Adult Study: ABT-414 Alone or ABT-414 Plus Temozolomide vs. Lomustine or Temozolomide for Recurrent Glioblastoma Pediatric Study: Evaluation of ABT-414 in Children With High Grade Gliomas

Study Purpose

This study was conducted to evaluate the efficacy and safety of depatuxizumab mafodotin (ABT-414) alone or with temozolomide versus temozolomide or lomustine alone in adult participants with recurrent glioblastoma. The study also included a substudy to evaluate safety, tolerability and pharmacokinetics of ABT-414 in a pediatric population.

Recruitment Criteria

Accepts Healthy Volunteers

Healthy volunteers are participants who do not have a disease or condition, or related conditions or symptoms

No
Study Type

An interventional clinical study is where participants are assigned to receive one or more interventions (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.


An observational clinical study is where participants identified as belonging to study groups are assessed for biomedical or health outcomes.


Searching Both is inclusive of interventional and observational studies.

Interventional
Eligible Ages N/A - 99 Years
Gender All
More Inclusion & Exclusion Criteria

Inclusion Criteria:

Adult participants (greater than or equal to 18 years old):
  • - Histologically confirmed de novo (primary) glioblastoma with unequivocal tumor progression or recurrence.
  • - In case of testing at the time of first progression: either at least 3 months after the end of radiotherapy or have tumor progression that is clearly outside the radiation field or have tumor progression unequivocally proven by surgery/biopsy.
  • - Absence of any psychological, familial, sociological or geographical factors potentially hampering compliance with the study protocol and follow-up schedule; such conditions should be assessed with the patient before registration in the trial.
  • - Availability of adequate biological material (formalin-fixed paraffin embedded [FFPE] tumor) for central testing of Epithelial Growth Factor Receptor (EGFR) amplification.
  • - Presence of EGFR amplification confirmed by central assessment; participants with undetermined EGFR status are excluded.
  • - World Health Organization (WHO) Performance status 0 - 2.
  • - No more than one line of chemotherapy (concurrent and adjuvant Temozolomide based chemotherapy including in combination with another investigational agent is considered one line of chemotherapy).
Chemotherapy must have been completed at least 4 weeks prior to randomization.
  • - Post surgery MRI within 48 hours following surgery, however an MRI scan has to be done within 2 weeks prior to randomization.
  • - Surgery completed at least 2 weeks before randomization and patients should have fully recovered as assessed by investigators.
  • - Renal function: calculated creatinine clearance ≥ 30 mL/min by the Cockcroft-Gault formula.
  • - Liver function: bilirubin < 1.5× upper limit of the normal range (ULN), alkaline phosphatase and transaminases (ASAT) < 2.5× ULN.
Pediatric sub-study participants (less than 18 years old):
  • - Histologically proven high grade glioma (HGG: WHO grade III glioma [e.
g anaplastic astrocytoma, anaplastic oligodendroglioma, anaplastic oligoastrocytoma], grade IV glioma [e.g. glioblastoma, gliosarcoma] or diffuse intrinsic pontine glioma [DIPG]).
  • - Must either have recurrent/progressive tumor or, if newly diagnosed, have completed any planned radiation therapy at least 4 weeks prior to first dose of ABT-414.
  • - The tumor tissue must have been determined to have EGFR amplification, (by local or other testing service).
  • - Availability of adequate biological material for retrospective confirmatory central testing of EGFR amplification.
  • - Participant has sufficiently recovered from previous therapy.
The investigator believes that benefit of treating the pediatric subject with ABT-414 outweighs the expected risks and that this treatment is in the best interests of the pediatric subject.
  • - Renal function: calculated creatinine clearance ≥ 30 mL/min by the Cockcroft-Gault formula for pediatric patients ≥12 years of age and estimated glomerular filtration rate ≥ 30 mL/min/1.73 m^2 by modified Schwartz equation for pediatric patients < 12 years of age.
  • - Liver function: Total bilirubin ≤ 1.5× upper limit of the normal range (ULN), Aspartate Aminotransferase (AST), and Alanine Aminotransferase (ALT) <= 3× ULN.
Participants with Gilbert's syndrome documented in medical history may be enrolled if total bilirubin is < 3 times ULN. Not allowed are participants with known chronic liver disease and/or cirrhosis.

