drugset / Trial / NCT02882217

Study to Assess Pharmacokinetics, Safety, and Tolerability of XC-8

NCT02882217 ↗

Phase 1 Completed 32 enrolled EURRUS Biotech GmbH
RandomizedParallel-groupQuadruple-blindBasic science

Summary

The study focusses on the evaluation of safety and tolerability of the XC8. The design of the study involves sequential dosing of cohorts (group of volunteers), taking increasing doses of the product after receiving conclusion and recommendation for further continuation of the study from the Dose Escalation Committee.

Timeline

Start
2016-08
Primary completion
2017-05
Completion
2017-05

Drugs

EvaluationDrugModalityDoseRoute
Comparator XC8 Unknown 10 mg Oral
Comparator XC8 Unknown 50 mg Oral
Comparator XC8 Unknown 200 mg Oral

Indications