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    The EU Clinical Trials Register currently displays   40640   clinical trials with a EudraCT protocol, of which   6630   are clinical trials conducted with subjects less than 18 years old.
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    EudraCT Number:2013-003884-71
    Sponsor's Protocol Code Number:LPS13649
    National Competent Authority:Spain - AEMPS
    Clinical Trial Type:EEA CTA
    Trial Status:Ongoing
    Date on which this record was first entered in the EudraCT database:2014-10-03
    Trial results View results
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    A. Protocol Information
    A.1Member State ConcernedSpain - AEMPS
    A.2EudraCT number2013-003884-71
    A.3Full title of the trial
    A long-term follow-up study for Multiple Sclerosis patients who have completed the alemtuzumab Extension Study (CAMMS03409)
    Estudio de seguimiento a largo plazo para pacientes con Esclerosis Múltiple que han completado el estudio de extensión de alemtuzumab (CAMMS03409)
    A.3.1Title of the trial for lay people, in easily understood, i.e. non-technical, language
    Phase IIIB-IV long term follow-up study for patients who participated in CAMMS03409
    Estudio fase IIIB-IV de seguimiento a largo plazo para pacientes que participaron en el estudio CAMMS03409
    A.3.2Name or abbreviated title of the trial where available
    A.4.1Sponsor's protocol code numberLPS13649
    A.5.3WHO Universal Trial Reference Number (UTRN)U1111-1148-2987
    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 SponsorGenzyme Corporation
    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 supportGenzyme Corporation
    B.4.2CountryUnited States
    B.5 Contact point designated by the sponsor for further information on the trial
    B.5.1Name of organisationsanofi-aventis, s.a.
    B.5.2Functional name of contact pointUnidad Estudios Clínicos
    B.5.3 Address:
    B.5.3.1Street Addressc/ Josep Pla nº2, 4ª planta
    B.5.3.2Town/ cityBarcelona
    B.5.3.3Post code08019
    B.5.4Telephone number93 485 94 00
    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 Yes
    D. name Lemtrada
    D. of the Marketing Authorisation holderGenzyme Therapeutics Ltd.
    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 nameLemtrada
    D.3.2Product code GZ402673
    D.3.4Pharmaceutical form 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 INNalemtuzumab
    D.3.9.1CAS number 216503-57-0
    D.3.9.2Current sponsor codeGZ402673
    D.3.9.4EV Substance CodeSUB12459MIG
    D.3.10 Strength
    D.3.10.1Concentration unit mg/ml milligram(s)/millilitre
    D.3.10.2Concentration typeequal
    D.3.10.3Concentration number10
    D.3.11 The IMP contains an:
    D.3.11.1Active substance of chemical origin No
    D.3.11.2Active substance of biological/ biotechnological origin (other than Advanced Therapy IMP (ATIMP) Yes
    The IMP is a:
    D.3.11.3Advanced Therapy IMP (ATIMP) No
    D. cell therapy medicinal product No
    D. therapy medical product No
    D. Engineered Product No
    D. ATIMP (i.e. one involving a medical device) No
    D. 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 Yes
    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 Yes
    D. medicinal product typeHumanised Monoclonal Antibody
    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
    Relapsing-remitting multiple sclerosis
    Esclerosis múltiple en remisión de recaídas
    E.1.1.1Medical condition in easily understood language
    Relapsing-remitting multiple sclerosis
    Esclerosis múltiple en remisión de recaídas
    E.1.1.2Therapeutic area Diseases [C] - Nervous System Diseases [C10]
    MedDRA Classification
    E.1.2 Medical condition or disease under investigation
    E.1.2Version 17.0
    E.1.2Level PT
    E.1.2Classification code 10063399
    E.1.2Term Relapsing-remitting multiple sclerosis
    E.1.2System Organ Class 10029205 - Nervous system disorders
    E.1.3Condition being studied is a rare disease No
    E.2 Objective of the trial
    E.2.1Main objective of the trial
    To evaluate long-term safety of alemtuzumab
    Evaluar la seguridad a largo plazo de alemtuzumab
    E.2.2Secondary objectives of the trial
    - To evaluate long term efficacy of alemtuzumab
    - To evaluate the safety profile of patients who received other Disease Modifying Treatment's (DMT) following alemtuzumab treatment
    - To evaluate patient-reported Quality of Life (QoL) outcomes and health resource utilization of patients who received alemtuzumab
    - To evaluate as needed re-treatment with alemtuzumab and other DMTs
    Evaluar la eficacia a largo plazo de alemtuzumab
    Evaluar el perfil de seguridad de los pacientes que hayan recibido otros tratamientos modificadores de la enfermedad (TME) tras el tratamiento con alemtuzumab.
