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New treatment option for Clinical Stage IV Cutaneous Melanoma AJCC v8
Official title Binimetinib and Encorafenib for the Treatment of Metastatic Melanoma and Central Nervous System Metastases
ClinicalTrials.gov ID: NCT05026983
What this study is testing
What is Binimetinib?
Binimetinib is an investigational medicine, given as an once-daily pill taken by mouth, being studied as a potential treatment for clinical stage iv cutaneous melanoma ajcc v8.
Also referred to as ARRY-162, ARRY-438162.
Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.
- What it's testing
- This phase II trial studies the effects of binimetinib and encorafenib in treating patients with melanoma that has spread to the central nervous system (metastases). Binimetinib and encorafenib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.
- Phase 2: a mid-size study of how well it works
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- Able to provide written informed consent.
- Age \>= 18 years at the time of informed consent
- Histologically confirmed diagnosis of melanoma
- Presence of BRAFV600 mutation in tumor tissue previously determined by a local assay (including immunohistochemistry [IHC]) at any time prior to...
- Cohort A: BRAF V600 mutant melanoma patients with progressive central nervous system (CNS) metastases. This includes patients with parenchymal brain...
You likely can't join if
- Evidence of active infection =\< 7 days prior to initiation of study drug therapy (does not apply to viral infections that are presumed to be...
- Use of non-oncology vaccines containing live virus for prevention of infectious diseases within 30 days of prior to study drug. Dead virus vaccines...
- Inability to swallow and retain study treatment
- Known history of testing positive for human immunodeficiency virus (HIV) or known acquired immunodeficiency syndrome (AIDS) even if fully...
- Impaired cardiovascular function or clinically significant cardiovascular disease including, but not limited to, the following:
- History of acute coronary syndromes (including myocardial infarction, unstable angina, coronary artery bypass grafting, coronary angioplasty or...
See the full eligibility criteria
Who can join
- Able to provide written informed consent.
- Age \>= 18 years at the time of informed consent
- Histologically confirmed diagnosis of melanoma
- Presence of BRAFV600 mutation in tumor tissue previously determined by a local assay (including immunohistochemistry [IHC]) at any time prior to Screening or during Screening
- Cohort A: BRAF V600 mutant melanoma patients with progressive central nervous system (CNS) metastases. This includes patients with parenchymal brain metastases and/or LMD
- Cohort A: Prior therapy with Food and Drug Administration (FDA)-approved BRAF inhibitors (+/- MEK inhibitors) is required
- No washout period is required
- Cohort A: Prior therapy with immunotherapy or other investigational agents is allowed
- Washout period of 14 days since last dose
- Cohort B: BRAF V600 mutant melanoma patients who are treatment naive to BRAF/MEK inhibitors with CNS metastases, including LMD. Prior treatment with immunotherapy is permitted
- For patients with parenchymal brain metastases (mets) without LMD
- Metastatic disease to the brain with at least 1 progressing parenchymal brain lesion \>= 0.5 cm and =\< 3 cm, defined as a magnetic resonance imaging (MRI) contrast-enhancing lesion that may be accurately measured in at...
- For patients with LMD
- Patients must have investigator assessed radiographic and/or CSF cytological evidence of LMD
- Patients must have an Eastern Cooperative Oncology Group (ECOG) performance status (PS) of =\< 2
- Patients may receive steroids to control symptoms related to CNS involvement
- For patients with parenchymal brain metastases the dose must be =\< 2 mg per 24 hours of dexamethasone (or the equivalent). Patient's symptoms should experience stability of neurological symptoms for at least 7 days, or...
- For patients with LMD: the dose must be =\< 4 mg per 24 hours of dexamethasone (or the equivalent). Physiologic replacement doses for adrenal insufficiency is allowed on this protocol
- Radiation therapy:
- For patients with parenchymal brain mets: prior radiation therapy, including stereotactic (SRS) or whole brain radiation (WBXRT) is allowed, but patient must be progressing in or having at least 1 new CNS lesion. Prior...
- For patients with LMD: Patients who have received radiation to brain and/or spine, including WBXRT, SRS, or SBRT, are eligible, but must have completed radiation treatment at least 7 days prior to the start of treatment.
