Study of Pharmacokinetics and Metabolism on [(14)C]ADC189

AnDiCon Biotech

Status and phase

Completed

Phase 1

Conditions

Metabolism

Pharmacokinetics

Treatments

Drug: [(14)C]ADC189

Study type

Interventional

Funder types

Industry

Identifiers

NCT06360796

2023-ADC189-I-010

Details and patient eligibility

About

This study is designed to determined the metabolism, excretion, and substance balance of almonertinib of ADC189. The pharmacokinetic characteristics and safety profile of ADC189 was investigated following a single oral dose (45 mg/100 µCi) in healthy Chinese male participants.

Full description

This study adopted a single-center, open, non-randomized, single-dose design. Six to eight healthy Chinese male subjects were planned to be enrolled, and the final aim is to collect all required samples and data from at least 6 subjects.

After each subject take a single oral dose of 45 mg (about 100 μCi) [14C]ADC189 on Day 1, whole blood, plasma, urine and feces samples were collected at specified time points during the study. The total radioactivity was measured to calculate the ratio of total radioactivity of whole blood to total radioactivity of plasma, pharmacokinetic parameters, recovery rate and excretion pathway data of total radioactivity in whole blood and plasma. Meanwhile, the radioactive metabolite spectrum and structural identification of main metabolites in plasma, urine and feces were performed to obtain the pathway and characteristics of main metabolic elimination of ADC189 in human body, as well as circulating metabolites ≥10% of total radioactivity exposure in plasma.

Enrollment

6 patients

Sex

Male

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

1. healthy Chinese male subjects within 18 to 45 years old inclusive;
1. body weight over 50 Kg, and within a BMI range of 19.0 to 26.0 kg/m2 inclusive;
1. has no sperm donation plan, no family planning and voluntarily adopts strict contraceptive methods during the study period and within six months after the completion of the trial;
1. able to comprehend and willing to sign an Informed Consent Form (ICF).

Exclusion criteria

1. history or presence of an abnormal ECG;
1. participation in more than 1 other radiolabeled investigational study drug trial within 12 months prior to Check-in;
1. exposure to significant radiation within 12 months prior to Check-in;
1. participation in any other investigational study drug trial;
1. use of any prescription medications/products within 14 days prior to Check-in;
1. use of any drug that affects drug metabolism enzymes or transporters (P-gp and BCRP) in the 30 days prior to taking the study drug, as detailed in Appendix 5;
1. receipt of blood products within 1 month prior to Check-in.