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

2026年6月1日 更新者: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.

調査の概要

研究の種類

介入

入学 (推定)

8

段階

  • フェーズ 1

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

    • Jiangsu
      • Suzhou、Jiangsu、中国、215000
        • the First Affiliated Hospital of Soochow University
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人

健康ボランティアの受け入れ

はい

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:基礎科学
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Single Dose Zorifertinib Group
Single oral administration of 200 mg/5 µCi [¹⁴C]Zorifertinib in healthy male subjects under fasting condition

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Total radioactive recovery and cumulative total radioactive recovery in urine and feces at each time interval
時間枠: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
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
Peak Plasma Concentration (Cmax)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • 主任研究者:Liyan Miao, Ph.D.、the First Affiliated Hospital of Soochow University

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年6月1日

一次修了 (推定)

2026年8月1日

研究の完了 (推定)

2026年8月1日

試験登録日

最初に提出

2026年5月20日

QC基準を満たした最初の提出物

2026年5月27日

最初の投稿 (実際)

2026年6月2日

学習記録の更新

投稿された最後の更新 (実際)

2026年6月3日

QC基準を満たした最後の更新が送信されました

2026年6月1日

最終確認日

2026年5月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • AZD3759-CIT-101

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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[14C]Zorifertinib Oral Formulationの臨床試験

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