Tracking Information

First Submitted Date ^ICMJE

June 28, 2019

First Posted Date ^ICMJE

July 2, 2019

Last Update Posted Date

April 1, 2021

Actual Study Start Date ^ICMJE

February 25, 2020

Estimated Primary Completion Date

September 30, 2024 (Final data collection date for primary outcome measure)

Current Primary Outcome Measures ^ICMJE

Recommended Phase 2 Dose [ Time Frame: Up to 12 months ]
Evaluating the number and frequency of adverse events as determined by the National Cancer Institute Common Toxicity Criteria for Adverse Events (NCI-CTCAE) version (v)5.0 by investigator's assessment will be used to determine the recommended phase 2 dose for future studies.
Number of Participants with Dose Limiting Toxicities [ Time Frame: Up to 28 days ]
A dose limiting toxicity (DLT) is generally defined as a grade 3 or higher, treatment-related adverse event that is attributable to the study treatment during the first 28 days of therapy (Cycle 1). The dose limiting toxicity will be based on the tolerability observed during cycle 1 of treatment/observation. Adverse events will be assessed by the investigators using NCI-CTCAE v5.0.
Number of Total Treatment-Emergent Adverse Events (AEs) [ Time Frame: From treatment initiation through study completion, an average of 1 year ]
Treatment Emergent AEs will be defined by the NCI CTCAE v5.0 as AEs newly occuring after the patient has begun study treatment.
Number of Treatment-Emergent Adverse Events by Grade [ Time Frame: From treatment initiation through study completion, an average of 1 year ]
Severity grade will be defined by the NCI CTCAE v5.0.
Number of Grade 3 or Greater Treatment-Emergent Adverse Events by CTCAE v5.0 [ Time Frame: From treatment initiation through study completion, an average of 1 year ]
Severity grade will be defined by the NCI CTCAE v5.0.
Number of Serious Treatment-Emergent Adverse Events by CTCAE v5.0 [ Time Frame: From treatment initiation through study completion, an average of 1 year ]
Severity grade will be defined by the NCI CTCAE v5.0.
Number of Treatment-Emergent Adverse Events with an Outcome of Death by CTCAE v5.0 [ Time Frame: From treatment initiation through study completion, an average of 1 year ]
Severity grade will be defined by the NCI CTCAE v5.0.
Number of Treatment-Emergent Adverse Events Leading to Discontinuation of Study Treatment [ Time Frame: From treatment initiation through study completion, an average of 1 year ]
Severity grade will be defined by the NCI CTCAE v5.0.
Number of Treatment-Emergent Adverse Events Resulting in Interruption, Reduction, or Delay of study treatment [ Time Frame: From treatment initiation through study completion, an average of 1 year ]
Severity grade will be defined by the NCI CTCAE v5.0.

