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    Summary
    EudraCT Number:2012-002807-17
    Sponsor's Protocol Code Number:ACR/GLYCALCH/1220
    National Competent Authority:Germany - BfArM
    Clinical Trial Type:EEA CTA
    Trial Status:Completed
    Date on which this record was first entered in the EudraCT database:2012-07-16
    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 ConcernedGermany - BfArM
    A.2EudraCT number2012-002807-17
    A.3Full title of the trial
    A monocenter, double-blind, randomized study to assess the antiperspirant efficacy of glycopyrrolate 2% versus Aluminium chlorohydrate 15% after topical applications on axilla of healthy volunteers
    A.3.1Title of the trial for lay people, in easily understood, i.e. non-technical, language
    A monocenter, double-blind, randomized study to assess the antiperspirant efficacy of glycopyrrolate 2% versus Aluminium chlorohydrate 15% after topical applications on axilla of healthy volunteers
    A.4.1Sponsor's protocol code numberACR/GLYCALCH/1220
    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 SponsorL’OREAL RECHERCHE
    B.1.3.4CountryFrance
    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 supportL'OREAL RECHERCHE
    B.4.2CountryFrance
    B.5 Contact point designated by the sponsor for further information on the trial
    B.5.1Name of organisationL’OREAL RECHERCHE
    B.5.2Functional name of contact pointProject Manager L'Oreal Recherche
    B.5.3 Address:
    B.5.3.1Street AddressRue du Général Roguet 90
    B.5.3.2Town/ cityCLICHY Cedex
    B.5.3.3Post code92583
    B.5.3.4CountryFrance
    B.5.4Telephone number+33(0)147563539
    B.5.5Fax number+33(0)147564824
    B.5.6E-mailRDeDORMAEL@rd.loreal.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 nameglycopyrrolate 2%
    D.3.4Pharmaceutical form Cutaneous solution
    D.3.4.1Specific paediatric formulation No
    D.3.7Routes of administration for this IMPTopical use (Noncurrent)
    D.3.8 to D.3.10 IMP Identification Details (Active Substances)
    D.3.8INN - Proposed INNGLYCOPYRRONIUM BROMIDE
    D.3.9.1CAS number 596-51-0
    D.3.9.4EV Substance CodeSUB07951MIG
    D.3.10 Strength
    D.3.10.1Concentration unit % (W/V) percent weight/volume
    D.3.10.2Concentration typeequal
    D.3.10.3Concentration number2
    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.IMP: 2
    D.1.2 and D.1.3IMP RoleComparator
    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 nameEmulsion of aluminum chlorohydrate 15 %
    D.3.2Product code 266603 4
    D.3.4Pharmaceutical form Cutaneous solution
    D.3.4.1Specific paediatric formulation No
    D.3.7Routes of administration for this IMPCutaneous use
    D.3.8 to D.3.10 IMP Identification Details (Active Substances)
    D.3.8INN - Proposed INNAluminum chlorohydrate
    D.3.9.1CAS number 1327-41-9
    D.3.9.3Other descriptive nameALUMINIUM HYDROCHLORIDE
    D.3.9.4EV Substance CodeSUB12824MIG
    D.3.10 Strength
    D.3.10.1Concentration unit % (W/V) percent weight/volume
    D.3.10.2Concentration typeequal
    D.3.10.3Concentration number15
    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
    The study will be performed in healthy volunteers
    E.1.1.1Medical condition in easily understood language
    The study will be performed in healthy volunteers
    E.1.1.2Therapeutic area Diseases [C] - Skin and Connective Tissue Diseases [C17]
    MedDRA Classification
    E.1.3Condition being studied is a rare disease No
    E.2 Objective of the trial
    E.2.1Main objective of the trial
    The main objective of this study is to assess the antiperspirant efficacy of glycopyrrolate 2% on the axillae of healthy volunteers, after topical applications and compare to the positive control Aluminum chlorohydrate 15 %
    E.2.2Secondary objectives of the trial
    The secondary objective is to assess the safety of the different study products
    E.2.3Trial contains a sub-study No
    E.3Principal inclusion criteria
    The prescribing information for Robinul (Glycopyrrolate) in particular
    contraindications, warnings and precautions, adverse reactions and drug
    interactions are to be considered.
    • Men and Female from 18 to 45 years old;
    • The physical examination and medical history must be without disease
    findings unless the investigator considers an abnormality to be irrelevant to
    the outcome of the clinical trial;
    • Casual Heart rate 48-76 beats/min; Systolic blood pressure 90-135 mm Hg;
    Diastolic blood pressure 60-80 mm Hg;
    • Skin type I to III according to the Fitzpatrick classification;
    • Body Mass Index (BMI) between 20 – 28
    • Experience in sauna use: at least one sauna visit within the last year;
    • Intact, healthy skin in the investigational areas (axilla);
    • Willing and able to fulfil the study requirements and schedule;
    • Informed about the study objectives and procedures, and able to understand
    them;
    • Written informed consent obtained;
    E.4Principal exclusion criteria
    • Female in pregnancy (positive urine pregnancy-test performed at screening, D22 before randomization and at D34) or lactation, or without effective contraception;
    • Symptoms or illnesses which may lead to adverse events resulting from glycopyrrolate and sauna use (such as cardiovascular diseases, prolonged QT-interval, hypertension, coronary deficiency, varicose vein, respiratory or gastrointestinal troubles, claustrophobia, diabetes, tiredness, glaucoma, thyroid diseases, atopic dermatitis, obstructive disorders of the lower urinary tract);
    • Subject with a perspiration level below 100 mg of sweat per axilla after 20 minute collection time. This will be evaluated at D22 before randomization.
    • Dermatological disorders influencing the investigational areas (presence of, acne, rosacea, sunburn, excess pilosity, eczema, urticaria etc. in the investigational area.);
    • Medical history of skin cancer;
    • History of allergy, hypersensitivity to any medicinal or cosmetic product, deodorants or antiperspirants;
    • History of allergy or contra-indication to glycopyrrolate or any serious reaction to one of the components of the investigational products;
    • Subject with neuromuscular or auto-immune disease (including Myasthenia Gravis) or any acute or chronic illness, or any long term concomitant medical condition which may expose the subject if participating in the study or may interfere with the study conduct, from investigator point of view;
    • Having used within the 8 past weeks before the inclusion diazepam,verapamil, glycopyrrolate or compounds such as botulinum toxin or having planned to use these treatments during the study;
    • Having used within the 4 past weeks before inclusion any topical or systemic treatment, drug (anti-inflammatory drugs, corticoids, retinoids, on the investigational areas, that would interfere with the study assessments and/or investigational products, or having planned to use these treatments during the study;
    • Having used within the 3 past weeks before inclusion any cosmetic on the investigational areas, that would interfere with the study assessments and/or investigational products, or having planned to use these treatments during the study;
    • Any physical treatment (like laser or electric depilation) under the arm within the last 6 months, or having planned to use these treatment during the study;
    • Having planned U.V. exposure on the investigational areas (sunlight or sunbeds) during the study;
    • Having planned to perform intensive sport (> 5 hours per week) from D0 to D34)
    • Having planned to practice swimming, sauna or hammam during the treatment period (D22 to D34)
    • Deprivation of freedom by an administrative or legal decision;
    • Unable to be contacted by phone in case of emergency;
    • Having participated within the 30 days before inclusion or currently participating in another clinical study.
    E.5 End points
    E.5.1Primary end point(s)
    The primary end point is to show a significant reduction in sweat
    production by the study product in comparison with the contralateral control field treated with Aluminum chlorohydrate 15 %.
    E.5.1.1Timepoint(s) of evaluation of this end point
    On study days 26 and 29 and 24, 48 and 72 hours after the last application of products.
    E.5.2Secondary end point(s)
    Adverse Events and local intolerances
    E.5.2.1Timepoint(s) of evaluation of this end point
    Study days 22 to 34
    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 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 Yes
    E.8.1.1Randomised Yes
    E.8.1.2Open No
    E.8.1.3Single blind No
    E.8.1.4Double blind Yes
    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 Yes
    E.8.2.3.1Comparator description
    Other cosmetical product
    E.8.2.4Number of treatment arms in the trial1
    E.8.3 The trial involves single site in the Member State concerned Yes
    E.8.4 The trial involves multiple sites in the Member State concerned No
    E.8.5The trial involves multiple Member States No
    E.8.6 Trial involving sites outside the EEA
    E.8.6.1Trial being conducted both within and outside the EEA No
    E.8.6.2Trial being conducted completely outside of the EEA No
    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
    The end of the trial is last visit of the last subject undergoing the trial.
    E.8.9 Initial estimate of the duration of the trial
    E.8.9.1In the Member State concerned years0
    E.8.9.1In the Member State concerned months2
    E.8.9.1In the Member State concerned 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: 33
    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 Yes
    F.3.2Patients No
    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 state33
    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)
    not aplicable as only healthy volunteers are included
    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 Decision2012-12-17
    N.Ethics Committee Opinion of the trial applicationFavourable
    N.Ethics Committee Opinion: Reason(s) for unfavourable opinion
    N.Date of Ethics Committee Opinion2012-10-15
    P. End of Trial
    P.End of Trial StatusCompleted
    P.Date of the global end of the trial2014-02-13
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