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    Summary
    EudraCT Number:2014-003773-42
    Sponsor's Protocol Code Number:PM1183-B-005-14
    National Competent Authority:Germany - BfArM
    Clinical Trial Type:EEA CTA
    Trial Status:Ongoing
    Date on which this record was first entered in the EudraCT database:2016-06-20
    Trial 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 ConcernedGermany - BfArM
    A.2EudraCT number2014-003773-42
    A.3Full title of the trial
    A Multicenter Phase II Clinical Trial of Lurbinectedin (PM01183) in Selected
    Advanced Solid Tumors.
    A.3.1Title of the trial for lay people, in easily understood, i.e. non-technical, language
    Clinical Trial of Lurbinectedin (PM01183) in Selected Advanced Solid
    Tumors.
    A.3.2Name or abbreviated title of the trial where available
    N.A.
    A.4.1Sponsor's protocol code numberPM1183-B-005-14
    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 SponsorPharma Mar S.A.
    B.1.3.4CountrySpain
    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 supportPharma Mar, S.A.
    B.4.2CountrySpain
    B.5 Contact point designated by the sponsor for further information on the trial
    B.5.1Name of organisationPharma Mar, S.A.
    B.5.2Functional name of contact pointClinical Trials
    B.5.3 Address:
    B.5.3.1Street AddressAvda de los Reyes, 1, Polígono Industrial “La Mina”
    B.5.3.2Town/ cityColmenar Viejo (Madrid)
    B.5.3.3Post code28770
    B.5.3.4CountrySpain
    B.5.4Telephone number+34918466087
    B.5.5Fax number+34918466003
    B.5.6E-mailclinicaltrials@pharmamar.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 nameLurbinectedin
    D.3.2Product code PM01183
    D.3.4Pharmaceutical form Powder for concentrate for solution for infusion
    D.3.4.1Specific paediatric formulation No
    D.3.7Routes of administration for this IMPIntravenous use
    D.3.8 to D.3.10 IMP Identification Details (Active Substances)
    D.3.8INN - Proposed INNlurbinectedin
    D.3.9.1CAS number 497871-47-3
    D.3.9.2Current sponsor codePM01183
    D.3.9.3Other descriptive nameLURBINECTEDIN
    D.3.9.4EV Substance CodeSUB31196
    D.3.10 Strength
    D.3.10.1Concentration unit mg milligram(s)
    D.3.10.2Concentration typeequal
    D.3.10.3Concentration number4
    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
    Selected Advanced Solid Tumors.
    E.1.1.1Medical condition in easily understood language
    Selected Advanced Solid Tumors.
    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 10048683
    E.1.2Term Advanced cancer
    E.1.2System Organ Class 100000020935
    E.1.3Condition being studied is a rare disease No
    E.2 Objective of the trial
    E.2.1Main objective of the trial
    To assess the antitumor activity of lurbinectedin (PM01183) in terms of
    overall response rate (ORR), according to RECIST v 1.1 in the following
    advanced solid tumors: small cell lung cancer (SCLC), head and neck
    carcinoma (H&N), neuroendocrine tumors (NETs), biliary tract
    carcinoma, endometrial carcinoma, BRCA 1/2-associated metastatic
    breast carcinoma, carcinoma of unknown primary site, germ cell tumors
    (GCTs) and Ewing´s family of tumors (EFTs).
    E.2.2Secondary objectives of the trial
    *Characterize the antitumor activity of PM01183 in terms of duration of
    response (DR), clinical benefit (ORR or stable disease (SD) lasting over
    four months (SD>=4 months)), progression-free survival (PFS) and one-year overall survival (1y-OS) in each cohort of advanced solid tumors [overall survival (OS) instead of 1y-OS in the cohort of SCLC patients].
    *Characterize the plasma pharmacokinetics (PK) of PM01183.
    *Conduct an exploratory pharmacogenomic (PGx) and pharmacogenetic
    analysis.
    *Evaluate the safety profile of PM01183 in this patient population.
    E.2.3Trial contains a sub-study Yes
    E.2.3.1Full title, date and version of each sub-study and their related objectives
    An exploratory pharmacogenomic (PGx) and pharmacogenetic sub-study.
    E.3Principal inclusion criteria
    1)Age >/= 18 years.
    2)Voluntary signed informed consent (IC) of the patient before any study-specific procedure.
