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CompletedNCT05802628

Salivary Drug Concentration Exploratory Study of Cetylpyridinium Chloride Buccal Tablets

A Single-arm, Open-label Study to Explore the Salivary Concentration of Cetylpyridinium Chloride Buccal Tablets After Single-dose Administration in Healthy Subjects

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
10 (actual)
Sponsor
Peking University People's Hospital · Academic / Other
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The study is a single-arm, open-label study to explore the salivary concentration of Cetylpyridinium Chloride Buccal Tablets after single-dose administration in Healthy Subjects

Detailed description

Primary Objective: To observe the concentration of the investigational product in the saliva of healthy subjects. Secondary purpose: To observe the safety of the investigational product in healthy subjects.

Conditions

Interventions

TypeNameDescription
DRUGCetylpyridinium Chloride Buccal TabletsSubjects administrated single dose of Cetylpyridinium Chloride Buccal Tablet

Timeline

Start date
2023-04-10
Primary completion
2023-04-18
Completion
2023-04-18
First posted
2023-04-06
Last updated
2023-07-12

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05802628. Inclusion in this directory is not an endorsement.

Salivary Drug Concentration Exploratory Study of Cetylpyridinium Chloride Buccal Tablets (NCT05802628) · Clinical Trials Directory