MedPath

Study of Oral Atogepant Tablets to Assess Safety and Efficacy in Adult Participants With Migraine

Phase 3
Active, not recruiting
Conditions
Migraine
Interventions
Registration Number
NCT06241313
Lead Sponsor
AbbVie
Brief Summary

A migraine attack is a moderate or severe headache that usually occurs on one side of the head and is often accompanied by throbbing, sensitivity to light, sensitivity to sound, nausea, or other symptoms. The main goal of the study is to see if atogepant is effective, safe, and well-tolerated in treating migraine attacks quickly.

Atogepant is a medicine currently approved for the preventive treatment of migraine in adults and has been shown to be effective and well tolerated when taken daily to prevent migraine attacks. This study includes double-blind phase means that neither the participants nor the study doctors know who is given which study treatment (atogepant or placebo) followed by an open-label phase meaning that both participants and study doctors know which study treatment is given. All participants will receive atogepant during the open-label part of the study. This study will include 1300 participants aged 18-75 years with a history of migraine at approximately 160 sites across the world.

All participants will receive both atogepant and placebo to treat qualifying migraines. At the start of the study, participants will be randomized to 1 of 4 dosing sequences to determine when they will receive atogepant and when they will receive placebo during the study. After treating 4 qualifying migraine attacks, participants will receive open-label atogepant for any additional migraine attacks they have until the end of the study (Week 24).

There may be a bigger responsibility for participants in this study than there would be in participants receiving standard of care treatment. participants will attend regular visits during the study at a hospital or clinic, as well as telephone visits, and the effects of treatment will be checked by completion of questionnaires in an electronic diary, medical assessments, blood tests, and checking for side effects.

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
1300
Inclusion Criteria
  • History of migraine (with or without aura) according to the International Classification of Headache Disorders 3rd Edition (ICHD-3) for >= 12 months prior to Visit 1/Screening.
  • History of 2 to 8 migraine attacks of moderate to severe headache pain in each of the 3 months prior to Visit 1/Screening per investigator judgment.
  • Migraine onset before the age of 50.
  • History of migraines lasting between 4 and 72 hours when untreated or treated unsuccessfully and migraine episodes separated by at least 48 hours of headache pain freedom.
Exclusion Criteria
  • History of an average of 15 or more headache days per month in the 6 months prior to Visit 1/Screening per the investigator's judgment, or a current diagnosis of chronic migraine as defined by ICHD-3.
  • Require hospital/emergency room treatment for migraine attacks on 3 or more occasions within 6 months prior to Visit 1/Screening.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Sequence 3AtogepantParticipants will receive both atogepant and placebo to treat qualifying migraines.
Sequence 3Placebo for AtogepantParticipants will receive both atogepant and placebo to treat qualifying migraines.
Sequence 1Placebo for AtogepantParticipants will receive both atogepant and placebo to treat qualifying migraines.
Sequence 4AtogepantParticipants will receive both atogepant and placebo to treat qualifying migraines.
Sequence 4Placebo for AtogepantParticipants will receive both atogepant and placebo to treat qualifying migraines.
Sequence 2Placebo for AtogepantParticipants will receive both atogepant and placebo to treat qualifying migraines.
Sequence 2AtogepantParticipants will receive both atogepant and placebo to treat qualifying migraines.
Sequence 1AtogepantParticipants will receive both atogepant and placebo to treat qualifying migraines.
Primary Outcome Measures
NameTimeMethod
Percentage of Participants Achieving Pain Freedom at 2 Hours After the Double-Blind (DB) Dose for the First AttackApproximately 16 Weeks

Pain freedom is defined as a reduction in headache severity from moderate/severe at baseline (predose) to no pain.

Secondary Outcome Measures
NameTimeMethod
Percentage of Participants With Absence of Most Bothersome Migraine-associated Symptom (MBS) at 2 Hours After the Double-Blind (DB) Dose for the First AttackApproximately 16 Weeks

Percentage of Participants With Absence of Most Bothersome Migraine-associated Symptom (MBS) will be assessed.

Percentage of Participants Achieving Pain Relief at 2 Hours After the Double-Blind (DB) Dose for the First AttackApproximately 16 Weeks

Pain relief is defined as the reduction of a moderate/severe migraine headache at baseline \[predose\] to a mild headache or to no headache.

Percentage of Participants Achieving Sustained Pain Relief From 2 to 24 Hours After DB Dose for the First AttackApproximately 16 Weeks

Sustained pain relief is defined as pain relief at 2 hours after the DB dose with no administration of rescue medication and no occurrence of a moderate/severe headache from 2 to 24 hours.