    3)Pathologically proven diagnosis of any of the following malignancies:
    a)Small cell lung cancer (SCLC).
    b)Head and neck carcinoma (H&N). Salivary glands tumors are excluded.
    c)Neuroendocrine tumors (NETs), grade 2 and 3 according to World
    Health Organization (WHO) classification.
    d)Biliary tract carcinoma.
    e)Endometrial carcinoma.
    f)BRCA 1/2- associated metastatic breast carcinoma.
    g)Carcinoma of unknown primary site.
    h)Germ cell tumor (GCTs), excluding immature teratoma, or teratoma
    with malignant transformation.
    i)Ewing's family of tumors (EFTs).4)Prior treatment. Patients must have received:
    a)SCLC: one prior chemotherapy-containing line.
    b)H&N: one or two prior chemotherapy-containing lines.
    c)NETs: one or two prior chemotherapy-containing lines. No more than three prior hormone or biological therapy lines.
    d)Biliary tract carcinoma: one or two prior chemotherapy-containing
    lines.
    e)Endometrial carcinoma: one prior chemotherapy-containing line.
    f)BRCA 1/2-associated metastatic breast carcinoma: at least one but no
    more than three prior chemotherapy-containing lines.
    g)Carcinoma of unknown primary site: one or two prior chemotherapycontaining
    lines.
    h)GCTs: no limit of prior therapy (patients with no other clinical
    therapeutic options).
    i)EFTs: no more than two prior chemotherapy-containing lines in the
    metastatic/recurrent setting.
    5)Measurable disease as defined by RECIST v.1.1, and documented
    progression before study entry.
    6)Eastern Cooperative Oncology Group (ECOG) performance status (PS) </= 2.
    7)Adequate major organ function:
    a)Hemoglobin >/= 9 g/dl, prior red blood cell (RBC) transfusions are
    allowed if clinically indicated; absolute neutrophil count (ANC) >/= 2.0 x 109/l; and platelet count >/= 100 x 109/l.
    b)Alanine aminotransferase (ALT), and aspartate aminotransferase (AST) </= 3.0 x upper limit of normal (ULN).
    c)Total bilirubin </= 1.5 x ULN, or direct bilirubin </= ULN.
    d)Albumin >/= 3 g/dl.
    e)Serum creatinine </= 1.5 x ULN or creatinine clearance >/= 30 ml/min.
    f)Creatine phosphokinase (CPK) </= 2.5 x ULN.
    8)Washout periods prior to Day 1 of Cycle 1:
    a)At least three weeks since the last chemotherapy (six weeks if therapy contained nitrosureas or systemic mitomycin C).
    b)At least four weeks since the last monoclonal antibody (MAb)-containing therapy, or radiotherapy (RT) > 30 gray (Gy).
    c)At least two weeks since the last biological/investigational therapy
    (excluding MAbs) or palliative RT (</= 10 fractions or </= 30 Gy total dose).
    9)Grade </= 1 toxicity due to any previous cancer therapy according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE, v.4). Grade 2 is allowed in case of alopecia and/or peripheral sensory neuropathy.
    10)Women of childbearing potential must have pregnancy excluded by appropriate testing before study entry. Fertile women must agree to use a medically acceptable method of contraception throughout the treatment period and for at least three months after treatment
    discontinuation. Fertile men must agree to refrain from fathering a child or donating sperm during the trial and for four months after the last infusion.
    E.4Principal exclusion criteria
    1)Prior treatment with PM01183 or trabectedin.
    2)Prior or concurrent malignant disease unless in complete remission for more than five years, except treated in situ carcinoma of the cervix, basal or squamous cell skin carcinoma, and in situ transitional cell bladder carcinoma.
    3)Known central nervous system (CNS) involvement. In patients with
    SCLC, brain computed tomography (CT)-scan or magnetic resonance
    imaging(MRI) results must be provided at baseline.
    4)Relevant diseases or clinical situations which may increase the
    patient´s risk:
    a)History within the last year or presence of unstable angina, myocardial infarction, congestive heart failure, or clinically relevant valvular heart disease or symptomatic arrhythmia or any asymptomatic ventricular arrhythmia requiring ongoing treatment.
    b)Grade >/= 3 dyspnea or daily intermittent oxygen requirement within two weeks prior to the study treatment onset.
    c)Active infection.
    d)Unhealed wounds or presence of any external drainage.
    e)Known chronic active hepatitis or cirrhosis.
    f)Immunocompromised patients, including known infection by human
    immunodeficiency virus (HIV).
    5)Women who are pregnant or breast-feeding, and fertile patients (men and women) who are not using an effective method of contraception. *
    6)Impending need for RT (e.g., painful bone metastasis and/or risk of
    spinal cord compression).
