drugset / Trial / NCT05826600

A Study of OMX-0407 in Patients With Previously Treated Solid Tumours That Can't be Removed Surgically

NCT05826600 ↗

Phase 1/2 Terminated 68 enrolled iOmx Therapeutics AG
NaSequentialOpen-labelTreatment

Summary

The main purpose of the dose escalation phase of the study is to determine the safety of different doses of OMX-0407. The dose expansion (phase Ib) part of the study will evaluate efficacy, safety and tolerability at a dose determined in the dose escalation,

Timeline

Start
2023-03-30
Primary completion
2026-04-02
Completion
2026-04-02

Outcome

Outcome not reported

Stopped (Business): “Study terminated as part of strategic considerations and not based on safety concerns.”

Drugs

EvaluationDrugModalityDoseRoute
Subject OMX-0407 Unknown 10 mg Oral
Subject OMX-0407 Unknown 100 mg Oral

Indications