tTF-NGR Phase I Study

PHASE1CompletedINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

March 1, 2017

Primary Completion Date

November 5, 2019

Study Completion Date

November 5, 2019

Conditions
Malignant Solid TumorsLymphomas
Interventions
BIOLOGICAL

tTF-NGR

tTF-NGR will be given as 1-hour infusion via central venous access once daily for 5 days with a subsequent rest period of 2 weeks and following cycles with dose escalation of 0.5 mg/m2 upon judgement of tolerability and therapeutic activity. Starting dose will be 1 mg/m2/day. Dose-escalation is stopped before the maximum number of 8 escalation steps if tumor response, tumor progression or a Dose-Limiting Toxicity (DLT) is observed.

Trial Locations (1)

48149

University Hospital Muenster, Münster

All Listed Sponsors
collaborator

Deutsche Krebshilfe e.V., Bonn (Germany)

OTHER

lead

University Hospital Muenster

OTHER

NCT02902237 - tTF-NGR Phase I Study | Biotech Hunter | Biotech Hunter