A Study to Evaluate the Effect of a Single Oral Dose of ZX-7101A on the QTc Interval in Healthy Subjects

Influenza, Human Clinical Trial

— QTc-ZX-7101A  

Official title:

A Study to Evaluate the Effect of a Single Oral Dose of ZX-7101A on the QTc Interval in Healthy Subjects

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT05955027
• Other study ID #: ZX-7101A-206
• Status: Not yet recruiting
• Phase: Phase 1
• Start date: August 15, 2023
• Est. completion date: May 7, 2024

Study information

• Verified date: June 2023
• Source: Nanjing Zenshine Pharmaceuticals
• Contact: Zhang Jing, Doctor
• Phone: 52887926
• Email: Zhangj_fudan[@]163.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the effect of a single oral dose of ZX-7101A on the QTc interval in healthy subjects.

Description:

Day 1, Oral fasting administration of ZX-7101A tablets 80mg, 160mg and placebo, 6 visit periods were set from days 2 to 15(Day2, Day3, Day5, Day7, Day10, Day15)

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 24
• Est. completion date: May 7, 2024
• Est. primary completion date: March 7, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

• Healthy male or female subjects, 18-45 years of age, inclusive, at the time of signing the ICF.

• Weight: Male weight =50 kg, female weight =45 kg, BMI between 19.0 and 28.0 kg/m2 (including cut-off value), BMI= weight (kg)/height 2 (m2).

• The investigator judged the subjects to be in good overall health based on their medical history, physical examination, vital signs, 12-lead electrocardiogram, laboratory tests (routine blood work, urine work, blood biochemistry, coagulation function), viral serology, and chest X-ray results (normal or abnormal test results have no clinical significance).

• Female subjects of childbearing potential and male subjects with a partner of childbearing potential who voluntarily signed ICF should be no fertile, sperm/egg donation for 6 months (female) or 90 days (male) from the beginning to the last dose, and voluntary use highly effective contraception (including partner) (non-drug contraception is required during the trial).

• Fully understand the trial content and possible adverse reactions, have the ability to communicate with researchers normally, while complying with study requirements, follow protocol procedures and restrictions, and be able to visit on time.

Exclusion Criteria:

• Subjects with a prior or present history of clinically abnormal metabolic, liver, kidney, hematological, pulmonary, cardiovascular, gastrointestinal, urinary, endocrine, neurological, or psychiatric disease who were judged by the investigator to be unsuitable for participation in this study.

• Subjects with digestive tract disease or any condition that may affect drug absorption, such as a history of liver and gallbladder disease, gastrointestinal disease, gastrointestinal surgery (except appendectomy) or a history of chronic pancreatitis, idiopathic acute pancreatitis, or habitual diarrhea.

• Subjects with electrolyte metabolism disorders such as hyperkalemia, hypokalemia, hypermagnesia, hypomagnesia, hypercalcemia or hypocalcemia.

• Subjects who have a history of other risk factors for tachycardia, or a family history of a first-degree relative (i.e. biological parent, sibling, or child) of short QT syndrome, long QT syndrome, or sudden unexplained death in young age (=40 years).

• Allergic constitutions (such as allergies to two or more drugs, foods, and pollen), or determined by the investigator, may be allergic to the investigational product or any component of the investigational product.

• Subjects who have got acute respiratory infections within 2 weeks before screening; Or have a history of fungal infection.

• For patients with abnormal vital signs (blood pressure, pulse rate, ear temperature) and clinically significant results, the abnormal values of each vital sign are: Body temperature (ear temperature) >37.5 ?; Systolic blood pressure (recumbent) <90 mmHg or =140 mmHg;Diastolic blood pressure (lying) <50 mmHg or =90 mmHg; Pulse rate (lying position) <50 beats/min or >100 beats/min.

• QTcF interval > 450ms or < 300 ms (Fridericia's correction), or QRS>120ms.

• Subjects who have abnormal liver function: alanyl aminotransferase (ALT) or aspartate aminotransferase (AST) higher than the upper limit of normal or serum total bilirubin (TBIL) greater than 1.5 times the upper limit of normal, who judged clinical significance by investigators.

• Subjects estimate glomerular filtration rate <90 mL/min/1.73 m2.

• Subjects virus serological test (hepatitis B virus surface antigen, hepatitis C virus antibody, human immunodeficiency virus antibody, treponema pallidum specific antibody TPPA) positive results.

• Subjects with a history of drug abuse (morphine, dimethylene dioxyamphetamine, methamphetamine, THC, ketamine, cocaine) or who screened positive for drug abuse.

• Women who are pregnant or breastfeeding, or who test positive for blood pregnancy.

• Subjects who have used any P-gp or CYP inducer or inhibitor within 30 days before screening, or any prescription or Chinese herbal medicine within 4 weeks before the start of the trial, or over-the-counter or health care products (including polyvalent cations and metal supplements, etc.) within 2 weeks before the start of the trial; It should have a longer time interval if the elimination half-life is longer-at least 5 elimination half-lives for the drug.

• Subjects who consumed more than 14 units of alcohol per week in the 6 months prior before screening (1 unit of alcohol =360mL beer or 45mL spirits with 40% alcohol or 150mL wine) or had a positive alcohol breath test or could not abstain during the trial.

• Subjects who smoked more than 5 cigarettes per day in the 3 months prior before screening or habitually used nicotine-containing products or could not give up during the trial.

Related Conditions & MeSH terms

• Influenza, Human

Intervention

Drug:
• ZX-7101A
a drug to treat influenza, oral
• Placebo
placebo control, oral

Locations

Country	Name	City	State
China	Huashan Hospital affiliated to Fudan University	Shanghai	Shanghai

Sponsors (1)

Lead Sponsor	Collaborator
Nanjing Zenshine Pharmaceuticals

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	??QTc -Placebo-corrected, baseline-adjusted QTc interval (??QTc)	Placebo-corrected, baseline-adjusted QTc interval (??QTc) at designed time after single oral administration of ZX-7101A tablets 80mg and 160mg in healthy Chinese adults. ??QTc:The change of QTc interval from baseline value (?QTc) at each time point after administration was calculated, and then the difference of ?QTc between the experimental group and the placebo group at each time point was calculated(??QTc).	Day1, Day2, Day3, Day5, Day7, Day10, Day15
Secondary	T wave	T-wave morphology,or absence	Day1, Day2, Day3, Day5, Day7, Day10, Day15
Secondary	PK parameters	Cmax of prodrug ZX-7101A and active metabolite ZX-7101 (mother drug)	Day1, Day2, Day3, Day5, Day7, Day10, Day15
Secondary	TEAE	Rate of Treatment-Emergent Adverse Events(TEAE)	Day1, Day2, Day3, Day5, Day7, Day10, Day15
Secondary	U wave	U-wave presence and absence	Day1, Day2, Day3, Day5, Day7, Day10, Day15
Secondary	PK parameters	AUC0-t of prodrug ZX-7101A and active metabolite ZX-7101 (mother drug)	Day1, Day2, Day3, Day5, Day7, Day10, Day15
Secondary	PK parameters	AUCinf of prodrug ZX-7101A and active metabolite ZX-7101 (mother drug)	Day1, Day2, Day3, Day5, Day7, Day10, Day15
Secondary	PK parameters	Tmax of prodrug ZX-7101A and active metabolite ZX-7101 (mother drug)	Day1, Day2, Day3, Day5, Day7, Day10, Day15