CompletedPhase 2NCT01752400
Official study title

AUY922 for Advanced ALK-positive NSCLC

Study summary

This research study is a Phase II clinical trial, which tests the safety and effectiveness of an investigational drug to learn whether the drug works in treating a specific cancer. "Investigational" means that the drug is being studied and that research doctors are trying to find out more about it-such as the safest dose to use, the side effects it may cause and if the drug is effective for treating your type of cancer. It also means that the FDA has not yet approved the drug for your type of cancer or for any use outside of research studies. It has been found that some people with NSCLC have a change (mutation) in a certain gene called the ALK gene. This mutated gene helps cancer cells grow. There is a drug (crizotinib) that has been approved by the FDA for the treatment of people with NSCLC who have mutations in the ALK gene. Most people respond to crizotinib initially. Over time, however, patients may stop responding (become resistant) to crizotinib because of additional changes in the ALK gene that makes crizotinib ineffective. AUY922 is an investigational drug that may stop cancer cells from growing abnormally. This drug has been used in other research studies. Information from those other research studies suggests that AUY922 may be effective in killing cancer cells that have become resistant to drugs like crizotinib. Only participants with changes in the ALK gene will be allowed to participate in this study. The purpose of this study is to test the safety of AUY922 and determine how well AUY922 treats participants with advanced, ALK-positive NSCLC.

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Key things to know

Main goalTreatment

This describes the study’s primary purpose.

What is being studiedAUY922

The study team can explain what participation involves.

Who it may be forNon-small cell lung cancer (NSCLC) · ALK

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Mar 29, 2018 · Source: ClinicalTrials.gov

Is enrollment open?Completed

Ask the study team to confirm whether enrollment is open.

What kind of study?Phase 2

Interventional

Where is it offered?4 U.S. locations

Locations may change over time.

Who runs it?Massachusetts General Hospital

Study sponsor

01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Phase 2
Sponsor
Massachusetts General Hospital
Interventions being studied
Drug: AUY922
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

The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.

Requirements people may need to meetInclusion criteria
  • Histologically or cytologically confirmed advanced NSCLC
  • Tumor characterized by abnormalities in ALK
  • Required to provide archival tissue in the form of 5 formalin fixed paraffin embedded sections
  • Have acquired resistance to treatment with an ALK-TKI
  • At least one measurable lesion as defined by RECIST criteria
  • Life expectancy of at least 12 weeks
Reasons someone may not be able to joinExclusion criteria
  • Pregnant or breastfeeding
  • Discontinued ALK TKI more than four weeks prior to enrollment
  • Unresolved diarrhea greater than or equal to CTCAE grade 1
  • Not willing to use double barrier methods of contraception
  • Prior anti-neoplastic treatment with any HSP90 or HDAC inhibitor compound
  • Have received cytoxic chemotherapy in the intervening period since discontinuation of an ALK-TKI
  • Have undergone major surgery within 2 weeks prior to starting study drug
  • Any concurrent or uncontrolled illness
  • Any known disorders due to a deficiency in bilirubin glucuronidation
  • Taking therapeutic doses of warfarin
  • Any serious cardiac disorders or abnormalities
  • Concurrent malignancies or invasive cancers diagnosed within the past 2 years except for adequately treated basal cell cancer of the skin or in situ cancers
  • Known to be HIV positive
  • Known hypersensitivity to any of the study drugs or their excipients
  • Participation in another clinical study within 30 days before the first study treatment

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

  • Massachusetts General HospitalBoston, Massachusetts
  • Beth Isreal Deaconess Medical CenterBoston, Massachusetts
  • Brigham and Women's HospitalBoston, Massachusetts
  • Dana-Farber Cancer InstituteBoston, Massachusetts

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Mar 29, 2018. Always confirm current availability with the study team.

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