Binimetinib And Hydroxychloroquine In Treating Patients With KRAS Mutant Metastatic Pancreatic Cancer

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Study Registration Dates	Results Reporting Dates	Study Record Updates
First Submitted 2019-08-22	Results First Submitted N/A	Last Update Submitted that met QC Criteria 2025-05-13
First Submitted that Met QC Criteria 2019-10-16	Results First Submitted that Met QC Criteria N/A	Last Update Posted (ACTUAL) 2025-05-16
First Posted (ACTUAL) 2019-10-18	Results First Posted N/A	Last Verified 2025-05

Design Details

Primary Purpose:
Treatment

Allocation:
Na

Interventional Model:
Single Group

Masking:
None

Arms and Interventions

Participant Group/Arm	Intervention/Treatment
EXPERIMENTAL: Treatment (binimetinib, hydroxychloroquine) Patients receive binimetinib PO BID and hydroxychloroquine PO BID on days 1-14. Cycles repeat every 14 days in the absence of disease progression or unacceptable toxicity.	DRUG: Binimetinib Given PO DRUG: Hydroxychloroquine Given PO

Participant Group/Arm

Intervention/Treatment

EXPERIMENTAL: Treatment (binimetinib, hydroxychloroquine)

Patients receive binimetinib PO BID and hydroxychloroquine PO BID on days 1-14. Cycles repeat every 14 days in the absence of disease progression or unacceptable toxicity.

DRUG: Binimetinib

Given PO

DRUG: Hydroxychloroquine

Given PO

Primary Outcome Measures	Measure Description	Time Frame
Maximum tolerated dose (MTD)	Will employ the Bayesian optimal interval (BOIN) design to find the MTD.	Up to 30 days

Secondary Outcome Measures	Measure Description	Time Frame
Response rate		Up to 1 year
Incidence of adverse events	Toxicity will be assessed using common toxicity criteria version 5.	Up to 1 year
Progression free survival	To determine the ability of the combination to halt tumor growth.	Up to 1 year
Overall survival	To assess the overall survival of patients treated on this regimen.	Up to 1 year

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person’s general health condition or prior treatments.

Ages Eligible for Study:
ALL

Sexes Eligible for Study:
18 Years

Accepts Healthy Volunteers:

Have histologically or cytologically confirmed diagnosis of pancreatic adenocarcinoma based on pathology report with radiologically identified metastases that meet Response Evaluation Criteria in Solid Tumors (RECIST) criteria.
Be willing and able to provide written informed consent for the trial.
Have at least one measurable lesion by RECIST criteria.
Have had prior treatment with at least one line of therapy for metastatic disease.
Have had tumor mutation profiling from any Clinical Laboratory Improvement Act (CLIA) certified laboratory demonstrating a KRAS mutation. Liquid biopsy demonstrating KRAS mutation will be considered acceptable.
Have a performance status of 0 or 1 on the Eastern Cooperative Oncology Group (ECOG) performance scale.
Absolute neutrophil count (ANC) >= 1500/uL (specimens must be collected within 10 days prior to the start of trial treatment).
Platelets >= 100,000/uL (specimens must be collected within 10 days prior to the start of trial treatment).
Hemoglobin >= 9.0 g/dL (specimens must be collected within 10 days prior to the start of trial treatment).
Creatinine OR measured or calculated creatinine clearance (glomerular filtration rate [GFR] can also be used in place of creatinine or creatinine clearance [CrCl]) =< 1.5 x upper limit of normal (ULN) OR >= 50 mL/min for subjects with creatinine level > 1.5 x ULN (specimens must be collected within 10 days prior to the start of trial treatment).
Total bilirubin =< 1.5 x ULN (specimens must be collected within 10 days prior to the start of trial treatment).
Indirect bilirubin =< ULN (specimens must be collected within 10 days prior to the start of trial treatment).
Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT]), and alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase [SGPT]) =< 2.5 x ULN (=< 5 x ULN for subjects with liver metastases) (specimens must be collected within 10 days prior to the start of trial treatment).
Alkaline phosphatase =< 2.5 x ULN (=< 5 x ULN for subjects with liver metastases) (specimens must be collected within 10 days prior to the start of trial treatment).
Serum albumin > 3.3 mg/dl (specimens must be collected within 10 days prior to the start of trial treatment).
International normalized ratio (INR) OR prothrombin time (PT), activated partial thromboplastin time (aPTT) =< 1.5 x ULN unless subject is receiving anticoagulant therapy as long as PT or aPTT is within therapeutic range of intended use of anticoagulants (specimens must be collected within 10 days prior to the start of trial treatment).
Female subjects of childbearing potential must have a negative urine or serum pregnancy test prior to the start of treatment.
The participant is deemed by the investigator to have the ability to be compliant with scheduled visits, treatment plan, and study procedures.
Male and female subjects of childbearing potential must agree to use an adequate method of contraception starting with the first dose of trial therapy through 30 days after the last dose of trial therapy. Note: Abstinence is acceptable if this is the usual lifestyle and preferred contraception for the subject. Acceptable methods of contraception are listed in the protocol text.

