CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 2 enrolled
Drug / intervention
Sipuleucel-T +2 morebiological
Likely dose
Not stated in 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/NCT02159950
NCT02159950Phase 2Completed

A Phase II Randomized Open Label Study of Sipuleucel-T vs. Sipuleucel-T and Tasquinimod in Patients With Metastatic Castrate-Resistant Prostate Cancer (CRPC)

Roswell Park Cancer Institute·interventional·Posted Jun 10, 2014·Updated Apr 27, 2023

In Brief

A Phase 2 clinical trial evaluating Laboratory Biomarker Analysis, Sipuleucel-T, and 1 other intervention for Hormone-Resistant Prostate Cancer and 3 related conditions. Completed, enrolled 2 participants across 1 site.

Detailed Summary

This randomized phase II trial studies how well sipuleucel-T with or without tasquinimod works in treating patients with hormone-resistant prostate cancer that has spread to other parts of the body. Vaccines made from a person's tumor cells and white blood cells may help the body build an effective immune response to kill tumor cells. Tasquinimod may stop the growth of prostate cancer by blocking the growth of new blood vessels necessary for tumor growth. It is not yet known whether sipuleucel-T is more effective with or without tasquinimod in treating prostate cancer.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
CollaboratorsActive Biotech AB

Timeline

Phase 2CompletedFinished
201520162017201820192020202120222023202420252026
First PostedJun 10, 2014
Enrollment StartJan 1, 2015
Primary CompletionJul 1, 2015
TodayJul 2, 2026
Enrollment to primary: 6 monthsPosted 12.1 years ago

Interventions

Laboratory Biomarker Analysisother

Correlative studies

Sipuleucel-Tbiological

Given IV

Tasquinimoddrug

Given PO