TVB-2640 for the Treatment of Patients with Metastatic or Advanced KRAS Mutant Non-Small Cell Lung Cancers

Inclusion Criteria

• Metastatic or advanced stage, histologically or cytologically confirmed NSCLC and molecular identification of KRAS mutation. * KRAS mutant NSCLC must be refractory, relapsed, and/or intolerant (including contraindications to) of combination platinum-doublet chemotherapy and immune checkpoint inhibitor therapy * Molecular characterization (tissue- or blood-based [i.e., cell-free/circulating tumor DNA]) must have been performed and must have demonstrated an oncogenic KRAS mutation (e.g., exon 12, 13, 61, or 117 mutation detected by sequencing) by a Clinical Laboratory Improvement Act (CLIA)-certified assay (source documentation required). KRAS mutations at other codons require review and approval by Study Chair
• Subjects' EGFR mutation and ALK gene rearrangement status must be known prior to study entry. Subjects with EGFR mutation or ALK gene rearrangement must have progressed after appropriate Food and Drug Administration (FDA)-approved targeted therapy options prior to eligibility
• Patient has evidence of disease progression on most recent line of therapy
• Patient has measurable disease by Response Evaluation Criteria in Solid Tumors (RECIST) version (v)1.1 (Eisenhauer, 2009)
• Age >= 18 years
• Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
• Predicted life expectancy of >= 3 months
• Absolute neutrophil count >= 1,500/mcL
• Platelets >= 75,000/mcL
• Total bilirubin < 2 X institutional upper limit of normal
• Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =< 5 X institutional upper limit of normal
• Serum creatinine =< 1.5 X institutional upper limit of normal
• Left ventricular ejection fraction (LVEF) >= 50%
• Corrected QT using Fridericia's formula (QTcF) < 470 msec
• Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry, for the duration of study participation, and for 90 days following completion of therapy. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately * A female of child-bearing potential is any woman (regardless of sexual orientation, having undergone a tubal ligation, or remaining celibate by choice) who meets the following criteria: ** Has not undergone a hysterectomy or bilateral oophorectomy; or ** Has not been naturally postmenopausal for at least 12 consecutive months (i.e., has had menses at any time in the preceding 12 consecutive months)
• No significant ischemic heart disease or myocardial infarction within 6 months of first dose of TVB-2640 and with current adequate cardiac function
• Ability to understand and the willingness to sign a written informed consent

Exclusion Criteria

• Patient is unable to swallow oral medications or has impairment of gastrointestinal (GI) function or GI disease that may significantly alter drug absorption such as active inflammatory bowel disease, uncontrolled nausea, vomiting, diarrhea, or malabsorption syndrome
• Patient has a history of risk factors for torsade de pointes such as uncontrolled heart failure, severe hypokalemia with potassium less than 3 mM/L, history of long QT syndrome or require use during study participation of concomitant medications known to prolong QT/corrected QT (QTc) interval
• Patients who require use of strong CYP3A4/5 agonists or inhibitors during study participation
• Patient has uncontrolled or severe intercurrent medical condition including uncontrolled brain metastases. Patients with stable brain metastases either treated or untreated, on a stable dose of steroids/anticonvulsants, with no dose increase within 4 weeks before the first dose of TVB-2640, and no anticipated dose change, are allowed
• Patient underwent major surgery within 4 weeks before the first dose of TVB-2640 or received cancer-directed therapy either chemotherapy, radiotherapy, hormonal therapy, biologic or immunotherapy, etc. or an investigational drug or device within 2 weeks (6 weeks for mitomycin C and nitrosoureas) or 5 half-lives of that agent, whichever is shorter before the first dose of TVB-2640. In addition, any drug-related toxicity, with the exception of alopecia, an endocrinopathy controlled with replacement therapy, or a clinically stable toxicity not expected to increase from study therapy (e.g., cisplatin-associated ototoxicity) should have recovered to =< grade 1
• If female, patient is pregnant or breast-feeding
• Patient has evidence of a serious active infection-infection requiring treatment with intravenous antibiotics
• Patient has known immunodeficiency virus- human immunodeficiency virus (HIV) or hepatitis B or C infection, as such patients may be at increased risk for toxicity due to concomitant treatment and disease-related symptoms may preclude accurate assessment of the safety of TVB-2640
• Patient has an important medical illness or abnormal laboratory finding that, in the investigator’s opinion, would increase the risk of participating in this study
• Patients with prior or concurrent malignancy whose natural history or treatment has the potential to interfere with the safety or efficacy assessment of the investigational agent
• History of clinically significant dry eye (xerophthalmia) or other corneal abnormality or, if a contact lens wearer, does not agree to abstain from contact lens use from baseline through the last study drug dose
• Patient has a known allergy or hypersensitivity to components of TVB-2640
• Patient has a prior history of hypersensitivity, drug/radiation-induced, or other immune-mediated pneumonitis