Overview

Study to Determine the Safety, Maximum Tolerated Dose, Pharmacokinetics of Sorafenib (BAY43-9006)

Status:
Completed
Trial end date:
2008-04-01
Target enrollment:
Participant gender:
Summary
The primary objective of the study was to define the safety profile and maximum tolerated dose (MTD) of sorafenib tablets in combination with carboplatin and paclitaxel chemotherapy in patients with advanced, refractory solid tumors. The secondary objectives were evaluation of pharmacokinetics (PK) and tumor response of these patients being treated with sorafenib in combination with paclitaxel and carboplatin.
Phase:
Phase 1
Details
Lead Sponsor:
Bayer
Collaborators:
Amgen
Onyx Pharmaceuticals
Treatments:
Albumin-Bound Paclitaxel
Carboplatin
Niacinamide
Paclitaxel
Sorafenib