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Trial record 72 of 106 for:    "Kennedy disease"

Ribociclib and Bicalutamide in AR+ TNBC

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ClinicalTrials.gov Identifier: NCT03090165
Recruitment Status : Active, not recruiting
First Posted : March 24, 2017
Last Update Posted : February 22, 2019
Sponsor:
Collaborators:
Novartis
Big Ten Cancer Research Consortium
Information provided by (Responsible Party):
Ruth O'Regan, M.D., Big Ten Cancer Research Consortium

Brief Summary:
This is an open label, multi-institutional, single arm phase II trial of ribociclib in combination with bicalutamide in advanced AR+ triple-negative breast cancer. No randomization or blinding is involved.

Condition or disease Intervention/treatment Phase
Triple Negative Breast Cancer Drug: ribociclib Drug: Bicalutamide Phase 1 Phase 2

Detailed Description:

OUTLINE: This is a multi-center study.

INVESTIGATIONAL TREATMENT:

  • bicalutamide - 150mg po daily D1 - D28 (Cycle = 28 days)
  • ribociclib po daily D1 - D21 of 28 day cycle

PHASE I SAFETY RUN-IN COHORT:

The maximum tolerated dose (MTD) of bicalutamide in combination with ribociclib will be determined using a standard "3+3" design. The first cohort of 3 subjects will receive ribociclib 400mg po daily D1 - D21 of a 28 day cycle (Dose Level 1). If no DLTs are experienced then the next cohort of 3 subjects will receive ribociclib 400mg po daily D1 - D28 of a 28 day cycle (Dose Level 2). If no DLTs are experienced then the next cohort of 3 subjects will receive ribociclib 600mg po daily D1 - D21 of a 28 day cycle (Dose Level 3). If no DLTs are experienced on Dose Level 3, then 3 additional subjects should be treated at this level before declaring MTD.

DLTs will be assessed within the first cycle (28 days).

PHASE II INVESTIGATIONAL TREATMENT:

  • co-therapy bicalutamide 150mg po daily D1 - D28
  • ribociclib po at the RP2D as determined in the Phase I Safety Run-In Cohort

Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1 within 28 days prior to registration

Life expectancy of > 12 weeks as determined by the treating physician.

Hematological:

  • White blood cell (WBC) ≥4 × 10^9/L
  • Absolute Neutrophil Count (ANC) ≥1.5 × 10^9/L
  • Hemoglobin (Hb) ≥9 g/dL
  • Platelets (Plt) ≥100 × 10^9/L

Renal:

  • Creatinine ≤1.5 mg/dL OR
  • Calculated creatinine clearance ≥50 ml/min using the Cockcroft-Gault formula

Hepatic:

  • Bilirubin ≤upper limit of normal (ULN)*
  • Aspartate aminotransferase (AST) ≤2.5 × ULN or ≤5 × ULN if liver mets.
  • Alanine aminotransferase (ALT) ≤2.5 × ULN or ≤5 × ULN if liver mets. * For subjects with Gilbert's syndrome, this will apply to direct bilirubin only.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 11 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Masking Description: Open Label
Primary Purpose: Treatment
Official Title: A Phase I/II, Single Arm, Non-randomized Study of Ribociclib (LEE011), a CDK 4/6 Inhibitor, in Combination With Bicalutamide, an Androgen Receptor (AR) Inhibitor, in Advanced AR+ Triple-negative Breast Cancer: Big Ten Cancer Research Consortium BRE15-024
Actual Study Start Date : March 2, 2017
Estimated Primary Completion Date : September 2019
Estimated Study Completion Date : September 2019

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Breast Cancer

Arm Intervention/treatment
Experimental: Arm A - Phase I

Dose Escalation Cohort 1 will consist of 3-6 patients who will receive bicalutamide 150mg PO daily on days 1-28 of a 28 day cycle and ribociclib 400mg PO daily on days 1-21 of a 28 day cycle.

Cohort 2 will consist of 3-6 patients who will receive bicalutamide 150mg PO daily on days 1-28 of a 28 day cycle and ribociclib 400mg PO daily on days 1-28 of a 28 day cycle.

