drugset / Trial / NCT02191852

Pharmacokinetic Study of Seresis® in the Skin in Healthy Young Female Volunteers

NCT02191852 ↗

Phase 1 Completed 8 enrolled Boehringer Ingelheim
NaSingle-groupOpen-labelTreatment

Summary

Study to evaluate the total antioxidant capacity of Seresis® (with Thiobarbituric acid reactive substances (TBARS) assays)) in the skin; as well as in buccal mucosa cells (BMCs) and in plasma, compared to baseline values; furthermore to detect the quantitative enrichment of individual antioxidant compounds contained in the product and to investigate whether or not some of them accumulate in target tissues such as skin, BMCs and plasma

Timeline

Start
1999-06
Primary completion
1999-10
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject Seresis® Unknown — —

Indications

No indication recorded.