Original Primary Outcome Measures ^ICMJE

Recommended Phase 2 Dose of Brigatinib in Combination with Binimetinib [ Time Frame: Up to 12 months ]
Will be measured by evaluating the number and frequency of adverse events as determined by the National Cancer Institute Common Toxicity Criteria for Adverse Events (NCI-CTCAE) version (v)5.0 by investigator's assessment and to determine the recommended phase 2 dose for future studies.
Number of Participants with Dose Limiting Toxicities [ Time Frame: Up to 28 days ]
A dose limiting toxicity (DLT) is generally defined as a grade 3 or higher, treatment-related adverse event that is attributable to the study treatment during the first 28 days of therapy (Cycle 1). The dose limiting toxicity will be based on the tolerability observed during cycle 1 of treatment/observation. Adverse events will be assessed by the investigators using NCI-CTCAE v5.0.
Number of All Treatment-Emergent Adverse Events by CTCAE v5.0 [ Time Frame: From treatment initiation through study completion, an average of 1 year ]
Severity grade will be defined by the NCI CTCAE v5.0.
Number of Treatment-Emergent Adverse Events by CTCAE v5.0 Grade [ Time Frame: From treatment initiation through study completion, an average of 1 year ]
Severity grade will be defined by the NCI CTCAE v5.0.
Number of Grade 3 or Greater Treatment-Emergent Adverse Events by CTCAE v5.0 [ Time Frame: From treatment initiation through study completion, an average of 1 year ]
Severity grade will be defined by the NCI CTCAE v5.0.
Number of Serious Treatment-Emergent Adverse Events by CTCAE v5.0 [ Time Frame: From treatment initiation through study completion, an average of 1 year ]
Severity grade will be defined by the NCI CTCAE v5.0.
Number of Treatment-Emergent Adverse Events with an Outcome of Death by CTCAE v5.0 [ Time Frame: From treatment initiation through study completion, an average of 1 year ]
Severity grade will be defined by the NCI CTCAE v5.0.
Number of Treatment-Emergent Adverse Events Leading to Discontinuation of Brigatinib and Binimetinib by CTCAE v5.0 [ Time Frame: From treatment initiation through study completion, an average of 1 year ]
Severity grade will be defined by the NCI CTCAE v5.0.
Number of Treatment-Emergent Adverse Events Resulting in Interruption, Reduction or Delay of Brigatinib or Binimetinib by CTCAE v5.0 [ Time Frame: From treatment initiation through study completion, an average of 1 year ]
Severity grade will be defined by the NCI CTCAE v5.0.

Change History

Current Secondary Outcome Measures ^ICMJE

Objective Response Rate (ORR) Assessed by Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 [ Time Frame: From treatment initiation through study completion, an average of 1 year ]
RECIST v1.1 will be used to determine the overall response rate defined as participants with a complete response (CR) or a partial response (PR). Point estimate and 95% exact binomial confidence interval (CI) will be obtained for ORR.
Median Depth of Response Assessed by RECIST v1.1 [ Time Frame: From treatment initiation through study completion, an average of 1 year ]
Will be defined as maximal reduction in tumor size based on Response Evaluation Criteria in Solid Tumors (RECIST) measurement. Median and inter-quartile range will be used to describe the depth of response (the maximal reduction in tumor size based on RECIST measurement).
Area Under the Plasma Concentration versus Time Curve (AUC) of Brigatinib [ Time Frame: At pre-dose, 0.5, 1, 2, 4, 6, 8 and 24 hours post-dose on days 1 and 15 of cycle 1 ]
Plasma concentration assessment (pharmacokinetic data) of brigatinib during coadministration with binimetinib will be determined by assay at various timepoints. The assay will be done by Takeda / their designated vendor.
Median Progression Free Survival (PFS) [ Time Frame: Up to 6 months ]
PFS is measured as the time from start of treatment to time of disease progression at 6 months. Kaplan-Meier method will be used to describe the describe the median PFS with 95% CI.
Median Overall Survival (OS) [ Time Frame: Up to 12 months ]
Overall Survival is measures as the time from start of treatment to time of death, or lost to follow-up. Kaplan-Meier method will be used to describe the describe the median OS at 12 months with 95% CI.

Original Secondary Outcome Measures ^ICMJE

Objective Response Rate (ORR) Assessed by Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 [ Time Frame: From treatment initiation through study completion, an average of 1 year ]
Point estimate and 95% exact binomial confidence interval (CI) will be obtained for ORR.
Median Depth of Response Assessed by RECIST v1.1 [ Time Frame: From treatment initiation through study completion, an average of 1 year ]
Will be defined as maximal reduction in tumor size based on Response Evaluation Criteria in Solid Tumors (RECIST) measurement. Median and inter-quartile range will be used to describe the depth of response (the maximal reduction in tumor size based on RECIST measurement).
Area Under the Plasma Concentration versus Time Curve (AUC) of Brigatinib [ Time Frame: At pre-dose, 0.5, 1, 2, 4, 6, 8 and 24 hours post-dose on days 1 and 15 of cycle 1 ]
Plasma concentration assessment (pharmacokinetic data) of brigatinib during coadministration with binimetinib will be determined by assay at various timepoints. The assay will be done by Takeda / their designated vendor.
Progression Free Survival (PFS) [ Time Frame: Time from start of treatment to time of disease progression, assessed at 6 months ]
Kaplan-Meier method will be used to describe the describe PFS at 6 months months with their median and 95% CI.
Overall Survival (OS) [ Time Frame: At 12 months ]
Kaplan-Meier method will be used to describe the describe OS at 12 months with their median and 95% CI.

