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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00127595
Other study ID # GEMOX
Secondary ID
Status Terminated
Phase Phase 2
First received August 5, 2005
Last updated August 23, 2005
Start date January 2002
Est. completion date April 2005

Study information

Verified date August 2005
Source Gustave Roussy, Cancer Campus, Grand Paris
Contact n/a
Is FDA regulated No
Health authority France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Study type Interventional

Clinical Trial Summary

This is a phase II monocentric study of oxaliplatin (Ox) in combination with gemcitabine (Gem; GEMOX) in patients (pts) with advanced/metastatic transitional cell carcinoma (TCC) of the urothelial tract.


Recruitment information / eligibility

Status Terminated
Enrollment 28
Est. completion date April 2005
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Transitional cell carcinoma

- Histologically-proven

- Locally advanced unresectable or metastatic

- With at least one measurable target

- Informed consent signed

Exclusion Criteria:

- Previous chemotherapy

- Previous radiotherapy

- Performance status >=2

- Peripheral neuropathy >=1

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
gemcitabine, oxaliplatin


Locations

Country Name City State
France Institut Gustave Roussy Villejuif

Sponsors (1)

Lead Sponsor Collaborator
Gustave Roussy, Cancer Campus, Grand Paris

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary response rate (Response Evaluation Criteria in Solid Tumors [RECIST] criteria)
Secondary overall survival
Secondary disease free survival
Secondary toxicity
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