drugset / Trial / NCT01134250

Combination Therapy of F16IL2 and Paclitaxel in Solid Tumour Patients

NCT01134250

Phase 1/2 Completed 48 enrolled Philogen S.p.A.
NaSingle-groupOpen-labelTreatment

Summary

This Phase Ib/II study is an open label, multicenter study. The study is divided in two parts: Phase I: an open-label, dose escalation study of F16IL2 in combination with paclitaxel for patients with solid tumours, bladder cancer, breast cancer, metastatic melanoma, mesothelioma, NSCLC, prostate cancer and sarcoma amenable to taxane therapy. Phase II: a prospective, single-arm, multicentre study of a fixed dose of F16IL2 in combination with paclitaxel, equivalent to stage 1 of the Simon two-stage phase II design, for patients with metastatic melanoma, breast cancer and NSCLC amenable to taxane therapy.

Timeline

Start
2008-08-06
Primary completion
2014-04-07
Completion
2014-04-07

Drugs

EvaluationDrugModalityDoseRoute
Subject F16IL2 Protein / enzyme biologic 5e+06 iu Intravenous
Subject F16IL2 Protein / enzyme biologic 3.5e+07 iu Intravenous
Subject Paclitaxel Small molecule 60 mg/m2 Intravenous
Subject Paclitaxel Small molecule 90 mg/m2 Intravenous