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Recruiting Phase 1

PSTB100 Study in Healthy Adult Subjects

NCT07702279 · tracked via the Priya Life Science Australia tracker
Sponsor
Prospect Therapeutics (Nanjing) Limited
Phase
Phase 1
Started
2026-07-14
Last updated
2026-09-04

Condition(s) studied

Healthy Adult Subjects

Investigational drug(s) / intervention(s)

PSTB100 tabletsPSTB100 tablets

PSTB100 tablets: PSTB100 tablets

PSTB100 tablets: dose 1 once daily, dose 2 once daily, dose 3 once daily

Study summary

This study is a randomized, double-blind, placebo-controlled, dose-escalation, first-in-human clinical trial in healthy adults, designed to assess the safety, tolerability, and PK characteristics of PSTB100 tablets.

Eligibility

Sex
ALL
Min age
18 Years
Max age
55 Years
Healthy volunteers
Accepted
Inclusion Criteria: * 1.Healthy subjects aged 18-55 years (inclusive) at screening, with no gender restriction. Cohort 8 will enroll only male subjects aged 18-45 years (inclusive) at screening. * 2.Body Mass Index (BMI) of 18.0 to 32.0 kg/m² (inclusive), and 19.0 to 26.0 kg/m² (inclusive) for Cohort 8. * 3.Good health status confirmed by medical history, vital signs, physical examination, 12-lead ECG, laboratory tests (blood routine, biochemistry, coagulation function, urinalysis), etc., with no clinically significant abnormalities. * 4.Fully informed about the study, voluntary participation, and signed Informed Consent Form (ICF). * 5\. Women of childbearing potential who have no pregnancy plan from the screening period until 1 month after the end of the trial, and agree to use contraceptive methods as detailed further in the protocol (see Appendix 3) from signing the ICF until 30 days after last dose. * 6.Males who agree to use contraception as detailed further in the protocol (see Appendix 3) with partners of childbearing potential from signing ICF until 90 days after last dose. Exclusion Criteria: * 1.Females who are pregnant (positive or clinically abnormal pregnancy test result), lactating, or planning to become pregnant. * 2.Pulse rate ≤50 beats/min or \>100 beats/min at screening. * 3.Systolic blood pressure \<90 mmHg or ≥140 mmHg, or diastolic blood pressure \<60 mmHg or ≥90 mmHg at screening. * 4.History or current presence of clinically significant diseases or abnormalities in cardiovascular, respiratory, digestive, endocrine, metabolic, neurological, dermatological, ophthalmological, infectious, or psychiatric systems, including but not limited to history of eczema, no use of steroid creams for 3 months prior to screening; current or history of attention deficit hyperactivity disorder (ADHD), anxiety or depression (no use of antidepressants for at least 6 months prior to screening); Gilberts syndrome. Subjects with previous non-severe diseases or cured acute diseases may be enrolled if the assessor confirms no impact on the clinical trial. * 5.Use of tobacco, coffee, St. John's wort, grapefruit, grapefruit juice, cranberry juice, or strenuous exercise within 24 hours before enrollment. * 6.6.Suspected or confirmed allergy to any ingredient of the investigational product, or any known allergy history (however, subjects with mild allergies such as to pollen, cats or dust, which is fully resolved or without any treatment for more than 3 years can be enrolled). * 7.Previous surgery that may affect the clinical trial results (including but not limited to cholecystectomy, subtotal gastrectomy; excluding minor surgeries such as subcutaneous lipoma resection). 8.Use of any medication within 14 days before the study drug administration, including over-the-counter drugs and herbal medicines (except vitamins and calcium tablets), or dietary supplement within 7 days before the study drug administration. * 9.Blood loss or blood donation exceeding 400 mL within 30 days before screening (physiological blood loss excluded). * 10.Participation in any clinical trial of investigational drugs or medical devices within 3 months (or within 5 half-lives of investigational drugs, whichever is longer) before screening (excluding subjects who failed screening). * 11.History of alcohol abuse. Subjects who consumed more than 14 standard alcohol units weekly within the past year (1 standard unit ≈ 250 mL of 5% beer; 100 mL of 12.5% wine; 30 mL of 42% spirits) or who refuse to abstain from alcohol during the trial. * 12.History of smoking abuse (average ≥ 5 cigarettes daily within 1 month before screening) or refusal to abstain from smoking during the trial. * 13.History of drug abuse or positive urine drug screening result during screening (subjects with positive cotinine at screening \[D-28\~D-2\] will be not excluded if a negative cotinine is obtained on D-1). * 14.Breath alcohol test with positive result at screening. * 15.Clinically abnormal results of HBsAg, anti-HBcAb, anti-TP (if applicable), anti-HCV, anti-HIV, or QuantiFERON Gold. * 16.History of severe/serious bacterial infection, recurrent (\>3× per year) bacterial infections, or herpes simplex virus (HSV) infection. * 17.Subjects who received live vaccine within 4 weeks of screening, or plan to receive live vaccine during and up to 4 weeks after the last dose of investigational product. * 18.Subjects for Cohort 8 will be excluded if: * Experienced cold, infection, etc., within 4 weeks before screening. * Have contraindications or are unsuitable for lumbar puncture. * 19\. Any other situation that the researcher considers may bring safety risks to the subject, interfere with the study, or that the subject may not complete the study or comply with the requirements (due to management reasons, dysphagia, or other reasons).

