ADVANCED-2
Basic Study Information
Purpose:
TARA-002-101-Ph2 is an open-label study to investigate the safety and anti-tumor activity
of intravesical instillation of TARA-002 in adults 18 years of age or older with high-grade
CIS NMIBC (± Ta/T1).
The purpose of this Phase 2 study (TARA-002-101-Ph2) is to further assess the safety
and anti-tumor activity of TARA-002 at the RP2D which has been established in the
Phase 1a dose finding study (TARA-002-101-Ph1a).
This Phase 2 study includes participants with CIS NMIBC (± Ta/T1) with active disease
(defined as disease present at last tumor evaluation prior to signing ICF).
Participants will be enrolled into one of 2 cohorts:
Cohort A:
* Participants with CIS (± Ta/T1) who are BCG naive, or
* Participants with CIS (± Ta/T1) who are BCG exposed and have not received intravesical
BCG for at least 24 months prior to the most recent CIS diagnosis
Cohort B:
* Participants with persistent or recurrent CIS (± Ta/T1) who are BCG unresponsive
within 12 months of completion of adequate BCG therapy (minimum 5/6 doses induction
and 2/3 doses maintenance or 2/6 doses reinduction)
Location: University of Rochester, Department of Urology
Lead Researcher (Principal Investigator)
Lead Researcher:
William Tabayoyong
Study Contact Information
Study Contact: Clinical Trials Office
Study Location: Wilmot Cancer Institute, Â鶹ÊÓƵ
Study Email: WCICTOResearch@urmc.rochester.edu
Additional Study Details
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