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NCT07422142

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

Not yet recruiting Phase 1 Last updated 19 February 2026
What this trial tests

Phase 1 trial testing gastrodin injection;placebo in Delirium in 54 participants. Not yet recruiting.

Timeline
1 March 2026
Primary endpoint
30 September 2026
30 September 2026

Quick facts

Lead sponsorKunming Pharmaceuticals, Inc.
PhasePhase 1
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment54
Start date1 March 2026
Primary completion30 September 2026
Estimated completion30 September 2026
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Kunming Pharmaceuticals, Inc. — full company profile →

Who can join

Adults 18 to 65, any sex, with Delirium. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Delirium

Currently open trials in the same condition.

Other Kunming Pharmaceuticals, Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07422142.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing