interventional clinical trials that were approved in the European Union (EU)/European Economic Area (EEA) under the Clinical Trials Directive 2001/20/EC
clinical trials conducted outside the EU/EEA that are linked to European paediatric-medicine development
EU/EEA interventional clinical trials approved under or transitioned to the Clinical Trial Regulation 536/2014 are publicly accessible through the
Clinical Trials Information System (CTIS).
The EU Clinical Trials Register currently displays
44341
clinical trials with a EudraCT protocol, of which
7370
are clinical trials conducted with subjects less than 18 years old.
The register also displays information on
18700
older paediatric trials (in scope of Article 45 of the Paediatric Regulation (EC) No 1901/2006).
Phase 1 trials conducted solely on adults and that are not part of an agreed paediatric investigation plan (PIP) are not publicly available (see
Frequently Asked Questions ).
Full Title: An Open-label, Single-arm, Multicohort, Phase 2 Study to Assess the Efficacy and Safety of Tabelecleucel in Subjects with Epstein-Barr Virus-associated Diseases
Medical condition: • EBV+ primary imunodeficiency lymphoproliferative disease (LPD)
• EBV+ LPD in the setting of acquired (non-congenital) immunodeficiency
• EBV+ post-transplant LPD involving the central nervous ...
Disease:
Version
SOC Term
Classification Code
Term
Level
21.1
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly
Gender: Male, Female
Trial protocol:FR(Trial now transitioned)AT(Trial now transitioned)BE(Trial now transitioned)IT(Trial now transitioned)ES(Ongoing)
Trial results:(No results available)
EudraCT Number: 2013-000225-30
Sponsor Protocol Number: DMA-Clin-199-2013-001
Start Date*: 2013-04-12
Sponsor Name:DiaMedica USA Inc.
Full Title: A DOUBLE-BLINDED, PLACEBO-CONTROLLED, SINGLE DOSE AND MULTIPLE-DOSE STUDY TO EVALUATE THE SAFETY, TOLERABILITY, PHARMACOKINETICS, PHARMACODYNAMICS AND PROOF OF CONCEPT OF DM-199 IN HEALTHY SUBJECTS...
Sponsor Name:Pfizer Inc. 235 East 42nd Street, New York, NY 10017
Full Title: A Phase 1B/2 Study To Evaluate The Safety And Efficacy of PF-04449913, An Oral Hedgehog Inhibitor, In Combination With Intensive Chemotherapy, Low Dose ARA-C Or Decitabine In Patients With Acute My...
Medical condition: Acute myeloid leukemia or myelodysplastic syndrome
Disease:
Version
SOC Term
Classification Code
Term
Level
20.0
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10000886
Acute myeloid leukemia
LLT
20.0
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Sponsor Name:Grupo Español de Tumores Neuroendocrinos
Full Title: A Phase II randomized double-blind study of Santostatin LAR in combination with Axitinib versus Placebo in patients with progressive advanced well-differentiated neuroendocrine carcinomas of non-pa...
Medical condition: Patients with progressive advanced well-differentiated neuroendocrine carcinomas of non-pancreatic origin (carcinoids)
Disease:
Version
SOC Term
Classification Code
Term
Level
14.1
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Sponsor Name:Princess Maxima Center for Pediatric Oncology in The Netherlands
Full Title: A Phase I/II study of Brigatinib in pediatric and young adult patients with ALK+ Anaplastic Large Cell Lymphoma, Inflammatory Myofibroblastic Tumors or other solid tumors
Medical condition: relapsed/refractory ALK rearranged** or ALK mutated tumors, including relapsed/refractory ALK+ALCL and ALK+IMT.
Disease:
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults
Gender: Male, Female
Trial protocol:NL(Trial now transitioned)FR(Trial now transitioned)ES(Ongoing)DK(Trial now transitioned)SE(Trial now transitioned)IT(Trial now transitioned)DE(Trial now transitioned)NO(Prematurely Ended)BE(Trial now transitioned)FI(Trial now transitioned)PL(Trial now transitioned)AT(Ongoing)CZ(Trial now transitioned)
Trial results:(No results available)
EudraCT Number: 2019-003117-33
Sponsor Protocol Number: Pevonedistat-2002
Start Date*: Information not available in EudraCT
Sponsor Name:Millennium Pharmaceuticals, Inc.
Full Title: A Randomized, Open-label, Controlled, Phase 2 Study of Pevonedistat, Venetoclax, and Azacitidine Versus Venetoclax Plus Azacitidine in Adults With Newly Diagnosed Acute Myeloid Leukemia Who Are Unf...
Medical condition: Acute Myeloid Leukemia (AML)
Disease:
Version
SOC Term
Classification Code
Term
Level
21.0
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10000886
Acute myeloid leukemia
LLT
20.1
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10024330
Leukemia acute
LLT
21.1
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10024348
Leukemia myelogenous
LLT
Population Age: Adults, Elderly
Gender: Male, Female
Trial protocol:PL(Trial now transitioned)IT(Trial now transitioned)FR(Completed)
Trial results:(No results available)
EudraCT Number: 2009-017098-40
Sponsor Protocol Number: DEC-MDS
Start Date*: 2010-07-09
Sponsor Name:King's College London
[...]
1. King's College London 2. King's College Hospital NHS Foundation Trust
Full Title: Use of Decitabine in Myelodysplastic Syndrome (MDS) Following Azacitidine (AZA) Failure (DEC-MDS)
Medical condition: Myelodysplastic Syndromes
Acute Myeloid Leukaemia
Chronic Myelomonocytic Leukaemia
Disease:
Version
SOC Term
Classification Code
Term
Level
14.1
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10054350
Chronic myelomonocytic leukemia
LLT
14.1
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10000886
Acute myeloid leukemia
LLT
14.1
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10000880
Acute myeloid leukaemia
PT
14.1
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10028533
Myelodysplastic syndrome
PT
14.1
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Sponsor Name:Incyte Biosciences International Sàrl
Full Title: A Phase 1/2 Study Exploring the Safety, Tolerability, and Efficacy of INCAGN01876 in Combination With Immune Therapies in Subjects With Advanced or Metastatic Malignancies.
Medical condition: Phase 1: advanced or metastatic cervical cancer, endometrial cancer, gastric cancer, hepatocellular carcinoma, melanoma (mucosal or cutaneous), Merkel cell carcinoma, mesothelioma, MSI-H colorectal...
Disease:
Version
SOC Term
Classification Code
Term
Level
20.0
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10041067
Small cell lung cancer
PT
20.0
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10060121
Squamous cell carcinoma of head and neck
PT
20.0
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10014733
Endometrial cancer
PT
20.0
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10027407
Mesothelioma malignant
PT
20.0
100000017553
10064467
Urothelial carcinoma
LLT
20.0
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10073071
Hepatocellular carcinoma
PT
20.0
100000018529
10027150
Melanoma malignant
LLT
20.0
100000018548
10064025
Merkel cell carcinoma
LLT
20.0
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10017758
Gastric cancer
PT
20.0
100000020977
10008229
Cervical cancer
LLT
20.0
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10061873
Non-small cell lung cancer
PT
11.0
100000005104
10038408
Renal cell carcinomas
HLT
20.0
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10061451
Colorectal cancer
PT
20.0
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10075566
Triple negative breast cancer
PT
20.0
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Full Title: A Phase 1/2, Multicenter, Open-label Study of FT 2102 as a Single Agent and in Combination with Azacitidine or Cytarabine in Patients with Acute Myeloid Leukemia or Myelodysplastic Syndrome with an...
Medical condition: Relapsed/refractory Acute Myeloid Leukemia (AML) or Myelodysplastic Syndrome (MDS).
Disease:
Version
SOC Term
Classification Code
Term
Level
21.1
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10028533
Myelodysplastic syndrome
PT
21.0
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10000886
Acute myeloid leukemia
LLT
21.0
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10060558
Acute myeloid leukemia recurrent
LLT
Population Age: Adults, Elderly
Gender: Male, Female
Trial protocol:DE(Completed)ES(Ongoing)GB(GB - no longer in EU/EEA)IT(Completed)
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• EEA CTAs: Date study was authorised to proceed • Outside EU/EEA: Date study was submitted in EudraCT