AUY922 in Patient With Stage IV NSCLC

• Status: Completed
• Trial end date: 2017-02-01
• Target enrollment: 0
• Participant gender: All

Summary

This is an open-label, single-arm, multicenter phase II trial in patients with stage IV EGFR T790M, EGFR exon 20 and other uncommon, HER2, or BRAF-mutated; ALK, ROS1, or RET-rearranged NSCLC.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: National Taiwan University Hospital

Criteria

Inclusion Criteria:

• Histologically or cytologically proven diagnosis of stage IV NSCLC (AJCC 7th) which had been treated with one systemic therapy.

• One of the molecular alterations as follows:

• EGFR mutations in exon 20 T790M.

• EGFR mutations in exon 20; in-frame duplication and/or insertion (e.g. A767_V769dupASV or H773_V774insH) or point mutations other than T790M; or other uncommon mutations.

• HER2 mutation in exon 20; in-frame duplication and/or insertion (e.g. YVMA 776-779 ins).

• BRAF mutation in exon 15; point mutation (e.g. V600E) or in exon 11; point mutation (e.g. G469A, D594G).

• ALK translocation resulting in EML4-ALK, KIF5B-ALK, or TFG-ALK fusion as determined by an ALK break apart FISH assay and defined by an increase in the distance of 5' and 3' ALK probes (split 5'-3') or the loss of the 5' probe (single 3'). Positive ALK results from other methods such as immunohistochemistry (IHC) or reverse transcriptase polymerase chain reaction testing may also be acceptable.

• ROS1 translocation resulting in CD74-ROS1 or SLC34A2-ROS1, etc.

• RET translocation resulting in KIF5B-RET fusion, etc.

• Patients with brain metastases are eligible if treated and neurologically stable for at least 2 weeks and is not taking any steroid.

• Any prior chemotherapy, targeted therapy (monoclonal antibodies), or major surgeries must have had completed at least 4 weeks before initiation of study medication. Any prior targeted therapy (tyrosine kinase inhibitors), radiotherapy or minor surgeries must have had completed at least 2 weeks before initiation of study medication. Any acute toxicity must have recovered to <=grade 1 (except for alopecia).

• Patients must have measurable or evaluable disease as per RECIST version 1.1.

• 20 years of age or older

• ECOG performance status 0-2

• Adequate organ function as defined by the following criteria:

• Bone marrow function

• Hemoglobin >=8.0 g/dL

• Absolute neutrophil count (ANC) >=1500/uL

• Platelets >=100,000/uL

• Hepatic function

• Serum aspartate transaminase (AST) and serum alanine transaminase (ALT) <=3.0 x upper limit of normal (ULN) or AST and ALT <=5.0 x ULN if there is liver metastasis

• Total serum bilirubin <=1.5 x ULN Renal function

• Creatinine <= 1.5 x ULN or creatinine clearance >=45 mL/min

• Able to communicate well with the investigator, to understand and comply with the requirements of the study. Understand and sign the written informed consent.

• Patients must use effective methods of contraception during the study period and for at least 90 days following study completion (excluding surgically sterile male patients, surgically sterile or postmenopausal female patients).

Exclusion Criteria:

• Currently on other therapeutic clinical trials

• Prior treatment of HSP90 inhibitors

• Any of the following within 3 months before initiation of study medication

• Myocardial infarction

• Unstable angina

• Coronary artery bypass graft

• Congestive heart failure NYHA functional class III or IV

• Cerebral vascular accident

• Transient ischemic attack

• Uncontrolled hypertension at screening

• Ongoing cardiac arrhythmias of NCI CTCAE grade >=2

• Active infection requiring antibiotics

• Pregnancy or breast feeding

• Prior malignancy within the past 5 years (excluding non-melanoma skin cancer, cervical carcinoma in situ, superficial bladder cancer, and early prostate cancer).

• Active hepatitis B or C; positive HIV test result.