Exclusion Criteria:

Adult population (greater than or equal to 18 years old):
  • - Prior treatment with nitrosoureas.
  • - Prior treatment with bevacizumab.
  • - Previous exposure to Epithelial Growth Factor Receptor (EGFR) targeted agents, including EGFRvIII targeting agents.
  • - Prior discontinuation of temozolomide chemotherapy for toxicity reasons.
  • - Prior Radiation Therapy (RT) with a dose over 65 Gy to the brain, stereotactic radiosurgery or brachytherapy unless the recurrence is histologically proven.
  • - Previous other malignancies, except for any previous malignancy which was treated with curative intent more than 5 years prior to randomization, and except for adequately controlled limited basal cell carcinoma of the skin, squamous carcinoma of the skin or carcinoma in situ of the cervix.
  • - Women of childbearing potential must have a negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent units of HCG) within 72 hours prior to randomization.
  • - No history of wheat allergies and Coeliac disease.
  • - No EIAED, patients who require anti-convulsant therapy must be taking non-enzyme inducing antiepileptic drugs (non-EIAED).
Patients previously on EIAED must be fully switched to non-EIAED at least 2 weeks prior to randomization. Pediatric sub-study (less than 18 years old):
  • - (For recurrent disease) No prior RT with a dose over 65 Gy to the brain, stereotactic radiosurgery or brachytherapy unless the recurrence is histologically proven.
  • - No current or recent (within 4 weeks or 5 half-lives [whichever is shorter] before enrollment) treatment with another investigational drug.
  • - Female participants of childbearing potential must have a negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent units of HCG) within 72 hours prior to randomization.

Trial Details

Trial ID:

This trial id was obtained from ClinicalTrials.gov, a service of the U.S. National Institutes of Health, providing information on publicly and privately supported clinical studies of human participants with locations in all 50 States and in 196 countries.

NCT02343406
Phase

Phase 1: Studies that emphasize safety and how the drug is metabolized and excreted in humans.

Phase 2: Studies that gather preliminary data on effectiveness (whether the drug works in people who have a certain disease or condition) and additional safety data.

Phase 3: Studies that gather more information about safety and effectiveness by studying different populations and different dosages and by using the drug in combination with other drugs.

Phase 4: Studies occurring after FDA has approved a drug for marketing, efficacy, or optimal use.

Phase 2
Lead Sponsor

The sponsor is the organization or person who oversees the clinical study and is responsible for analyzing the study data.

AbbVie
Principal Investigator

The person who is responsible for the scientific and technical direction of the entire clinical study.

AbbVie Inc.
Principal Investigator Affiliation AbbVie
Agency Class

Category of organization(s) involved as sponsor (and collaborator) supporting the trial.

Industry, Other
Overall Status Completed
Countries Australia, Austria, Belgium, Canada, Czechia, Finland, France, Germany, Hungary, Ireland, Italy, Korea, Republic of, Mexico, Netherlands, Poland, Singapore, Spain, Switzerland, Taiwan, United Kingdom, United States
Conditions

The disease, disorder, syndrome, illness, or injury that is being studied.

Glioblastoma
Additional Details

The study objectives were to assess whether depatuxizumab mafodotin (ABT-414) alone or in combination with temozolomide (TMZ) improved overall survival (OS), progression-free survival (PFS), tumor response, quality of life, neurological deterioration-free survival (NDFS), and steroid use compared to standard treatment with lomustine single agent or TMZ re-challenge in adult subjects ≥ 18 years of age with centrally-confirmed recurrent epidermal growth factor receptor (EGFR)-amplified glioblastoma. The safety, pharmacokinetics, and efficacy of depatuxizumab mafodotin in children <18 years of age was evaluated in a pediatric substudy. The EMEA-001732-PIP02-15 pediatric investigation plan was withdrawn on 07 July 2019 due to the discontinuation of the depatuxizumab mafodotin research program.

