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This trial is complete. It is no longer accepting participants. Results may be available on ClinicalTrials.gov.

NCT01772797

NCT01772797
Completed Phase 1 🇦🇺 Australian site

Who may be able to join

Who might be able to join this trial:

  • You have advanced or spreading non-small cell lung cancer (NSCLC) that got worse during or after treatment with a specific type of targeted therapy called an ALK inhibitor
  • Your tumor has been tested and shows a specific genetic change (called an ALK rearrangement) in 15% or more of the tumor cells, measured by a test called FISH
  • Your disease can be tracked and measured using standard imaging scans (confirm with trial site)

Who may not be able to join:

  • You have cancer that has spread to the brain and is causing symptoms, or requires increasing doses of steroids or other brain-focused treatments to keep it under control
  • You have a history of serious scarring or inflammation of the lung tissue, including significant lung damage from previous radiation treatment
  • You have significant heart problems (confirm with trial site)
  • Your liver, kidneys, or other organs are not working well enough, based on blood test results (confirm with trial site)
  • You are taking certain medications that strongly affect how the body processes drugs, and you cannot stop taking them at least one week before starting the trial
  • You are taking certain other medications that are broken down by the same pathways in the body, and you cannot stop them at least one week before starting the trial (confirm with trial site)
  • You have significant, uncontrolled digestive system problems or disease affecting your stomach or intestines
  • You have previously been treated with a type of drug called an HSP90 inhibitor
  • You received radiation treatment to the lung within 4 weeks before starting the trial, or you have not yet recovered from side effects of previous radiation therapy
  • You are currently pregnant or breastfeeding
  • You have a history of pancreatitis (inflammation of the pancreas), or have had abnormal blood levels of certain digestive enzymes (amylase or lipase) due to a pancreas condition

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

Phase 1: approximately ~10% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.

Trial details

Status
Completed
Phase
Phase 1
Sponsor
Novartis Pharmaceuticals
Registry
clinicaltrials_gov
Start date
1 June 2013
Est. completion
1 January 2016

Where this trial is recruiting

🇦🇺 Australia 🇮🇹 Italy 🇸🇬 Singapore 🇪🇸 Spain 🇺🇸 United States

1 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Incidence rate of Dose Limiting Toxicities (DLT)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

View original record on ClinicalTrials.gov