Has pancreatic tumor other than adenocarcinoma, including: acinar cell carcinoma, pancreaticoblastoma, malignant cystic neoplasms, endocrine neoplasms, squamous cell carcinoma, ampulla of Vater, periampullary, duodenal, or common bile duct malignancies. Poorly differentiated carcinoma may be included at the discretion of the investigator if histologic features suggest the possibility of adenocarcinoma.
Is currently participating in or has participated in a study of an investigational agent or has used an investigational treatment within 2 weeks prior to the anticipated first dose of study treatment.
Received anticancer therapy including chemotherapy, immunotherapy, or antineoplastic biologic drugs (e.g. erlotinib) within 14 days of the anticipated start of study treatment.
Have undergone major surgery (e.g. inpatient procedures) =< 6 weeks prior to the start of study treatment or who have not recovered from side effects of earlier such procedures.
Have undergone radiation within 7 days prior to the start of treatment.
Patient has not recovered to =< grade 1 from toxic effects of prior therapy before starting study treatment. Note that alopecia, neuropathy, myalgias, and endocrinopathy are exceptions to this criteria.
Impaired cardiovascular function or clinically significant cardiovascular disease including, but not limited to, any of the following:

History of acute coronary syndromes (including myocardial infarction, unstable angina, coronary artery bypass grafting, coronary angioplasty or stenting) < 6 months prior to screening;
Congestive heart failure requiring treatment (New York Heart Association grade >= 2);
Left ventricular ejection fraction (LVEF) < 50% as determined by multigated acquisition scan (MUGA) or echocardiography (ECHO);
Uncontrolled hypertension defined as persistent systolic blood pressure >= 150 mmHg or diastolic blood pressure >= 100 mmHg despite current therapy;
History or presence of clinically significant cardiac arrhythmias (including resting bradycardia, uncontrolled atrial fibrillation or uncontrolled paroxysmal supraventricular tachycardia);
Triplicate average baseline corrected QT (QTc) interval >= 480 ms.
Impairment of gastrointestinal function or disease which may significantly alter the absorption of study drug (e.g., active ulcerative disease, uncontrolled vomiting or diarrhea, malabsorption syndrome, small bowel resection with decreased intestinal absorption), or recent (=< 3 months) history of a partial or complete bowel obstruction, or other conditions that will interfere significantly with the absorption of oral drugs.
Had a solid organ or hematologic transplant.
Concurrent neuromuscular disorder that is associated with elevated creatine kinase (CK) (e.g., inflammatory myopathies, muscular dystrophy, amyotrophic lateral sclerosis, spinal muscular atrophy).
Has required treatment for other malignancies within 1 year prior to first dose of study treatment, with the exception of curatively treated basal cell carcinoma of the skin, squamous cell carcinoma of the skin and/or curatively resected tumors of low invasive potential (e.g., in situ cervical and/or breast cancers).
Has a history of central nervous system (CNS) metastases and/or carcinomatous meningitis.
History or current evidence of retinal vein occlusion (RVO) or current risk factors for RVO (e.g., uncontrolled glaucoma or ocular hypertension, history of hyperviscosity or hypercoagulability syndromes); history of retinal degenerative disease.
Has an active infection requiring systemic therapy.
Chronic use of steroids for pain or emesis management.
Has known ophthalmologic disease that, in the opinion of investigators, would pose an increased risk of visual disturbances during the study. This includes a history or current evidence of retinal vein occlusion (RVO) or current risk factors for RVO (e.g., uncontrolled glaucoma or ocular hypertension, history of hyperviscosity or hypercoagulability syndromes); history of retinal degenerative disease. The routine use of eyeglasses does not in itself disqualify patient participation.
Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.
Is pregnant or breastfeeding, or expecting to conceive or father children within the projected duration of the trial, starting with the screening visit through 30 days after the last dose of trial treatment.
Has a known history of human immunodeficiency virus (HIV) infection (HIV 1/2 antibodies) (No HIV screening is required for patients with no known diagnosis).
Has a history of the following liver diseases:

