Pemetrexed Disodium and Hsp90 Inhibitor AUY922 in Treating Patients With Previously Treated Stage IV Non-Small Cell Lung Cancer

Study summary

This phase I trial studies the side effects and the best dose of Hsp90 inhibitor AUY922 when given together with pemetrexed disodium in treating patients with previously treated stage IV non-small cell lung cancer. Hsp90 inhibitor AUY922 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as pemetrexed disodium, work in different ways to stop the growth of tumor cell, either by killing the cells or stopping them from dividing. Giving Hsp90 inhibitor AUY922 together with pemetrexed disodium may kill more tumor cells

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Key things to know

Main goalTreatment

This describes the study’s primary purpose.

What is being studiedHsp90 inhibitor AUY922 and pemetrexed disodium

Plus 2 other study approaches.

Who it may be forNon-small cell lung cancer (NSCLC) · Metastatic or stage IV · Recurrent or relapsed

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Sep 3, 2020 · Source: ClinicalTrials.gov

Is enrollment open?Completed

Ask the study team to confirm whether enrollment is open.

What kind of study?Phase 1

Interventional

Where is it offered?1 U.S. location

Locations may change over time.

Who runs it?Jonsson Comprehensive Cancer Center

Study sponsor

Study overview

What this study is about

Purpose: Treatment
Study type: Interventional
Phase: Phase 1
Sponsor: Jonsson Comprehensive Cancer Center
Interventions being studied: Drug: Hsp90 inhibitor AUY922; Drug: pemetrexed disodium; Other: pharmacological study; Other: laboratory biomarker analysis

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How this study is categorized

These labels come from structured fields and exact terms in the public record.

Cancer type

Non-small cell lung cancer (NSCLC)→

Disease setting

Metastatic or stage IV→Recurrent or relapsed→

Treatment approach

Chemotherapy→

Study topics

After prior treatment→

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

Ability to understand the purpose and risks of the study and provide signed and dated informed consent and authorization to use protected health information (PHI) in accordance with national and local subject privacy regulations
Histologically- or cytologically-confirmed stage IV non-squamous, NSCLC who have progressed after at least one prior line of treatment; in the expansion phase, participants are only eligible if their molecular category has not been fully enrolled (10 participants with epidermal growth factor receptor (EGFR) mutations, 5 participants with anaplastic lymphoma receptor tyrosine kinase (ALK) gene rearrangement, 5 participants with wild type v-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog (KRAS), EGFR and ALK)
At least one measurable lesion as defined by modified RECIST version 1.1; previously irradiated lesions are not measurable unless the lesion is new or has demonstrated clear progression after radiation
Last chemotherapy or treatment with another systemic anti-cancer agent must have stopped \>= 4 weeks prior to enrollment (or \>= 5 half-lives for oral tyrosine-kinase inhibitors or 2 weeks for palliative radiotherapy); participants must have recovered (Common Terminology Criteria for Adverse Events \[CTCAE\] =\< 1 or baseline) from acute toxicities of any previous therapy (with the exception of alopecia)
Eastern Cooperative Oncology Group (ECOG) performance status =\< 2
Expected survival time of \>= 3 months in the opinion of the investigator
Absolute neutrophil count (ANC) \>=1.5 x 10\^9/L
Hemoglobin (Hgb) \>= 9 g/dl
Platelets (plt) \>= 100 x 10\^9/L
Potassium within normal limits
Total calcium (corrected for serum albumin) within normal limits or corrected with supplements
Magnesium within lower limits or corrected with supplements
Phosphorus within lower limits or corrected with supplements
Aspartate aminotransferase (AST)/serum glutamic oxaloacetic transaminase (SGOT) and alanine aminotransferase (ALT)/serum glutamate pyruvate transaminase (SGPT) =\< 1.5 x upper limit of normal (ULN)
AST/SGOT and ALT/SGPT =\< 2.5 x upper limit of normal (ULN) if liver metastases are present
Serum bilirubin =\< 1.5 x ULN
Serum creatinine =\< 1.5 x ULN or 24-hour clearance \>= 50 ml/min
Negative serum or urine pregnancy test; the serum pregnancy test must be obtained prior to the first administration of AUY922 (=\< 14 days prior to dosing) in all pre-menopausal women and women \< 2 years after the onset of menopause
Ability to provide a formalin-fixed, paraffin-embedded (FFPE) tumor tissue sample containing representative tumor tissue from a previously obtained biopsy/resection that meets specific tissue sample requirements at screening

