drugset / Trial / NCT02431364

Trial of Safety and Tolerability of Oral Verdinexor (KPT-335) in Healthy Adults

NCT02431364 ↗

Phase 1 Terminated 33 enrolled Karyopharm Therapeutics Inc
RandomizedSequentialDouble-blindBasic science

Summary

This is a randomized, double-blind, sequential, dose-escalation, Phase 1 trial to evaluate the safety and tolerability of verdinexor. Verdinexor or placebo will be given on Days 1 and 3 to healthy adult participants.

Timeline

Start
2015-05-26
Primary completion
2015-10-01
Completion
2015-10-01

Outcome

Outcome not reported

Stopped: “Administrative reason”

Drugs

EvaluationDrugModalityDoseRoute
Subject Verdinexor Small molecule 5 mg Oral
Subject Verdinexor Small molecule 10 mg Oral
Subject Verdinexor Small molecule 20 mg Oral
Subject Verdinexor Small molecule 40 mg Oral

Indications

No indication recorded.