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A Pharmacokinetic Study of Erlotinib in Cancer Patients with Advanced Solid Tumors, with Adequate and Moderately Impaired Hepatic Function

This trial is complete
The study has ended normally, and participants are no longer being examined or treated (that is, the last participant's last visit has occurred).

Clinicaltrials.gov ID

The unique identification code given to each clinical study upon registration at ClinicalTrials.gov.
NCT00139620

Astellas Study ID

The unique identification code given by the study sponsor.

OSI-774-104

EudraCT ID

The unique identification code given to each clinical study upon registration at EudraCT (European Union Drug Regulating Authorities Clinical Trials Database).

2006-002363-59

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Condition

Advanced/Metastatic Cancer

Phase

These clinical trials are usually the first time an experimental treatment is studied in a small group of people.

Phase 1

Age

18 Years - N/A N/A

Sex

Female & Male

Product

N/A

Type

A type of clinical study in which participants are assigned to groups that receive one or more intervention/treatment (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.

Interventional

Trial Dates

Aug 2005 - Jun 2007

Masking

None (Open Label)

Enrollment number

39

An Open-Label Study to Characterize the Pharmacokinetic Parameters of Erlotinib (Tarceva®, OSI-774) in Cancer Patients with Advanced Solid Tumors, with Adequate and Moderately Impaired Hepatic Function

Study summary

Study documents

Study Documents, including study results, are available after a study is completed or terminated, according to Astellas Transparency policy.

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Locations

Mayo Clinic

Rochester, United States, 55905

Premiere Oncology

Santa Monica, United States, 90404

UPMC Cancer Pavilion

Pittsburgh, United States, 15232

University of Colorado Health Sciences Center

Aurora, United States, 80010

The Beatson West of Scotland Cancer Centre

Glasgow, United Kingdom, G12 0YN

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