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Summary

Eligibility
for people ages 18 years and up
Location
at San Francisco, California and other locations
Dates
study started
estimated completion:
Principal Investigator

Description

Summary

The purpose of this study is to explore the safety, tolerability, pharmacokinetics, immunogenicity and preliminary efficacy of INCB024360 administered in combination with MEDI4736 in subjects with selected advanced solid tumors.

Official Title

A Phase 1/2 Study Exploring the Safety, Tolerability, and Efficacy of Epacadostat (INCB024360) in Combination With Durvalumab (MEDI4736) in Subjects With Selected Advanced Solid Tumors (ECHO-203)

Keywords

Selected Advanced Solid Tumors Non-small Cell Lung Cancer Melanoma Head and Neck Cancer Gastric Cancer Gastroesophageal Cancer Urothelial Cancer Triple Negative Breast Cancer Antibodies, Monoclonal

Eligibility

You can join if…

Open to people ages 18 years and up

  • Male or female subjects, age 18 years or older
  • Histologically or cytologically confirmed diagnosis of selected locally advanced or metastatic solid tumors
  • Must have failed at least 1 prior treatment regimen for locally advanced or metastatic disease or be intolerant to treatment or refuse standard treatment

You CAN'T join if...

  • Laboratory and medical history parameters not within protocol-defined range
  • Participation in any other study in which receipt of an investigational study drug occurred within 28 days or 5 half-lives (whichever is longer) prior to first dose
  • Prior treatment with immune checkpoint inhibitors (eg, anti-CTLA-4, anti-PD-1,anti-PD-L1, and any other antibody or drug specifically targeting T-cell co-stimulation) or an IDO inhibitor (exception is tumor types in which a PD-1 pathway targeted agent is approved, e.g. melanoma, non-small cell lung cancer.)
  • Receipt of any anticancer medication in the 21 days prior to receiving the first dose of study medication
  • Has an active or inactive autoimmune process
  • Evidence of interstitial lung disease or active, non-infectious pneumonitis
  • Prior radiotherapy within 2 weeks of initiating treatment; Must have recovered from all radiation-related toxicities, not require corticosteroids, and not have had radiation pneumonitis
  • Untreated central nervous system (CNS) metastases or CNS metastases that have progressed
  • Currently pregnant or breastfeeding

Locations

  • San Francisco, California, United States
  • Denver, Colorado, United States
  • Dallas, Texas, United States
  • Houston, Texas, United States
  • Chicago, Illinois, United States
  • Louisville, Kentucky, United States
  • Huntersville, North Carolina, United States
  • Winston-Salem, North Carolina, United States
  • Tampa, Florida, United States
  • Durham, North Carolina, United States
  • Sarasota, Florida, United States
  • Port Saint Lucie, Florida, United States
  • Miami, Florida, United States
  • Barcelona, Spain
  • Pamplona, Spain
  • Turin, Italy

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Incyte Corporation
ID
NCT02318277
Phase
Phase 1/2
Lead Scientist
Alain Algazi
Study Type
Interventional
Last Updated
May 1, 2017
I’m interested in this study!