CompletedPhase 1 / Phase 2NCT00994123

A Study of MM-121 Combination Therapy in Patients With Advanced Non-Small Cell Lung Cancer

A Phase 1-2 study of MM-121 in combination with standard therapy for non-small cell lung cancer (NSCLC).

Checked against the public recordLast updated Aug 22, 2016 · Source: ClinicalTrials.gov

StatusCompleted
PhasePhase 1 / Phase 2
U.S. locations38
SponsorMerrimack Pharmaceuticals
01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Phase 1 / Phase 2
Sponsor
Merrimack Pharmaceuticals
Interventions being studied
Drug: MM-121; 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

Inclusion Criteria: * Patients with locally advanced or metastatic non-small cell lung cancer. * Patients must be \>/= 18 years of age. * Patients must have adequate Performance Status (PS) as measured by ECOG and adequate end organ function. Exclusion Criteria: * Patients with a recent history (within 5 years) of another malignancy. * Patients who are pregnant or nursing. * Patients with clinically significant heart failure. * Patients with clinically significant eye or gastrointestinal abnormalities.

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

  • Study locationBirmingham, Alabama
  • Study locationTucson, Arizona
  • Study locationLoma Linda, California
  • Study locationSacramento, California
  • Study locationSan Francisco, California
  • Study locationAurora, Colorado
  • Study locationTampa, Florida
  • Study locationAtlanta, Georgia
  • Study locationLafayette, Indiana
  • Study locationBoston, Massachusetts
  • Study locationSt Louis, Missouri
  • Study locationBuffalo, New York

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Aug 22, 2016. Always confirm current availability with the study team.

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