Current Other Pre-specified Outcome Measures

Not Provided

Original Other Pre-specified Outcome Measures

Not Provided

Descriptive Information

Brief Title ^ICMJE

Brigatinib and Binimetinib in Treating Patients With Stage IIIB-IV ALK or ROS1-Rearranged Non-small Cell Lung Cancer

Official Title ^ICMJE

A Phase I Study of Brigatinib With Binimetinib in Advanced ALK- or ROS1-Rearranged Non-Small Cell Lung Cancer (NSCLC)

Brief Summary

This phase I trial studies the side effects and best dose of brigatinib and binimetinib in treating patients with stage IIIB-IV non-small cell lung cancer and a type of gene mutation called a rearrangement in the ALK or ROS1 genes. Brigatinib and binimetinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.

Detailed Description

PRIMARY OBJECTIVES:

I. To determine the safety and tolerability of brigatinib in combination with binimetinib in stage IIIB or IV anaplastic lymphoma kinase (ALK) or ROS1 rearranged non-small cell lung cancer (NSCLC) and the recommended phase 2 dose.

SECONDARY OBJECTIVES:

I. To determine preliminary efficacy of brigatinib in combination with binimetinib in any line of treatment.

II. To characterize the pharmacokinetic parameters of brigatinib in combination with binimetinib.

EXPLORATORY OBJECTIVES:

I. To assess circulating tumor deoxyribonucleic acid (DNA) (ctDNA) utility in evaluating treatment response.

II. To evaluate the blockade of downstream signaling indicating response or resistance to treatment of immunohistochemistry (IHC) for phosphatidylinositol 3-kinase (PI3K)/Protein kinase B (AKT)/Mitogen-activated protein kinase (MAPK) pathway activity evaluation.

OUTLINE: This a dose-escalation study.

Patients receive brigatinib orally (PO) once daily (QD) and binimetinib PO twice daily (BID) on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up for 30 days and then every 6 months for 12 months.

Study Type ^ICMJE

Interventional

Study Phase ^ICMJE

Phase 1

Study Design ^ICMJE

Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment

Condition ^ICMJE

ALK Gene Rearrangement
Lung Non-Small Cell Carcinoma
Progressive Disease
ROS1 Gene Rearrangement
Stage IIIB Lung Cancer
Stage IIIC Lung Cancer
Stage IV Lung Cancer
Stage IVA Lung Cancer
Stage IVB Lung Cancer

Intervention ^ICMJE

Drug: Binimetinib
Given PO
Other Names:
- ARRY-162
- ARRY-438162
- MEK162
Drug: Brigatinib
Given PO
Other Names:
- Alunbrig
- AP 26113
- AP-26113
- AP26113

Study Arms ^ICMJE

Experimental: Treatment (brigatinib, binimetinib)

Patients receive brigatinib PO QD and binimetinib PO BID on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity.

Interventions:

Drug: Binimetinib
Drug: Brigatinib

Publications *

Not Provided

* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.

Recruitment Information

Recruitment Status ^ICMJE

Recruiting

Estimated Enrollment ^ICMJE

18

Original Estimated Enrollment ^ICMJE

Same as current

Estimated Study Completion Date ^ICMJE

September 30, 2024

Estimated Primary Completion Date

September 30, 2024 (Final data collection date for primary outcome measure)

Eligibility Criteria ^ICMJE

Inclusion Criteria:

