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Not Yet RecruitingNCT07422142

A Phase I Clinical Study to Evaluate the Safety, Tolerability, and Pharmacokinetic Profile of Gastrodin Injection in Healthy Chinese Subjects

Status
Not Yet Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
54 (estimated)
Sponsor
Kunming Pharmaceuticals, Inc. · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

This is a single-center, double-blind study to evaluate the safety, tolerability, pharmacokinetics of Gastrodin Injection in healthy Subjects

Conditions

Interventions

TypeNameDescription
DRUGgastrodin injection;placeboSingle-dose intravenous administration of gastrodin injection or placebo
DRUGgastrodin injection;placeboMultiple-dose intravenous administration of gastrodin injection or placebo

Timeline

Start date
2026-03-01
Primary completion
2026-09-30
Completion
2026-09-30
First posted
2026-02-19
Last updated
2026-02-19

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07422142. Inclusion in this directory is not an endorsement.

A Phase I Clinical Study to Evaluate the Safety, Tolerability, and Pharmacokinetic Profile of Gastrodin Injection in Hea (NCT07422142) · Clinical Trials Directory