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Material Balance of [14C]Zorifertinib in Healthy Adult Male Participants in China

2026. július 6. frissítette: Alpha Biopharma (Jiangsu) Co., Ltd.

Phase I Clinical Study on Material Balance of [14C]Zorifertinib in Healthy Adult Male Participants in China

This is a single-center, single-dose, open-label, Phase I study to evaluate the mass balance, biotransformation, pharmacokinetic characteristics, excretion pathways, and safety of a single oral 200 mg/5 µCi dose of [14C]Zorifertinib in healthy Chinese adult male participants. The study includes a screening period (Day -14 to Day -1) and a dosing and observation period (Day 1 to Day 14). Blood, urine, and feces samples will be collected to measure radioactivity, drug concentrations, and metabolites. Safety will be assessed by adverse events, vital signs, laboratory tests, 12-lead ECG, and ophthalmic examinations. The target total radioactivity recovery is ≥90% of the administered dose.

A tanulmány áttekintése

Tanulmány típusa

Beavatkozó

Beiratkozás (Becsült)

8

Fázis

  • 1. fázis

Kapcsolatok és helyek

Ez a rész a vizsgálatot végzők elérhetőségeit, valamint a vizsgálat lefolytatásának helyére vonatkozó információkat tartalmazza.

Tanulmányi kapcsolat

Tanulmányi helyek

    • Jiangsu
      • Suzhou, Jiangsu, Kína, 215000
        • Toborzás
        • The First Affiliated Hospital of Soochow University
        • Kapcsolatba lépni:

Részvételi kritériumok

A kutatók olyan embereket keresnek, akik megfelelnek egy bizonyos leírásnak, az úgynevezett jogosultsági kritériumoknak. Néhány példa ezekre a kritériumokra a személy általános egészségi állapota vagy a korábbi kezelések.

Jogosultsági kritériumok

Tanulmányozható életkorok

  • Felnőtt

Egészséges önkénteseket fogad

Igen

Leírás

Inclusion Criteria:

  1. Healthy Chinese males;
  2. Age at the time of signing the informed consent form: 18-45 years (inclusive);
  3. Body mass index (BMI) ranging from 19-26 kg/m2 (inclusive), with a body weight of no less than 50 kg;
  4. Fully understand the purpose and requirements of this study and voluntarily sign the informed consent form;
  5. Be able to communicate well with the investigators and complete the trial according to the protocol.
  6. The 14C content in plasma and urine samples obtained during screening are within general environmental 14C background levels. Directly analyzed plasma samples must have values ≤150 pMC, and urine samples containing petroleum-based carbon carriers must have values ≤50 pMC.

Exclusion Criteria:

Ancillary Examinations:

  1. Abnormal findings from comprehensive physical examination, vital signs, laboratory tests (hematology, blood biochemistry, coagulation function, urinalysis, routine stool + occult blood, thyroid function), 12-lead ECG, chest X-ray (posteroanterior view), abdominal ultrasound, digital rectal examination, etc., that are judged by the investigator as clinically significant.
  2. Resting corrected QT interval (Fridericia correction, QTcF = QT/RR1/3) obtained from 12-lead ECG >450 ms in males, or other abnormalities judged by the investigator as clinically significant.
  3. Positive result for any of the following: hepatitis B surface antigen or hepatitis B e antigen, hepatitis C virus antibody, Treponema pallidum antibody, or human immunodeficiency virus antigen/antibody combination test (HIV-Ag/Ab).
  4. Abnormal findings from ophthalmic examination (slit lamp, intraocular pressure, fundus photography) that are clinically significant.

    Medication History:

  5. Use of any drugs that inhibit or induce the drug-metabolizing enzyme CYP3A4 within 30 days prior to the screening period.
  6. Use of any prescription drugs, over-the-counter drugs, herbal medicines, or food supplements (e.g., vitamins, calcium supplements) within 14 days prior to the screening period.

