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A Phase 1 Dose-escalation Study of OSI-906 and Erlotinib (Tarceva®)

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.
NCT00739453

Astellas Study ID

The unique identification code given by the study sponsor.

OSI-906-103

EudraCT ID

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

2008-001743-20

Follow Trial

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

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

Oct 2008 - Mar 2012

Masking

None (Open Label)

Enrollment number

95

A Phase I Dose-escalation Study of OSI-906 and Erlotinib (Tarceva®) in Patients with Advanced Solid Tumors

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

University of Colorado Health Science Center

Aurora, United States, 80045

Johns Hopkins Sidney Kimmel Comprehensive Cancer Center

Baltimore, United States, 21231

Hudson-Webber Cancer Research Center, Karmanos Cancer Institute

Detroit, United States, 48201

University of Oxford Department of Medical Oncology

Oxford, United Kingdom, OX3 7LJ

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