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    The EU Clinical Trials Register currently displays   43839   clinical trials with a EudraCT protocol, of which   7280   are clinical trials conducted with subjects less than 18 years old.   The register also displays information on   18700   older paediatric trials (in scope of Article 45 of the Paediatric Regulation (EC) No 1901/2006).

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    Summary
    EudraCT Number:2014-004010-28
    Sponsor's Protocol Code Number:I3Y-MC-JPBO
    National Competent Authority:Belgium - FPS Health-DGM
    Clinical Trial Type:EEA CTA
    Trial Status:Completed
    Date on which this record was first entered in the EudraCT database:2015-02-10
    Trial results View results
    Index
    A. PROTOCOL INFORMATION
    B. SPONSOR INFORMATION
    C. APPLICANT IDENTIFICATION
    D. IMP IDENTIFICATION
    D.8 INFORMATION ON PLACEBO
    E. GENERAL INFORMATION ON THE TRIAL
    F. POPULATION OF TRIAL SUBJECTS
    G. INVESTIGATOR NETWORKS TO BE INVOLVED IN THE TRIAL
    N. REVIEW BY THE COMPETENT AUTHORITY OR ETHICS COMMITTEE IN THE COUNTRY CONCERNED
    P. END OF TRIAL
    Expand All   Collapse All
    A. Protocol Information
    A.1Member State ConcernedBelgium - FPS Health-DGM
    A.2EudraCT number2014-004010-28
    A.3Full title of the trial
    A Phase 2 Study of Abemaciclib in Patients with Brain Metastases Secondary to Hormone Receptor Positive Breast Cancer, Non-small Cell Lung Cancer, or Melanoma
    A.3.1Title of the trial for lay people, in easily understood, i.e. non-technical, language
    A Study of Abemaciclib (LY2835219) in Participants With Breast Cancer, Non-Small Cell Lung Cancer, or Melanoma That Has Spread to the Brain
    A.4.1Sponsor's protocol code numberI3Y-MC-JPBO
    A.5.2US NCT (ClinicalTrials.gov registry) numberNCT02308020
    A.7Trial is part of a Paediatric Investigation Plan No
    A.8EMA Decision number of Paediatric Investigation Plan
    B. Sponsor Information
    B.Sponsor: 1
    B.1.1Name of SponsorEli Lilly and Company
    B.1.3.4CountryUnited States
    B.3.1 and B.3.2Status of the sponsorCommercial
    B.4 Source(s) of Monetary or Material Support for the clinical trial:
    B.4.1Name of organisation providing supportEli Lilly and Company
    B.4.2CountryUnited Kingdom
    B.5 Contact point designated by the sponsor for further information on the trial
    B.5.1Name of organisationEli Lilly
    B.5.2Functional name of contact pointClinical Trial Registry Office
    B.5.3 Address:
    B.5.3.1Street AddressLilly Corporate Center, DC 1526
    B.5.3.2Town/ cityIndianapolis
    B.5.3.3Post code46285
    B.5.3.4CountryUnited States
    B.5.6E-mailEU_Lilly_Clinical_Trials@lilly.com
    D. IMP Identification
    D.IMP: 1
    D.1.2 and D.1.3IMP RoleTest
    D.2 Status of the IMP to be used in the clinical trial
    D.2.1IMP to be used in the trial has a marketing authorisation No
    D.2.5The IMP has been designated in this indication as an orphan drug in the Community No
    D.2.5.1Orphan drug designation number
    D.3 Description of the IMP
    D.3.1Product nameAbemaciclib
    D.3.2Product code LY2835219
    D.3.4Pharmaceutical form Capsule
    D.3.4.1Specific paediatric formulation No
    D.3.7Routes of administration for this IMPOral use
    D.3.8 to D.3.10 IMP Identification Details (Active Substances)
    D.3.8INN - Proposed INNNot available
    D.3.9.1CAS number 1231929-97-7
    D.3.9.3Other descriptive nameLY2835219
    D.3.9.4EV Substance CodeSUB88440
    D.3.10 Strength
    D.3.10.1Concentration unit mg milligram(s)
    D.3.10.2Concentration typeequal
    D.3.10.3Concentration number50
    D.3.11 The IMP contains an:
    D.3.11.1Active substance of chemical origin Yes
    D.3.11.2Active substance of biological/ biotechnological origin (other than Advanced Therapy IMP (ATIMP) No
    The IMP is a:
    D.3.11.3Advanced Therapy IMP (ATIMP) No
    D.3.11.3.1Somatic cell therapy medicinal product No
    D.3.11.3.2Gene therapy medical product No
