Status:
COMPLETED
Study of Vicinium for Treating Patients With Non-Invasive Urothelial Carcinoma In Situ
Lead Sponsor:
Sesen Bio, Inc.
Conditions:
Urinary Bladder Cancer
Bladder Cancer
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
The purpose of this study is to evaluate the efficacy and tolerability of Vicinium when administered as a monotherapy intravesical instillation in patients with non-invasive urothelial carcinoma in si...
Detailed Description
A phase II study was performed to assess the efficacy and tolerability of intravesical Vicinium in patients with urothelial carcinoma in situ of the bladder. Bacillus Calmette-Guérin treatment had pre...
Eligibility Criteria
Inclusion
- Disease Characteristics
- The patient must be male or female 18 years of age or older.
- The patient must have histologically-confirmed Transitional Cell Carcinoma (TCC) of the bladder.
- The patient must have histologically-confirmed carcinoma in situ (CIS), with or without non-invasive papillary disease
- The patient must have immunohistochemically-confirmed EpCAM positive disease.
- The patient must have a life expectancy of at least 12 months.
- Prior/Concurrent Therapy
- The patient must have, within the last 24 months, failed to respond to at least 1 cycle of treatment with BCG (with or without interferon) or be intolerant to BCG treatment.
- The patient must have had a transurethral resection of the bladder tumour (TURBT) mapping the location of tumour and quantifying the area of bladder affected.
- The patient must have documented residual CIS (i.e. unresectable disease) prior to study drug administration.
- Patient Characteristics
- The patient must have adequate organ function, as defined by the clinical trial protocol
- Other
- The patient must have the ability to understand and sign an Independent Ethics Committee or Institutional Review Board (IEC/IRB)- approved informed consent document indicating that the patient (or legally acceptable representative) has been informed of all the pertinent aspects of the trial prior to enrollment and is willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures.
Exclusion
- The patient has evidence of urethral or upper tract transitional cell carcinoma (TCC) by biopsy or upper tract radiological imaging (i.e. intravenous pyelogram, computed tomography (CT) urogram, or retrograde pyelogram) within the past 2 years
- The patient has hydronephrosis
- The patient has had prior intravesical chemotherapy or investigational or anti-cancer treatments within the last 2 months, inclusive of single-dose adjuvant intravesical chemotherapy immediately post-TURBT
- The patient has existing severe urinary tract infection or recurrent severe bacterial cystitis
- The patient has active, uncontrolled impairment of the renal, hepatobiliary, cardiovascular, gastrointestinal, urogenital, neurologic or hematopoietic systems which, in the opinion of the investigator, would predispose the patient to the development of complications from the administration of intravesical therapy and/or general anesthesia
- Any patient who, in the opinion of the investigator, cannot tolerate intravesical administration or intravesical surgical manipulation (cystoscopy, biopsy) due to the presence of concomitant serious illness (i.e. uncontrolled cardiac or respiratory disorders)
- The patient is pregnant or breast feeding
- Women of reproductive age (who are not either medically or surgically incapable or bearing children) and all men may not participate unless agreeing to use double barrier contraception, or commit to abstinence during the period of therapy
Key Trial Info
Start Date :
March 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 1 2009
Estimated Enrollment :
46 Patients enrolled
Trial Details
Trial ID
NCT00462488
Start Date
March 1 2007
End Date
October 1 2009
Last Update
May 12 2020
Active Locations (21)
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1
Southeastern Research Group, Inc.
Tallahassee, Florida, United States, 32308
2
Johns Hopkins Medical Institutions
Baltimore, Maryland, United States, 21287
3
Lawrenceville Urology
Lawrenceville, New Jersey, United States, 08648
4
Duke University Medical Center
Durham, North Carolina, United States, 27710