    Evaluar los resultados en cuanto a la calidad de vida (CdV) notificados por los pacientes y la utilización de los recursos sanitarios por parte de pacientes que hayan recibido alemtuzumab.
    Evaluar en caso necesario la repetición del tratamiento con alemtuzumab y otros TME.
    E.2.3Trial contains a sub-study No
    E.3Principal inclusion criteria
    - Patient has completed at least 48 months of the Extension Study CAMMS03409
    - Signed written informed consent form
    - Que el paciente haya completado al menos 48 meses del Estudio de Extensión CAMMS03409.
    - Firmar el formulario de consentimiento informado (FCI).
    E.4Principal exclusion criteria
    - Patient participating in another investigational interventional study
    - Que el paciente esté participando en otro estudio de intervención en fase de investigación.
    E.5 End points
    E.5.1Primary end point(s)
    - Incidence, duration, grade/intensity, relationship to study drug, and outcome of the following: Serious Adverse Events; Adverse Events
    - Incidence, nature, seriousness, grade/intensity, relationship to study drug, and outcome of the following adverse events of special interest: Specific autoimmune mediated conditions, Infusion-associated reactions, Malignancy, Infections
    - Changes in laboratory parameters
    - Incidencia, duración, grado/intensidad, relación con el fármaco del estudio y desenlace de lo siguiente: Acontecimientos Adversos Graves (AAG), Acontecimientos Adversos (AA)
    - Incidencia, carácter, gravedad, grado/intensidad, relación con el fármaco del estudio y desenlace de los Acontecimientos Adversos de Interés Especial (AAIE) siguientes: Afecciones autoinmunes, Reacciones asociadas a la infusión (RAI), Neoplasia maligna, Infecciones
    - Cambios en los parámetros analíticos
    E.5.1.1Timepoint(s) of evaluation of this end point
    Final analysis at study completion (Up to a maximum of 5.5 years). Yearly interim analysis.
    Análisis final a la finalización del estudio (hasta un máximo de 5.5 años)
    Analisis intermedio anual
    E.5.2Secondary end point(s)
    - Annualized relapse rate (ARR)
    - Proportion of participants relapse free
    - Change over time in Expanded Disability Status Scale (EDSS) scores
    - Change over time in brain imaging findings
    - Change over time in self-reported quality of life (QoL) as assessed by the Medical Outcome Study (MOS) 36-Item Short-Form Health Survey (SF-36) Version 2
    - Change over time in the Functional Assessment of Multiple Sclerosis (FAMS)
    - Change over time in the EuroQoL in 5 Dimensions (EQ-5D)
    - Pharmaco-economic evaluation (Modified Health Resources Utilization Questionnaire (HRUQ) / Health Related Productivity Questionnaire (HRPQ))
    - Tasa anualizada de recaídas (TAR)
    - Proporción de pacientes sin recaídas
    - Cambio a lo largo del tiempo en las puntuaciones de la Escala Ampliada del Estado de Discapacidad (Expanded Disability Status Scale, EDSS)
    - Cambio a lo largo del tiempo en los hallazgos de las resonancias magnéticas cerebrales
    - Cambio a lo largo del tiempo en la calidad de vida (CdV) autonotificada y evaluada mediante la versión 2 del Cuestionario de Salud Abreviado de 36 Ítems
    - Cambio a lo largo del tiempo en la Evaluación Funcional de la Esclerosis Múltiple
    - Cambio a lo largo del tiempo en el cuestionario EuroQoL en 5 dimensiones (EQ-5D).