    Medical and Surgical History:

  7. History of any clinically serious disease or condition that the investigator believes may affect the trial results, including but not limited to circulatory, respiratory, endocrine, nervous, digestive, urinary, hematologic, immune, psychiatric, or metabolic diseases;
  8. History of dysphagia or any condition that may affect drug absorption, e.g., gastrectomy, cholecystectomy, gastric bypass, duodenotomy, colectomy, inflammatory bowel disease;
  9. History of organic heart disease, heart failure, myocardial infarction, angina pectoris, arrhythmia, ventricular tachycardia, clinically symptomatic AV block, long QT syndrome, or family history of long QT syndrome (evidenced by genetic proof or sudden cardiac death of a close relative at a young age);
  10. Major surgery within 6 months prior to the screening period, or surgical incision not fully healed; Major surgery includes, but is not limited to, any procedure with significant bleeding risk, prolonged general anesthesia, incisional biopsy, or significant traumatic injury;
  11. Allergic constitution, e.g., known history of allergy to two or more substances; Or judged by the investigator as potentially allergic to the investigational drug;
  12. Hemorrhoids or perianal diseases with regular/ongoing hematochezia, irritable bowel syndrome, inflammatory bowel disease.

    Lifestyle Habits:

  13. Habitual constipation or diarrhea;
  14. Alcoholism or regular alcohol consumption within 6 months prior to screening, i.e., alcohol intake exceeding 14 units per week (1 unit = 360 mL beer, or 45 mL spirit with 40% alcohol, or 150 mL wine), or a breath alcohol test result ≥20 mg/dL at screening, or inability to abstain from alcohol during the trial period;
  15. Smoking >5 cigarettes per day or habitual use of nicotine-containing products within 3 months prior to screening, or inability to abstain during the trial period;
  16. Drug abuse or use of soft drugs (e.g., cannabis) within 3 months prior to screening, or use of hard drugs (e.g., amphetamines, phencyclidine) within 1 year prior to screening; Or positive urine screen for drugs of abuse during the screening period;
  17. Habitual consumption of grapefruit juice or excessive tea, coffee, and/or caffeinated beverages, and inability to abstain during the study period.

    Others:

  18. Participation in a radiolabeled drug trial within 1 year prior to screening, or participation in a 14C-labeled breath test within 3 months prior to screening;
  19. History of needle phobia or blood phobia, difficulty with blood collection, or inability to tolerate venous puncture;
  20. Participation in any other clinical trial (including drug and device trials) within 3 months prior to the screening period;
  21. Vaccination within 1 month prior to screening, or planned vaccination during the study period;
  22. Plan to father a child or donate sperm during the study period or within 1 year after study completion, or disagreement to use strict contraceptive measures (see Appendix 1) for themselves and their partners during the study period and within 1 year after study completion;
  23. Blood loss or blood donation of ≥400 mL within 3 months prior to screening, or blood transfusion within 1 month;
  24. Any other factor that, in the investigator's opinion, makes the participant unsuitable for participation in this trial.

Tanulási terv

Ez a rész a vizsgálati terv részleteit tartalmazza, beleértve a vizsgálat megtervezését és a vizsgálat mérését.

Hogyan készül a tanulmány?

Tervezési részletek

  • Elsődleges cél: Alapvető tudomány
  • Kiosztás: N/A
  • Beavatkozó modell: Egyetlen csoportos hozzárendelés
  • Maszkolás: Nincs (Open Label)

Fegyverek és beavatkozások

Résztvevő csoport / kar
Beavatkozás / kezelés
Kísérleti: Single Dose Zorifertinib Group
Single oral administration of 200 mg/5 µCi [¹⁴C]Zorifertinib in healthy male subjects under fasting condition

Mit mér a tanulmány?