    D.3.11.3.3Tissue Engineered Product No
    D.3.11.3.4Combination ATIMP (i.e. one involving a medical device) No
    D.3.11.3.5Committee on Advanced therapies (CAT) has issued a classification for this product No
    D.3.11.4Combination product that includes a device, but does not involve an Advanced Therapy No
    D.3.11.5Radiopharmaceutical medicinal product No
    D.3.11.6Immunological medicinal product (such as vaccine, allergen, immune serum) No
    D.3.11.7Plasma derived medicinal product No
    D.3.11.8Extractive medicinal product No
    D.3.11.9Recombinant medicinal product No
    D.3.11.10Medicinal product containing genetically modified organisms No
    D.3.11.11Herbal medicinal product No
    D.3.11.12Homeopathic medicinal product No
    D.3.11.13Another type of medicinal product No
    D.8 Information on Placebo
    E. General Information on the Trial
    E.1 Medical condition or disease under investigation
    E.1.1Medical condition(s) being investigated
    Brain tumours, Breast Cancer, Non-Small Cell Lung Cancer, Melanoma
    E.1.1.1Medical condition in easily understood language
    Breast Cancer, Non-Small Cell Lung Cancer, Melanoma
    E.1.1.2Therapeutic area Diseases [C] - Cancer [C04]
    MedDRA Classification
    E.1.2 Medical condition or disease under investigation
    E.1.2Version 20.0
    E.1.2Level LLT
    E.1.2Classification code 10027475
    E.1.2Term Metastatic breast cancer
    E.1.2System Organ Class 100000020826
    E.1.3Condition being studied is a rare disease No
    E.2 Objective of the trial
    E.2.1Main objective of the trial
    The primary objective of this study is to evaluate abemaciclib with
    respect to OIRR (complete response [CR] + partial response [PR]) based
    on tumor assessments and Response Assessment in Neuro-Oncology
    brain metastases response assessment criteria (RANO-BM):
    • in patients with brain metastases secondary to HR+, HER2+ breast
    cancer.
    • in patients with brain metastases secondary to HR+, HER2- breast
    cancer.
    • in patients with brain metastases secondary to NSCLC.
    • in patients with brain metastases secondary to melanoma.
    E.2.2Secondary objectives of the trial
    Evaluate abemaciclib with respect to:
    - Intracranial disease per RANO-BM
    - Best overall intracranial response (BOIR)
    - Duration of intracranial response (DOIR) (CR + PR)
    - Intracranial disease control rate (IDCR) (CR + PR + stable disease
    [SD])
    - Intracranial clinical benefit rate (ICBR) (CR + PR + SD ≥6 months)
    Overall
    - Overall survival (OS)
    - Objective response rate (ORR) per Response Evaluation Criteria in Solid
    Tumors (RECIST) v1.1 and RANO-BM
    - Disease control rate (DCR) (CR+ PR+ SD) per RECIST v1.1 and RANOBM
    - Progression free survival (PFS) per RECIST v1.1 and RANO-BM
    - Change in symptoms as assessed by MD Anderson Symptom Inventory
    – Brain Tumor (MDASI-BT)
    - Safety and tolerability
    - PK of abemaciclib and its metabolites
    E.2.3Trial contains a sub-study No
    E.3Principal inclusion criteria
    Patients are eligible to be included in the study only if they meet all of
    the following criteria:
    [1] have brain metastases secondary to histologically or cytologically confirmed HR+ breast cancer, NSCLC, or melanoma.
    For Parts A and B: have confirmed HR+ breast cancer. To fulfill the
    requirement for HR+ disease, a breast cancer must express, at least 1 of
    the hormone receptors (ER or progesterone receptor [PgR]). For ER and PgR assays to be considered positive, ≥1% of tumor cell nuclei must be
    immunoreactive by immunohistochemistry (IHC) (Hammond et al.
    2010).
    For Part A: have HR+ breast cancer with confirmed HER2
    overexpression (HER2+) status. To fulfill the requirement for HER2+
    disease, tumor tissue must demonstrate 3+ by IHC or gene amplification
    by in-situ hybridization (ISH) (Wolff et al. 2013).
    For Part B: have HR+ breast cancer which does not demonstrate HER2
    overexpression (HER2-) by either IHC or ISH.