Hepatitis B (defined as hepatitis B surface antigen [HBsAg] reactive),
Hepatitis C (defined as detectable hepatitis C virus [HCV] ribonucleic acid [RNA]),
Primary biliary cholangitis,
Primary sclerosing cholangitis,
History of immune mediated cholangitis.
Of note, patients with a history of bacterial cholangitis are eligible if the infection has been fully resolved prior to the screening visit. An exception is made for hepatitis C patients who have undergone treatment and who have negative serologic testing for at least one year.
Has a known history of active TB (Mycobacterium Tuberculosis).
Is unable to tolerate a contrast enhanced computed tomography (CT) or magnetic resonance imaging (MRI) for staging/restaging purposes.
In the estimation of the treating physician or primary investigator, have had a clinical deterioration of their ECOG performance within the month prior to enrollment. Evidence for such deterioration shall be documented in the patient's medical record.
Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the subject's participation for the full duration of the trial, or is not in the best interest of the subject to participate, in the opinion of the treating investigator. Evidence for such abnormalities/conditions will be documented in the patient's medical record.
Has a history of thromboembolic or cerebrovascular events =< 12 weeks prior to the first dose of study treatment. Examples include transient ischemic attacks, cerebrovascular accidents, hemodynamically significant (i.e. massive or sub-massive) deep vein thrombosis or pulmonary emboli. Note: Patients with either deep vein thrombosis or pulmonary emboli that does not result in hemodynamic instability are allowed to enroll as long as they are on a stable dose of anticoagulants for at least 4 weeks. Also note: Patients with thromboembolic events related to indwelling catheters or other procedures may be enrolled. Finally: patients with stable mesenteric thrombosis that predate study assessment (eg portal vein thrombus) may be enrolled.
Has a history of active bleeding requiring transfusion within a 3 month period prior to screening. (Transfusions attributed to chemotherapy related anemia do not meet this exclusion criterion.)
Known cases of drug-induced hepatobiliary toxicities (other than a radiological finding of fatty liver).
Has had prior treatment with a MEK or ERK inhibitor.
Partial or complete bowel obstruction.
Impaired gastrointestinal function that may significantly alter the absorption of binimetinib (e.g., ulcerative diseases, uncontrolled vomiting, malabsorption syndrome, small bowel resection with decreased intestinal absorption) or baseline diarrhea >= grade 1.
Use of digoxin, mefloquine, cyclosporine, methotrexate, fexofenadine, quinidine, talinolol, vinblastine, coumestrol, daidzein, dantrolene, estrone-3-sulfate, genistein, prazosin, sulfasalazine, or antiepileptics if used for seizures (ok to use the latter if part of a pain regimen). Prior loperamide use for diarrhea is permitted at enrollment but should be changed to diphenoxylate / atropine before initiation of treatment.
Has a history of psoriatic arthritis requiring systemic treatment.
Has a history of porphyria.
(Expansion phase only) Inability to safely undergo tumor biopsies (e.g. requirement for antiplatelet therapy).

Collaborators and Investigators

Publications

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