Arms & Interventions

Arms

Experimental: ABT-414/temozolomide

Depatuxizumab mafodotin (ABT-414) administered once every 2 weeks in combination with temozolomide (TMZ) to adult participants

Experimental: ABT-414_adult

Depatuxizumab mafodotin (ABT-414) administered once every 2 weeks to adult participants

Active Comparator: Control_lomustine

Adult participants relapsing during temozolomide (TMZ) treatment or within the first 16 weeks after the first day of the last TMZ cycle received lomustine on Day 1 of every 42-day treatment period until one of the treatment withdrawal criteria was met, up to a maximum of 1 year.

Active Comparator: Control_ temozolomide

Adult participants relapsing 16 weeks or more after the first day of the last temozolomide (TMZ) cycle received TMZ on Day 1 to Day 5 for the first 28-day cycle, with dose escalation in subsequent cycles in case of adequate tolerance and treatment continuing until one of the treatment withdrawal criteria was met.

Experimental: ABT-414_ pediatric

Depatuxizumab mafodotin (ABT-414) administered once every 2 weeks to pediatric participants. Temozolomide (TMZ) was only allowed for pediatric participants if its use was in accordance with local clinical practice, and was not considered an investigational product for the study (unless this was a local requirement).

Interventions

Drug: - Depatuxizumab mafodotin

Adults: intravenous administration (1.25 mg/kg or 1.0 mg/kg body weight) over 30 to 40 minutes once every 2 weeks until one of the treatment withdrawal criteria was met. The dose was 1.25 mg/kg in the original protocol (Version 1) and Version 2, Amendment 1, and was lowered to 1.0 mg/kg in protocol Version 3, Amendment 2. Pediatric participants: Intravenous administration (1.0 mg/kg body weight for those who were 6 to 17 years old at the date of first dose, or 1.3 mg/kg for those who were 0 to 5 years old) over 30 to 40 minutes or as directed by the guidelines once every 2 weeks until one of the treatment withdrawal criteria was met, for a maximum of one year. If used in combination with temozolomide, depatuxizumab mafodotin was dosed on Day 1 and Day 15 of the TMZ cycle (assuming a standard regimen of 200 mg/m^2/day for 5 days of each 28-day cycle; for other TMZ schedules, timing of the depatuxizumab mafodotin dosing schedule were to be discussed with the medical monitor).

Drug: - Temozolomide

Capsules administered orally, 150 mg/m^2 on Days 1-5 for the first 28-day cycle, with dose escalation to 200 mg/m^2 in subsequent cycles in case of adequate tolerance until one of the treatment withdrawal criteria was met.

Drug: - Lomustine

Capsules administered orally, 110 mg/m^2 on Day 1 of every 42-day treatment period. Treatment continued until one of the treatment withdrawal criteria was met, for a maximum of one year.

Contact a Trial Team

If you are interested in learning more about this trial, find the trial site nearest to your location and contact the site coordinator via email or phone. We also strongly recommend that you consult with your healthcare provider about the trials that may interest you and refer to our terms of service below.