    7)Limitation of the patient's ability to comply with the treatment or to follow-up the protocol.
    * Women of childbearing potential (WOCBP) must agree to use an effective contraception method to avoid pregnancy during the course of the trial (and for at least three months after the last infusion). Valid methods to determine the childbearing potential, adequate contraception and requirements for WOCBP partners are described in the study protocol, appendix 2. Fertile men must agree to refrain from fathering a child or donating sperm during the trial and for four months after the last infusion.
    E.5 End points
    E.5.1Primary end point(s)
    Overall Response Rate (ORR) in each tumor type. ORR is defined as the
    percentage of patients with a confirmed response, either complete (CR)
    or partial (PR), according to the RECIST (v. 1.1).
    E.5.1.1Timepoint(s) of evaluation of this end point
    Along the study.
    E.5.2Secondary end point(s)
    Efficacy:
    * Duration of Response (DR), defined as the time between the
    date when the response criteria (PR or CR, whichever one is first reached) are fulfilled to the first date when PD, recurrence or death is documented.
    * Clinical Benefit, defined as ORR or stable disease lasting over four months (SD >/= 4 months).
    * Progression-free Survival (PFS), defined as the period of time from the date of first infusion to the date of PD, death (of any cause), or last tumor evaluation.
    * PFS4/PFS6, defined as the Kaplan-Meier estimates of the probability of being free from progression and death after the first infusion at these time points (4 and 6 months).
    * OS6/OS12, defined as the Kaplan-Meier estimates of the probability of being alive after the first infusion at these time points (6 and 12 months)(overall survival in the cohort of SCLC patients).

    Plasma Pharmacokinetics (PK) of PM01183
    Non-compartmental (NCA) PK parameters: area under the curve (AUC), maximum plasma concentration (Cmax), clearance (CL) and half-life (t1/2).
    Population PK parameters of the compartment model to be developed (initially based on Volumes and Clearance), and PK/PD correlation parameters, if applicable.

    Pharmacogenetics
    This analysis will be performed in those patients who signed the IC for the pharmacogenetic sub-study. The presence or absence of known polymorphisms from a single sample collected at any time during the study, but preferably just before treatment start in Cycle 1, will be assessed to explain the individual variability in the main PK parameters.

    Pharmacogenomics (PGx):
    This exploratory analysis will be performed in those patients treated in any arm who signed the IC for the PGx sub-study. mRNA or protein
    expression levels of factors involved in DNA repair mechanisms, or
    related to the mechanism of action of lurbinectedin, will be evaluated
    from prior available tumor tissue samples obtained at diagnosis or
    relapse. Their mutational status might be also analyzed. Their
    correlation with the clinical response and outcome after treatment will be assessed.

    Safety Profile:
    * Clinical examinations. Clinical assessment of AEs and serious adverse events (SAEs).
    * Changes in laboratory parameters (hematological and biochemical, including liver function tests).
    * Reasons for treatment discontinuations.
    * Reasons for dose reduction and treatment delays.
    E.5.2.1Timepoint(s) of evaluation of this end point
    Along the study.
    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 Yes
    E.6.11Pharmacogenomic Yes
    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 trial1
    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 concerned2
    E.8.5The trial involves multiple Member States Yes
    E.8.5.1Number of sites anticipated in the EEA21
    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
    Switzerland
    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
    When all evaluable patients have at least 12 months of follow-up, and
    all patients in the SCLC cohort have been followed up until death.
    E.8.9 Initial estimate of the duration of the trial
    E.8.9.1In the Member State concerned years3
    E.8.9.1In the Member State concerned months0
    E.8.9.1In the Member State concerned days0
    E.8.9.2In all countries concerned by the trial years4
    E.8.9.2In all countries concerned by the trial months0
    E.8.9.2In all countries concerned by the trial days0
    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: 137
    F.1.3Elderly (>=65 years) Yes
    F.1.3.1Number of subjects for this age range: 188
    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 state10
    F.4.2 For a multinational trial
    F.4.2.1In the EEA 235
    F.4.2.2In the whole clinical trial 325
    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)
    None.
    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 Decision2016-09-02
    N.Ethics Committee Opinion of the trial applicationFavourable
    N.Ethics Committee Opinion: Reason(s) for unfavourable opinion
    N.Date of Ethics Committee Opinion2016-09-01
    P. End of Trial
    P.End of Trial StatusOngoing
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