Cohort 3 will consist of 3-6 patients who will receive bicalutamide 150mg PO daily on days 1-28 of a 28 day cycle and ribociclib 600mg PO daily on days 1-21 of a 28 day cycle.

Experimental: Arm B - Phase II Investigational Treatment The maximum safe dose of ribociclib in combination with bicalutamide will be given to up to 46 patients.

Drug: ribociclib
400mg PO
Other Name: LEE011

Drug: ribociclib
600mg PO
Other Name: LEE011

Drug: Bicalutamide
150mg PO




Primary Outcome Measures :
  1. Phase I: Maximum Tolerated Dose [ Time Frame: D1 of treatment to end of cohort cycle (assessed at 28 days) ]
    Phase I: Maximum tolerated dose (MTD) for subjects receiving ribociclib and bicalutamide without experiencing dose-limiting toxicity(s) (DLT) per Common Terminology Criteria for Adverse Events (CTCAE) v4

  2. Phase II: Clinical benefit rate (CBR) of treatment combination [ Time Frame: D1 of treatment to end of 4 treatment cycles (assessed at 16 weeks) ]
    Compare sum of confirmed complete plus partial responses plus stable disease per response evaluation criteria in solid tumors (RECIST) 1.1 criteria


Secondary Outcome Measures :
  1. Phase I: Objective Response Rate (ORR) [ Time Frame: 2 years ]
    The objective response rate is the proportion of all subjects with confirmed PR or CR according to RECIST 1.1, from the start of treatment until disease progression/recurrence (taking as reference for progressive disease the smallest measurements recorded since the start of treatment).

  2. Phase I: Duration of Response [ Time Frame: 2 years ]
    Duration of overall response—the period measured from the time that measurement criteria are met for complete or partial response (whichever status is recorded first) until the date that recurrent or progressive disease is objectively documented (taking as reference for progressive disease the smallest measurements recorded since treatment started).

  3. Phase I: Assess Safety and Tolerability By summarizing counts and percentages grade 3-5 adverse events (NCI CTCAE Version 4) [ Time Frame: 2 years ]
    By summarizing counts and percentages grade 3-5 adverse events (NCI CTCAE Version 4)

  4. Phase I: Ribociclib pharmacokinetics [ Time Frame: 2 months ]
    Time points: Peak Plasma Concentration (Cmax) Pre dose and 2-hours post-dose (±15 min) pharmacokinetic samples will be collected on Cycle 1 Day 1, Cycle 1 Day 15, Cycle 2 Day 1 and Cycle 2 Day 15.

  5. Phase II: Progression Free Survival (PFS) [ Time Frame: 2 years ]
    PFS will be summarized using Kaplan-Meier estimates of the median survival times.

  6. Phase II: Objective Response Rate (ORR) [ Time Frame: 2 years ]
    by RECIST 1.1 on treatment with combination of bicalutamide and ribociclib in advanced AR+ TNBC

  7. Phase II: Overall Survival (OS) [ Time Frame: 5 years ]
    Overall survival is defined by the date of treatment initiation to date of death from any cause.

  8. Phase II: Clinical Benefit Rate (CBR) at 16 weeks based on degree of Androgen Receptor (AR) expression by Immunohistochemistry (IHC) [ Time Frame: 16 weeks ]
    CBR at 16 weeks based on degree of AR expression by IHC (AR >0% vs. AR ≥10%).

  9. Phase II: Progression Free Survival (PFS) based on degree of AR expression by IHC [ Time Frame: 2 years ]
    PFS based on degree of AR expression by IHC (AR >0% vs. AR ≥10%).