Elsődleges eredményintézkedések

Eredménymérő
Intézkedés leírása
Időkeret
Total radioactive recovery and cumulative total radioactive recovery in urine and feces at each time interval
Időkeret: Pre-dose up to 312 hours after dosing, or until termination criteria met
Pre-dose up to 312 hours after dosing, or until termination criteria met
Percentage of total radioactivity exposure (%AUC), percentage of parent drug and its metabolites (%Dose), and metabolite identification
Időkeret: Pre-dose up to 312 hours after dosing, or until termination criteria met
Percentage of total radioactivity exposure (%AUC) accounted for by parent drug and its metabolites in plasma. Percentage of administered dose (%Dose) accounted for by parent drug and its metabolites in urine and faeces. Identification of metabolites in plasma, urine, and feces
Pre-dose up to 312 hours after dosing, or until termination criteria met
Peak Plasma Concentration (Cmax)
Időkeret: Pre-dose up to 120 hours after dosing,or until termination criteria met
Pharmacokinetic parameters of total radioactivity in plasma and whole blood (if applicable)
Pre-dose up to 120 hours after dosing,or until termination criteria met
Time to Peak Concentration (Tmax)
Időkeret: Pre-dose up to 120 hours after dosing,or until termination criteria met
Pharmacokinetic parameters of total radioactivity in plasma and whole blood (if applicable)
Pre-dose up to 120 hours after dosing,or until termination criteria met
Area under the plasma concentration versus time curve (AUC)
Időkeret: Pre-dose up to 120 hours after dosing,or until termination criteria met
Pharmacokinetic parameters of total radioactivity in plasma and whole blood (if applicable)
Pre-dose up to 120 hours after dosing,or until termination criteria met
Elimination Half-Life (t1/2)
Időkeret: Pre-dose up to 120 hours after dosing,or until termination criteria met
Pharmacokinetic parameters of total radioactivity in plasma and whole blood (if applicable)
Pre-dose up to 120 hours after dosing,or until termination criteria met
Terminal Rate Constant (λz)
Időkeret: Pre-dose up to 120 hours after dosing,or until termination criteria met
Pharmacokinetic parameters of total radioactivity in plasma and whole blood (if applicable)
Pre-dose up to 120 hours after dosing,or until termination criteria met
Apparent Volume of Distribution (Vz/F)
Időkeret: Pre-dose up to 120 hours after dosing,or until termination criteria met
Pharmacokinetic parameters of total radioactivity in plasma and whole blood (if applicable)
Pre-dose up to 120 hours after dosing,or until termination criteria met
Apparent Clearance (CLz/F)
Időkeret: Pre-dose up to 120 hours after dosing,or until termination criteria met
Pharmacokinetic parameters of total radioactivity in plasma and whole blood (if applicable)
Pre-dose up to 120 hours after dosing,or until termination criteria met
Mean Residence Time (MRT)
Időkeret: Pre-dose up to 120 hours after dosing,or until termination criteria met
Pharmacokinetic parameters of total radioactivity in plasma and whole blood (if applicable)
Pre-dose up to 120 hours after dosing,or until termination criteria met
Whole blood / plasma total radioactivity ratio
Időkeret: Pre-dose up to 120 hours after dosing,or until termination criteria met
Pre-dose up to 120 hours after dosing,or until termination criteria met

