CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 51 enrolled
Drug / intervention
sorafenibdrug
Likely dose
Sorafenib 800 mg orally once daily until progressionAI-extracted
Key inclusion· 7
  • Histologically confirmed soft tissue sarcoma of specific types: angiosarcoma (cutaneous or visceral), malignant hemangiosarcoma, malignant hemangiopericytoma, or grade 3-4 leiomyosarcoma or liposarcoma
  • Unresectable residual, metastatic, or recurrent disease documented by radiography
  • Measurable disease by imaging or physical examination
  • Archived paraffin-embedded tumor sections available
Key exclusion· 9
  • Known brain metastases
  • History of thromboembolic disease
  • Uncontrolled hypertension
  • Prior sorafenib or inhibitors of VEGFR or MAPK pathway

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

Search/NCT00217620
NCT00217620Phase 2Completed

Phase II Trial of BAY-9006 (NSC #724772) in Advanced Soft Tissue Sarcomas

National Cancer Institute (NCI)·interventional·Posted Sep 22, 2005·Updated May 15, 2014

In Brief

A Phase 2 clinical trial evaluating sorafenib for Sarcoma. Completed, enrolled 51 participants across 184 sites.

Detailed Summary

RATIONALE: Sorafenib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. PURPOSE: This phase II trial is studying how well sorafenib works in treating patients with advanced soft tissue sarcomas.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSarcoma
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedSep 22, 2005
Enrollment StartMar 1, 2006
Primary CompletionApr 1, 2008
Study CompletionSep 1, 2012
TodayJul 2, 2026
Enrollment to primary: 2.1 yearsPosted 20.8 years ago

Interventions

sorafenibdrug

800 mg per day, daily until progression