drugset / Trial / NCT02191241

Pharmacokinetics of a Single Oral Dose of 1,800 mg Red Vine Leaf Extract (Antistax®)

NCT02191241 ↗

Phase 1 Completed 12 enrolled Boehringer Ingelheim
NaSingle-groupOpen-label

Summary

To describe the plasma and urinary pharmacokinetics of quercetin glucuronide and kaempferol glucuronide after the administration of a single peroral dose of 1,800mg Red Vine Leaf Extract (Antistax®). Additionally, the trial evaluated the safety and tolerability of this dose in healthy subjects.

Timeline

Start
2001-08
Primary completion
2004-09
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject Red Vine Leaf Extract Unknown 1800 mg Oral

Indications

No indication recorded.