclusion Criteria:

1. Current or history of any clinically significant disease or disorder which, in the opinion of the investigator, may either put the subject at risk because of participation in the study, or influence the results or the subject's ability to participate in the study

2. History of any type of cancer.

3. Subjects considered unlikely to comply with study procedures, restrictions and requirements

4. Any clinically significant illness, medical/surgical procedure or trauma within 4 weeks of the administration of investigational product that is likely to introduce additional risk factors, jeopardize study integrity, or to interfere with the study assessments or procedures

5. Any clinically significant abnormalities in clinical chemistry, haematology, coagulation or urinalysis results at the time of screening visit as judged by the investigator

6. Any positive result on screening for serum hepatitis B surface antigen, hepatitis C antibody or human immunodeficiency virus (HIV)

7. After 10 minutes of supine rest, abnormal vital signs defined as any of the following:

1. Systolic blood pressure > 140 mm Hg (average of two measurements)

2. Diastolic blood pressure > 90 mm Hg (average of two measurements)

3. Heart rate < 40 or > 85 beats per minute (average of two measurements)

4. Body temperature (auricular) =38oC

8. Prolonged QTcF interval (>450 ms), clinically significant cardiac arrhythmia or any other clinically significant abnormalities in the resting ECG as judged by the investigator

9. Intake of any medication, vitamin or mineral supplement product that could affect the outcome of the study, within 2 weeks prior to the first study treatment administration or less than 5 times the half-life of the medication. Possible prior use of enzyme inducing drugs will be considered case-by-case by the investigator.

10. Any blood donation/blood loss > 250 ml during the 3 months prior to screening

11. Has received another new chemical entity (defined as a compound which has not been approved for marketing) or has participated in any other clinical trial that included drug treatment within 3 months of the administration of investigational product in this study. Subjects consented and screened but not dosed in previous phase I studies can be included in this study.

12. Current or history of alcohol or drug abuse within the last 5 years, current excessive use of alcohol (current regular alcohol drinking of more than 24 units/week) or use of illicit drugs.

13. Positive screen for drugs of abuse at screening or on admission to the unit or positive breath test result for alcohol at screening or on admission to the unit prior to the administration of investigational product.

14. Known allergy to the components used in the formulation of GT-002.

15. Current smokers or users of nicotine products. Irregular use of nicotine (e.g. smoking, snuffing, and chewing tobacco) up to five doses per week is allowed before screening visit.

16. Intake of >5 cups of coffee/day or the corresponding amount of other caffeine containing beverages (e.g. energy drinks containing caffeine) during the study.

17. Subjects who have planned any scheduled invasive treatment or medical/surgical procedure during the study period.

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Related Conditions & MeSH terms

• Safety and Tolerability

Intervention

Drug:
• GT-002
Single ascending dose
• Placebo oral capsule
Comparator single ascending dose

Locations

Country	Name	City	State
Finland	CRST Oy, Clinical Research Services Turku	Turku

Sponsors (2)

Lead Sponsor	Collaborator
Gabather AB	Smerud Medical Research International AS

Country where clinical trial is conducted

Finland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Adverse Events (AEs)	To evaluate the safety and tolerability GT-002 in healthy subjects by assessing the number, severity and type of adverse events, including changes in vital signs, physical examinations, laboratory safety tests and ECGs	Day 1 to day 3
Secondary	Pharmacokinetic parameter AUCt	Area under the curve from the time of dosing until the last quantifiable concentration	Day1 to day 3
Secondary	Pharmacokinetic parameter AUC0-24	Area under the curve from the time of dosing until 24 hours post dosing	Day1 to day 2
Secondary	Pharmacokinetic parameter AUC0-infinity	Area under the curve from the time of dosing extrapolated to infinity	day 1 to day 3
Secondary	Pharmacokinetic parameter Cmax	Maximum concentration (Cmax)	Day 1 to day 3
Secondary	tmax	Time to maximum concentration	Day 1 to day 3
Secondary	t1/2	Apparent terminal elimination half-life	Day 1 to day 3