Clinical trial

The Mass Balance Study of [14C]JT001 in Chinese Healthy Adult Male Subjects

Name
JT016-001-I
Description
This study is a single center, single dose, non-randomized, open design clinical study.By quantitative analysis of the biological samples of subjects after oral administration of \[14C\]JT001, the data of human radioactive excretion rate and the main excretion pathway will be obtained. The main metabolites ,metabolic pathways and elimination pathways of JT001 will be identified.
Trial arms
Trial start
2023-03-18
Estimated PCD
2023-06-15
Trial end
2023-10-15
Status
Recruiting
Phase
Early phase I
Treatment
[14C]JT001
Subjects will receive approximately 300 mg/100 µCi of \[14C\]JT001 orally.
Arms:
[14C]JT001
Size
6
Primary endpoint
Total radioactive recovery
1 month
cumulative excretion rate of total radioactive material in fecal matter
1 month
Peak concentration(Cmax)
1 month
time to peak(Tmax)
1 month
elimination half life(t1/2)
1 month
Major metabolites in human plasma, urine, and feces by liquid chromatography-mass spectrometry (LC-MS/MS)
1 month
Eligibility criteria
Inclusion Criteria: 1. Healthy adult males 2. Age: 18-45 years old 3. Body weight: Body mass index (BMI) is between 19.0 and 26.0 kg/m2 (including boundary values), and the body weight of the subject is not less than 50.0 kg; 4. Voluntarily sign informed consent; 5. Subjects were able to complete the trail according to protocol. Exclusion Criteria: 1. Physical examination, vital signs, routine laboratory examination, imaging examination abnormal and clinically significant 2. The electrocardiogram was abnormal and was considered clinically significant by the investigators, or has a history of organic heart disease 3. Has hepatitis B (HBV) or hepatitis C (HCV) or HIV antibody and syphilis antibody positive; 4. Any drug that inhibits or induces the drug transporters P-gp and BCRP has been used within 30 days prior to the screening period 5. Any conditions that may affect drug absorption. 6. Previous antineoplastic therapy meets washout requirements. 7. Hemorrhoids or perianal disease with regular/ongoing blood in the stool, irritable bowel syndrome, inflammatory bowel disease 8. Habitual constipation or diarrhea. 9. Significant radioactive exposure within 1 year.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE1'], 'designInfo': {'allocation': 'NA', 'interventionModel': 'SINGLE_GROUP', 'interventionModelDescription': 'Single Group', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 6, 'type': 'ESTIMATED'}}
Updated at
2023-04-07

1 organization

1 product

1 indication

Product
[14C]JT001