Adelaide, SA, AUSTRALIA; Research Center
Investigational Oral Medication for RRMS
Adelaide, SA, AUSTRALIA; Research Center
Investigational Oral Medication for RRMS
Adelaide, SA, Australia; Royal Adelaide Hospital
A research study for patients with symptoms of overactive
bladder.
Camperdown, NSW, AUSTRALIA; Research Center
Investigational Oral Medication for RRMS
Chatswood, NSW, AUSTRALIA; Research Center
Investigational Oral Medication for RRMS
Clayton, VIC, AUSTRALIA; Research Center
Investigational Oral Medication for RRMS
Fitzroy, VIC, AUSTRALIA; Research Center
Investigational Oral Medication for RRMS
Geelong, VIC, AUSTRALIA; Research Center
Investigational Oral Medication for RRMS
Heidelberg, VIC, AUSTRALIA; Research Center
Investigational Oral Medication for RRMS
Kogarah, NSW, AUSTRALIA; Research Center
Investigational Oral Medication for RRMS
Liverpool, NSW, AUSTRALIA; Research Center
Investigational Oral Medication for RRMS
Melbourne, VIC, AUSTRALIA; Research Center
Investigational Oral Medication for RRMS
Newcastle, NSW, AUSTRALIA; Research Center
Investigational Oral Medication for RRMS
Graz, STYRIA, AUSTRIA; Research Center
Investigational Oral Medication for RRMS
Innsbruck, TYROL, AUSTRIA; Research Center
Investigational Oral Medication for RRMS
Linz, UPPER AUSTRIA, AUSTRIA; Research Center
Investigational Oral Medication for RRMS
Wien, VIENNA, AUSTRIA; Research Center
Investigational Oral Medication for RRMS
Gomel, HOMYELRSKAYA, BELARUS; Research Center
Investigational Oral Medication for RRMS
Gomel, HOMYELRSKAYA, BELARUS; Research Center
Investigational Oral Medication for RRMS
Minsk, MINSK, BELARUS; Research Center
Investigational Oral Medication for RRMS
Minsk, MINSK, BELARUS; Research Center
Investigational Oral Medication for RRMS
Vitebsk, VITSYEBSKAYA, BELARUS; Research Center
Investigational Oral Medication for RRMS
Vitebsk, VITSYEBSKAYA, BELARUS; Research Center
Investigational Oral Medication for RRMS
Antwerpen, ANTWERPEN, BELGIUM; Research Center
Investigational Oral Medication for RRMS
Brugge, WEST-VLAANDEREN, BELGIUM; Research Center
Investigational Oral Medication for RRMS
Charleroi, HAINAUT, BELGIUM; Research Center
Investigational Oral Medication for RRMS
Diepenbeek, LIMBURG, BELGIUM; Research Center
Investigational Oral Medication for RRMS
Edegem, Belgium; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Leuven, FLEMISH BRABANT, BELGIUM; Research Center
Investigational Oral Medication for RRMS
Liège, LIEGE, BELGIUM; Research Center
Investigational Oral Medication for RRMS
Lommel, LIMBURG, BELGIUM; Research Center
Investigational Oral Medication for RRMS
Lommel, LIMBURG, BELGIUM; Research Center
Investigational Oral Medication for RRMS
Overpelt, Belgium; UCB Clinical Trial Call Center
Placebo Controlled Study in Subjects With Relapsing Forms of MS to Evaluate the Safety, Tolerability and Effects of CDP323
Sijsele-Damme, Belgium; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Sijsele-Damme, WEST-VLAANDEREN, BELGIUM; Research Center
Investigational Oral Medication for RRMS
Sijsele-Damme,WEST-VLAANDEREN, BELGIUM; Research Center
Investigational Oral Medication for RRMS
St. Truiden, Belgium; UCB Clinical Trial Call Center
Placebo Controlled Study in Subjects With Relapsing Forms of MS to Evaluate the Safety, Tolerability and Effects of CDP323
Woluwe, BRUSSELS, BELGIUM; Research Center
Investigational Oral Medication for RRMS
Woluwe, BRUSSELS, BELGIUM; Research Center
Investigational Oral Medication for RRMS
Banja Luka, Republic Srpska, Bosnia; Research Center
Investigational Oral Medication for RRMS
Banja Luka, Republic Srpska, Bosnia; Research Center
Investigational Oral Medication for RRMS
Sarajevo, B&H Federation, Bosnia; Research Center
Investigational Oral Medication for RRMS
Tuzla, B&H Federation, Bosnia; Research Center
Investigational Oral Medication for RRMS
Campinas, SAO PAULO, BRAZIL; Research Center
Investigational Oral Medication for RRMS
Porto Alegre, RIO GRANDE DO SUL, BRAZIL; Research Center
Investigational Oral Medication for RRMS
São Paulo, SAO PAULO, BRAZIL; Research Center
Investigational Oral Medication for RRMS
Plovdiv, BULGARIA; Research Center
Investigational Oral Medication for RRMS
Rousse, BULGARIA; Research Center
Investigational Oral Medication for RRMS
Rousse, BULGARIA; Research Center
Investigational Oral Medication for RRMS
Sofia, BULGARIA; Research Center
Investigational Oral Medication for RRMS
Sofia, Bulgaria; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Sofia, BULGARIA; Research Center
Investigational Oral Medication for RRMS
Stara Zagora, BULGARIA; Research Center
Investigational Oral Medication for RRMS
Varna, BULGARIA; Research Center
Investigational Oral Medication for RRMS
Varna, BULGARIA; Research Center
Investigational Oral Medication for RRMS
Burnaby, BC, CANADA; Research Center
Investigational Oral Medication for RRMS
Edmonton, AB, Canada; Research Center
Investigational Oral Medication for RRMS
Gatineau, QC, CANADA; Research Center
Investigational Oral Medication for RRMS
Halifax, NS, CANADA; Research Center
Investigational Oral Medication for RRMS
Levis, PQ, CANADA; Research Center
Investigational Oral Medication for RRMS
Montreal, QC, CANADA; Research Center
Investigational Oral Medication for RRMS
Montreal, QC, Canada; Research Center
Investigational Oral Medication for RRMS
Ottawa, ON, CANADA; Research Center
Investigational Oral Medication for RRMS
Quebec, QC, CANADA; Research Center
Investigational Oral Medication for RRMS
Regina, SK, CANADA; Research Center
Investigational Oral Medication for RRMS
Sherbrooke, QC, CANADA; Research Center
Investigational Oral Medication for RRMS
Toronto, ON, Canada; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Vancouver, BC, Canada; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Victoria, BC, Canada; Can-Med Clinical Research Inc.
A research study for patients with symptoms of overactive bladder
Victoria, BC, Canada; Dr. Steinhoff Clinical Research
A research study for patients with symptoms of overactive
bladder.
San José, San José, COSTA RICA; Research Center
Investigational Oral Medication for RRMS
Osijek, Osijek-Baranja, CROATIA; Research Center
Investigational Oral Medication for RRMS
Osijek, Osijek-Baranja, CROATIA; Research Center
Investigational Oral Medication for RRMS
Rijeka, Primorje-Gorski Kotar, CROATIA; Research Center
Investigational Oral Medication for RRMS
Rijeka, Primorje-Gorski Kotar, CROATIA; Research Center
Investigational Oral Medication for RRMS
Zagreb, CROATIA; Research Center
Investigational Oral Medication for RRMS
Zagreb, CROATIA; Research Center
Investigational Oral Medication for RRMS
Brno, CZECH REPUBLIC; Research Center
Investigational Oral Medication for RRMS
Jihlava, CZECH REPUBLIC; Research Center
Investigational Oral Medication for RRMS
Opava, CZECH REPUBLIC; Research Center
Investigational Oral Medication for RRMS
Ostrava, Czech Republic; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Ostrava, CZECH REPUBLIC; Research Center
Investigational Oral Medication for RRMS
Ostrava, North Moravia, CZECH REPUBLIC; Research Center
Investigational Oral Medication for RRMS
Ostrava-Moravska Ostrava, CZECH REPUBLIC; Research Center
Investigational Oral Medication for RRMS
Pardubice, Czech Republic; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Plzen, CZECH REPUBLIC; Research Center
Investigational Oral Medication for RRMS
Prague, Czech Republic; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Praha, Czech Republic; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Praha 2, CZECH REPUBLIC; Research Center
Investigational Oral Medication for RRMS
Praha 2, CZECH REPUBLIC; Research Center
Investigational Oral Medication for RRMS
Praha 5, PRAHA, CZECH REPUBLIC; Research Center
Investigational Oral Medication for RRMS
Teplice, CZECH REPUBLIC; Research Center
Investigational Oral Medication for RRMS
Teplice, Czech Republic; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Arhus, Denmark; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Kuressaare, ESTONIA; Research Center
Investigational Oral Medication for RRMS
Parnu, ESTONIA; Research Center
Investigational Oral Medication for RRMS
Tallinn, ESTONIA; Research Center
Investigational Oral Medication for RRMS
Tartu, ESTONIA; Research Center
Investigational Oral Medication for RRMS
Helsinki, Finland; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Turku, Finland; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Bobigny, FRANCE; Research Center
Investigational Oral Medication for RRMS
Bordeaux, France; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Bordeaux, FRANCE; Research Center
Investigational Oral Medication for RRMS
Caen cedex, FRANCE; Research Center
Investigational Oral Medication for RRMS
Caen Cedex 9, France; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Clermont Ferrand, FRANCE; Research Center
Investigational Oral Medication for RRMS
Clermont-Ferrand Cedex1, France; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Dijon, FRANCE; Research Center
Investigational Oral Medication for RRMS
Dijon, FRANCE; Research Center
Investigational Oral Medication for RRMS
Lille cedex, FRANCE; Research Center
Investigational Oral Medication for RRMS
Lyon, France; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Lyon cedex 03, FRANCE; Research Center
Investigational Oral Medication for RRMS
Marseille Cedex 9, FRANCE; Research Center
Investigational Oral Medication for RRMS
Montpellier, FRANCE; Research Center
Investigational Oral Medication for RRMS
Montpellier Cedex, France; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Montpellier cedex 5, FRANCE; Research Center
Investigational Oral Medication for RRMS
Nancy cedex, FRANCE; Research Center
Investigational Oral Medication for RRMS
Nice, FRANCE; Research Center
Investigational Oral Medication for RRMS
Nimes, France; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Nîmes, FRANCE; Research Center
Investigational Oral Medication for RRMS
Paris, FRANCE; Research Center
Investigational Oral Medication for RRMS
Rennes, FRANCE; Research Center
Investigational Oral Medication for RRMS
Strasbourg, ALSACE, FRANCE; Research Center
Investigational Oral Medication for RRMS
Bad Neustadt/Saale, BAYERN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Bamberg, BAYERN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Bayreuth, BAYERN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Berg, Starnberger See, GERMANY; Research Center
Investigational Oral Medication for RRMS
Berlin, Germany; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Berlin, Germany; UCB Clinical Trial Call Center
Placebo Controlled Study in Subjects With Relapsing Forms of MS to Evaluate the Safety, Tolerability and Effects of CDP323
Berlin BERLIN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Berlin, BERLIN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Bochum, NORDRHEIN-WESTFALEN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Düsseldorf, NORDRHEIN-WESTFALEN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Düsseldorf, NORDRHEIN-WESTFALEN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Erbach, GERMANY; Research Center
Investigational Oral Medication for RRMS
Erlangen, BAYERN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Essen, NORDRHEIN-WESTFALEN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Gießen, HESSEN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Halle (Saale), SACHSEN-ANHALT, GERMANY; Research Center
Investigational Oral Medication for RRMS
Halle (Saale), SACHSEN-ANHALT, GERMANY; Research Center
Investigational Oral Medication for RRMS
Hamburg, Germany; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Hamburg, HAMBURG, GERMANY; Research Center
Investigational Oral Medication for RRMS
Hanburg, GERMANY; Research Center
Investigational Oral Medication for RRMS
Hanburg, GERMANY; Research Center
Investigational Oral Medication for RRMS
Hannover, NIEDERSACHSEN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Heidelberg, BADEN-WUTTEMBERG, GERMANY; Research Center
Investigational Oral Medication for RRMS
Jena, THURINGEN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Köln, NORDRHEIN-WESTFALEN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Leipzig, SACHSEN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Lengerich, GERMANY; Research Center
Investigational Oral Medication for RRMS
Magdeburg, SACHSEN-ANHALT, GERMANY; Research Center
Investigational Oral Medication for RRMS
Marburg, Germany; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Marburg, HESSEN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Minden, NORDRHEIN-WESTFALEN, GERMANY; Research Center
Investigational Oral Medication for RRMS
München, BAYERN, GERMANY; Research Center
Investigational Oral Medication for RRMS
München, BAYERN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Münster, NORDRHEIN-WESTFALEN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Osnabrück, NIEDERSACHSEN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Regensburg, Germany; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Regensburg, BAYERN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Regensburg, BAYERN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Schwerin, MECKLENBURG-VORPOMMERN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Siegen, Germany; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Tübingen, Germany; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Ulm, Germany; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Westerstede, NIEDERSACHSEN, GERMANY; Research Center
Investigational Oral Medication for RRMS
Athens, ATTICA, GREECE; Research Center
Investigational Oral Medication for RRMS
Athens, ATTICA, GREECE; Research Center
Investigational Oral Medication for RRMS
Guatemala, GREECE; Research Center
Investigational Oral Medication for RRMS
Guatemala City, GREECE; Research Center
Investigational Oral Medication for RRMS
Heraklion, GREECE; Research Center
Investigational Oral Medication for RRMS
Ioannina, GREECE; Research Center
Investigational Oral Medication for RRMS
Patras, GREECE; Research Center
Investigational Oral Medication for RRMS
Thessaloniki, GREECE; Research Center
Investigational Oral Medication for RRMS
Thessaloniki, GREECE; Research Center
Investigational Oral Medication for RRMS
Budapest, Hungary; UCB Clinical Trial Call Center
Placebo Controlled Study in Subjects With Relapsing Forms of MS to Evaluate the Safety, Tolerability and Effects of CDP323
Gyor, Hungary; UCB Clinical Trial Call Center
Placebo Controlled Study in Subjects With Relapsing Forms of MS to Evaluate the Safety, Tolerability and Effects of CDP323
Bangalore, INDIA; Research Center
Investigational Oral Medication for RRMS
Chandigarh, INDIA; Research Center
Investigational Oral Medication for RRMS
Chennai, INDIA; Research Center
Investigational Oral Medication for RRMS
Chennai, INDIA; Research Center
Investigational Oral Medication for RRMS
Coimbatore, INDIA; Research Center
Investigational Oral Medication for RRMS
Coimbatore, INDIA; Research Center
Investigational Oral Medication for RRMS
Delhi, INDIA; Research Center
Investigational Oral Medication for RRMS
Delhi, INDIA; Research Center
Investigational Oral Medication for RRMS
Hyderabad, INDIA; Research Center
Investigational Oral Medication for RRMS
Hyderabad, INDIA; Research Center
Investigational Oral Medication for RRMS
Jaipur, INDIA; Research Center
Investigational Oral Medication for RRMS
Kolkata, INDIA; Research Center
Investigational Oral Medication for RRMS
Kolkata, INDIA; Research Center
Investigational Oral Medication for RRMS
Lucknow, INDIA; Research Center
Investigational Oral Medication for RRMS
Lucknow, INDIA; Research Center
Investigational Oral Medication for RRMS
Mangalore, INDIA; Research Center
Investigational Oral Medication for RRMS
Mangalore, INDIA; Research Center
Investigational Oral Medication for RRMS
Mumbai, INDIA; Research Center
Investigational Oral Medication for RRMS
Mumbai, INDIA; Research Center
Investigational Oral Medication for RRMS
New Dehli, INDIA; Research Center
Investigational Oral Medication for RRMS
New Delhi, INDIA; Research Center
Investigational Oral Medication for RRMS
Pune, INDIA; Research Center
Investigational Oral Medication for RRMS
Pune, INDIA; Research Center
Investigational Oral Medication for RRMS
Cork, Cork, IRELAND; Research Center
Investigational Oral Medication for RRMS
Dublin, IRELAND; Research Center
Investigational Oral Medication for RRMS
Ashkelon, ISRAEL; Research Center
Investigational Oral Medication for RRMS
Beer Yaakov, ISRAEL; Research Center
Investigational Oral Medication for RRMS
Holon, ISRAEL; Research Center
Investigational Oral Medication for RRMS
Jerusalem, ISRAEL; Research Center
Investigational Oral Medication for RRMS
Safed, ISRAEL; Research Center
Investigational Oral Medication for RRMS
Tel Hashomer, ISRAEL; Research Center
Investigational Oral Medication for RRMS
Milan, Italy; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Roma, Italy; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Roma, ITALY; Research Center
Investigational Oral Medication for RRMS
Almata, KAZAKHSTAN; Research Center
Investigational Oral Medication for RRMS
Almaty, KAZAKHSTAN; Research Center
Investigational Oral Medication for RRMS
Almaty, KAZAKHSTAN; Research Center
Investigational Oral Medication for RRMS
Astana, KAZAKHSTAN; Research Center
Investigational Oral Medication for RRMS
Karaganda, KAZAKHSTAN; Research Center
Investigational Oral Medication for RRMS
Karaganda, KAZAKHSTAN; Research Center
Investigational Oral Medication for RRMS
Symkent, KAZAKHSTAN; Research Center
Investigational Oral Medication for RRMS
Riga, LATVIA; Research Center
Investigational Oral Medication for RRMS
Skopje, Macedonia; Research Center
Investigational Oral Medication for RRMS
Skopje, Macedonia; Research Center
Investigational Oral Medication for RRMS
Aguascalientes, Mexico; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Aguascalientes, Aguascalientes, MEXICO; Research Center
Investigational Oral Medication for RRMS
Chihuahua, Mexico; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Chihuahua, MEXICO; Research Center
Investigational Oral Medication for RRMS
Chihuahua, Chih, MEXICO; Research Center
Investigational Oral Medication for RRMS
Guadalajara, Jal, MEXICO; Research Center
Investigational Oral Medication for RRMS
Guadalajara, JALISCO, MEXICO; Research Center
Investigational Oral Medication for RRMS
Merida, Yuc, MEXICO; Research Center
Investigational Oral Medication for RRMS
Mexico D.F, MEXICO; Research Center
Investigational Oral Medication for RRMS
Mexico, 14000, MEXICO; Research Center
Investigational Oral Medication for RRMS
Mexico, DISTRITO FEDERAL, MEXICO; Research Center
Investigational Oral Medication for RRMS
Monterrey, NL, MEXICO; Research Center
Investigational Oral Medication for RRMS
Monterrey, NUEVO LEON, MEXICO; Research Center
Investigational Oral Medication for RRMS
Morelia, Michoacan, MEXICO; Research Center
Investigational Oral Medication for RRMS
Puebla, PUEBLA, MEXICO; Research Center
Investigational Oral Medication for RRMS
San Luis Potosi, SAN LUIS POTOSI, MEXICO; Research Center
Investigational Oral Medication for RRMS
Tijuana,Baja California, MEXICO; Research Center
Investigational Oral Medication for RRMS
Chisinau, MOLDOVA; Research Center
Investigational Oral Medication for RRMS
Chisinau, MOLDOVA; Research Center
Investigational Oral Medication for RRMS
Breda, Netherlands; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Breda, Netherlands; UCB Clinical Trial Call Center
Placebo Controlled Study in Subjects With Relapsing Forms of MS to Evaluate the Safety, Tolerability and Effects of CDP323
Breda, NOORD-BRABANT, NETHERLANDS; Research Center
Investigational Oral Medication for RRMS
Nieuwegein, Netherlands; UCB Clinical Trial Call Center
Placebo Controlled Study in Subjects With Relapsing Forms of MS to Evaluate the Safety, Tolerability and Effects of CDP323
Nijmegen, Netherlands; UCB Clinical Trial Call Center
Placebo Controlled Study in Subjects With Relapsing Forms of MS to Evaluate the Safety, Tolerability and Effects of CDP323
Sittard, LIMBURG, NETHERLANDS; Research Center
Investigational Oral Medication for RRMS
Christchurch, NEW ZEALAND; Research Center
Investigational Oral Medication for RRMS
Grafton, Auckland, NEW ZEALAND; Research Center
Investigational Oral Medication for RRMS
Hamilton, NEW ZEALAND; Research Center
Investigational Oral Medication for RRMS
Hamilton, NEW ZEALAND; Research Center
Investigational Oral Medication for RRMS
Bialystok, PODLASKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Bialystok, PODLASKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Bydgoszcz, KUJAWSKO-POMORSKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Bydgoszcz, KUJAWSKO-POMORSKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Gdansk, Poland; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Gdansk, POMORSKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Gdansk, POMORSKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Katowice, SLASKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Katowice, SLASKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Kraków, MALOPOLSKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Kraków, MALOPOLSKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Lodz, Poland; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Lódz, LODZKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Lódz, LODZKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Lublin, Poland; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Lublin, DOLNOSLASKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Lublin, DOLNOSLASKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Poznan, WIELKOPOLSKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Poznan, WIELKOPOLSKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Sosnowiec, SLASKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Sosnowiec, SLASKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Szczecin, POLAND; Research Center
Investigational Oral Medication for RRMS
Szczecin, POLAND; Research Center
Investigational Oral Medication for RRMS
Warszawa, Poland; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Warszawa, MAZOWIECKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Warszawa, MAZOWIECKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Wroclaw, DOLNOSLASKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Wroclaw, DOLNOSLASKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Zabrze, SLASKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Zabrze, SLASKIE, POLAND; Research Center
Investigational Oral Medication for RRMS
Guaynabo, PUERTO RICO; Research Center
Investigational Oral Medication for RRMS
Guaynabo, Puerto Rico; Research Site
New Oral Investigational Treatment Laquinimod for Relapsing-Remitting Multiple Sclerosis
Bucresti, ROMANIA; Research Center
Investigational Oral Medication for RRMS
Bucuresti, Romania; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Bucuresti, ROMANIA; Research Center
Investigational Oral Medication for RRMS
Bucuresti, ROMANIA; Research Center
Investigational Oral Medication for RRMS
Cluj-Napoca, Cluj, ROMANIA; Research Center
Investigational Oral Medication for RRMS
Iasi, ROMANIA; Research Center
Investigational Oral Medication for RRMS
Oradea, ROMANIA; Research Center
Investigational Oral Medication for RRMS
Targu Mures, Romania; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Timisoara, Timis, ROMANIA; Research Center
Investigational Oral Medication for RRMS
Tirgu Mures, ROMANIA; Research Center
Investigational Oral Medication for RRMS
Ekaterinburg, Russian Federation; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Kazan, Russian Federation; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Moscow, Russian Federation; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Nizhny Novgorod, Russian Federation; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Novosibirsk, Russian Federation; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Tyumen, Russian Federation; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Belgrade, SERBIA; Research Center
Investigational Oral Medication for RRMS
Belgrade, SERBIA; Research Center
Investigational Oral Medication for RRMS
Kragujevac, SERBIA; Research Center
Investigational Oral Medication for RRMS
Kragujevac, SERBIA; Research Center
Investigational Oral Medication for RRMS
Nis, SERBIA; Research Center
Investigational Oral Medication for RRMS
Nis, SERBIA; Research Center
Investigational Oral Medication for RRMS
Novi Sad, SERBIA; Research Center
Investigational Oral Medication for RRMS
Novi Sad, SERBIA; Research Center
Investigational Oral Medication for RRMS
Banska Bystrica, Slovakia; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Bratislava, Slovakia; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Bratislava, SLOVAKIA; Research Center
Investigational Oral Medication for RRMS
Bratislava, SLOVAKIA; Research Center
Investigational Oral Medication for RRMS
Kosice, Slovakia; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Kosice, SLOVAKIA; Research Center
Investigational Oral Medication for RRMS
Kosice, SLOVAKIA; Research Center
Investigational Oral Medication for RRMS
Martin, Zilina, SLOVAKIA; Research Center
Investigational Oral Medication for RRMS
Martin, Zilina, SLOVAKIA; Research Center
Investigational Oral Medication for RRMS
Nitra, Slovakia; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Ruzomberok, SLOVAKIA; Research Center
Investigational Oral Medication for RRMS
Cape Town, Western Cape, SOUTH AFRICA; Research Center
Investigational Oral Medication for RRMS
Durban, KwaZulu-Natal, SOUTH AFRICA; Research Center
Investigational Oral Medication for RRMS
Parow, Western Cape, SOUTH AFRICA; Research Center
Investigational Oral Medication for RRMS
Rosebank, SOUTH AFRICA; Research Center
Investigational Oral Medication for RRMS
Barcelona, Spain; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Barcelona, BARCELONA, SPAIN; Research Center
Investigational Oral Medication for RRMS
Córdoba, CORDOBA, SPAIN; Research Center
Investigational Oral Medication for RRMS
Madrid, Spain; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Madrid, MADRID, SPAIN; Research Center
Investigational Oral Medication for RRMS
Malaga, Spain; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Málaga, MALAGA, SPAIN; Research Center
Investigational Oral Medication for RRMS
Oviedo, Spain; UCB Clinical Trial Call Center
Placebo Controlled Study in Subjects With Relapsing Forms of MS to Evaluate the Safety, Tolerability and Effects of CDP323
Santiago de Compostela, LA CORUNA, SPAIN; Research Center
Investigational Oral Medication for RRMS
Sevilla, Spain; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Sevilla, ANDALUCÍA, SPAIN; Research Center
Investigational Oral Medication for RRMS
Valencia, Spain; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Basel, Switzerland; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Basel, BASEL, SWITZERLAND; Research Center
Investigational Oral Medication for RRMS
Lausanne, Switzerland; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Sankt Gallen, SANKT GALLEN, SWITZERLAND; Research Center
Investigational Oral Medication for RRMS
Zurich, Switzerland; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Zürich, ZURICH, SWITZERLAND; Research Center
Investigational Oral Medication for RRMS
Adana, ADANA, TURKEY; Research Center
Investigational Oral Medication for RRMS
Istanbul, TURKEY; Research Center
Investigational Oral Medication for RRMS
Izmir, TURKEY; Research Center
Investigational Oral Medication for RRMS
Trabzon, TURKEY; Research Center
Investigational Oral Medication for RRMS
Kharkiv, KHARKIV, UKRAINE; Research Center
Investigational Oral Medication for RRMS
Kharkiv, KHARKIV, UKRAINE; Research Center
Investigational Oral Medication for RRMS
Kharkov, Ukraine; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Kiev, Ukraine; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Kyiv, KIEV, UKRAINE; Research Center
Investigational Oral Medication for RRMS
Kyiv, KIEV, UKRAINE; Research Center
Investigational Oral Medication for RRMS
Kyiv, KIEV, UKRAINE; Research Center
Investigational Oral Medication for RRMS
Lviv, LVIV, UKRAINE; Research Center
Investigational Oral Medication for RRMS
Lviv, LVIV, UKRAINE; Research Center
Investigational Oral Medication for RRMS
Odessa, ODESSA, UKRAINE; Research Center
Investigational Oral Medication for RRMS
Odessa, ODESSA, UKRAINE; Research Center
Investigational Oral Medication for RRMS
Poltava, POLTAVA, UKRAINE; Research Center
Investigational Oral Medication for RRMS
Poltava, POLTAVA, UKRAINE; Research Center
Investigational Oral Medication for RRMS
Propetrovsk, Ukraine; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Simferopol, CRIMEA, UKRAINE; Research Center
Investigational Oral Medication for RRMS
Vinnitsa, VINNYTSYA, UKRAINE; Research Center
Investigational Oral Medication for RRMS
Vinnytsya, Ukraine; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Zaporozhye, ZAPORIZHZHYA, UKRAINE; Research Center
Investigational Oral Medication for RRMS
Zaporozhye, ZAPORIZHZHYA, UKRAINE; Research Center
Investigational Oral Medication for RRMS
Croydon, Surrey, United Kingdom; UCB Clinical Trial Call Center
Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study in Subjects With Relapsing Forms of Multiple Sclerosis to Evaluate the Effects of Different CDP323 Doses on Biomarker Patterns as Well as on Safety and Tolerability.
Liverpool, United Kingdom; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
London, ENGLAND, UNITED KINGDOM; Research Center
Investigational Oral Medication for RRMS
Newcastle, United Kingdom; UCB Clinical Trial Call Center
Placebo Controlled Study in Subjects With Relapsing Forms of MS to Evaluate the Safety, Tolerability and Effects of CDP323
Newcastle upon Tyne, United Kingdom; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Newcastle upon Tyne, ENGLAND, UNITED KINGDOM; Research Center
Investigational Oral Medication for RRMS
Nottingham, United Kingdom; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Oxford, ENGLAND, UNITED KINGDOM; Research Center
Investigational Oral Medication for RRMS
Sheffield, United Kingdom; Research Site:
A Dose-Finding Study of Ocrelizumab in Patients With Relapsing-Remitting Multiple Sclerosis.
Sheffield, United Kingdom; UCB Clinical Trial Call Center
Placebo Controlled Study in Subjects With Relapsing Forms of MS to Evaluate the Safety, Tolerability and Effects of CDP323
Sheffield, ENGLAND, UNITED KINGDOM; Research Center
Investigational Oral Medication for RRMS
Staffordshire, ENGLAND, UNITED KINGDOM; Research Center
Investigational Oral Medication for RRMS
Tooting, London, United Kingdom; UCB Clinical Trial Call Center
Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study in Subjects With Relapsing Forms of Multiple Sclerosis to Evaluate the Effects of Different CDP323 Doses on Biomarker Patterns as Well as on Safety and Tolerability.