Participants must have histologically or cytological confirmed stage IIIB/IV NSCLC
Documented ALK-rearrangement (or ROS1- rearrangement) break-apart fluorescence in situ hybridization (FISH) (in >= 15% or tumor cells), or next generation sequencing assay performed on tumor sample or cell free DNA in a Clinical Laboratory Improvement Act (CLIA)-approved laboratory
At least one prior ALK or ROS1 targeted tyrosine kinase inhibitor (TKI). With progression or intolerance of most recent regimen
Dose Escalation Phase Only: At least one prior ALK or ROS1 targeted TKI. With progression or intolerance of most recent regimen.
Dose Expansion Phase Only: In addition to the criteria in Exclusion Criteria # 3, ALK+ patients with no prior chemotherapy, immunotherapy, radiation therapy or other systemic therapy are also allowed.
Measurable or evaluable disease defined by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria
Age >= 18 years
Life expectancy of at least 3 months
Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
Leukocytes >= 3,000/microliter (mcL)
Absolute neutrophil count >=1,500/mcL
Platelets >= 75,000/mcL
Hemoglobin (Hgb) >= 9 gm/dL
Total bilirubin within normal institutional limits
Aspartate aminotransferase (AST) (serum glutamic-oxaloacetic transaminase (SGOT)) =< 5 x institutional upper limit of normal
Alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase (SGPT)) =< 5 x institutional upper limit of normal if there are liver metastases
Creatinine within normal institutional limits OR
Creatinine clearance >= 50 mL/min/1.73 m^2 for participants with creatinine levels above institutional normal
Female participants who:
- Are postmenopausal for at least 1 year before the screening visit, OR
- Are surgically sterile, OR
- If they are of childbearing potential, agree to practice 2 effective methods of contraception, at the same time, from the time of signing the informed consent through 4 months after the last dose of the study drugs, or
- Agree to completely abstain from heterosexual intercourse
Male participants, even if surgically sterilized (i.e., status post-vasectomy), who:
- Agree to practice effective barrier contraception during the entire study treatment period and through 4 months after the last dose of the study drugs, or
- Agree to completely abstain from heterosexual intercourse
Negative pregnancy testing required at screening and cycle 1 day 1 for women of childbearing potential
Ability to understand a written informed consent document, and willingness to sign it
Able to swallow and retain orally administered medication and does not have any clinically significant gastrointestinal abnormalities that may alter absorption such as malabsorption syndrome or major resection of the stomach or bowels
Participant is deemed by the investigator to have the initiative and means to be compliant with the protocol (treatment and follow-up)

Exclusion Criteria:

