Bladder Cancer Clinical Trial

Vinflunine in Patients With Locally Advanced or Metastatic Transitional Cell Carcinoma of the Urothelium

Summary

The purpose of this clinical research study is to learn if vinflunine can shrink or slow the growth of the cancer or increase survival in patients with transitional cell carcinoma of the urothelium. The safety of this treatment will also be studied.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Clinical diagnosis of transitional cell carcinoma of the urothelium that is locally advanced or metastatic (i.e. patients cannot be candidates for local/regional control of disease).
Relapse or progression within 12.5 months of prior cisplatin or carboplatin containing chemotherapy regimen.
Adequate performance status (Karnofsky greater or equal to 80).

Exclusion Criteria:

Receipt of more than 1 prior chemotherapy regimen in any setting.
Prior discontinuation of platinum due solely to toxicity.
Current neuropathy greater or equal to CTC grade 2.
Prior radiation to greater or equal to 30% of bone marrow.
Inadequate hematologic function: ANC <1,500 cells/mm3, Platelet<100,000 cells/mm3.
Inadequate hepatic function: total bilirubin > 1.5 times ULN, ALT/AST > 2.5 times ULN or > 5 times ULN in case of liver metastasis.
Inadequate renal function: creatinine clearance <20 ml/min.
Prior allergy to any vinca-alkaloid.

Study is for people with:

Bladder Cancer

Phase:

Phase 2

Estimated Enrollment:

150

Study ID:

NCT00101608

Recruitment Status:

Completed

Sponsor:

Bristol-Myers Squibb

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There is 1 Location for this study

See Locations Near You

Local Institution
Beverly Hills California, , United States
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La Jolla California, , United States
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Los Angeles California, , United States
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Santa Monica California, , United States
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Stanford California, , United States
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Vallejo California, , United States
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Aurora Colorado, , United States
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New Haven Connecticut, , United States
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Washington District of Columbia, , United States
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Jacksonville Florida, , United States
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Miami Florida, , United States
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Atlanta Georgia, , United States
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Honolulu Hawaii, , United States
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Chicago Illinois, , United States
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Joliet Illinois, , United States
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Urbana Illinois, , United States
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Louisville Kentucky, , United States
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Baltimore Maryland, , United States
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Burlington Massachusetts, , United States
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Ann Arbor Michigan, , United States
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Detroit Michigan, , United States
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Kansas City Missouri, , United States
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St. Louis Missouri, , United States
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Las Vegas Nevada, , United States
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Lebanon New Hampshire, , United States
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Bronx New York, , United States
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Buffalo New York, , United States
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New York New York, , United States
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Charlotte North Carolina, , United States
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Durham North Carolina, , United States
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Cincinnati Ohio, , United States
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Philadelphia Pennsylvania, , United States
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Pittsburgh Pennsylvania, , United States
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Providence Rhode Island, , United States
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Nashville Tennessee, , United States
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Dallas Texas, , United States
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Seattle Washington, , United States
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Milwaukee Wisconsin, , United States
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Liverpool New South Wales, , Australia
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Sydney New South Wales, , Australia
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Taree New South Wales, , Australia
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Waratah New South Wales, , Australia
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Westmead New South Wales, , Australia
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Adelaide South Australia, , Australia
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Linz , , Austria
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Salzburg , , Austria
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Edmonton Alberta, , Canada
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London Ontario, , Canada
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Toronto Ontario, , Canada
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Montreal Quebec, , Canada
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Caen , , France
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Le Mans Cedex 2 , , France
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Nice , , France
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Paris , , France
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Toulouse , , France
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Ilion , , Greece
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Jakarta , , Indonesia
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Genova , , Italy
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Milan , , Italy
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Roma , , Italy
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Rome , , Italy
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Viterbo , , Italy
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Seoul , , Korea, Republic of
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Cebu City , , Philippines
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Quezon City , , Philippines
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Quezon , , Philippines
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Singapore , , Singapore
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Murcia , , Spain
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Palma De Mallorca , , Spain
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Santander , , Spain
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Sevilla , , Spain
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Linkoping , , Sweden
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Uppsala , , Sweden
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Aarau , , Switzerland
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Bangkok , , Thailand

How clear is this clinincal trial information?

Study is for people with:

Bladder Cancer

Phase:

Phase 2

Estimated Enrollment:

150

Study ID:

NCT00101608

Recruitment Status:

Completed

Sponsor:


Bristol-Myers Squibb

How clear is this clinincal trial information?

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