Expanded Access Multicenter Study of Lucanix® (Belagenpumatucel-L)

NCT01279798 · Status: NO_LONGER_AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2011-03-01

No results posted yet for this study

Summary

This is an expanded access protocol designed to make Lucanix® available to subjects with advanced non-small cell lung cancer (NSCLC) who are not eligible for the Phase III Protocol, NR001-03. A total of 45 patients will be enrolled into the study.

Conditions

Interventions

BIOLOGICAL

Lucanix® (belagenpumatucel-L)

Subjects will receive up to 12 monthly (28-35 day interval) Lucanix injections at a dose of 2.5 × 10e7 cells per injection.

Sponsors & Collaborators

  • NovaRx Corporation

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01279798 on ClinicalTrials.gov