Másodlagos eredményintézkedések

Eredménymérő
Intézkedés leírása
Időkeret
Peak Plasma Concentration (Cmax)
Időkeret: Pre-dose up to 120 hours after dosing,or until termination criteria met
Pharmacokinetic parameters for zorifertinib, its metabolite (AZ'1168), and other major metabolites (if applicable) in plasma
Pre-dose up to 120 hours after dosing,or until termination criteria met
Time to Peak Concentration (Tmax)
Időkeret: Pre-dose up to 120 hours after dosing,or until termination criteria met
Pharmacokinetic parameters for zorifertinib, its metabolite (AZ'1168), and other major metabolites (if applicable) in plasma
Pre-dose up to 120 hours after dosing,or until termination criteria met
Area under the plasma concentration versus time curve (AUC)
Időkeret: Pre-dose up to 120 hours after dosing,or until termination criteria met
Pharmacokinetic parameters for zorifertinib, its metabolite (AZ'1168), and other major metabolites (if applicable) in plasma
Pre-dose up to 120 hours after dosing,or until termination criteria met
Elimination Half-Life (t1/2)
Időkeret: Pre-dose up to 120 hours after dosing,or until termination criteria met
Pharmacokinetic parameters for zorifertinib, its metabolite (AZ'1168), and other major metabolites (if applicable) in plasma
Pre-dose up to 120 hours after dosing,or until termination criteria met
Terminal Rate Constant (λz)
Időkeret: Pre-dose up to 120 hours after dosing,or until termination criteria met
Pharmacokinetic parameters for zorifertinib, its metabolite (AZ'1168), and other major metabolites (if applicable) in plasma
Pre-dose up to 120 hours after dosing,or until termination criteria met
Apparent Volume of Distribution (Vz/F)
Időkeret: Pre-dose up to 120 hours after dosing,or until termination criteria met
Pharmacokinetic parameters for zorifertinib, its metabolite (AZ'1168), and other major metabolites (if applicable) in plasma
Pre-dose up to 120 hours after dosing,or until termination criteria met
Apparent Clearance (CLz/F)
Időkeret: Pre-dose up to 120 hours after dosing,or until termination criteria met
Pharmacokinetic parameters for zorifertinib, its metabolite (AZ'1168), and other major metabolites (if applicable) in plasma
Pre-dose up to 120 hours after dosing,or until termination criteria met
Mean Residence Time (MRT)
Időkeret: Pre-dose up to 120 hours after dosing,or until termination criteria met
Pharmacokinetic parameters for zorifertinib, its metabolite (AZ'1168), and other major metabolites (if applicable) in plasma
Pre-dose up to 120 hours after dosing,or until termination criteria met
Incidence and severity of Adverse Events (AEs)
Időkeret: Pre-dose up to 312 hours after dosing, or until termination criteria met
All adverse events were classified according to the CTCAE (version: 6.0)
Pre-dose up to 312 hours after dosing, or until termination criteria met

Együttműködők és nyomozók

Itt találhatja meg a tanulmányban érintett személyeket és szervezeteket.

Nyomozók

  • Kutatásvezető: Liyan Miao, Ph.D., The First Affiliated Hospital of Soochow University

Tanulmányi rekorddátumok

Ezek a dátumok nyomon követik a ClinicalTrials.gov webhelyre benyújtott vizsgálati rekordok és összefoglaló eredmények benyújtásának folyamatát. A vizsgálati feljegyzéseket és a jelentett eredményeket a Nemzeti Orvostudományi Könyvtár (NLM) felülvizsgálja, hogy megbizonyosodjon arról, hogy megfelelnek-e az adott minőség-ellenőrzési szabványoknak, mielőtt közzéteszik őket a nyilvános weboldalon.

Tanulmány főbb dátumok

Tanulmány kezdete (Tényleges)

2026. július 6.

Elsődleges befejezés (Becsült)

2026. augusztus 1.

A tanulmány befejezése (Becsült)

2026. augusztus 1.

Tanulmányi regisztráció dátumai

Először benyújtva

2026. május 20.

Először nyújtották be, amely megfelel a minőségbiztosítási kritériumoknak

2026. május 27.

Első közzététel (Tényleges)

2026. június 2.

Tanulmányi rekordok frissítései

Utolsó frissítés közzétéve (Tényleges)

2026. július 8.

Az utolsó frissítés elküldve, amely megfelel a minőségbiztosítási kritériumoknak

2026. július 6.

Utolsó ellenőrzés

2026. július 1.

Több információ

A tanulmányhoz kapcsolódó kifejezések

Egyéb vizsgálati azonosító számok

  • AZD3759-CIT-101

Gyógyszer- és eszközinformációk, tanulmányi dokumentumok

Egy amerikai FDA által szabályozott gyógyszerkészítményt tanulmányoz

Nem

Egy amerikai FDA által szabályozott eszközterméket tanulmányoz

Nem

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