Tolerability and Pharmacokinetics of Hypidone Hydrochloride in Healthy Subjects

Major Depressive Disorder Clinical Trial

Official title:

A Multiple-Dose Study to Evaluate the Tolerability and Pharmacokinetics of Hypidone Hydrochloride Tablets in Chinese Healthy Subjects

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04598607
• Other study ID #: HYP104-CTP
• Secondary ID: 2017ZX09309012
• Status: Completed
• Phase: Phase 1
• Start date: October 30, 2020
• Est. completion date: January 15, 2021

Study information

• Verified date: August 2021
• Source: Zhejiang Huahai Pharmaceutical Co., Ltd.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will investigate the tolerability and pharmacokinetics of Hypidone Hydrochloride by multiple doses in 36 healthy male and female subjects who are of 18 to 55 years old.

Description:

This is a double-blind, placebo-controlled, randomized, multiple-dose, single center study. 36 male and female healthy subjects will be enrolled in this study. Within 14 days prior to study drug administration, subjects will be screened based on the inclusion and exclusion criteria. The study will be performed in 3 groups of 12 subjects each. In each group of 12 subjects, 10 subjects will be randomly assigned to receive Hypidone Hydrochloride and 2 subjects to receive matching placebo.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 36
• Est. completion date: January 15, 2021
• Est. primary completion date: January 11, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

1. Chinese healthy subjects, male to female ratio is 1:1;

2. 18 = age =55;

3. Female body weight is not less than 45kg, male body weight is not less than 50kg, BMI is between 18.5~28.0 kg/m2 (including upper and lower limits);

4. Understand and sign informed consent, and participate in clinical trials voluntarily.

Exclusion Criteria:

1. Those who have a history of major diseases such as cardiovascular system, respiratory system, liver, kidney, endocrine system, digestive system, blood and lymphatic system, immune system, nervous system, skeletal system and psychiatry, and who are judged unfit to participate in this study;

2. Any condition or condition that may significantly affect drug absorption, distribution, metabolism, and excretion, such as a history of gastrointestinal surgery (gastrectomy, gastroenterostomy, enterectomy, etc.);

3. General physical examination, vital signs and other abnormalities judged by clinicians as clinically significant;

4. resting pulse rate <55 times/min or >100 times/min;Sitting systolic pressure <90mmHg or >140mmHg, diastolic pressure <60mmHg or >90mmHg;

5. The laboratory examination indicates that the subject has abnormalities that the researcher has determined to be clinically significant;

6. ALT or Cr and BUN exceeding the upper limit of normal value;Urine protein test results "++" or above;

7. Serum virology test (HBs antigen, HCV antibody, syphilis serum reaction (Trust test) and HIV antibody test) with positive results;

8. Abnormal electrocardiogram (ECG) at screening stage is of clinical significance, such as QTc interval =450ms in men and QTc interval =470ms in women, and the researchers think it is not suitable to be included;

9. patients who had taken any prescription drugs, non-prescription drugs, Chinese herbs, vitamins and other dietary supplements in the two weeks prior to enrollment, and the researchers believe that this situation may affect the evaluation results of this study.

10. Those who have taken food or drink (such as grapefruit) containing enzymes that can induce or inhibit liver metabolism within 1 week before starting the administration of the test;

11. A history of severe allergy or has a history of allergy to two or more foods or drugs;

12. Subjects with a history of smoking 2 weeks before the screening period or subject with positive urine cotinine test during the admission review period;

13. A history of alcohol abuse and consume an average of more than 14 units of alcohol per week (1 unit =285ml beer or 25ml spirits or 150ml wine), or during the study subjects were unable to avoid alcohol consumption within 24 hours before and during the study period or alcohol breath test positive;

14. A history of drug abuse or drug abuse, or those with positive urine drug screening;

15. Pregnant or lactating women;

16. The subject or his/her spouse has a family planning plan within the next 6 months of the last use of the drug, and is unable to use the contraceptive method approved by the Study during the study period as directed by the investigator;

17. Those who had donated blood or lost blood =400mL in the 3 months before screening, and those who had donated blood =200mL in the 1 month before screening or had a history of component donation;

18. it is impossible to avoid using caffeinated drinks, strenuous exercise, or other factors affecting drug absorption, distribution, metabolism, and excretion within 24 hours before and during the trial;

19. Subjects who have participated in or are participating in other experimental drugs or unlisted drug trials within 3 months prior to screening;

20. Persons directly related to this clinical trial;

21. Subjects who, in the opinion of the investigator, have other factors that are not appropriate to participate in this study.

Related Conditions & MeSH terms

• Depressive Disorder
• Depressive Disorder, Major
• Major Depressive Disorder

Intervention

Drug:
• Hypidone Hydrochloride tablets
30mg(10mg×3), 40mg(10mg×4) or 50mg(10mg×5) Hypidone Hydrochloride tablets will be given orally once on day 1, day 9 and twice a day on day 3~8.
• Placebo
3, 4 or 5 tablets of placebo will be given orally once on day 1, day 9 and twice a day on day 3~8.

Locations

Country	Name	City	State
China	Shanghai Mental Health Center	Shanghai	Shanghai

Sponsors (1)

Lead Sponsor	Collaborator
Zhejiang Huahai Pharmaceutical Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Cmax	Peak Plasma Concentration	Day 1-11
Primary	Tmax	Time to Peak Plasma Concentration	Day 1-11
Primary	AUC	Area under the plasma concentration versus time curve	Day 1-11
Primary	T1/2	half-life	Day 1-11
Secondary	Percentage of subjects with treatment-emergent adverse events(TEAE)	Clinical significant Abnormal of Laboratory valuse, physical examination results, vital signs and ECG results will be recorded as TEAE.	Up to Day 15
Secondary	Percentage of subjects with abnormal Laboratory values	Laboratory tests including Hematology, Biochemistry and Urinalysis.	Up to Day 15
Secondary	Percentage of subjects with abnormal Physical examinations results	Physical examinations including Head and face, skin system, lymph nodes, eyes, ear, nose and throat, mouth, respiratory system, abdomen, cardiovascular system, musculoskeletal and nervous system.	Up to Day 15
Secondary	Percentage of subjects with abnormal Vital signs results	Vital signs including sitting blood pressure, pulse rate and ear temperature.	Up to Day 15
Secondary	Percentage of subjects with abnormal ECG(12-lead Electrocardiogram) results	ECG tests including heart rates, PR interval, QT interval, corrected QT interval.	Up to Day 15