Primary outcome measure(s)

  • Time to Reach Maximum Observed Plasma concentration (Tmax) — Part 1 : Pre- dose to 24 hours , 48 hours post dose, 72 hours post dose Part 2 : Pre- dose to 12 hours, and 24 hours post Day 1 dose to be collected within 15 minutes pre Day 2 dose
    PK characteristics after single dose
  • Maximum Observed PSTB100 Plasma Concentration (Cmax) — Part 1 : Pre- dose to 24 hours , 48 hours post dose, 72 hours post dose Part 2 : Pre- dose to 12 hours, and 24 hours post Day 1 dose to be collected within 15 minutes pre Day 2 dose
    PK characteristics after single dose
  • PSTB100 area under the plasma concentration-time curve (AUC0-24h, AUC0-t, AUC0-∞, etc.) — Part 1 : Pre- dose to 24 hours , 48 hours post dose, 72 hours post dose Part 2 : Pre- dose to 12 hours, and 24 hours post Day 1 dose to be collected within 15 minutes pre Day 2 dose
    PK characteristics after single dose
  • Plasma clearance (CL/F) — Part 1 : Pre- dose to 24 hours , 48 hours post dose, 72 hours post dose Part 2 : Pre- dose to 12 hours, and 24 hours post Day 1 dose to be collected within 15 minutes pre Day 2 dose
    PK characteristics after single dose
  • Plasma elimination half-life (T₁/₂) — Part 1 : Pre- dose to 24 hours , 48 hours post dose, 72 hours post dose Part 2 : Pre- dose to 12 hours, and 24 hours post Day 1 dose to be collected within 15 minutes pre Day 2 dose
    PK characteristics after single dose
  • Mean residence time (MRT) — Part 1 : Pre- dose to 24 hours , 48 hours post dose, 72 hours post dose Part 2 : Pre- dose to 12 hours, and 24 hours post Day 1 dose to be collected within 15 minutes pre Day 2 dose
    PK characteristics after single dose
  • Steady-state time to peak (Tmax,ss) — Pre- dose to 12 hours, 24 hours post day 1 dose, pre- day 4, pre- day 6, pre- day 7 to 24 hours post day 7 dose, 48 hours post day 7 dose.
    PK characteristics after multiple dose
  • Steady-state peak concentration (Cmax,ss) — Pre- dose to 12 hours, 24 hours post day 1 dose, pre- day 4, pre- day 6, pre- day 7 to 24 hours post day 7 dose, 48 hours post day 7 dose.
    PK characteristics after multiple dose
  • Steady-state trough concentration (Cmin,ss) — Pre- dose to 12 hours, 24 hours post day 1 dose, pre- day 4, pre- day 6, pre- day 7 to 24 hours post day 7 dose, 48 hours post day 7 dose.
    PK characteristics after multiple dose
  • Average steady-state plasma concentration (Cav,ss) — Pre- dose to 12 hours, 24 hours post day 1 dose, pre- day 4, pre- day 6, pre- day 7 to 24 hours post day 7 dose, 48 hours post day 7 dose.
    PK characteristics after multiple dose
  • Area under the steady-state plasma concentration-time curve (AUCss) — Pre- dose to 12 hours, 24 hours post day 1 dose, pre- day 4, pre- day 6, pre- day 7 to 24 hours post day 7 dose, 48 hours post day 7 dose.
    PK characteristics after multiple dose
  • Fluctuation factor (DF) between trough and peak concentrations; — Pre- dose to 12 hours, 24 hours post day 1 dose, pre- day 4, pre- day 6, pre- day 7 to 24 hours post day 7 dose, 48 hours post day 7 dose.
    PK characteristics after multiple dose
  • Accumulation ratios Rac:Cmax — Pre- dose to 12 hours, 24 hours post day 1 dose, pre- day 4, pre- day 6, pre- day 7 to 24 hours post day 7 dose, 48 hours post day 7 dose.
    PK characteristics after multiple dose
  • Accumulation ratios Rac:AUC. — Pre- dose to 12 hours, 24 hours post day 1 dose, pre- day 4, pre- day 6, pre- day 7 to 24 hours post day 7 dose, 48 hours post day 7 dose.
    PK characteristics after multiple dose

Trial sites (1)

FacilityCityRegionStatus
Nucleus Network Pty Ltd Brisbane Queensland Recruiting

More Prospect Therapeutics (Nanjing) Limited trials in Australia

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07702279 on ClinicalTrials.gov ↗ ← All trials in Australia