A Trial of HRS-7450 in Chinese Healthy Volunteers

Launched by FUJIAN SHENGDI PHARMACEUTICAL CO., LTD. · Oct 13, 2023

Keywords

ClinConnect Summary

This clinical trial is studying a new medication called HRS-7450 to see how safe it is for healthy people. The researchers want to find out how well the drug is tolerated when given in increasing doses compared to a placebo (a pill with no active ingredients). This is the first time this drug will be tested in humans, and it is focused on healthy volunteers between the ages of 18 and 45 who meet certain health criteria.

To join the trial, participants must be in good health, with specific weight and body mass index (BMI) requirements, and must agree to use effective birth control during the study. People with certain health issues, allergies, or who have taken other medications recently may not be eligible. If someone decides to participate, they will need to provide written consent and will be closely monitored for their safety throughout the study. Since the trial is not yet recruiting, interested individuals will need to wait until it begins to learn more about taking part.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. Healthy male and female subjects between 18 and 45 years of age (inclusive) at the screening visit
• • 2. Female weighed ≥ 45 kg, male weighed ≥ 50 kg, and all weighed ≤ was 90 kg, and a BMI between 18-28 kg/m²(inclusive)
• • 3. Subjects with fertility promised to have no fertility, sperm or egg donation plan and voluntarily take efficient contraceptive measures ( including partners ) within two weeks before screening and 6 months after the last administration
• • 4. Able to provide written, informed consent prior to initiation of any trial-related procedures, and able, in the opinion of the Principal Investigator, to comply with all the requirements of the trial
• Exclusion Criteria:
• • 1. Subjects with a history of drug allergy, or a history of allergy ( asthma, urticaria, eczema, etc. ), or allergic constitution ( such as allergies to two or more drugs, food, and pollen ) or intolerance to any ingredients of the study drug
• • 2. Subjects with heart, respiration, endocrine, metabolism, kidney, liver, gastrointestinal tract, skin, infection, malignant tumor, blood, nervous system disease or mental illness, metabolic dysfunction prior to screening or administration
• • 3. The results of physical examination, vital sign examination, laboratory examination, etc. during the screening are deemed clinically significant
• • 4. Subjects with risk factors for torsades de pointes ventricular tachycardia, or had a family history of short QT syndrome, long QT syndrome, unexplained sudden death in youth ( ≤ 40 years old ), drowning or sudden infant death syndrome in first-degree relatives ( i.e., biological parents, siblings or children )
• • 5. Subjects with hyperkalemia, hypokalemia, hypermagnesemia, hypomagnesemia, hypercalcemia or hypocalcemia are deemed clinically significant
• • 6. ECG examination is clinical significant, such as QTcF \> 470ms
• • 7. Subjects with gastrointestinal, urinary and other bleeding tendencies or other high-risk bleeding tendencies within 3 weeks before screening; or those who have arterial puncture within the past 1 week that does not easily compress the hemostatic site were included
• • 8. ALT, AST, total bilirubin, direct bilirubin and indirect bilirubin exceeded the upper limit of normal value during screening visit
• • 9. Positive test for human immunodeficiency virus (HIV-1 and HIV-2), hepatitis B surface antigen (HBsAg), anti-hepatitis C virus (anti-HCV) or syphilis at the Screening Visit.
• • 10. Subjects who underwent surgery within 3 months before screening or schedule to have surgery during the trial, or those who have previously had surgery that may affect the PK profile or safety evaluation significantly of the study drug
• • 11. Subjects who received any IMP within 3 months before the screening visit or planned to participate in other clinical trials during the trial
• • 12. Received any drug that inhibits or induces liver metabolism of the drug within 1 month prior to screening visit
• • 13. Received any prescription drugs (including vaccines) or non-prescription medications, and herbal supplements within 2 weeks prior to screening visit
• • 14. Blood donation or blood loss≥200 mL within 3 month before screening, or schedule to donate blood during the trial or within 1 month after the end of the trial.
• • 15. Had taken a special diet (including dragon fruit, mango, grapefruit, and/or xanthine diet, chocolate) and/or consumed excessive amounts of tea, coffee, grapefruit/grapefruit juice, and/or caffeinated beverages (averaging more than 8 cups per day of 200 ml each) in the 2 weeks prior to screening visit
• • 16. History of alcohol abuse \[more than 14 units of alcohol intake in one week (1 unit of alcohol equivalent to 285 mL of beer, 25 mL of spirits, or 100ml of wine), more than twice a week\]
• • 17. More than 10 cigarettes( or equivalent tobacco)per day in the 3 months prior to screening or unable to quit smoking during the trial period
• • 18. Positive urine drug test at the Screening Visit History of drug abuse within the past 5 years
• • 19. Pregnant or lactating women, or pregnancy test positive
• • 20. Can not tolerate venipuncture or have a history of needle sickness and blood
• • 21. Subjects with history of phlebitis
• • 22. In the opinion of the Investigator, subjects should be excluded in this trial