CI

At a glance

ClinicalIndex Comparison Record
Phase 2Unknown· 120 target
Drug / intervention
low-dose-bevacizumab/pemetrexed +1 moredrug
Likely dose
low-dose-bevacizumab/pemetrexed 2 mg/kgfrom 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/NCT02829008
NCT02829008Phase 2Unknown

A Phase 2 Clinical Trial:Low -Dose-bevacizumab and Pemetrexed Versus Treatment of Physician's Choice in Metastatic HER2-negative Breast Cancer Patients After Failure of Taxanes and Anthracycline-containing Regimens

Chinese Academy of Medical Sciences·interventional·Posted Jul 12, 2016·Updated Jul 12, 2016

In Brief

A Phase 2 clinical trial evaluating low-dose-bevacizumab/pemetrexed and Treatment of physician's choice for Metastatic Breast Cancer. Targeting 120 participants across 1 site.

Detailed Summary

This is a single-center, open, randomized, controlled phase 2 clinical trial designed to compare low-dose-bevacizumab and pemetrexed with TPC in metastatic HER2-negative breast cancer patients after failure of taxanes and anthracycline-containing regimens.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Phase 2UnknownOverdue
20162017201820192020202120222023202420252026
First PostedJul 12, 2016
Enrollment StartApr 1, 2016
Primary CompletionApr 1, 2018
Study CompletionApr 1, 2020
TodayJul 1, 2026
Enrollment to primary: 2 yearsPosted 10.0 years ago

Interventions

low-dose-bevacizumab/pemetrexeddrug

Bevacizumab is administrated at a dose of 2 mg/kg once weekly by intravenous transfusion, which is on day 1, 8 and 15, and pemetrexed is given at a dose of 500mg/m2 once on the first day by intravenous transfusion, and repeated every three weeks, too.

Treatment of physician's choicedrug

The clinicians can select any drug or regimen that has been approved in metastatic cancer at present, including monotherapy, combination therapy, target therapy and palliative therapy. Specific agents include taxanes, capecitabine, gemcitabine, vinorelbine, cisplatin,carboplatin, nutrient solutions, and so on. These agents can be administered as monotherapy or in combination.