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

1 de junho de 2026 atualizado por: 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.

Visão geral do estudo

Tipo de estudo

Intervencional

Inscrição (Estimado)

8

Estágio

  • Fase 1

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Locais de estudo

    • Jiangsu
      • Suzhou, Jiangsu, China, 215000
        • The First Affiliated Hospital of Soochow University
        • Contato:

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto

Aceita Voluntários Saudáveis

Sim

Descrição

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.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Ciência básica
  • Alocação: N / D
  • Modelo Intervencional: Atribuição de grupo único
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Single Dose Zorifertinib Group
Single oral administration of 200 mg/5 µCi [¹⁴C]Zorifertinib in healthy male subjects under fasting condition

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Total radioactive recovery and cumulative total radioactive recovery in urine and feces at each time interval
Prazo: 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
Prazo: 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)
Prazo: 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)
Prazo: 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)
Prazo: 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)
Prazo: 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)
Prazo: 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)
Prazo: 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)
Prazo: 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)
Prazo: 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
Prazo: 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

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Peak Plasma Concentration (Cmax)
Prazo: 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)
Prazo: 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)
Prazo: 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)
Prazo: 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)
Prazo: 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)
Prazo: 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)
Prazo: 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)
Prazo: 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)
Prazo: 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

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

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

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de junho de 2026

Conclusão Primária (Estimado)

1 de agosto de 2026

Conclusão do estudo (Estimado)

1 de agosto de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

20 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

27 de maio de 2026

Primeira postagem (Real)

2 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

3 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

1 de junho de 2026

Última verificação

1 de maio de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • AZD3759-CIT-101

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

Ensaios clínicos em Metástases do Sistema Nervoso Central (SNC)

Ensaios clínicos em [14C]Zorifertinib Oral Formulation

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