Study Details

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Study of Intermittent OSI-906 Dosing

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.
NCT00514306

Astellas Study ID

The unique identification code given by the study sponsor.

OSI-906-102

EudraCT ID

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

2006-005938-20

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

Jul 2007 - Sep 2010

Masking

None (Open Label)

Enrollment number

79

A Phase I Dose Escalation Study of Intermittent Oral OSI-906 dosing 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

MD Anderson Cancer Center

Houston, United States, 77030

Drug Development Unit, Royal Marsden Hospital

Sutton, United Kingdom, SM2 5PT

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