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Clinical Trials/NCT05851261
NCT05851261
Completed
Phase 1

Phase I Clinical Study to Evaluate the Safety, Tolerance, Pharmacokinetics Characteristics of Single and Multiple Administration of Oral PA3670 Tablets in Chinese Healthy Subjects and the Effect of Food on Pharmacokinetics

Zhejiang Palo Alto Pharmaceuticals, Inc.1 site in 1 country60 target enrollmentApril 13, 2023
InterventionsPA3670
DrugsPA3670

Overview

Phase
Phase 1
Intervention
PA3670
Conditions
Chronic HBV Infection
Sponsor
Zhejiang Palo Alto Pharmaceuticals, Inc.
Enrollment
60
Locations
1
Primary Endpoint
Number of subjects experiencing adverse events (AEs)
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The primary objectives of this study are to evaluate the safety and tolerance of single and multiple oral administration of PA3670 tablets in Chinese adult healthy subjects and the effect of food on pharmacokinetics of PA3670 tablets in Chinese adult healthy subjects.

Detailed Description

Stage I: Single dose, Single Ascending Dose (SAD) This is a randomized, double-blind, placebo-controlled, dose-escalation clinical trial. The objective is to evaluate the safety, tolerability and pharmacokinetics characteristics of PA3670 tablets in Chinese healthy subjects. There are three dose groups of PA3670(5 mg、15 mg、30 mg) proposed to be tested sequentially in this study. A total of 30 healthy subjects are planned to be enrolled in this study and will be randomly assigned to the corresponding dose group in equal proportion, stratified by gender (male vs female). 10 subjects in each dose group are randomly assigned in a ratio of 4:1 to receive PA3670 tablets or placebo. All subjects will be dosed in a single dose, and the dose-related safety, tolerability and PK of PA3670 will be evaluated. Stage Ⅱ: Multiple dose This is a randomized, double-blind, placebo-controlled, multiple dose clinical trial. A total of 10 subjects are planned to be enrolled in this study and will be randomly assigned in a ratio of 4:1 to receive 15mg PA3670 tablets or placebo. All subjects will be dosed for 9 consecutive days, and safety, tolerability and PK of PA3670 will be evaluated. Stage Ⅲ: Study on the effect of food on Pharmacokinetics This is a randomized, open, two group crossover clinical trial. A total of 20 subjects are planned to be enrolled in this study, and will be randomly assigned to a dosing order (i.e. fasting administration followed by high-fat meal administration, or high-fat meal administration followed by fasting administration) in a ratio of 1:1. Subjects will be dosed 15 mg PA3670 tablets in a single dose, and the food-related PK of PA1010 will be evaluated.

Registry
clinicaltrials.gov
Start Date
April 13, 2023
End Date
December 19, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Sponsor
Zhejiang Palo Alto Pharmaceuticals, Inc.
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Healthy male and female subjects aged from 18 to 65 (inclusive);
  • Male weight ≥ 50 kg, female weight ≥ 45 kg, and body mass index (BMI) between 19 and 28 kg/m2 (including the critical value);
  • Be able to complete the test according to the study protocol;
  • Voluntary participation and signing of informed consent.

Exclusion Criteria

  • There are any medical conditions that the investigator thinks may increase the risk of the subject participating in the study (especially the history of esophageal or gastrointestinal ulcer), may interfere with drug absorption, distribution, metabolism or excretion, or may weaken the compliance of the study protocol;
  • Allergic to the study drug or any component of the study drug, or allergic (refers to allergic to 2 or more kinds of food, drugs or environmental substances);
  • The vital signs, physical examination, laboratory examination (blood routine test, blood biochemistry, urine routine test, blood coagulation function, etc.), chest X-ray examination, abdominal B-ultrasound (liver, gallbladder, pancreas, spleen, kidney), 12 lead ECG, etc. in the screening period were judged abnormal and had clinical significance;
  • Those who are positive for hepatitis B surface antigen, hepatitis C virus antibody, treponema pallidum antibody and HIV antibody;
  • Those who regularly drank alcohol within 3 months before screening, i.e., those who drank more than 14 units of alcohol every week (1 unit=360 mL of beer with 5% alcohol content, 45 mL of spirits with 40% alcohol content, or 150 mL of wine with 12% alcohol content), or those who had positive alcohol breath test in the baseline period or could not stop drinking alcohol during the study period;
  • Those who smoke ≥ 5 cigarettes a day within 3 months before screening, those who are positive for nicotine test in the baseline period, or those who cannot stop using any tobacco products during the test period;
  • Those who have a history of drug abuse and drug abuse in the past two years, or who are positive for urine screening of drug abuse at baseline (including morphine, methamphetamine, ketamine, benzodiazepine, cocaine, tetrahydrocannabinol acid);
  • Those who have used any drugs (prescription drugs, over-the-counter drugs, Chinese herbal medicine, vaccines) or health products within 4 weeks before screening and during screening;
  • Those who take any food or drink rich in caffeine and xanthine (coffee, tea, cola, chocolate, seafood, animal liver, etc.) within 48 hours before the first use of the study drug, or do not agree to stop eating the above diet during the test period;
  • Female subjects had unprotected sex in the past two weeks; Male subjects (or their partners) or female subjects who have fertility plans or donated sperm and eggs during the whole test period and within 3 months after administration, and who are unwilling to take one or more physical contraceptive measures or are breastfeeding during the test period;