    For Part C: have HR+ breast cancer, NSCLC, or melanoma with brain
    lesions for which surgical resection is clinically indicated and agree to
    provide posttreatment (5 to 14 days after initiating abemaciclib) brain
    tumor tissue.
    For Part D: have NSCLC of any subtype.
    For Part E: have melanoma of any subtype
    For Part F: have HR+ breast cancer, NSCLC, or melanoma with
    leptomeningeal metastases by documented positive CSF cytology or by
    clinical signs and symptoms associated with abnormal magnetic
    resonance imaging (MRI) features. Concomitant parenchymal brain
    metastases are allowed (not required), but must be stable for at least 4
    weeks following whole brain radiotherapy (WBRT) or stereotactic
    radiosurgery (SRS).
    [2] Deleted criterion.
    [3] For Parts A,B, D and E: have ≥1 new or not previously irradiated
    measurable metastatic brain lesion ≥10 mm in the longest diameter (LD) and ≥5 mm in
    the perpendicular plane or a progressive previously irradiated metastatic brain lesion on radiographic imaging by gadolinium-enhanced magnetic resonance imaging (Gd MRI).
    For Part C (surgical): have metastatic brain lesion(s) for which surgical
    resection is clinically indicated.
    [4] have completed local therapy (surgical resection or SRS) ≥
    14 days prior to initiating abemaciclib and recovered from all acute
    effects. Patients are not required to have received prior local therapy for
    study participation.
    [5] if receiving concomitant corticosteroids, must be on a stable or
    decreasing dose for at least 7 days prior to the baseline Gd-MRI.
    [6] have a Karnofsky performance status of ≥70 (see Attachment 4).
    [7] have a life expectancy ≥12 weeks.
    [8] for HR+ breast cancer patients in Parts A, B and F: if currently receiving endocrine therapy, a patient may continue to receive the same endocrine therapy provided that extracranial disease is stable for at least 3 months and CNS disease progression has occurred while on this
    endocrine therapy. If these conditions are not met, patients must discontinue endocrine therapy prior to initiation of abemaciclib. Part C patients may continue or initiate endocrine therapy concurrently with abemaciclib and need not meet the above conditions.
    For HER2+ breast cancer patients in Parts A, C, and F: patients may
    receive concurrent treatment (ongoing or initiated simultaneously with
    abemaciclib) with trastuzumab. Concurrent treatment with trastuzumab emtansine (T-DM1) is not allowed.
    For NSCLC patients in Parts D, and F: if currently receiving
    gemcitabine or pemetrexed (single-agent or in combination with another
    XML File Identifier: WIkDUrCUKE2gFU7qidPCYUEI6YA=
    Page 11/24 therapy), a patient may continue to receive 1 of these 2 therapies as a single agent provided that extracranial disease is stable for at least 6
    weeks and CNS disease progression has occurred while on this therapy.
    Combination therapies (aside from gemcitabine or pemetrexed) must be
    discontinued for at least 14 days prior to initiation of abemaciclib. Part C patients may continue or initiate gemcitabine
    or pemetrexed (as single agents) concurrently with abemaciclib and need not meet the above conditions.
    [9] have discontinued all previous therapies for cancer (including cytotoxic chemotherapy, targeted therapy [including, but not limited to, everolimus], radiotherapy, immunotherapy, and investigational therapy) for at least 14 days prior to receiving abemaciclib and recovered from the acute effects of therapy (treatment related toxicity resolved to baseline) except for residual alopecia or peripheral neuropathy.
    [10] for HER2+ breast cancer patients in Parts A, C, and F: patients receiving concurrent trastuzumab, must have left ventricular ejection fraction within investigative site's normal range.
    E.4Principal exclusion criteria
    Patients will be excluded from the study if they meet any of the
    following criteria:
    [16] require immediate local therapy, including but not limited to
    WBRT, SRS, or surgical resection, for treatment of brain metastases.
    [17] require concurrent anticancer treatment at any time during the
    study treatment period.
    [18] are taking concurrent enzyme-inducing antiepileptic drugs
    (EIAED).
    [19] have evidence of significant (ie, symptomatic) intracranial
    hemorrhage.
    [20] for Parts A, B, C, D, and E: have evidence of leptomeningeal
    metastases by clinical signs and symptoms associated with abnormal
    MRI features or by documented CSF cytology.
    [21] have experienced >2 seizures within 4 weeks prior to study entry.
