drugset / Trial / NCT02279602

Rollover Protocol for Subjects Who Have Responded on Study 4218s - A Phase 2 Study

NCT02279602

Phase 2 Completed 7 enrolled Mateon Therapeutics
NaSingle-groupOpen-labelTreatment

Summary

Subjects achieving a clinical response in study OX4218s with a biomarker reduction or symptom response are eligible to enroll in this rollover study to continue once every three weeks fosbretabulin infusions for up to one year.

Timeline

Start
2014-12
Primary completion
2016-08
Completion
2016-08

Drugs

EvaluationDrugModalityDoseRoute
Subject fosbretabulin Small molecule 60 mg/m2