Palo Alto, California

Status

Address

Lucile Packard Children's Hosp /ID# 153678

Palo Alto, California, 34304

Children's Hospital Colorado /ID# 153677, Aurora, Colorado

Status

Address

Children's Hospital Colorado /ID# 153677

Aurora, Colorado, 80045

Aurora, Colorado

Status

Address

Univ of Colorado Cancer Center /ID# 134882

Aurora, Colorado, 80045

Denver, Colorado

Status

Address

Sarah Cannon Research Institute at HealthONE - Denver /ID# 141798

Denver, Colorado, 80218

Chicago, Illinois

Status

Address

Rush University Medical Center /ID# 137542

Chicago, Illinois, 60612

Dana-Farber Cancer Institute /ID# 154210, Boston, Massachusetts

Status

Address

Dana-Farber Cancer Institute /ID# 154210

Boston, Massachusetts, 02215

Lake Success, New York

Status

Address

Long Island Brain Tumor Center /ID# 134496

Lake Success, New York, 11042

Weill Cornell Medicine /ID# 152656, New York, New York

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Address

Weill Cornell Medicine /ID# 152656

New York, New York, 10032-3725

Cleveland Clinic Main Campus /ID# 137540, Cleveland, Ohio

Status

Address

Cleveland Clinic Main Campus /ID# 137540

Cleveland, Ohio, 44195

University of Pittsburgh MC /ID# 134491, Pittsburgh, Pennsylvania

Status

Address

University of Pittsburgh MC /ID# 134491

Pittsburgh, Pennsylvania, 15260

Tennessee Oncology, PLLC /ID# 134492, Nashville, Tennessee

Status

Address

Tennessee Oncology, PLLC /ID# 134492

Nashville, Tennessee, 37203

Dallas, Texas

Status

Address

UT Southwestern Medical Center /ID# 136718

Dallas, Texas, 75390-7208

Swedish Medical Center /ID# 136719, Seattle, Washington

Status

Address

Swedish Medical Center /ID# 136719

Seattle, Washington, 98104

International Sites

Port Macquarie Base Hospital /ID# 134569, Port Macquarie, New South Wales, Australia

Status

Address

Port Macquarie Base Hospital /ID# 134569

Port Macquarie, New South Wales, 2444

Sydney Children's Hospital /ID# 153533, Randwick, New South Wales, Australia

Status

Address

Sydney Children's Hospital /ID# 153533

Randwick, New South Wales, 2031

Royal North Shore Hospital /ID# 147092, Saint Leonards, New South Wales, Australia

Status

Address

Royal North Shore Hospital /ID# 147092

Saint Leonards, New South Wales, 2065

Calvary Mater Newcastle /ID# 134570, Waratah, New South Wales, Australia

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Address

Calvary Mater Newcastle /ID# 134570

Waratah, New South Wales, 2298

Wollongong, New South Wales, Australia

Status

Address

Southern Medical Day Care Ctr /ID# 134495

Wollongong, New South Wales, 2500

Herston, Queensland, Australia

Status

Address

Royal Brisbane and Women's Hospital /ID# 147091

Herston, Queensland, 4029

Royal Adelaide Hospital /ID# 135208, Adelaide, South Australia, Australia

Status

Address

Royal Adelaide Hospital /ID# 135208

Adelaide, South Australia, 5000

Royal Hobart Hospital /ID# 135209, Hobart, Tasmania, Australia

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Address

Royal Hobart Hospital /ID# 135209

Hobart, Tasmania, 7000

Geelong, Victoria, Australia

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Address

Barwon Health University Hospital Geelong /ID# 134493

Geelong, Victoria, 3220

Royal Children's Hospital /ID# 157624, Melbourne, Victoria, Australia

Status

Address

Royal Children's Hospital /ID# 157624

Melbourne, Victoria, 3052

St. Pölten, Niederoesterreich, Austria

Status

Address

University Hospital St. Polten /ID# 139070

St. Pölten, Niederoesterreich, 3100

LKH-Univ. Klinikum Graz /ID# 139071, Graz, Austria

Status

Address

LKH-Univ. Klinikum Graz /ID# 139071

Graz, , 8036

Linz, Austria

Status

Address

Kepler Universitätsklinikum GmbH - Neuromed Campus /ID# 139068

Linz, , 4020

Woluwe-Saint-Lambert, Bruxelles-Capitale, Belgium

Status

Address

Cliniques Universitaires Saint Luc /ID# 139391

Woluwe-Saint-Lambert, Bruxelles-Capitale, 1200

Grand Hôpital de Charleroi /ID# 139342, Charleroi, Hainaut, Belgium

Status

Address

Grand Hôpital de Charleroi /ID# 139342

Charleroi, Hainaut, 6000

UZ Gent /ID# 152944, Gent, Oost-Vlaanderen, Belgium

Status

Address

UZ Gent /ID# 152944

Gent, Oost-Vlaanderen, 9000

AZ St-Jan Brugge-Oostende AV /ID# 137927, Brugge, West-Vlaanderen, Belgium

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Address

AZ St-Jan Brugge-Oostende AV /ID# 137927

Brugge, West-Vlaanderen, 8000

ZNA Middelheim /ID# 137926, Antwerp, Belgium

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Address

ZNA Middelheim /ID# 137926

Antwerp, , 2020

UZ Leuven /ID# 137925, Leuven, Belgium

Status

Address

UZ Leuven /ID# 137925

Leuven, , 3000

Montreal, Quebec, Canada

Status

Address

Montreal Neurological Institut /ID# 136309

Montreal, Quebec, H3A 2B4

Fakultni Nemocnice v Motole /ID# 139509, Prague 5, Praha 5, Czechia

Status

Address

Fakultni Nemocnice v Motole /ID# 139509

Prague 5, Praha 5, 150 06

Masarykuv onkologikcy ustav /ID# 139508, Brno, Czechia

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Address

Masarykuv onkologikcy ustav /ID# 139508

Brno, , 656 53

FN Hradec Kralove /ID# 139510, Hradec Kralove, Czechia

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Address

FN Hradec Kralove /ID# 139510

Hradec Kralove, , 500 05

Univ Hosp Ostrava-Poruba /ID# 139507, Ostrava, Czechia

Status

Address

Univ Hosp Ostrava-Poruba /ID# 139507

Ostrava, , 708 52

Helsinki, Finland

Status

Address

Helsinki Univ Central Hospital /ID# 140078

Helsinki, , 00290

Helsinki, Finland

Status

Address

Helsinki Univ Central Hospital /ID# 153069

Helsinki, , 00290

Turku University Hospital /ID# 140861, Turku, Finland

Status

Address

Turku University Hospital /ID# 140861

Turku, , 20520

Lille CEDEX, Hauts-de-France, France

Status

Address

CHRU Lille - Hôpital Claude Huriez /ID# 137916

Lille CEDEX, Hauts-de-France, 59045

Centre Oscar Lambret /ID# 169619, Lille, Hauts-de-France, France

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Address

Centre Oscar Lambret /ID# 169619

Lille, Hauts-de-France, 59020

CHU-Hopital Avicenne /ID# 137910, Bobigny, Ile-de-France, France

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Address

CHU-Hopital Avicenne /ID# 137910

Bobigny, Ile-de-France, 93000

Gustave Roussy /ID# 137912, Villejuif, Ile-de-France, France

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Address

Gustave Roussy /ID# 137912

Villejuif, Ile-de-France, 94805

St Herblain CEDEX, Loire-Atlantique, France

Status

Address

Institut de Cancer de l'Ouest /ID# 137914

St Herblain CEDEX, Loire-Atlantique, 44805

Hopital de la Timone /ID# 137911, Marseille CEDEX 05, Provence-Alpes-Cote-d Azur, France

Status

Address

Hopital de la Timone /ID# 137911

Marseille CEDEX 05, Provence-Alpes-Cote-d Azur, 13385

CHU de Nice /ID# 137917, Nice CEDEX 1, Provence-Alpes-Cote-d Azur, France

Status

Address

CHU de Nice /ID# 137917

Nice CEDEX 1, Provence-Alpes-Cote-d Azur, 06002

Centre Leon Berard /ID# 137918, Lyon CEDEX 08, Rhone, France

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Address

Centre Leon Berard /ID# 137918

Lyon CEDEX 08, Rhone, 69373

Angers, France

Status

Address

Institut de Cancer de l'Ouest /ID# 137909

Angers, , 49055

Hospices Civils de Lyon /ID# 137913, Bron, France

Status

Address

Hospices Civils de Lyon /ID# 137913

Bron, , 69500

Hopital Pitie Salpetriere /ID# 145887, Paris, France

Status

Address

Hopital Pitie Salpetriere /ID# 145887

Paris, , 75651

Heidelberg, Baden-Wuerttemberg, Germany

Status

Address

Universitaetsklinik Heidelberg /ID# 137924

Heidelberg, Baden-Wuerttemberg, 69120

Ratisbon, Bayern, Germany

Status

Address

Universitatsklinik Regensburg /ID# 137920

Ratisbon, Bayern, 93053

Hamburg, Germany

Status

Address

Univ Klinik Eppendorf Hamburg /ID# 137921

Hamburg, , 20246

Munich, Germany

Status

Address

LMU Klinikum der Universität München /ID# 137922

Munich, , 80337

Tuebingen, Germany

Status

Address

Universitatsklinikum Tubingen /ID# 137923

Tuebingen, , 72076

Pecsi Tudomanyegyetem /ID# 136111, Pécs, Pecs, Hungary

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Address

Pecsi Tudomanyegyetem /ID# 136111

Pécs, Pecs, 7624

Semmelweis Egyetem /ID# 152578, Budapest, Hungary

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Address

Semmelweis Egyetem /ID# 152578

Budapest, , 1085

Budapest, Hungary

Status

Address

National Institute of Oncology /ID# 135970

Budapest, , 1122

Budapest, Hungary

Status

Address

Orszagos Klinikai Idegtudomany /ID# 135971

Budapest, , 1145

Debrecen, Hungary

Status

Address

Debreceni Egyetem Klinikai Központ /ID# 135969

Debrecen, , 4032

Cork University Hospital /ID# 136828, Cork, Ireland

Status

Address

Cork University Hospital /ID# 136828

Cork, , T12 E8YV

Beaumont Hospital /ID# 136829, Dublin, Ireland

Status

Address

Beaumont Hospital /ID# 136829

Dublin, , D09 XR63

Bologna, Italy

Status

Address

Ospedale Bellaria.Azienda USL IRCCS.Istituto delle Scienze Neurologiche di Bolog /ID# 138335

