CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 83 enrolled
Drug / intervention
Sorafenib (Nexavar, BAY43-9006) + Dacarbazine (DTIC)drug
Likely dose
Sorafenib (Nexavar, BAY43-9006) + Dacarbazine (DTIC) 1000 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00492297
NCT00492297Phase 2Completed

A Phase II, Multi-center, Open-label, Uncontrolled Study to Evaluate the Efficacy and Safety of BAY 43-9006 Given Daily in Combination With Repeated 21-Day Cycles of Dacarbazine (DTIC) Chemotherapy in Subjects With Advanced Metastatic Melanoma.

Bayer·interventional·Posted Jun 27, 2007·Updated Oct 31, 2014

In Brief

A Phase 2 clinical trial evaluating Sorafenib (Nexavar, BAY43-9006) + Dacarbazine (DTIC) for Melanoma. Completed, enrolled 83 participants across 12 sites in 2 countries.

Detailed Summary

The purpose of this study is to see whether a new type of anti-cancer drug, known as BAY 43-9006, can be given safely and with good effect in combination with dacarbazine (DTIC). DTIC is the current standard chemotherapy drug given for melanoma that has spread through the body. Although this drug can be effective on its own and is generally well tolerated, not all patients will benefit, so there is a need to test new drugs and drug combinations for treating melanoma.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMelanoma
CountriesFrance, United Kingdom
Collaborators--

Timeline

Phase 2CompletedFinished
20052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJun 27, 2007
Enrollment StartApr 1, 2005
Primary CompletionJun 1, 2008
Study CompletionJul 1, 2008
TodayJul 2, 2026
Enrollment to primary: 3.2 yearsPosted 19.0 years ago

Interventions

Sorafenib (Nexavar, BAY43-9006) + Dacarbazine (DTIC)drug

Dacarbazine 1000 mg/m\^2 on day one of repeated 21 day cycles, in combination with daily continuous oral sorafenib (Nexavar, BAY 43-9006), 400 mg twice a day (bid)