Percentage of Participants Achieving Sustained Pain Relief From 2 to 48 Hours After DB Dose for the First AttackApproximately 16 Weeks

Sustained pain relief is defined as pain relief at 2 hours after the DB dose with no administration of rescue medication and no occurrence of a moderate/severe headache from 2 to 24 hours.

Percentage of Participants With Use of Rescue Medication Within 24 Hours After DB Dose for the First AttackApproximately 16 Weeks

Percentage of participants with use of rescue medication within 24 hours after the DB dose for the first attack will be assessed.

Percentage of Participants With Ability to Function Normally at 2 Hours After DB Dose for the First AttackApproximately 16 Weeks

Percentage of participants with ability to function normally at 2 hours after the DB dose for the first attack will be assessed.

Percentage of Participants Achieving Sustained Pain Freedom From 2 to 48 Hours After DB Dose for the First AttackApproximately 16 Weeks

Sustained pain freedom is defined as pain freedom at 2 hours after the DB dose with no administration of rescue medication and no occurrence of a mild/moderate/severe headache from 2 to 24 hours.

Percentage of Participants With Absence of Photophobia at 2 Hours After the DB Dose for the First AttackApproximately 16 Weeks

Photophobia is defined as sensitivity to light.

Percentage of Participants With Absence of Phonophobia at 2 Hours After the DB Dose for the First AttackApproximately 16 Weeks

Phonophobia is defined as sensitivity to sound.

Percentage of Participants Achieving Pain Freedom at 8 Hours After the DB Dose for the First AttackApproximately 16 Weeks

Pain freedom is defined as a reduction in headache severity from moderate/severe at baseline (predose) to no pain.

Percentage of Participants With Ability to Function Normally at 8 Hours After DB Dose for the First AttackApproximately 16 Weeks

Percentage of participants with ability to function normally at 8 hours after the DB dose for the first attack will be assessed.

Percentage of Participants Achieving Pain Relief at 1 Hour After the Double-Blind (DB) Dose for the First AttackApproximately 16 Weeks

Pain relief is defined as the reduction of a moderate/severe migraine headache at baseline \[predose\] to a mild headache or to no headache.

Percentage of Participants With Absence of Nausea at 2 Hours After the Double-Blind (DB) Dose for the First AttackApproximately 16 Weeks

Percentage of participants with absence of nausea at 2 hours after the DB dose for the first attack.

Percentage of Participants Achieving Pain Relief at 30 Minutes After the Double-Blind (DB) Dose for the First AttackApproximately 16 Weeks

Pain relief is defined as the reduction of a moderate/severe migraine headache at baseline \[predose\] to a mild headache or to no headache.

Percentage of Participants With Ability to Function Normally at 1 Hour After DB Dose for the First AttackApproximately 16 Weeks

Percentage of participants with ability to function normally at 1 hour after the DB dose for the first attack will be assessed.

Percentage of Participants Achieving Pain Freedom at 2 Hours After Receiving DB Atogepant for at least 2 out of 3 AttacksApproximately 16 Weeks

Pain freedom is defined as a reduction in headache severity from moderate/severe at baseline (predose) to no pain.

Percentage of Participants Achieving Sustained Pain Freedom From 2 to 24 Hours After DB Dose for the First AttackApproximately 16 Weeks

Sustained pain freedom is defined as pain freedom at 2 hours after the DB dose with no administration of rescue medication and no occurrence of a mild/moderate/severe headache from 2 to 24 hours.

Percentage of Participants Achieving Sustained Pain Relief From 2 to 48 Hours After Receiving DB Atogepant for at least 2 out of 3 AttacksApproximately 16 Weeks

Sustained pain relief is defined as pain relief at 2 hours after the DB dose with no administration of rescue medication and no occurrence of a moderate/severe headache from 2 to 24 hours.

Percentage of Participants Achieving Sustained Pain Freedom From 2 to 24 Hours After Receiving DB Atogepant for at least 2 out of 3 AttacksApproximately 16 Weeks

Sustained pain freedom is defined as pain freedom at 2 hours after the DB dose with no administration of rescue medication and no occurrence of a mild/moderate/severe headache from 2 to 24 hours.

Percentage of Participants Achieving Sustained Pain Freedom From 2 to 48 Hours After Receiving DB Atogepant for at least 2 out of 3 AttacksApproximately 16 Weeks

Sustained pain freedom is defined as pain freedom at 2 hours after the DB dose with no administration of rescue medication and no occurrence of a mild/moderate/severe headache from 2 to 24 hours.

Percentage of Participants Achieving Pain Relief at 2 Hours After Receiving Double-Blind (DB) Atogepant for at least 2 out of 3 AttacksApproximately 16 Weeks

Pain relief is defined as the reduction of a moderate/severe migraine headache at baseline \[predose\] to a mild headache or to no headache.

Percentage of Participants Achieving Sustained Pain Relief From 2 to 24 Hours After Receiving DB Atogepant for at least 2 out of 3 AttacksApproximately 16 Weeks

Sustained pain relief is defined as pain relief at 2 hours after the DB dose with no administration of rescue medication and no occurrence of a moderate/severe headache from 2 to 24 hours.

Trial Locations

Locations (148)

Unidade Local de Saude de Santo Antonio, E.P.E. /ID# 258140

🇵🇹

Porto, Portugal

Semmelweis Egyetem /ID# 258800

🇭🇺

Budapest, Hungary

UNO Medical Trials /ID# 259186

🇭🇺

Budapest, Hungary

S-Medicon Kft /ID# 258547

🇭🇺

Budapest, Hungary

Istituto Neurologico Mediterraneo Neuromed /ID# 258593

🇮🇹

Pozzilli, Isernia, Italy

ASL 1 Abruzzo - Ospedale SS. Filippo and Nicola /ID# 258590

🇮🇹

Avezzano, L Aquila, Italy

IRCCS Ospedale San Raffaele /ID# 258592

🇮🇹

Milan, Milano, Italy

Istituto Auxologico Italiano - Irccs /ID# 258623

🇮🇹

Milan, Milano, Italy

A.O.U. CITTA' DELLA SALUTE E DELLA SCIENZA DI TORINO - Ospedale Molinette /ID# 258591

🇮🇹

Torino, Piemonte, Italy

Univ. of Bologna-IRCCS-Istituto delle Scienze Neurologiche /ID# 261089

🇮🇹

Bologna, Italy

ASST degli Spedali Civili di Brescia /ID# 258594

🇮🇹

Brescia, Italy

ICOT Istituto Marco Pasquali /ID# 258621

🇮🇹

Latina, Italy

Fondazione Mondino Istituto Neurologico Nazionale a Carattere Scientifico IRCCS /ID# 258589

🇮🇹

Pavia, Italy

Fondazione Policlinico Universitario Campus Bio-Medico /ID# 258588

🇮🇹

Roma, Italy

H.-Hartziekenhuis Lier /ID# 257577

🇧🇪

Lier, Belgium

Cabinet Prive Dr Sava /ID# 257581

🇧🇪

Saint-Nicolas, Belgium

Ospedale San Paolo - ASL2 /ID# 258622

🇮🇹

Savona, Italy

Tokyo Dental College Ichikawa General Hospital /ID# 259570

🇯🇵

Ichikawa-shi, Chiba, Japan

Higashi Sapporo Neurology And Neurosurgery Clinic /ID# 262708

🇯🇵

Sapporo-shi, Hokkaido, Japan

The first affiliated hospital of bengbu medical college /ID# 258758

🇨🇳

Bengbu, Anhui, China

Peking University Third Hospital /ID# 259573

🇨🇳

Beijing, Beijing, China

The University Of Hong Kong - Shenzhen Hospital /ID# 258462

🇨🇳

Shenzhen, Guangdong, China

Hebei General Hospital /ID# 258583

🇨🇳

Shijiazhuang, Hebei, China

Zhengzhou People's Hospital /ID# 258670

🇨🇳

Zhengzhou, Henan, China

Zhuzhou Central Hospital /ID# 260076

🇨🇳

Zhuzhou, Hunan, China

The Second Affiliated Hospital of Soochow University /ID# 259551

🇨🇳

Suzhou, Jiangsu, China

Jiangxi Pingxiang People's Hospital /ID# 258652

🇨🇳

Pingxiang, Jiangxi, China

Beijing Friendship Hospital /ID# 258830

🇨🇳

Beijing, Beijing, China

The Second Xiangya Hospital of Central South University /ID# 260623

🇨🇳

Changsha, Hunan, China

The Second Affiliated Hospital of Nanjing Medical University /ID# 258648

🇨🇳

Nanjing, Jiangsu, China

Ikeda Neurosurgical Clinic /ID# 259085

🇯🇵

Kasuga-shi, Fukuoka, Japan

Xuanwu Hospital Capital Medical University /ID# 258510

🇨🇳

Beijing, Beijing, China

Chinese PLA General Hospital /ID# 257540

🇨🇳

Beijing, Beijing, China

Guangzhou First People's Hospital /ID# 258656

🇨🇳

Guangzhou, Guangdong, China

The First Affiliated Hospital of Soochow University /ID# 258783

🇨🇳

Suzhou, Jiangsu, China

Umenotsuji Clinic /ID# 258717

🇯🇵

Kochi-shi, Kochi, Japan

Sendai Headache and Neurology Clinic Medical Corporation /ID# 258862

🇯🇵

Sendai-shi, Miyagi, Japan

Peking University First Hospital /ID# 258672

🇨🇳

Xicheng District, Beijing, China

Fujian Medical University Union Hospital /ID# 259575

🇨🇳

Fuzhou, Fujian, China

The First Affiliated Hospital of Xiamen University /ID# 259576

🇨🇳

Xiamen, Fujian, China

Lanzhou University Second Hospital /ID# 259667

🇨🇳

Lanzhou, Gansu, China

Tominaga Clinic /ID# 258553

🇯🇵

Osaka-shi, Osaka, Japan

DOI Internal Medicine-Neurology Clinic /ID# 259009

🇯🇵

Hiroshima, Japan

Tatsuoka Neurology Clinic /ID# 258771

🇯🇵

Kyoto, Japan

Hallym University Dongtan Sacred Heart Hospital /ID# 257999

🇰🇷

Hwaseong, Gyeonggido, Korea, Republic of

The Second Affiliated Hospital of Guangzhou Medical University /ID# 258638

🇨🇳

Guangzhou, Guangdong, China

Usuda Clinic Of Internal Medicine /ID# 260422

🇯🇵

Setagaya-ku, Tokyo, Japan

Tokyo Headache Clinic /ID# 258534

🇯🇵

Shibuya-ku, Tokyo, Japan

Nagaseki Headache Clinic /ID# 259214

🇯🇵

Kai, Yamanashi, Japan

The Affiliated Hospital of Guizhou Medical University /ID# 259536

🇨🇳

Guiyang, Guizhou, China

Hainan General Hospital /ID# 259548

🇨🇳

Haikou, Hainan, China

The Third Xiangya Hospital of Central South University /ID# 258787

🇨🇳

Changsha, Hunan, China

The First Hospital of Jilin University /ID# 259585

🇨🇳

Changchun, Jilin, China

Chonnam National University Hospital /ID# 259154

🇰🇷

동구, Jeonranamdo, Korea, Republic of

Nowon Eulji Medical Center, Eulji University /ID# 258000

🇰🇷

Seoul, Seoul Teugbyeolsi, Korea, Republic of

Seoul National University Hospital /ID# 258002

🇰🇷

Seoul, Seoul Teugbyeolsi, Korea, Republic of

Kangbuk Samsung Hospital /ID# 258001

🇰🇷

Seoul, Seoul Teugbyeolsi, Korea, Republic of

Yonsei University Health System Severance Hospital /ID# 257998

🇰🇷

Seoul, Korea, Republic of

Vitamed Galaj i Cichomski Sp.j. /ID# 258278

🇵🇱

Bydgoszcz, Kujawsko-pomorskie, Poland

Athleticomed Sp. z o.o /ID# 258253

🇵🇱

Bydgoszcz, Kujawsko-pomorskie, Poland

Indywidualna Praktyka Lekarska dr hab. med. Anna Szczepanska-Szerej /ID# 258281

🇵🇱

Lublin, Lubelskie, Poland

Linden Sp. z o.o. sp.k. /ID# 258283

🇵🇱

Krakow, Malopolskie, Poland

Instytut Zdrowia Dr Boczarska Jedynak /ID# 258248

🇵🇱

Oświęcim, Malopolskie, Poland

Centrum Badan Klinicznych PI-House sp. z o.o. /ID# 258250

🇵🇱

Gdansk, Pomorskie, Poland

Silmedic Sp. z o.o. /ID# 258249

🇵🇱

Katowice, Slaskie, Poland

Solumed Centrum Medyczne /ID# 258288

🇵🇱

Poznan, Wielkopolskie, Poland

Clinical Research Center Sp. z.o.o. Medic-R sp. k /ID# 258268

🇵🇱

Poznan, Wielkopolskie, Poland

MIGRE Polskie Centrum Leczenia Migreny Anna Gryglas-Dworak /ID# 258287

🇵🇱

Wroclaw, Poland

Unidade Local de Saude do Alto Ave, EPE /ID# 257986

🇵🇹

Guimaraes, Braga, Portugal

Unidade Local de Saude de Almada-Seixal, EPE /ID# 257987

🇵🇹

Almada, Portugal

Hospital da Luz Lisboa /ID# 257983

🇵🇹

Lisboa, Portugal

Unidade Local de Saude de Santa Maria, EPE /ID# 257989

🇵🇹

Lisboa, Portugal

Unidade Local de Saude da Arrabida, EPE /ID# 258139

🇵🇹

Setubal, Portugal

University Hospital Bratislava - Hospital ak. L. Derera /ID# 257947

🇸🇰

Bratislava, Bratislavsky Kraj, Slovakia

Neurologicka a algeziologicka ambulancia, SANERA /ID# 259176

🇸🇰

Prešov, Presovsky Kraj, Slovakia

Liptovska nemocnica s poliklinikou MUDr. Ivana Stodolu Liptovsky Mikulas /ID# 258315

🇸🇰

Liptovsky Mikulas, Zilinsky Kraj, Slovakia

MUDr. Beata Dupejova neurologicka ambulancia s.r.o. /ID# 257901

🇸🇰

Banska Bystrica, Slovakia

Univerzitna nemocnica - Nemocnica svateho Michala a.s. /ID# 257909

🇸🇰

Bratislava, Slovakia

Poliklinika Bezrucova (Cliniq s.r.o.) /ID# 257961

🇸🇰

Bratislava, Slovakia

Hospital Universitario Marques de Valdecilla /ID# 257658

🇪🇸

Santander, Cantabria, Spain

Clinica Universidad de Navarra - Pamplona /ID# 257656

🇪🇸

Pamplona, Navarra, Spain

Hospital Universitario Vall d'Hebron /ID# 257652

🇪🇸

Barcelona, Spain

Hospital Universitario La Paz /ID# 257654

🇪🇸

Madrid, Spain

Hospital Universitario Virgen del Rocio /ID# 257657

🇪🇸

Sevilla, Spain

Hospital Universitario y Politecnico La Fe /ID# 257655

🇪🇸

Valencia, Spain

Hospital Clinico Universitario de Valladolid /ID# 257653

🇪🇸

Valladolid, Spain

Karolinska Universitetssjukhuset - Huddinge /ID# 258837

🇸🇪

Huddinge, Stockholms Lan, Sweden

Neurology Clinic /ID# 258835

🇸🇪

Stockholm, Stockholms Lan, Sweden

Hospital Clinico Universitario Lozano Blesa /ID# 257661

🇪🇸

Zaragoza, Spain

CTC EbbePark Linkoping /ID# 261170

🇸🇪

Linköping, Sweden

Kuang-Tien General Hospital /ID# 258063

🇨🇳

Taichung City, Taichung, Taiwan

Tri-Service General Hospital /ID# 258064

🇨🇳

Taipei City, Taiwan

Linkou Chang Gung Memorial Hospital /ID# 259171

🇨🇳

Taoyuan City, Taiwan

Skaneuro Privatmottagning /ID# 258833

🇸🇪

Lund, Skane Lan, Sweden

North Coast Medical Ltd - Newquay Health Centre /ID# 260019

🇬🇧

Newquay, Cornwall, United Kingdom

The Adam Practice /ID# 258190

🇬🇧

Poole, Dorset, United Kingdom

Re:Cognition Health Birmingham /ID# 258186

🇬🇧

Birmingham, United Kingdom

Optimuskliniken /ID# 258834

🇸🇪

Upplands Vasby, Sweden

Taipei Veterans General Hospital /ID# 258062

🇨🇳

Taipei City, Taipei, Taiwan

China Medical University Hospital /ID# 258417

🇨🇳

Taichung, Taiwan

Re:Cognition Health Bristol /ID# 258187

🇬🇧

Bristol, United Kingdom

Royal Primary Care Ashgate /ID# 258923

🇬🇧

Derbyshire, United Kingdom

Re:Cognition Health - Guildford /ID# 258188

🇬🇧

Guildford, United Kingdom

Primary Care Sheffield /ID# 259448

🇬🇧

Sheffield, United Kingdom

St Pancras Clinical Research /ID# 258183

🇬🇧

London, United Kingdom

The University of Nottingham Health Service /ID# 259380

🇬🇧

Nottingham, United Kingdom

Universitair Ziekenhuis Antwerpen /ID# 257582

🇧🇪

Edegem, Antwerpen, Belgium

Universitair Ziekenhuis Brussel /ID# 257584

🇧🇪

Jette, Bruxelles-Capitale, Belgium

Jessa Ziekenhuis /ID# 257578

🇧🇪

Hasselt, Limburg, Belgium

AZ Sint-Jan Brugge /ID# 257585

🇧🇪

Brugge, Belgium

AZ Groeninge /ID# 257586

🇧🇪

Kortrijk, Belgium

CHR de la Citadelle /ID# 257587

🇧🇪

Liege, Belgium

Gartnavel General Hospital /ID# 259384

🇬🇧

Glasgow, Glasgow City, United Kingdom

The Second hospital of Jilin university /ID# 258556

🇨🇳

Changchun, Jilin, China

General Hospital of Northern Theater Command /ID# 259556

🇨🇳

Shenyang, Liaoning, China

West China Hospital, Sichuan University /ID# 258664

🇨🇳

Chengdu, Sichuan, China

Shaanxi Provincial People'S Hospital /ID# 259529

🇨🇳

XI An, Shaanxi, China

Second Hospital of Shanxi Medical University /ID# 259669

🇨🇳

Taiyuan, Shanxi, China

Tianjin People's Hospital /ID# 258625

🇨🇳

Tianjin, Tianjin, China

Tianjin Medical University General Hospital /ID# 259513

🇨🇳

Tianjin, Tianjin, China

The second affiliated hospital of Zhejiang University school of medicine /ID# 258860

🇨🇳

Hangzhou, Zhejiang, China

The First Affiliated Hospital of Wenzhou Medical University /ID# 258939

🇨🇳

Wenzhou, Zhejiang, China

DADO MEDICAL s.r.o. /ID# 257672

🇨🇿

Praha, Czechia

Jávorszky Ödön Kórház /ID# 258969

🇭🇺

Vác, Pest, Hungary

Baotou Central Hospital /ID# 258786

🇨🇳

Baotou, China

FORBELI s.r.o. /ID# 259019

🇨🇿

Prague, Czechia

Fakultni Thomayerova nemocnice /ID# 259021

🇨🇿

Praha, Czechia

Neuropraxis Muenchen Sued /ID# 258077

🇩🇪

Unterhaching, Bayern, Germany

Cortex Study Center /ID# 259032

🇭🇺

Budapest, Hungary

The first people's Hospital Affiliated to Shanghai Jiaotong University /ID# 259554

🇨🇳

Shanghai, China

Fakultni Nemocnice Ostrava /ID# 259023

🇨🇿

Ostrava, Ostrava-mesto, Czechia

Praglandia /ID# 257667

🇨🇿

Prague, Praha 5, Czechia

INEP medical s.r.o. /ID# 257669

🇨🇿

Praha, Czechia

Kopfschmerzzentrum - Frankfurt /ID# 258019

🇩🇪

Frankfurt am Main, Hessen, Germany

Ambenet Hausarztpraxis /ID# 258075

🇩🇪

Leipzig, Sachsen, Germany

Vitos Orthopaedische Klinik Kassel gemeinnuetzige GmbH /ID# 258008

🇩🇪

Kassel, Germany

CCR Ostrava, s.r.o. /ID# 257743

🇨🇿

Ostrava, Ostrava-mesto, Czechia

Axon Clinical, s.r.o. /ID# 259024

🇨🇿

Praha, Czechia

Charite Universitaetsmedizin Berlin - Campus Mitte /ID# 258076

🇩🇪

Berlin, Germany

Velocity Clinical Research /ID# 258020

🇩🇪

Wiesbaden, Germany

NeuroHK s.r.o. /ID# 257671

🇨🇿

Hradec Kralove, Czechia

Clintrial s.r.o. /ID# 257663

🇨🇿

Prague 10, Czechia

Vestra Clinics s.r.o. /ID# 259022

🇨🇿

Rychnov nad Kneznou, Czechia

Studienzentrum Nord-West /ID# 258024

🇩🇪

Westerstede, Niedersachsen, Germany

Universitaetsklinikum Duesseldorf /ID# 258078

🇩🇪

Düsseldorf, Nordrhein-Westfalen, Germany

Schmerzklinik Kiel /ID# 258005

🇩🇪

Kiel, Schleswig-Holstein, Germany

Universitaetsklinikum Essen /ID# 258023

🇩🇪

Essen, Germany

Semmelweis Egyetem /ID# 258546

🇭🇺

Budapest, Hungary

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