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Not Yet RecruitingNCT06584058

HPP737 Substance Balance Study in Human

[14C] A Single-center, Nonrandomized, Open, Single-dose Substance Balance Study of HPP737 in Healthy Subjects

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
8 (estimated)
Sponsor
Newsoara Biopharma Co., Ltd. · Industry
Sex
Male
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

Main research purpose 1. Quantitative analysis of the total amount of radioactivity in excreta (urine and feces) of male healthy subjects after oral administration of \[14C\]HPP737, to obtain the cumulative excretion rate and main excretion routes of human radioactivity; 2. To identify the main metabolites in the offspring of \[14C\]HPP737 in healthy male subjects, and to determine the main biotransformation pathway and main metabolite structure; 3. To investigate the distribution of total radioactivity in whole blood and plasma and the pharmacokinetics of total plasma radioactivity in healthy male subjects after a single oral administration of \[14C\]HPP737. Participants will: 1. Take Investigational product once 2. Stay in the clinic about 7 days for checkups and tests 3. Report their symptoms

Conditions

Interventions

TypeNameDescription
DRUGHPP737\[14C\]HPP737 oral preparation, 20mg(150μCi), once

Timeline

Start date
2024-08-30
Primary completion
2025-07-30
Completion
2025-08-30
First posted
2024-09-04
Last updated
2024-09-04

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06584058. Inclusion in this directory is not an endorsement.