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Pegfilgrastim Given Same Day As or Day After Carboplatin and Docetaxel in Advanced Metastatic Non-Small Cell Lung Cancer (NSCLC)

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Amgen

Status

Completed

Conditions

Lung Cancer
Non-Small Cell Lung Cancer

Treatments

Other: PI Discretion

Study type

Observational

Funder types

Industry

Identifiers

NCT00094822
20030123

Details and patient eligibility

About

The purpose of this research study is to evaluate the safety and effectiveness of Neulasta® (pegfilgrastim) in reducing infection when given on the same day versus one day after the completion of chemotherapy (docetaxel and carboplatin) in patients with advanced or metastatic non-small cell lung cancer (NSCLC). This study is considered to be "investigational" because previous studies with Neulasta® used next day dosing and not same day dosing.

Enrollment

90 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Eligibility Criteria: - Age 18 years or older - Diagnosis of advanced or metastatic non-small cell lung cancer (NSCLC) - Have not received any prior chemotherapy - Have not received radiation therapy or undergone major surgery within the past 2 weeks

Trial design

90 participants in 2 patient groups

Pegfilgrastim
Treatment:
Other: PI Discretion
PLACEBO
Treatment:
Other: PI Discretion

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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