Single and Multiple Dose Safety, Tolerability, PK and Food Effect Study of HEC585 in Healthy Male and Female Subjects

NCT ID: NCT04512170

Last Updated: 2022-03-15

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 72 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-07-13
• Study Completion Date: 2021-08-23

Brief Summary

The Safety, Tolerability Pharmacokinetic and Food Effect Study of HEC585 in Healthy Male and Female Subjects

Conditions

Idiopathic Pulmonary Fibrosis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

A single dose HEC585（pilot trial arm）

Healthy subjects receive a single dose of HEC585

Group Type: EXPERIMENTAL

HEC585

Intervention Type: DRUG

single or Mulltiple doses up to 10 days

Single and Mulltiple doses HEC585（ Part 1, Cohort 1）

Healthy subjects receive Single and multiple doses of HEC585 or matching placebo

Group Type: EXPERIMENTAL

HEC585

Intervention Type: DRUG

single or Mulltiple doses up to 10 days

placebo

Intervention Type: DRUG

single or Mulltiple doses up to 10 days

Single and Mulltiple doses HEC585（ Part 1, Cohort 2）

Healthy subjects receive Single and multiple doses of HEC585 or matching placebo

Group Type: EXPERIMENTAL

HEC585

Intervention Type: DRUG

single or Mulltiple doses up to 10 days

placebo

Intervention Type: DRUG

single or Mulltiple doses up to 10 days

Single and Mulltiple doses HEC585（ Part 1, Cohort 3）

Healthy subjects receive Single and multiple doses of HEC585 or matching placebo

Group Type: EXPERIMENTAL

HEC585

Intervention Type: DRUG

single or Mulltiple doses up to 10 days

placebo

Intervention Type: DRUG

single or Mulltiple doses up to 10 days

Single dose of HEC585 （Part 2，Fed/Fasting）

Following an overnight fast of at least 10 hours, a single dose of HEC585 will be administered on 2 separate occasions (fasting and after meal) in a randomized crossover fashion with different food restrictions.

Group Type: EXPERIMENTAL

HEC585

Intervention Type: DRUG

single or Mulltiple doses up to 10 days

placebo

Intervention Type: DRUG

single or Mulltiple doses up to 10 days

two-period study at 400 mg dose group (part 3，Fed)

Healthy subjects receive Single/multiple doses of HEC585 or matching placebo in two cycles.

Group Type: EXPERIMENTAL

HEC585

Intervention Type: DRUG

single or Mulltiple doses up to 10 days

placebo

Intervention Type: DRUG

single or Mulltiple doses up to 10 days

Interventions

HEC585

single or Mulltiple doses up to 10 days

Intervention Type: DRUG

placebo

single or Mulltiple doses up to 10 days

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Subjects who are willing and are able to provide a written informed consent to participate in the study.

2. Without Plann for pregnancy or pregnant within 3 months after enrollment throughout the trial.

3. Subjects aged between 18 and 45 (both inclusive) years old.

4. Healthy volunteers has a body weight ≥50 kg (for male) or ≥ 45kg (for female) and body mass index ≥19 and ≤28 kg/m2 at screening.

5. Subjects, who are healthy, as having no clinically significant abnormalities in vital signs, physical examination, clinical laboratory test results, Chest X-ray and 12-lead electrocardiogram (ECG).

Exclusion Criteria

1. Subjects with a positive serology for human immunodeficiency virus (HIV) antibodies, hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibodies and/or TP antibodies at screening.

2. Subjects suffering from gastrointestinal diseases that can interfere with absorption or metabolism of drugs within 6 months before screening; and/or with history of central nervous system, cardiovascular system, digestive system, respiratory system, urinary system, blood system, immune system (such as thymus disease), reproductive system (such as prostate, testis, epididymis, ovarian disease); and/or thyroid disease or previous thyroid surgery, malignant tumor, metabolic disorder or others medical conditions (such as history of mental illness, etc.) that are not suitable for clinical trial participation.

3. Known allergic reactions or hypersensitivity to any excipient of the drug formulation(s)， anaphylaxis physique.

4. Use of any prescription or non-prescription medications within 14 days prior to initial dosing，Use of any medications known to inhibit or induce cytochrome P enzyme drug metabolism within 28 days prior to initial dosing.

5. Consume foods or beverages containing caffeine, xanthine, alcohol, and grapefruit within 48 hours prior to initial dosing.

6. Positive results from urine drug screen test.

7. History of alcoholism or drink regularly within 3 months prior to the study(defined as Alcohol consumption of > 21 units/week), or positive results from alcohol breath test.

8. Regular smoking of more than 10 cigarettes per day within 3 months before administration of study drug, or inability to refrain from smoking during the course of the study.

9. Donate blood or lose blood 400 mL or more within 1 month prior to initial dosing.

10. Subjects who plan to receive or have had organ transplants.

11. Females who are lactating/breastfeeding, or positive result from pregnancy test for women of child-bearing potential.

12. Subjects who participated in another clinical trial within 3 months prior to initial dosing.

13. Any other condition with in the opinion of the investigator would render the patient unsuitable for inclusion in the study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 45 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Sunshine Lake Pharma Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Shanghai Xuhui Central Hospital

Shanghai, , China

Countries

China

Other Identifiers

HEC585-P-02 / CRC-C1938

Identifier Type: -

Identifier Source: org_study_id