drugset / Trial / NCT06899230

Safety, Tolerability, and Pharmacokinetics (PK) of Single and Multiple Ascending Oral Doses of iQ-007

NCT06899230 ↗

Phase 1 Active not recruiting 72 enrolled iQure Australia Pty Ltd Avance Clinical Pty Ltd. · collab
RandomizedSequentialQuadruple-blindTreatment

Summary

This is a randomized, double-blind, placebo-controlled study conducted in healthy adult volunteers to assess the safety, tolerability and pharmacokinetics of iQ-007. iQ-007 may be indicated for use in patients with Focal Seizures and Drug-resistant Epilepsy (DRE).

Timeline

Start
2025-04-08
Primary completion
2026-01-29
Completion
2026-01-29

Drugs

EvaluationDrugModalityDoseRoute
Subject iQ-007 Unknown 200 mg Oral
Subject iQ-007 Unknown 600 mg Oral
Subject iQ-007 Unknown 2400 mg Oral
Subject iQ-007 Unknown 2800 mg Oral

Indications