- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07620951
Material Balance of [14C]Zorifertinib in Healthy Adult Male Participants in China
Phase I Clinical Study on Material Balance of [14C]Zorifertinib in Healthy Adult Male Participants in China
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Tipo di studio
Iscrizione (Stimato)
Fase
- Fase 1
Contatti e Sedi
Contatto studio
- Nome: John Ge, M.D.
- Numero di telefono: +86 (0)21-63862197
- Email: john.ge@alphabiopharma.com.cn
Luoghi di studio
-
-
Jiangsu
-
Suzhou, Jiangsu, Cina, 215000
- the First Affiliated Hospital of Soochow University
-
Contatto:
- Liyan Miao, Ph.D.
- Numero di telefono: 18915505252
- Email: miaolysuzhou@163.com
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Adulto
Accetta volontari sani
Descrizione
Inclusion Criteria:
- Healthy Chinese males;
- Age at the time of signing the informed consent form: 18-45 years (inclusive);
- Body mass index (BMI) ranging from 19-26 kg/m2 (inclusive), with a body weight of no less than 50 kg;
- Fully understand the purpose and requirements of this study and voluntarily sign the informed consent form;
- Be able to communicate well with the investigators and complete the trial according to the protocol.
- 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:
- 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.
- 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.
- 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).
Abnormal findings from ophthalmic examination (slit lamp, intraocular pressure, fundus photography) that are clinically significant.
Medication History:
- Use of any drugs that inhibit or induce the drug-metabolizing enzyme CYP3A4 within 30 days prior to the screening period.
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:
- 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;
- History of dysphagia or any condition that may affect drug absorption, e.g., gastrectomy, cholecystectomy, gastric bypass, duodenotomy, colectomy, inflammatory bowel disease;
- 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);
- 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;
- 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;
Hemorrhoids or perianal diseases with regular/ongoing hematochezia, irritable bowel syndrome, inflammatory bowel disease.
Lifestyle Habits:
- Habitual constipation or diarrhea;
- 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;
- 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;
- 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;
Habitual consumption of grapefruit juice or excessive tea, coffee, and/or caffeinated beverages, and inability to abstain during the study period.
Others:
- 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;
- History of needle phobia or blood phobia, difficulty with blood collection, or inability to tolerate venous puncture;
- Participation in any other clinical trial (including drug and device trials) within 3 months prior to the screening period;
- Vaccination within 1 month prior to screening, or planned vaccination during the study period;
- 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;
- Blood loss or blood donation of ≥400 mL within 3 months prior to screening, or blood transfusion within 1 month;
- Any other factor that, in the investigator's opinion, makes the participant unsuitable for participation in this trial.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Scienza basilare
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: Single Dose Zorifertinib Group
|
Single oral administration of 200 mg/5 µCi [¹⁴C]Zorifertinib in healthy male subjects under fasting condition
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Total radioactive recovery and cumulative total radioactive recovery in urine and feces at each time interval
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Peak Plasma Concentration (Cmax)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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
|
Collaboratori e investigatori
Investigatori
- Investigatore principale: Liyan Miao, Ph.D., the First Affiliated Hospital of Soochow University
Studiare le date dei record
Studia le date principali
Inizio studio (Stimato)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- AZD3759-CIT-101
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .