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Tolvaptan Phase 3 Efficacy and Safety Study in Autosomal Dominant Polycystic Kidney Disease (ADPKD) (TEMPO3:4)

30. maj 2017 opdateret af: Otsuka Pharmaceutical Development & Commercialization, Inc.

A Phase 3, Multi-center, Double-blind, Placebo-controlled, Parallel-arm Trial to Determine Long-term Safety and Efficacy of Oral Tolvaptan Tablets Regimens in Adult Subjects With Autosomal Dominant Polycystic Kidney Disease

This study's purpose is to evaluate the long-term safety and efficacy of tolvaptan versus placebo in patients with ADPKD.

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Detaljeret beskrivelse

This study evaluated whether or not tolvaptan is potentially beneficial, while maintaining an adequate safety profile, by reducing the rate of total kidney volume increase, while impacting the onset, severity, and progression of other important consequences of ADPKD.

During the 3-week titration phase, tolvaptan or placebo was titrated in weekly intervals from lowest to highest tolerated levels given in split-dose regimens of 45/15 mg, 60/30 mg and 90/30 mg orally upon awakening and approximately 9 hours later. As soon as a subject could not tolerate a given dose, the titration phase was over and the maintenance phase began at the dose level tolerated. The maintenance phase lasted to Month 36. Subjects were able to titrate down at any point during the study. Subjects were able to titrate up during the maintenance phase with Medical Monitor approval.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

1445

Fase

  • Fase 3

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

  • Argentina
      • Buenos Aires, Argentina, 1425
        • Instituto de Nefrología, Nefrology SA
      • Buenos Aires, Argentina, 1602
        • Hospital Municipal de Vicente Lopez, Dr Bernardo Houssay
      • Buenos Aires, Argentina, B1664INZ
        • Hosptial Universitario Austral
      • Cordoba, Argentina, X5000IUP
        • Sanatorio Allende
      • Cordoba, Argentina, X5016KEA
        • Hospital Privado-Centro Medico de Cordoba
  • Australien
      • Adelaide, Australien, 5000
        • Royal Adelaide Hospital
      • Adelaide, Australien, 5011
        • Queen Elizebeth Hospital
      • Brisbane, Australien, 4102
        • Princess Alexandra Hospital
      • Melbourne, Australien, 3050
        • Royal Melbourne Hospital
      • Melbourne, Australien, 3121
        • Melbourne Renal Research Group
      • Perth, Australien, 6054
        • Royal Perth Hospital
      • Sydney, Australien, 2065
        • Royal North Shore Hospital
      • Sydney, Australien, 2145
        • Westmead Hospital
  • Belgien
      • Brussel, Belgien, 1090
        • UZ Brussel
      • Brussels, Belgien, 1200
        • UCL-St Luc
      • Gent, Belgien, 9000
        • UZ Gent
  • Canada
    • Nova Scotia
      • Halifax, Nova Scotia, Canada, B3H1v8
        • Queen Elizabeth II Health Science Center, Division of Nephrology
    • Quebec
      • Montreal, Quebec, Canada, H3A1A1
        • Royal Victoria Hospital
      • Montreal, Quebec, Canada, H4J1C5
        • Hospital du Sacre- Coeur de Montreal
  • Danmark
      • Herlev, Danmark, 2730
        • Herlev Amtssygehus
      • Odense, Danmark, 5000
        • Odense Universitetshospital
  • Den Russiske Føderation
      • Kemerovo, Den Russiske Føderation, 650061
        • Kemerovo Medical Academy, Regional Clinical Hospital
      • Moscow, Den Russiske Føderation, 123060
        • City Clinical Hospital #52
      • St. Petersburg, Den Russiske Føderation, 191104
        • City Mariinskiy Hospital
      • St.-Petersburg, Den Russiske Føderation, 194291
        • Leningrad Regional Clinical Hospital
      • Tomsk, Den Russiske Føderation, 634063
        • Tomsk Regional Clinical Hospital
  • Det Forenede Kongerige
      • Belfast, Det Forenede Kongerige, BT9 7AB
        • Belfast City Hospital
      • Birmingham, Det Forenede Kongerige, B15 2TH
        • Oueen Elizabeth Hospital
      • Brighton, Det Forenede Kongerige, BN2 5BE
        • Sussex Renal Unit Royal Sussex County Hospital
      • Coventry, Det Forenede Kongerige, CV2 2DX
        • Uhcw Mhs Trust
      • Edinburgh, Det Forenede Kongerige, EH16 4SA
        • Royal Infirmary
      • Inverness, Det Forenede Kongerige, IV2 3UJ
        • Raigmore Hospital
      • London, Det Forenede Kongerige, NW3 2PF
        • Royal Free and University College Medical School
      • London, Det Forenede Kongerige, SE5-9RS
        • King's College Hospital
      • London, Det Forenede Kongerige, SW170RE
        • St. George's Hospital
      • Sheffield, Det Forenede Kongerige, S5 7AU
        • Royal Hallamshire Hospital
      • Swansea, Det Forenede Kongerige, SA6 6NL
        • Morriston Hospital
  • Forenede Stater
    • Alabama
      • Mobile, Alabama, Forenede Stater, 36617
        • University of South Alabama
      • Mobile, Alabama, Forenede Stater, 36608
        • Coastal Clinical Research
    • California
      • Riverside, California, Forenede Stater, 92503
        • Apex Research of Riverside
      • Stanford, California, Forenede Stater, 94305-5114
        • Stanford University Medical Center
    • Colorado
      • Denver, Colorado, Forenede Stater, 80262
        • University of Colorado Health Sciences Center
    • Connecticut
      • New Haven, Connecticut, Forenede Stater, 06510
        • Yale University School of Medicine
    • Florida
      • Jacksonville, Florida, Forenede Stater, 32216
        • Jacksonville Center for Clinical Research
      • Port Charlotte, Florida, Forenede Stater, 33952
        • Coastal Nephrology Associates Research Center, LLC
    • Georgia
      • Atlanta, Georgia, Forenede Stater, 30308
        • Emory University School of Medicine
    • Illinois
      • Chicago, Illinois, Forenede Stater, 60611
        • Northwestern University
    • Kansas
      • Kansas City, Kansas, Forenede Stater, 66160
        • University of Kansas Medical Center
    • Louisiana
      • Baton Rouge, Louisiana, Forenede Stater, 70809
        • Renal Associates of Baton Rough, L.L.C.
    • Maryland
      • Baltimore, Maryland, Forenede Stater, 21205
        • John Hopkins School of Medicine
    • Massachusetts
      • Boston, Massachusetts, Forenede Stater, 02215
        • Beth Israel Deaconess Medical Center
      • Boston, Massachusetts, Forenede Stater, 02111
        • Tufts- New England Medical Center
    • Minnesota
      • Rochester, Minnesota, Forenede Stater, 55905
        • Mayo Medical Center
    • New York
      • Buffalo, New York, Forenede Stater, 14215
        • Erie County Medical Center
      • Hawthorne, New York, Forenede Stater, 10532
        • Nephrology Associates of Westchester
      • New York, New York, Forenede Stater, 10032
        • Columbia University Medical Center
      • New York, New York, Forenede Stater, 10021
        • The Rogosin Institute
    • North Carolina
      • Chapel Hill, North Carolina, Forenede Stater, 27599
        • University of North Carolina, UNC, Kidney Center
      • Greenville, North Carolina, Forenede Stater, 27834
        • East Carolina University
    • Ohio
      • Cincinnati, Ohio, Forenede Stater, 45220
        • Kidney and Hypertension Center
      • Cleveland, Ohio, Forenede Stater, 44106
        • University Hospitals of Cleveland/Case
    • Oregon
      • Portland, Oregon, Forenede Stater, 97210
        • Northwest Renal Clinic, Inc.
    • Pennsylvania
      • Philadelphia, Pennsylvania, Forenede Stater, 19104
        • University of Pennsylvania Medical Center
    • South Carolina
      • Charleston, South Carolina, Forenede Stater, 29405
        • Charleston Nephrology Associates
    • Tennessee
      • Nashville, Tennessee, Forenede Stater, 37205
        • Nephrology Associates, P.C.
      • Nashville, Tennessee, Forenede Stater, 37232-1371
        • Vanderbilt University Medical Center
    • Virginia
      • Charlottesville, Virginia, Forenede Stater, 22908
        • University of Virginia, Nephrology Clinical Research Center
  • Frankrig
      • Bordeaux, Frankrig, 33076
        • CHU-Hopital Pellegrin
      • Caen Cedex, Frankrig, 14033
        • CHU - Hôpital Clémenceau
      • Lyon Cedex 3, Frankrig, 69437
        • Hôpital Edouard Herriot
      • Marseille, Frankrig, 13005
        • Hôpital de la Conception
      • Montpellier, Frankrig, 34295
        • CHU - Hôpital Lapeyronie
      • Paris, Frankrig, 75018
        • Hopital Bichat-Claude Bernard
      • Reims cedex, Frankrig, 51092
        • Centre Hospitalier Universitaire
      • Saint-Etienne Cedex 2, Frankrig, 42055
        • Chu - Hopital Nord
      • Toulouse Cedex 09, Frankrig, 31059
        • Hôpital Rangueil
  • Holland
      • Amsterdam, Holland, 1081 HV
        • VU Medisch Centrum
      • Groningen, Holland, 9713 GZ
        • UMCG Groningen
  • Italien
      • Bergamo, Italien, 24128
        • Ospedali Riuniti di Bergamo
      • Milano, Italien, 20132
        • Università Vita e Salute, Ospedale San Raffaele
      • Modena, Italien, 41100
        • Policlinico di Modena
      • Napoli, Italien, 80131
        • Policlinico
      • Pavia, Italien, 27100
        • IRCCS Fondazione Salvatore Maugeri
  • Japan
      • Chiba, Japan, 2608677
        • Chiba University Hospital
      • Chiba, Japan, 2608712
        • National Hospital Organization Chiba-East Hospital
      • Fukuoka, Japan, 8128582
        • Kyusyu University Hospital
      • Fukushima, Japan, 9601295
        • Fukushima Medical University Hospital
      • Hiroshima, Japan, 7348551
        • Hiroshima University Hospital
      • Kumamoto, Japan, 8608556
        • Kumamoto Univeristy Hospital
      • Kyoto, Japan, 6068507
        • Kyoto University Hospital
      • Kyoto, Japan, 612-8555
        • National Hospital Organization Kyoto Medical Center
      • Niigata, Japan, 9518520
        • Niigata University Medical & Dental Hospital
      • Osaka, Japan, 5500015
        • Ohno Memorial Hospital
      • Saitama, Japan, 3308503
        • Saitama Medical Center Jichi Medical University
    • Aichi
      • Toyoake, Aichi, Japan, 4701192
        • Fujita Health University Hospital
    • Hokkaido
      • Sapporo, Hokkaido, Japan, 608648
        • Hokkaido University Hospital
    • Kanagawa
      • Isehara, Kanagawa, Japan, 2591193
        • Tokai University Hospital
      • Kawasaki, Kanagawa, Japan, 2138587
        • Toranomon Hospital Kajigaya
      • Sagamihara, Kanagawa, Japan, 2288555
        • Kitasato University Hospital
    • Miyagi
      • Sendai, Miyagi, Japan, 9808574
        • Tohoku University Hospital
    • Osaka
      • Osaka-City, Osaka, Japan, 5458586
        • Osaka City University Hospital
      • Suita, Osaka, Japan, 5650871
        • Osaka University Hospital
    • Saitama
      • Kasukabe, Saitama, Japan, 3440035
        • Shuwa General Hospital
      • Kawagoe, Saitama, Japan, 3508500
        • Saitama Medical Center
    • Shizuoka
      • Hamamatsu, Shizuoka, Japan, 4313192
        • Hamamatsu University School of Medicine, University Hospital
    • Tochigi
      • Shimotsuke, Tochigi, Japan, 3290498
        • Jichi Medical School Hospital
    • Tokyo
      • Bunkyo-ku, Tokyo, Japan, 1138603
        • Nippon Medical School Hospital
      • Bunkyo-ku, Tokyo, Japan, 1138519
        • Tokyo Medical & Dental University Hospital, Faculty of Medicine
      • Itabashi-ku, Tokyo, Japan, 1738606
        • Teikyo University Hospital
      • Minato-Ku, Tokyo, Japan, 1058471
        • The Jikei University Hospital
      • Minato-ku, Tokyo, Japan, 1058470
        • Toranomon Hospital
      • Mitaka, Tokyo, Japan, 1818611
        • Kyorin University Hospital
      • Shinjuku-ku, Tokyo, Japan, 1628666
        • Tokyo Women's Medical University Hospital
  • Polen
      • Ciechanow, Polen, 06-400
        • Oddział Nefrologiczny Stacja Dializ
      • Gdansk, Polen, 80-952
        • Akademickie Centrum Kliniczne AMG
      • Gdansk, Polen, 80-952
        • Samodzielny Publiczny Szpital Kliniczny nr 1, Akademickie Centrum Kliniczne AMG
      • Krakow, Polen, 31-501
        • Samodzielny Publiczny Zaklad Opieki Zdrowotnej, Szpital Uniwersytecki w Krakowie
      • Lodz, Polen, 90-153
        • SOP ZOZ Uniwersytecki Szpital Kliniczny
      • Lublin, Polen, 20-954
        • Samodzielny Publiczny Szpital Kliniczny Nr 4 w Lublinie
      • Warsaw, Polen, 04-749
        • Międzyleski Szpital Specjalistyczny w Warszawie
      • Warsaw, Polen, 02-507
        • Klinika Chorób Wewnętrznych i Nefrologii
      • Warszawa, Polen, 03-401
        • Szpital Praski p.w. Przemienienia Panskiego, Samodzielny Publiczny Zaklad Opieki Zdrowotnej
      • Warszawa, Polen, 03-401
        • Szpital Praski, Samodzielny Publiczny ZOZ
      • Wroclaw, Polen, 50-417
        • Akademicki Szpital Kliniczny im J Mikulicza Radeckiego
  • Rumænien
      • Bucharest, Rumænien, 22328
        • Institutul Clinic Fundeni
      • Bucharest, Rumænien, 10731
        • Spitalul Clinic de Nefrologie Dr. Carol Davila
      • Iasi, Rumænien, 700503
        • Spitalul Clinic "C.I.Parhon"
  • Tyskland
      • Dresden, Tyskland, 1307
        • Universitätsklinikum Carl Gustav Carus
      • Düsseldorf, Tyskland, 40210
        • Nephrologische Gemeinschaftspraxis/Dialysezentrum
      • Essen, Tyskland, 45147
        • Klinik für Nieren- und Hochdruckkrankheiten
      • Freiburg, Tyskland, 78106
        • Universitätsklinikum Freiburg
      • Heidelberg, Tyskland, 69120
        • Universitätskliniken Heidelberg
      • Nuernberg, Tyskland, 90471
        • UH Erlangen/Nürnberg

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 50 år (Voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Legal adult age and able to give Informed Consent.
  • Adult subjects with a diagnosis of ADPKD. A diagnosis of ADPKD (age 18 or 20-50) required several cysts in each kidney (3 if by sonography, 5 if by CT or MRI) in those with a family history of ADPKD and 10 cysts (by any radiologic method) in each kidney and exclusion of other cystic kidney diseases if there was no family history.
  • Willingness to comply with reproductive precautions, if female.
  • Estimated creatinine clearance ≥ 60 mL/min. Estimated from serum creatinine during screening using Cockcroft-Gault with correction for gender and race, where possible.
  • Rapidly progressive kidney growth (total volume ≥ 750 cc) by magnetic resonance imaging (MRI) at randomization.

Exclusion Criteria:

  • Prior exposure to tolvaptan or other experimental PKD therapies.
  • Currently taking medication for purpose of affecting PKD cysts.
  • Women who are breast feeding and females of childbearing potential who are not using acceptable contraceptive methods.
  • In the opinion of the study investigator or sponsor may present a safety risk or confound study objectives.
  • Patients who are unlikely to adequately comply with study procedures.
  • Patients having contraindications to MRI.
  • Patients taking medications or having any illnesses likely to affect ADPKD outcomes.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Firedobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Tolvaptan
Participants received the highest tolerated split-dose regimen (upon awakening and 9 hours later) of tolvaptan 45/15 mg, 60/30 mg, or 90/30 mg orally for 36 months.
Medicin: Tolvaptan
Tolvaptan was supplied as tablets.
Andre navne:
  • OPC-41061
  • OPC-156
Placebo komparator: Placebo
Participants received placebo (upon awakening and 9 hours later) orally for 36 months.
Medicin: Placebo
Placebo was supplied as tablets.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Percentage Change Per Year in Total Kidney Volume From Baseline to Month 36
Tidsramme: Baseline to Month 36
Kidney volume was assessed in T1-weighted magnetic resonance images collected at each study site and sent to a central reviewing facility. At the central reviewing facility, blinded radiologists used proprietary software to measure the volume of both kidneys.
Baseline to Month 36

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Number of ADPKD Clinical Progression Events Per 100 Follow-up Years From Baseline to Month 36
Tidsramme: Baseline to Month 36
These ADPKD events in the key secondary Outcome Measure were selected on the basis of their potential relationship to progressing cystogenesis. Reducing the rate of cyst development and expansion would likely slow the progression of ADPKD. The 4 events were: (1) Onset or progression of hypertension (someone is hypertensive if they have > 139 mmHg systolic blood pressure [BP], > 89 mmHg diastolic BP, or if they are taking antihypertensive medication at any BP level); (2) severe renal pain requiring medical intervention; (3) worsening albuminuria (by category, see below); and (4) worsening renal function, defined as a 25% decrease in 1/serum creatinine from Baseline. Albuminuria was assessed using spot urine albumin/creatinine ratio measurements (all measurements in mg/mmol). Categories included normal (< 2.8 female or < 2.0 male), microalbuminuria (2.8-28 female or 2.0-20 male), and overt proteinuria (> 28 female or > 20 male.
Baseline to Month 36
Change in Renal Function Per Year From Week 3 to Month 36
Tidsramme: Week 3 to Month 36
Renal function was assessed using serum creatinine measurements and was estimated using 1/serum creatinine. The formula for 1/serum creatinine is: 1/Pcr, where Pcr = serum creatinine concentration (mg/dL). The change in renal function per year was based on the slope of change, obtained by regressing renal function data against time by subject.
Week 3 to Month 36
Change in Mean Arterial Blood Pressure Per Year in Non-hypertensive Participants From Baseline to Month 36
Tidsramme: Baseline to Month 36
For participants who were non-hypertensive (systolic BP ≤ 139 mmHg and diastolic BP ≤ 89 mmHg without taking antihypertensive medications) at baseline, mean arterial blood pressure was measured at scheduled clinic visits up to the point of exposure to antihypertensive therapy for any reason. The change in mean arterial blood pressure per year was based on the slope of blood pressure, obtained by regressing blood pressure against time by subject.
Baseline to Month 36
Area Under the Concentration-time Curve of Change in Renal Pain From Baseline to Month 36
Tidsramme: At screening, Baseline, Day 1, every 4 months up to month 36/early tremination (ET), follow-up visit 1 and 2
Change from baseline in renal pain was assessed by a 0 to 10 pain scale as average area under the concentration-time curve (AUC) between baseline and the last trial visit or the last visit prior to initiating medical (eg, narcotic or anti-nociceptives [eg, tricyclic antidepressants]) or surgical therapy for pain. In the pain scale, score 0 represented no pain at all and score 10 represented the worst pain. A negative change score indicates less pain. AUC of renal pain was derived from renal pain scores within treatment period and was calculated using the trapezoidal rule, by dividing the number of days between the first and last assessment.
At screening, Baseline, Day 1, every 4 months up to month 36/early tremination (ET), follow-up visit 1 and 2
Number of Hypertensive Events Per 100 Follow-up Years in Non-hypertensive Participants From Baseline to Month 36
Tidsramme: Baseline to Month 36
A hypertensive event was defined as a change from non-hypertensive (systolic BP ≤ 139 mmHg and diastolic BP ≤ 89 mmHg without taking antihypertensive medications) status to 1 of 3 conditions: (1) High pre-hypertensive (systolic BP [sBP] > 129 mmHg and/or diastolic BP [dBP] > 84 mmHg), (2) hypertensive (sBP > 139 mmHg and/or dBP > 89 mmHg), or (3) requiring antihypertensive therapy.
Baseline to Month 36
Percentage of Participants With a Clinically Sustained Decrease of Blood Pressure Leading to a Sustained Reduction in Antihypertensive Therapy From Baseline to Month 36
Tidsramme: Baseline to Month 36
Baseline to Month 36

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Otsuka Pharmaceutical Development & Commercialization, Inc.

Samarbejdspartnere

Otsuka Pharmaceutical Co., Ltd.

Efterforskere

  • Ledende efterforsker: Vicente Torres, MD, PhD, Mayo Medical Center
  • Studieleder: Frank Czerwiec, MD, PhD, Otsuka Pharmaceutical Development and Commercialization, Inc.
  • Studieleder: Osamu Sato, Otsuka Pharmaceutical Corporation, Ltd. Japan

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Generelle publikationer

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. januar 2007

Primær færdiggørelse (Faktiske)

1. januar 2012

Studieafslutning (Faktiske)

1. januar 2012

Datoer for studieregistrering

Først indsendt

26. januar 2007

Først indsendt, der opfyldte QC-kriterier

29. januar 2007

Først opslået (Skøn)

30. januar 2007

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

2. juli 2017

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

30. maj 2017

Sidst verificeret

1. maj 2017

Mere information

Begreber relateret til denne undersøgelse

Nøgleord

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • 156-04-251
  • 2006-002768-24 (EudraCT nummer)

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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