  10. Phase II: Estimate Duration of Response [ Time Frame: 2 years ]
    On treatment with combination of bicalutamide and ribociclib in advanced Androgen Receptor (AR)+ Triple Negative Breast Cancer (TNBC)

  11. Phase II: Evaluate Safety and Tolerability By summarizing counts and percentages grade 3-5 adverse events (NCI CTCAE Version 4) [ Time Frame: 2 years ]
    By summarizing counts and percentages grade 3-5 adverse events (NCI CTCAE Version 4)



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Metastatic or unresectable AR+ triple-negative breast cancer (TNBC); AR positivity assessed centrally and defined as immunohistochemical (IHC) staining of >0% of tumor nuclei.
  • Written informed consent and Health Insurance Portability and Accountability Act of 1996 (HIPAA) authorization for release of personal health information. NOTE: HIPAA authorization may be included in the informed consent or obtained separately.
  • One prior line of therapy is allowed.
  • Age ≥ 18 years at the time of consent.
  • Measurable disease according to RECIST 1.1 within 28 days prior to registration.
  • No active central nervous system (CNS) metastatic disease. NOTE: Subjects with CNS involvement must meet ALL of the following to be eligible:

    • At least 28 days from prior definitive treatment of their CNS disease by surgical resection, stereotactic body radiation therapy (SBRT) or whole brain radiation treatment (WBRT) at the time of registration
    • AND asymptomatic and off systemic corticosteroids and/or enzyme-inducing anti-epileptic medications for brain metastases for >14 days prior to registration.
  • Prior cancer treatment must be completed at least 14 days prior to registration and the subject must have recovered from all reversible acute toxic effects of the regimen (other than alopecia) to ≤grade 1 or to baseline prior to initiation of that therapy.
  • Screening rate-corrected QT interval (QTc) must be <450msec and a resting heart rate of at least 50-90 bpm via a standard 12-lead ECG within 28 days prior to registration.
  • Females of childbearing potential must have a negative serum pregnancy test within 7 days prior to registration. NOTE: Females are considered of child bearing potential unless they are surgically sterile (have undergone a hysterectomy, bilateral tubal ligation, or bilateral oophorectomy), or they are naturally postmenopausal for at least 12 consecutive months, or her male partner has had a vasectomy at least 6 months prior to screening (The sterilized male partner must be her only sexual partner.).
  • Females of childbearing potential and males must be willing to abstain from heterosexual activity or must agree to use adequate contraception (hormonal or barrier method) for the duration of study participation and for 3 weeks after discontinuation of study treatment.
  • As determined by the enrolling physician or protocol designee, ability of the subject to understand and comply with study procedures for the entire length of the study.
  • Able to swallow bicalutamide and ribociclib capsules/tablets.

Exclusion Criteria:

  • No prior therapy with AR antagonists including but not limited to bicalutamide, enzalutamide, abiraterone and orteronel.
  • No prior therapy with any CDK 4/6 inhibitors.
  • Active infection requiring systemic therapy.
  • Pregnant or breastfeeding (NOTE: breast milk cannot be stored for future use while the mother is being treated on study).
  • Known additional malignancy that is active and/or progressive requiring treatment; exceptions include basal cell or squamous cell skin cancer, in situ cervical or bladder cancer, or other cancer for which the subject has been disease-free for at least three years.
  • Treatment with any investigational drug within 14 days prior to registration or within 5 half-lives of the investigational product, whichever is longer.
  • Subject who has received radiotherapy <14 days prior to registration, and who has not recovered to grade 1 or better from related side effects of such therapy (exceptions include alopecia).
  • Subject has had major surgery within 14 days prior to registration or has not recovered from major side effects of the surgery (tumor biopsy is not considered as major surgery).
  • Known hypersensitivity to any of the excipients of ribociclib or bicalutamide.
  • Any impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of the study drugs (e.g., ulcerative diseases, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome, or small bowel resection).
  • Known history of HIV infection (testing not mandatory).
  • Any concurrent severe and/or uncontrolled medical condition that would, in the investigator's judgment, cause unacceptable safety risks, contraindicate subject participation in the clinical study or compromise compliance with the protocol (e.g. chronic pancreatitis, chronic active hepatitis, active untreated or uncontrolled fungal, bacterial or viral infections, etc.).
  • Subjects with any of the following conditions are excluded:

    • Serious or non-healing wound, ulcer, or bone fracture.
    • History of abdominal fistula, gastrointestinal perforation, or intra- abdominal abscess within 28 days prior to registration.
    • Any history of cerebrovascular accident (CVA) or transient ischemic attack within 12 months prior to registration.
    • Any history of arterial or venous thrombosis/thromboembolic event, including pulmonary embolism within the past 12 months prior to registration.
    • History of acute coronary syndromes (including myocardial infarction, unstable angina, coronary artery bypass grafting, coronary angioplasty, or stenting) or symptomatic pericarditis within 6 months prior to registration.
    • Symptomatic congestive heart failure (New York Heart Association III-IV) or documented cardiomyopathy with left ventricular ejection fraction (LVEF) <50% as determined by Multiple Gated acquisition (MUGA) scan or echocardiogram (ECHO) at screening. MUGA/ ECHO to be performed within 28 days prior to registration.
    • Clinically significant cardiac arrhythmias (e.g. ventricular tachycardia), complete left bundle branch block, high-grade AV block (e.g. bifascicular block, Mobitz type II and third-degree AV block).
    • Any episode of atrial fibrillation in the prior 12 months.
    • Long QT syndrome or family history of idiopathic sudden death or congenital long QT syndrome.
    • Concomitant use of medication(s) with a known risk to prolong the QT interval and/or known to cause Torsades de Pointe that cannot be discontinued (within 5 half-lives or 7 days prior to starting study drug) or replaced by safe alternative medication.
    • Systolic blood pressure (SBP) >160 mmHg or <90 mmHg at screening.
  • Currently receiving any known strong inducers or inhibitors of CYP3A4/5 which cannot be discontinued 7 days prior to starting study drug
  • Subject is currently receiving or has received systemic corticosteroids <14 days prior to starting study drugs. The following uses of corticosteroids are permitted: single doses, topical applications (e.g., for rash), inhaled sprays (e.g., for obstructive airways diseases), eye drops or local injections (e.g., intra-articular).
  • Subject is currently receiving warfarin or other coumarin-derived anticoagulant for treatment, prophylaxis or otherwise. Therapy with heparin, low molecular weight heparin (LMWH), or fondaparinux is allowed.
  • Subject with a Child-Pugh score B or C.
  • Subjects taking herbal supplements (St. John's Wort, gingko biloba, etc.) should discontinue these supplements 14 days prior to study registration.
  • Consumption of grapefruit, grapefruit hybrids, pummelos, star-fruit, Seville oranges or products containing the juice of each within 7 days prior to study registration.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03090165


Locations
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United States, Illinois
University of Illinois Cancer Center
Chicago, Illinois, United States, 60612
United States, Michigan
Michigan State University
Lansing, Michigan, United States, 48910
United States, New Jersey
Rutgers Cancer Institute of New Jersey
New Brunswick, New Jersey, United States, 08903
United States, Pennsylvania
Penn State Cancer Institute
Hershey, Pennsylvania, United States, 17033
United States, Wisconsin
University of Wisconsin
Madison, Wisconsin, United States, 53792
Sponsors and Collaborators
Ruth O'Regan, M.D.
Novartis
Big Ten Cancer Research Consortium
Investigators
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Study Chair: Ruth O'Regan, MD Big Ten Cancer Research Consortium

Additional Information:
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Responsible Party: Ruth O'Regan, M.D., Sponsor Investigator, Big Ten Cancer Research Consortium
ClinicalTrials.gov Identifier: NCT03090165     History of Changes
Other Study ID Numbers: BTCRC BRE15-024
First Posted: March 24, 2017    Key Record Dates
Last Update Posted: February 22, 2019
Last Verified: February 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Ruth O'Regan, M.D., Big Ten Cancer Research Consortium:
Triple Negative Breast Neoplasms
ribociclib
LEE011
CDK 4/6 inhibitor
bicalutamide
Additional relevant MeSH terms:
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Breast Neoplasms
Triple Negative Breast Neoplasms
Neoplasms by Site
Neoplasms
Breast Diseases
Skin Diseases
Bicalutamide
Androgen Antagonists
Hormone Antagonists
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs
Antineoplastic Agents