CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 217 enrolled
Drug / intervention
SU011248 +1 moredrug
Likely dose
SU011248 37.5 mg orally daily in continuous regimen with 3-week cycles, escalable to 50 mg daily if minimal toxicitiesAI-extracted
Key inclusion· 4
  • Recurrent or metastatic breast cancer
  • ER, PR, and HER2-negative status (triple-negative)
  • Prior treatment with anthracycline and taxane in adjuvant or advanced disease setting
  • Relapse within 6 months of adjuvant chemotherapy and/or 1-2 prior chemotherapy regimens for advanced disease
Key exclusion· 2
  • More than two prior chemotherapy regimens for advanced disease
  • Uncontrolled or symptomatic brain metastases

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

Search/NCT00246571
NCT00246571Phase 2Completed

A Randomized Phase 2 Study Of SU011248 Versus Standard-Of-Care For Patients With Previously Treated, Advanced, Triple Receptor Negative (ER, PR, HER2) Breast Cancer

Pfizer·interventional·Posted Oct 31, 2005·Updated Jul 12, 2012

In Brief

A Phase 2 clinical trial evaluating SU011248 and Chemotherapy for Breast Neoplasms. Completed, enrolled 217 participants across 113 sites in 12 countries.

Detailed Summary

The purpose of this study is to compare progression free survival for SU011248 \[sutent (sunitinib malate)\] versus standard of care therapy in patients with previously treated, advanced, triple receptor negative (ER, PR, HER2) locally recurrent or metastatic breast cancer.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesBulgaria, Canada, Czechia, France, Germany, Hungary, Italy, Spain, Turkey (Türkiye), Ukraine, United Kingdom, United States
Collaborators--

Timeline

Phase 2CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedOct 31, 2005
Enrollment StartJan 1, 2006
Primary CompletionMay 1, 2010
Study CompletionJun 1, 2011
TodayJul 2, 2026
Enrollment to primary: 4.3 yearsPosted 20.7 years ago

Interventions

SU011248drug

SU011248 capsules administered orally, daily in a continuous regimen, 3-week cycles, starting dose of 37.5 mg daily. 1-week treatment rests and dose reductions allowed for dose-limiting toxicity. Dose escalate SU011248 to 50-mg daily if minimal toxicities . Study will continue until disease progression. Patients randomized to or crossed over to SU011248 may continue beyond the time of Response Evaluation Criterion in Solid Tumors (RECIST) -defined progression at the discretion of the investigator in the case of clinical benefit.

Chemotherapydrug

The choice of chemotherapy will be at the discretion of the investigator within the limits outlined below. 1. Capecitabine - 1000-1250 mg/m2 twice daily days 1-14 every 3 weeks 2. Vinorelbine - 25-30 mg/m2 rapid intravenous infusion or 60-80 mg/m2 oral weekly, expressed in 3-week cycles 3. Docetaxel - 75-100 mg/m2 every 3 weeks 4. Paclitaxel - 175-200 mg/m2 every 3 weeks 5. Paclitaxel - 80-90 mg/m2 weekly, in a continuous regimen expressed in 3-week cycles or administration of 3 weeks of treatment followed by 1 week of rest. Use of the 3/1 regimen will require extra care in scheduling disease assessments. 6. Gemcitabine - 800-1250 mg/m2 Days 1 and 8 every 3 weeks Study will continue until disease progression or it is in the best interest of the patient to discontinue based on achievement of maximum benefit or tolerability issues. At the time of progression patients randomized to chemotherapy will be offered crossover to single agent SU011248.