TerminatedPhase 3NCT01487174

KD019 Versus Erlotinib in Subjects With Stage IIIB/IV Non Small Cell Lung Cancer With Progression After First- or Second-Line Chemotherapy

This study involves treatment with KD019 or erlotinib in patients with Non-small cell lung cancer (NSCLC) who have progressed after first- or second- line chemotherapy. It is hypothesized that KD019 can prolong survival compared with erlotinib.

Checked against the public recordLast updated May 13, 2022 · Source: ClinicalTrials.gov

StatusTerminated
PhasePhase 3
U.S. locations2
SponsorKadmon Corporation, LLC
01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Phase 3
Sponsor
Kadmon Corporation, LLC
Interventions being studied
Drug: KD019; Drug: Erlotinib
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

For Eligibility subjects must have: * failed one or two previous courses of therapy. * have no active brain metastasis. Treated non-active brain metastasis are acceptable. * cannot have received an Epidermal Growth Factor Receptors inhibitor (Tarceva \[erlotinib\] or Iressa \[gefitinib\]) in the past. * has demonstrated progressive disease.

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Yale Cancer CenterNew Haven, Connecticut
  • San Juan Oncology AssociatesFarmington, New Mexico

Source and freshness
Processed from ClinicalTrials.gov. Last public update: May 13, 2022. Always confirm current availability with the study team.

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