    [22] have visceral crisis. Visceral crisis is not the mere presence of
    visceral metastases but implies severe organ dysfunction as assessed by
    symptoms and signs, laboratory studies, and rapid progression of the
    disease.
    [23] for Parts A, B, D, E, and F: have previously received treatment
    with any CDK4 and CDK6 inhibitor. Part C patients may have received
    prior palbociclib or ribociclib, but not abemaciclib, treatment.
    [24] have known contraindication to Gd-MRI.
    [25] deleted criterion.
    [26] are currently enrolled in a clinical trial involving an investigational
    product or nonapproved use of a drug or device (other than the study
    drug used in this study), or concurrently enrolled in any other type of
    medical research judged not to be scientifically or medically compatible
    with this study.
    [27] have received treatment with a drug that has not received regulatory approval for any indication within 14 days of the initial dose of abemaciclib.
    [28] have a personal history within the last 12 months of any
    ventricular arrhythmia (including but not limited to ventricular tachycardia and ventricular fibrillation) or sudden cardiac arrest.
    [29] have serious preexisting medical conditions that, in the judgment of the investigator, would preclude participation in this study (for example, history of major surgical resection involving the stomach or small bowel).
    [30] have a preexisting chronic condition resulting in baseline Grade 2
    or higher diarrhea.
    [31] have a history of any other cancer (except nonmelanoma skin
    cancer or carcinoma in-situ of the cervix), unless in complete remission with no therapy for a minimum of 3 years.
    [32] are lactating.
    [33] have an active systemic fungal and/or known viral infection (for
    example, human immunodeficiency virus antibodies, hepatitis B surface antigen, or hepatitis C antibodies). Screening is not required for enrollment.
    [34] have an acute bacterial infection requiring IV antibiotics.
    [35] have received recent (within 28 days of initial dose of abemaciclib) or concurrent yellow fever vaccination.
    E.5 End points
    E.5.1Primary end point(s)
    Objective Intracranial Response Rate (OIRR) assessed using RANO-BM
    E.5.1.1Timepoint(s) of evaluation of this end point
    Baseline to Objective Disease Progression (Approximately 6 Months)
    E.5.2Secondary end point(s)
    Best Overall Intracranial Response (BOIR)
    Duration of intracranial response (DOIR) (CR + PR) Intracranial disease control rate (IDCR)
    Intracranial Clinical Benefit Rate (ICBR)
    Overall Survival (OS)
    Objective Response Rate (ORR) Disease Control Rate (DCR) Progression Free Survival (PFS)
    Change from Baseline to End of Study in Neurologic Symptoms on the MD Anderson Symptom
    Inventory-Brain Tumor (MDASI-BT) Scale Pharmacokinetics (PK): Minimum Concentration (Cmin) of Abemaciclib
    and its Metabolites
    E.5.2.1Timepoint(s) of evaluation of this end point
    Baseline to Earliest Objective Progression or Start of New Anticancer Therapy (Approximately 6 Months)
    Date of Complete Response or Partial Response to Date of Objective Disease Progression or Death from Any Cause (Approximately 6 Months)
    Baseline to Disease Progression or Start of New Anticancer Therapy (Approximately 6 Months)
    Baseline to Death from Any Cause (Approximately 18 Months)
    Baseline to Disease Progression (Approximately 6 Months)
    Baseline to Disease Progression or Start of New Anticancer Therapy (Approximately 6 Months)
    Baseline to Objective Disease Progression or Death from Any Cause (Approximately 6 Months)
    Baseline, End of Study (Approximately 6 Months)
    Cycle 1 through Cycle 4 (Approximately 3 Months)
    E.6 and E.7 Scope of the trial
    E.6Scope of the trial
    E.6.1Diagnosis No
    E.6.2Prophylaxis No
    E.6.3Therapy Yes
    E.6.4Safety Yes
    E.6.5Efficacy Yes
    E.6.6Pharmacokinetic Yes
    E.6.7Pharmacodynamic No
    E.6.8Bioequivalence No
    E.6.9Dose response No
    E.6.10Pharmacogenetic No
    E.6.11Pharmacogenomic No
    E.6.12Pharmacoeconomic No
    E.6.13Others No
    E.7Trial type and phase
    E.7.1Human pharmacology (Phase I) No
    E.7.1.1First administration to humans No
    E.7.1.2Bioequivalence study No
    E.7.1.3Other No
    E.7.1.3.1Other trial type description