    - Se administrarán el Cuestionario de Utilización de los Recursos Sanitarios (Health Resources Utilization Questionnaire, HRUQ)
    E.5.2.1Timepoint(s) of evaluation of this end point
    Final analysis at study completion (Up to a maximum of 5.5 years). Yearly interim analysis.
    Análisis final a la finalización del estudio (hasta un máximo de 5.5 años)
    Analisis intermedio anual
    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 No
    E.6.4Safety Yes
    E.6.5Efficacy Yes
    E.6.6Pharmacokinetic No
    E.6.7Pharmacodynamic No
    E.6.8Bioequivalence No
    E.6.9Dose response No
    E.6.10Pharmacogenetic No
    E.6.11Pharmacogenomic No
    E.6.12Pharmacoeconomic Yes
    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. trial type description
    E.7.2Therapeutic exploratory (Phase II) No
    E.7.3Therapeutic confirmatory (Phase III) Yes
    E.7.4Therapeutic use (Phase IV) Yes
    E.8 Design of the trial
    E.8.1Controlled No
    E.8.1.1Randomised Information not present in EudraCT
    E.8.1.2Open Information not present in EudraCT
    E.8.1.3Single blind Information not present in EudraCT
    E.8.1.4Double blind Information not present in EudraCT
    E.8.1.5Parallel group Information not present in EudraCT
    E.8.1.6Cross over Information not present in EudraCT
    E.8.1.7Other Information not present in EudraCT
    E.8.2 Comparator of controlled trial
    E.8.2.1Other medicinal product(s) Information not present in EudraCT
    E.8.2.2Placebo Information not present in EudraCT
    E.8.2.3Other Information not present in EudraCT
    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 EEA52
    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
    Czech Republic
    Russian Federation
    United Kingdom
    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
    Última visita del último paciente
    E.8.9 Initial estimate of the duration of the trial
    E.8.9.1In the Member State concerned years5
    E.8.9.1In the Member State concerned months6
    E.8.9.1In the Member State concerned days0
    E.8.9.2In all countries concerned by the trial years5
    E.8.9.2In all countries concerned by the trial months6
    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: 799
    F.1.3Elderly (>=65 years) No
    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 For clinical trials recorded in the database before the 10th March 2011 this question read: "Women of childbearing potential" and did not include the words "not using contraception". An answer of yes could have included women of child bearing potential whether or not they would be using contraception. The answer should therefore be understood in that context. This trial was recorded in the database on 2014-10-03. Yes
    F.3.3.2Women of child-bearing potential using contraception Yes
    F.3.3.3Pregnant women Yes
    F.3.3.4Nursing women Yes
    F.3.3.5Emergency situation Yes
    F.3.3.6Subjects incapable of giving consent personally No
    F.3.3.7Others Yes
    F. of other specific vulnerable populations
    In case of treatment, cautionary measures from approved labelling or IB are applied
    F.4 Planned number of subjects to be included
    F.4.1In the member state9
    F.4.2 For a multinational trial
    F.4.2.1In the EEA 399
    F.4.2.2In the whole clinical trial 799
    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)
    Patients will be followed for 48-months after the last infusion of alemtuzumab received in the current trial setting. If the 48-month period of safety follow-up continues after the study ends, the patient will be followed by their physician in a regular healthcare setting, in line with the local approved Risk Minimization Plan for alemtuzumab, until the 48-month period is completed.
    Los pacientes serán seguidos durante 48 meses después de la última infusión de alemtuzumab recibido en el contexto del ensayo actual. Si el período de 48 meses de seguimiento de seguridad continúa después de que termine el estudio, el paciente será seguido por su médico en un centro de salud regular, en línea con el Plan de Minimización de Riesgos aprobada local para alemtuzumab, hasta que el período de 48 meses sea completado.
    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 Decision2014-12-01
    N.Ethics Committee Opinion of the trial applicationFavourable
    N.Ethics Committee Opinion: Reason(s) for unfavourable opinion
    N.Date of Ethics Committee Opinion2014-11-14
    P. End of Trial
    P.End of Trial StatusOngoing
    The status of studies in GB is no longer updated from 1.1.2021
    For the UK, as from 1.1.2021, EU Law applies only to the territory of Northern Ireland (NI) to the extent foreseen in the Protocol on Ireland/NI
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