Bologna, , 40139

Ospedale Generale di Bolzano /ID# 138338, Bolzano, Italy

Status

Address

Ospedale Generale di Bolzano /ID# 138338

Bolzano, , 39100

Milan, Italy

Status

Address

Fondazione IRCCS Istituto Neurologico Carlo Besta /ID# 140395

Milan, , 20133

Istituto Oncologico Veneto /ID# 138336, Padova, Italy

Status

Address

Istituto Oncologico Veneto /ID# 138336

Padova, , 35128

Rome, Italy

Status

Address

Azienda Ospedaliera Sant' Andrea /ID# 138337

Rome, , 00189

Seongnam, Gyeonggido, Korea, Republic of

Status

Address

Seoul National Univ Bundang ho /ID# 136841

Seongnam, Gyeonggido, 13620

Samsung Medical Center /ID# 136842, Seoul, Seoul Teugbyeolsi, Korea, Republic of

Status

Address

Samsung Medical Center /ID# 136842

Seoul, Seoul Teugbyeolsi, 06351

Seoul, Korea, Republic of

Status

Address

Seoul National University Hospital /ID# 136840

Seoul, , 03080

Hospital Zambrano Hellion /ID# 138076, San Pedro Garza García, Mexico

Status

Address

Hospital Zambrano Hellion /ID# 138076

San Pedro Garza García, , 66278

Amsterdam, Netherlands

Status

Address

Vrije Universiteit Medisch Centrum /ID# 137221

Amsterdam, , 1081 HV

Groningen, Netherlands

Status

Address

Universitair Medisch Centrum Groningen /ID# 138266

Groningen, , 9713 GZ

Erasmus Medisch Centrum /ID# 136981, Rotterdam, Netherlands

Status

Address

Erasmus Medisch Centrum /ID# 136981

Rotterdam, , 3015 CE

Haaglanden Medisch Centrum /ID# 137222, The Hague, Netherlands

Status

Address

Haaglanden Medisch Centrum /ID# 137222

The Hague, , 2512 VA

Utrecht, Netherlands

Status

Address

Universitair Medisch Centrum Utrecht /ID# 137219

Utrecht, , 3584 CX

Prinses Maxima Centrum /ID# 204409, Utrecht, Netherlands

Status

Address

Prinses Maxima Centrum /ID# 204409

Utrecht, , 3584 EA

Gdansk, Mazowieckie, Poland

Status

Address

Uniwersyteckie Centrum Kliniczne /ID# 137919

Gdansk, Mazowieckie, 80-214

Lodz, Poland

Status

Address

Wojewodzkie Wielospecjalistycz /ID# 137654

Lodz, , 93-509

National University Hospital /ID# 135951, Singapore, Singapore

Status

Address

National University Hospital /ID# 135951

Singapore, , 119074

Singapore, Singapore

Status

Address

National Cancer Ctr Singapore /ID# 135952

Singapore, , 169610

Singapore, Singapore

Status

Address

KK Women's & Children Hospital /ID# 153676

Singapore, , 229899

Badalona, Barcelona, Spain

Status

Address

Instituto Catalán de Oncología (ICO) Badalona /ID# 140976

Badalona, Barcelona, 08916

Pamplona, Navarra, Comunidad, Spain

Status

Address

Clinica Universitar de Navarra - Pamplona /ID# 140047

Pamplona, Navarra, Comunidad, 31008

Barcelona, Spain

Status

Address

Instituto Catalan de Oncologia (ICO) & Hosp. de Bellvitge /ID# 137688

Barcelona, , 08908

Hospital Universitario Nino /ID# 153800, Madrid, Spain

Status

Address

Hospital Universitario Nino /ID# 153800

Madrid, , 28009

Hosp Univ 12 de Octubre /ID# 137908, Madrid, Spain

Status

Address

Hosp Univ 12 de Octubre /ID# 137908

Madrid, , 28041

Lausanne, Switzerland

Status

Address

Centre Hospitalier Univ Vaudoi /ID# 137929

Lausanne, , 1011

University Hospital Zurich /ID# 137930, Zurich, Switzerland

Status

Address

University Hospital Zurich /ID# 137930

Zurich, , 8091

Taichung City, Taichung, Taiwan

Status

Address

China Medical University Hosp /ID# 136976

Taichung City, Taichung, 40447

National Taiwan Univ Hosp /ID# 136975, Taipei City, Taipei, Taiwan

Status

Address

National Taiwan Univ Hosp /ID# 136975

Taipei City, Taipei, 10002

Taichung City, Taiwan

Status

Address

Taichung Veterans General Hosp /ID# 136977

Taichung City, , 40705

Taipei Veterans General Hosp /ID# 136974, Taipei City, Taiwan

Status

Address

Taipei Veterans General Hosp /ID# 136974

Taipei City, , 11217

Taoyuan City, Taiwan

Status

Address

Linkou Chang Gung Memorial Ho /ID# 136944

Taoyuan City, , 33305

London, London, City Of, United Kingdom

Status

Address

Guy's and St Thomas' NHS Found /ID# 140312

London, London, City Of, SE1 9RT

Birmingham, United Kingdom

Status

Address

Univ Hospitals Birmingham NHS Foundation trust /ID# 136978

Birmingham, , B15 2TG

Gartnavel General Hospital /ID# 136979, Glasgow, United Kingdom

Status

Address

Gartnavel General Hospital /ID# 136979

Glasgow, , G12 0YN

Hull and East Yorkshire NHS /ID# 136917, Hull, United Kingdom

Status

Address

Hull and East Yorkshire NHS /ID# 136917

Hull, , HU8 9HE

University College Hospitals /ID# 136879, London, United Kingdom

Status

Address

University College Hospitals /ID# 136879

London, , NW1 2BU

Great Ormond St Hospital NHS /ID# 153421, London, United Kingdom

Status

Address

Great Ormond St Hospital NHS /ID# 153421

London, , WC1N 3JH

Manchester, United Kingdom

Status

Address

Christie NHS Foundation Trust /ID# 140313

Manchester, , M20 4BX

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