L19TNFα in Patients With Advanced Solid Tumors

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

34

Participants

Timeline

Start Date

September 30, 2007

Primary Completion Date

May 31, 2011

Study Completion Date

September 30, 2011

Conditions
Solid TumorsColorectal Cancer
Interventions
DRUG

L19TNFa

"Phase I: Sequential assignment of Patient cohorts to one of six dose levels of L19TNFa: 1.3, 2.6, 5.2, 7.8, 10.4, 13.0 µg/kg.~Phase II: The Recommended Dose (RD) of 13.0 µg/kg of L19TNFα determined in Phase I.~Schedule: Infusions of L19TNFα on days 1, 3 and 5 of each 21-day cycle. Patients may remain on treatment for a maximum of six 21-day cycles."

Trial Locations (2)

Unknown

A.O. UNIVERSITARIA OSPEDALI RIUNITI - OSPEDALE UMBERTO I DI ANCONA - ANCONA (Italy), Ancona

European Istitue of Oncology Milan (Italy), Milan

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

InnoPharma Inc.

INDUSTRY

collaborator

Eudax S.r.l.

INDUSTRY

lead

Philogen S.p.A.

INDUSTRY

NCT01253837 - L19TNFα in Patients With Advanced Solid Tumors | Biotech Hunter | Biotech Hunter