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
44334
clinical trials with a EudraCT protocol, of which
7366
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: Treatment of malignant mesothelioma with pemetrexed (Alimta) + platinum (4 courses) or pemetrexed (Alimta) + platinum (4 courses) followed by Caelyx single drug (4 courses).
Sponsor Name:Asklepios Fachkliniken München Gauting
Full Title: Pleurectomy/decortication and hypterthermic intrathoracic chemotherapy compared to pleurectomy/decortication in patients with malignant pleural mesothelioma
Medical condition: malignant pleuramesothelioma
Disease:
Version
SOC Term
Classification Code
Term
Level
16.1
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Full Title: A Randomized, Open-Label Phase II/III Study With Dendritic Cells Loaded With Allogeneic Tumour Cell Lysate (PheraLys) in Subjects With Mesothelioma as Maintenance Treatment (MesoPher) After Chemoth...
Medical condition: Pleural malignant mesothelioma.
Disease:
Version
SOC Term
Classification Code
Term
Level
21.0
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10027407
Mesothelioma malignant
PT
Population Age: Adults
Gender: Male, Female
Trial protocol:NL(Completed)GB(GB - no longer in EU/EEA)BE(Completed)FR(Completed)IT(Completed)
Full Title: A Phase 2, Multicenter Study of the EZH2 Inhibitor Tazemetostat in Adult Subjects with Relapsed or Refractory BAP1 deficientMalignant Mesothelioma
Medical condition: Part 1 – Subjects with relapsed or refractory malignant mesothelioma regardless of BAP1 status
Part 2 – Subjects with relapsed or refractory BAP1-deficient malignant mesothelioma
Disease:
Version
SOC Term
Classification Code
Term
Level
19.1
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10027414
Mesotheliomas malignant and unspecified
HLT
19.1
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10027407
Mesothelioma malignant
PT
19.1
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10027406
Mesothelioma
PT
19.1
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10027408
Mesothelioma malignant advanced
LLT
19.1
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10062474
Mesothelioma malignant localized
LLT
19.1
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
10027411
Mesothelioma malignant recurrent
PT
19.1
10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Sponsor Name:GRUPPO ONCOLOGICO ITALIANO DI RICERCA CLINICA (GOIRC)
Full Title: A double-blind, placebo controlled, randomized multicenter Phase II Study evaluating Gemcitabine with or without Ramucirumab as II line treatment for advanced malignant pleural mesothelioma
Medical condition: diffuse malignant pleural mesethelioma
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: Randomized, Double-Blind, Phase 2/3 Study in Subjects with Malignant Pleural Mesothelioma to Assess ADI-PEG 20 with Pemetrexed and Cisplatin (ATOMIC-Meso Phase 2/3 Study)
Medical condition: Advanced malignant pleural mesothelioma (MPM)
Disease:
Version
SOC Term
Classification Code
Term
Level
21.0
100000004864
10035605
Pleural mesothelioma malignant advanced
LLT
Population Age: Adults, Elderly
Gender: Male, Female
Trial protocol:GB(GB - no longer in EU/EEA)IT(Completed)
Trial results:(No results available)
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• EEA CTAs: Date study was authorised to proceed • Outside EU/EEA: Date study was submitted in EudraCT