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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00035061
Other study ID # 4698
Secondary ID H3E-MC-JMEU
Status Completed
Phase Phase 2
First received May 2, 2002
Last updated July 18, 2006

Study information

Verified date July 2006
Source Eli Lilly and Company
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

Patients with bladder cancer will be participating in this study for the treatment of abnormal cells in the bladder that have returned after initial treatment OR have moved to a new site in the body.


Other known NCT identifiers
  • NCT00039260

Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- You must have been diagnosed with bladder cancer that has recurred or moved to a new part of the body.

- You must have at least one tumor that can be physically measured or scanned by x-ray.

- You may not have had previous chemotherapy (drug) treatment OR you have had surgery followed by one chemotherapy treatment at least 4 months ago.

Exclusion Criteria:

- You may not have used an experimental medicine or device within the past month.

- Cancer that has spread to your brain.

- If you are unwilling or unable to take folic acid or vitamin B12 supplements.

Study Design

Primary Purpose: Treatment


Intervention

Drug:
pemetrexed


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Eli Lilly and Company

Country where clinical trial is conducted

United States, 

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