Reasons someone may not be able to joinExclusion criteria

Unresolved diarrhea \>= CTCAE (v4.0) grade 1
Pregnant or lactating women
Fertile women of childbearing potential (WCBP) not using (or refusing to use) adequate methods of contraception as agreed on between her and the consenting investigator; male participants not using (or refusing to use) a condom during intercourse
History of another primary cancer within 3 years prior to enrollment with the exception of curatively treated skin cancer (other than melanoma) or curatively treated cervical carcinoma in-situ
History of central nervous system (CNS) metastasis; Note: participants without clinical signs and symptoms of CNS involvement are not required to have magnetic resonance imaging (MRI) of the brain; (exception: participants with treated brain metastases who are asymptomatic, not currently on steroid therapy, and clinically stable for \>= 2 weeks will be eligible for protocol participation)
Prior treatment with pemetrexed
Prior anti-neoplastic treatment with any heat shock protein 90 (HSP90) or histone deacetylase (HDAC) inhibitor compound
Participants who have undergone any major surgery =\< 2 weeks prior to starting study drug or who have not recovered from side effects of such therapy
Last chemotherapy or treatment with another systemic anti-cancer agent must have stopped \>= 4 weeks prior to enrollment (or \>= 5 half-lives for oral tyrosine-kinase inhibitors); participants with EGFR mutations and ALK gene rearrangement who have not received a tyrosine kinase inhibitor targeting their molecular abnormality (e.g., erlotinib or crizotinib respectively); participants must have recovered (CTCAE =\< 1) from acute toxicities of any previous therapy (with the exception of alopecia)
Participants who have concurrent or uncontrolled illness that the investigator feels will impede study participation including, but not limited to:
Acute or chronic liver disease
Acute or chronic renal disease
Active or ongoing infection
Psychiatric illness/social situations that would limit compliance with study requirements
Participants with known disorders due to a deficiency in bilirubin glucuronidation (e.g. Gilbert's syndrome)
Intolerance of Vitamin B12, folic acid or dexamethasone
Participants with following cardiac criteria:
History of long QT syndrome
QTcF \>= 450 ms during screening electrocardiogram (ECG)
History of clinically manifest ischemic heart disease including myocardial infarction, stable or unstable angina pectoris, coronary arteriography or cardiac stress testing/imaging with findings consistent with infarction or clinically significant coronary occlusion ≤ 6 months prior to study start
History of heart failure or left ventricular (LV) dysfunction (LV ejection fraction \[EF\] =\< 45%) by multi gated acquisition scan (MUGA) or echocardiogram (ECHO)
Clinically significant ECG abnormalities including one or more of the following: left bundle branch block (LBBB), right bundle branch block (RBBB) with left anterior hemiblock (LAHB); ST segment elevations or depressions \> 1mm, or 2nd (Mobitz II) or 3rd degree atrioventricular block (AV) block
History and presence of atrial fibrillation, atrial flutter or ventricular arrhythmias including ventricular tachycardia or Torsades de pointes
Other clinically significant heart disease (e.g. congestive heart failure, uncontrolled hypertension, history of labile hypertension, or history of poor compliance with a hypertensive regimen)
Clinically significant resting bradycardia (\< 50 beats per minute)
Participants who are currently receiving treatment with any medication which has a relative risk or prolonging the QTcF interval or inducing Torsades de pointes (as listed in protocol) and cannot be switched or discontinued to an alternative drug prior to commencing AUY922 dosing
Participants who are on a cardiac pacemaker
Participants unwilling or unable to comply with the protocol
Participants known to be human immunodeficiency virus (HIV) positive; testing is not required in the absence of clinical signs and symptoms suggesting HIV infection
Any systemic anti-cancer treatment out of allowed timelines
Concurrent cytotoxic or immunosuppressive therapy for non-malignant disease (e.g., for rheumatoid arthritis or lupus)

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

Study sites

U.S. locations

Jonsson Comprehensive Cancer CenterLos Angeles, California

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Sep 3, 2020. Always confirm current availability with the study team.

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