    E.7.2Therapeutic exploratory (Phase II) Yes
    E.7.3Therapeutic confirmatory (Phase III) No
    E.7.4Therapeutic use (Phase IV) No
    E.8 Design of the trial
    E.8.1Controlled No
    E.8.1.1Randomised No
    E.8.1.2Open Yes
    E.8.1.3Single blind No
    E.8.1.4Double blind No
    E.8.1.5Parallel group No
    E.8.1.6Cross over No
    E.8.1.7Other No
    E.8.2 Comparator of controlled trial
    E.8.2.1Other medicinal product(s) No
    E.8.2.2Placebo No
    E.8.2.3Other No
    E.8.2.4Number of treatment arms in the trial6
    E.8.3 The trial involves single site in the Member State concerned No
    E.8.4 The trial involves multiple sites in the Member State concerned Yes
    E.8.4.1Number of sites anticipated in Member State concerned4
    E.8.5The trial involves multiple Member States Yes
    E.8.5.1Number of sites anticipated in the EEA6
    E.8.6 Trial involving sites outside the EEA
    E.8.6.1Trial being conducted both within and outside the EEA Yes
    E.8.6.2Trial being conducted completely outside of the EEA No
    E.8.6.3If E.8.6.1 or E.8.6.2 are Yes, specify the regions in which trial sites are planned
    Australia
    Austria
    Belgium
    Canada
    France
    Israel
    Italy
    New Zealand
    Spain
    United States
    E.8.7Trial has a data monitoring committee No
    E.8.8 Definition of the end of the trial and justification where it is not the last visit of the last subject undergoing the trial
    End of trial refers to the date of the last visit or last scheduled procedure for the last patient. The end of trial occurs after study completion and after the last patient has discontinued study treatment and completed any applicable continued access follow-up
    E.8.9 Initial estimate of the duration of the trial
    E.8.9.1In the Member State concerned years2
    E.8.9.1In the Member State concerned months3
    E.8.9.1In the Member State concerned days
    E.8.9.2In all countries concerned by the trial years2
    E.8.9.2In all countries concerned by the trial months3
    F. Population of Trial Subjects
    F.1 Age Range
    F.1.1Trial has subjects under 18 No
    F.1.1.1In Utero No
    F.1.1.2Preterm newborn infants (up to gestational age < 37 weeks) No
    F.1.1.3Newborns (0-27 days) No
    F.1.1.4Infants and toddlers (28 days-23 months) No
    F.1.1.5Children (2-11years) No
    F.1.1.6Adolescents (12-17 years) No
    F.1.2Adults (18-64 years) Yes
    F.1.2.1Number of subjects for this age range: 151
    F.1.3Elderly (>=65 years) Yes
    F.1.3.1Number of subjects for this age range: 100
    F.2 Gender
    F.2.1Female Yes
    F.2.2Male Yes
    F.3 Group of trial subjects
    F.3.1Healthy volunteers No
    F.3.2Patients Yes
    F.3.3Specific vulnerable populations Yes
    F.3.3.1Women of childbearing potential not using contraception No
    F.3.3.2Women of child-bearing potential using contraception Yes
    F.3.3.3Pregnant women No
    F.3.3.4Nursing women No
    F.3.3.5Emergency situation No
    F.3.3.6Subjects incapable of giving consent personally No
    F.3.3.7Others No
    F.4 Planned number of subjects to be included
    F.4.1In the member state20
    F.4.2 For a multinational trial
    F.4.2.1In the EEA 95
    F.4.2.2In the whole clinical trial 251
    F.5 Plans for treatment or care after the subject has ended the participation in the trial (if it is different from the expected normal treatment of that condition)
    Post-treatment discontinuation follow up starts just after the last dose of study drug and ends when final safety assessments are completed 30 days (±5) after last dose of study drug. Long term follow up begins after the day short term post discontinuation follow up visits is completed and continues until the patient’s death, lost to follow-up, or overall study completion.
    G. Investigator Networks to be involved in the Trial
    N. Review by the Competent Authority or Ethics Committee in the country concerned
    N.Competent Authority Decision Authorised
    N.Date of Competent Authority Decision2015-03-16
    N.Ethics Committee Opinion of the trial applicationFavourable
    N.Ethics Committee Opinion: Reason(s) for unfavourable opinion
    N.Date of Ethics Committee Opinion2015-04-16
    P. End of Trial
    P.End of Trial StatusCompleted
    P.Date of the global end of the trial2019-11-27
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