Arms & Interventions

PA3670 5 mg

Ten subjects will be randomly assigned in a ratio of 4:1 to receive 5 mg of PA3670 tablets or PA3670 placebo tablets. They will be administered a single dose and observed for four days.

Intervention: PA3670

PA3670 15 mg

Ten subjects will be randomly assigned in a ratio of 4:1 to receive 15 mg of PA3670 tablets or PA3670 placebo tablets. They will be administered a single dose and observed for four days.

Intervention: PA3670

PA3670 30 mg

Ten subjects will be randomly assigned in a ratio of 4:1 to receive 30 mg of PA3670 tablets or PA3670 placebo tablets. They will be administered a single dose and observed for four days.

Intervention: PA3670

PA3670 15 mg for 9days

Ten subjects will be randomly assigned at a 4: 1 ratio to receive either 15mg of PA3670 tablets or PA3670 placebo tablets, once daily for 9 days.

Intervention: PA3670

PA3670 15mg before and after meals

Ten subjects will be administered 15mg PA3670 after overnight fasting for 10 hours in the first cycle, and then will be administered 10mg PA3670 within 30 minutes after high-fat meal in the second cycle. They will receive a single dose in each cycle and will be observed for four days. The cleaning period between the two cycles is more than 7 days.

Intervention: PA3670

PA3670 15mg after and before meals

Ten subjects will be administered 15mg PA3670 within 30 minutes after the high-fat meal in the first cycle, and then will be administered 10mg PA3670 after overnight fasting 10 hours in the second cycle. They will receive a single dose in each cycle and will be observed for four days. The cleaning period between the two cycles is more than 7 days.

Intervention: PA3670

Outcomes

Primary Outcomes

Number of subjects experiencing adverse events (AEs)

Time Frame: 7 days or 15 days

An adverse event (AE) is defined as any untoward medical occurrence in a clinical study subject administered a medicinal product which does not necessarily have a causal relationship with this treatment.

Body temperature

Time Frame: Up to 72 hours after last dose

Vital sign-body temperature

Pulse rate

Time Frame: Up to 72 hours after last dose

Vital sign-Pulse rate

Breathing rate

Time Frame: Up to 72 hours after last dose

Vital sign-Breathing rate

Systolic and diastolic blood pressure

Time Frame: Up to 72 hours after last dose

Vital sign-Systolic and diastolic blood pressure

Number of subjects having abnormal hematology laboratory parameters

Time Frame: Up to 72 hours after last dose

Absolute and relative number of subjects with values below, within or above the normal range will be assessed.

Number of subjects with abnormal clinical chemistry parameters

Time Frame: Up to 72 hours after last dose

Absolute and relative number of subjects with values below, within or above the normal range will be assessed.

Number of subjects with abnormal values for urinalysis

Time Frame: Up to 72 hours after last dose

Absolute and relative number of subjects with values below, within or above the normal range will be assessed.

Number of subjects with abnormal with blood coagulation function

Time Frame: Up to 72 hours after last dose

Absolute and relative number of subjects with values below, within or above the normal range will be assessed.

ECG parameter-QTc interval

Time Frame: Up to 72 hours after last dose

A 12-lead electrocardiogram (ECG) will be recorded using an ECG machine that automatically measures QTc interval

ECG parameter-PR interval

Time Frame: Up to 72 hours after last dose

A 12-lead electrocardiogram (ECG) will be recorded using an ECG machine that automatically measures PR interval.

ECG parameter-QRS duration

Time Frame: Up to 72 hours after last dose

A 12-lead electrocardiogram (ECG) will be recorded using an ECG machine that automatically measures QRS duration

Secondary Outcomes

  • Pharmacokinetics of PA3670-Cmax(4 days or 12 days)
  • Pharmacokinetics of PA3670-Tmax(4 days or 12 days)
  • Pharmacokinetics of single dose of PA3670-AUC(4 days or 12 days)

Study Sites (1)

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