Is currently participating and receiving study therapy or has participated in a study of an investigational agent and received study therapy or used an investigational device within 7 days for prior TKI and 14 days for chemotherapy or radiation and 30 days for prior immunotherapy before the first dose of treatment
Prior treatment with either study drug as most recent treatment or prior discontinuation of either study drug due to toxicity
Known hypersensitivity to any study drug components
Known history of interstitial lung disease or interstitial pneumonitis, including clinically significant radiation pneumonitis
Known history of myositis
History of pancreatitis
History or current evidence of retinal vein occlusion (RVO) or current risk factors to RVO (e.g. uncontrolled glaucoma or ocular hypertension, history of hyperviscosity or hypercoagulability syndromes); history of retinal degenerative disease
Impaired cardiovascular function or clinically significant cardiovascular diseases, including any of the following:
- Symptomatic chronic heart failure grade >= 2, history or current evidence of clinically significant cardiac arrhythmia and/or conduction abnormality < 6 months prior to screening except atrial fibrillation and paroxysmal supraventricular tachycardia.
- Have significant, uncontrolled, or active cardiovascular disease, specifically including, but not restricted to:
  - Myocardial infarction (MI) within 6 months prior to the first dose of brigatinib
  - Unstable angina within 6 months prior to first dose
  - Symptomatic congestive heart failure requiring treatment (New York Heart Association grade >= 2), history or current evidence of clinically significant cardiac arrhythmia and/or conduction abnormality =< 6 months prior to Screening except atrial fibrillation and paroxysmal supraventricular tachycardia
  - 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 echocardiogram (ECHO)
  - QT interval corrected for heart rate using the Fridericia formula (QTcF) > 480 msec;
  - History of clinically significant atrial arrhythmia
  - Any history of ventricular arrhythmia
  - Cerebrovascular accident or transient ischemic attack within 6 months prior to first dose
Uncontrolled hypertension defined as persistent elevation of systolic blood pressure >= 150 mmHg or diastolic blood pressure >= 100 mmHg despite current therapy
History of chronic inflammatory bowel disease or Crohn?s disease requiring medical intervention (immunomodulatory or immunosuppressive medications or surgery) =< 12 months prior to first dose of study treatment
Impaired gastrointestinal (GI) function or disease that may significantly alter the absorption of binimetinib or brigatinib (e.g., ulcerative diseases, uncontrolled vomiting, malabsorption syndrome, small bowel resection with decreased intestinal absorption)
History of thromboembolic or cerebrovascular events =< 6 months prior to starting study treatment, including transient ischemic attacks, cerebrovascular accidents, deep vein thrombosis or pulmonary emboli
Current neuromuscular disorder(s) associated with elevated creatine kinase (CK) (e.g., inflammatory myopathies, muscular dystrophy, amyotrophic lateral sclerosis, spinal muscular atrophy)
Major surgery =< 3 weeks prior to starting study drugs, or persistent/ongoing side effects of major surgery
Pregnant or nursing (lactating) women
Other severe, acute, or chronic medical conditions including uncontrolled diabetes mellitus or psychiatric conditions or laboratory abnormalities that, in the opinion of the investigator, may increase the risk associated with study participation or may interfere with ability to participate actively in the study
History of another malignancy. Participants with fully resected non-melanoma skin cancer, indolent early stage second malignancies, or who have been disease free for > three years may be eligible following discussion with study principal investigator (PI)
Any symptomatic brain metastasis
- Note: Participants previously treated or untreated for this condition who are asymptomatic in the absence of corticosteroid and anti-epileptic therapy are allowed. Brain metastases must be stable for >= 2 weeks, with imaging (e.g., magnetic resonance imaging [MRI] or computed tomography [CT]) demonstrating no current evidence of progressive brain metastases at screening)
Participants receiving any medications or substances that are inhibitors or inducers of CYP3A enzyme(s) and CYP2C8 within 14 days of enrollment are ineligible
Human immunodeficiency virus (HIV)-positive patients on combination antiretroviral therapy are ineligible because of the potential for pharmacokinetic interactions. In addition, these patients are at increased risk of lethal infections when treated with marrow-suppressive therapy

Sex/Gender ^ICMJE

Sexes Eligible for Study:

All

Ages ^ICMJE

18 Years and older (Adult, Older Adult)

Accepts Healthy Volunteers ^ICMJE

No

Contacts ^ICMJE

Contact: Janna Blaauw

(415) 885-7820

janna.blaauw@ucsf.edu

Listed Location Countries ^ICMJE

United States

Removed Location Countries

Administrative Information

NCT Number ^ICMJE

NCT04005144

Other Study ID Numbers ^ICMJE

186517
NCI-2019-02315 ( Registry Identifier: CTRP (Clinical Trial Reporting Program) )

Has Data Monitoring Committee

Yes

U.S. FDA-regulated Product

Studies a U.S. FDA-regulated Drug Product:	Yes
Studies a U.S. FDA-regulated Device Product:	No
Product Manufactured in and Exported from the U.S.:	No

IPD Sharing Statement ^ICMJE

Plan to Share IPD:

No

Responsible Party

University of California, San Francisco

Study Sponsor ^ICMJE

University of California, San Francisco

Collaborators ^ICMJE

Takeda
Array BioPharma

Investigators ^ICMJE

Principal Investigator:

Collin Blakely, MD, PhD

University of California, San Francisco

PRS Account

University of California, San Francisco

Verification Date

March 2021

^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

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Brigatinib and Binimetinib in Treating Patients With Stage IIIB-IV ALK or ROS1-Rearranged Non-small Cell Lung Cancer

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