- Prior therapy with systemic immunotherapy or other investigational agents is allowed
- Washout period of 14 days since last dose
- Other cancer directed treatment:
- Concurrent treatment with other anti-cancer systemic therapies is not allowed. No other concomitant intrathecal therapy with another agent will be allowed. For patients that have received other systemic therapies, the...
- Patients that received previous intrathecal therapy must have received their last treatment \>= 7 days prior to the start of treatment
- Patients who have received systemic chemotherapy must have received their last treatment \>= 21 days prior to the start of treatment Patients must have appropriate laboratory parameters as defined below:
- Absolute neutrophil count (ANC) 1.5 X 10\^9/L
- Hemoglobin 9.0 g/dL
- Platelets 75 X 10\^9/L
- Prothrombin time (PT)/international normalized ratio (INR) and partial thromboplastin time (PTT) =\< 1.5 X upper limit of normal (ULN)
- Total bilirubin =\ 1.5 X ULN is acceptable if bilirubin is fractionated and direct bilirubin \< 35%)
- NOTE: Patients with documented Gilbert syndrome or hyperbilirubinemia due to non-hepatic cause (e.g., hemolysis, hematoma) may be enrolled following discussion and agreement with the primary investigator
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤2.5 X ULN, in patients with liver metastases ≤5 X ULN
- Albumin ≥2.5 g/dL
- Creatinine ≤ 1.5 X ULN OR calculated creatinine clearance ≥50 mL/min OR 24-hour urine creatinine clearance ≥50 mL/min
- Female patients of childbearing potential must have a negative serum and/or urine pregnancy test result
- Female patients of childbearing potential must agree to protocol-approved methods of contraception and to not donate ova from Screening until 30 days after the last dose of study drug. Male patients must agree to use...
- The patient is deemed by the Investigator to have the initiative and means to comply with scheduled visits, treatment plan and study procedures
What rules you out
- Evidence of active infection =\< 7 days prior to initiation of study drug therapy (does not apply to viral infections that are presumed to be associated with the underlying tumor type required for study entry)
- Use of non-oncology vaccines containing live virus for prevention of infectious diseases within 30 days of prior to study drug. Dead virus vaccines (e.g Flu) are allowed, even during treatment with study drug
- Inability to swallow and retain study treatment
- Known history of testing positive for human immunodeficiency virus (HIV) or known acquired immunodeficiency syndrome (AIDS) even if fully immunocompetent on antiretroviral therapy (ART)
- Impaired cardiovascular function or clinically significant cardiovascular disease including, but not limited to, 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)
- A left ventricular ejection fraction (LVEF) \< 50% as determined by multigated acquisition (MUGA) or echocardiogram (ECHO)
- History or presence of clinically significant cardiac arrhythmias (including resting bradycardia, uncontrolled atrial fibrillation or uncontrolled paroxysmal supraventricular tachycardia)
- Baseline Fridericia's correction formula (QTcF) interval \>= 480 msec. Can be repeated up to three times to confirm
- Concurrent neuromuscular disorder (e.g., inflammatory myopathies, muscular dystrophy, amyotrophic lateral sclerosis, spinal muscular atrophy)
- Impairment of gastrointestinal function or disease which may significantly alter the absorption of study treatment (e.g., uncontrolled nausea, vomiting or diarrhea; malabsorption syndrome; small bowel resection). Known...
- 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...
- Use of herbal supplements, medications or foods that are moderate or strong inhibitors or inducers of cytochrome P450 (CYP) 3A4/5 =\< 1 week prior to the start of study treatment
- History of a thromboembolic event \< 12 weeks prior to starting study treatment. Examples of thromboembolic events include transient ischemia attack, cerebrovascular accident, deep vein thrombosis or pulmonary embolism...
- Evidence of hepatitis B virus (HBV) or hepatitis C virus (HCV) infection
- NOTE: Patients with laboratory evidence of cleared HBV or HCV infection may be enrolled
- NOTE: Patients with no prior history of HBV infection who have been vaccinated against HBV and who have a positive antibody against hepatitis B surface antigen as the only evidence of prior exposure may enroll
- Pregnancy or breastfeeding or patients who plan to become pregnant during the duration of the study
- Other severe, acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or study treatment administration or that may interfere with the...
The study team makes the final eligibility decision.
Where it's taking place
- Houston, Texas, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Houston, Texas, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.