- Trials with a EudraCT protocol (887)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
887 result(s) found for: Bone marrow biopsy.
Displaying page 8 of 45.
EudraCT Number: 2016-005019-42 | Sponsor Protocol Number: ET16-132 | Start Date*: 2018-02-14 | |||||||||||
Sponsor Name:Centre Léon Bérard | |||||||||||||
Full Title: A European, multicenter, randomized, open-label, Phase II trial aiming to assess the clinical and biological activity of an anti-PD-L1 (atezolizumab) in operable localized soft tissue sarcomas pati... | |||||||||||||
Medical condition: localised and operable soft tissue sarcomas | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005325-12 | Sponsor Protocol Number: CFZ014 | Start Date*: 2015-08-10 | |||||||||||
Sponsor Name:Onyx Therapeutics, Inc. | |||||||||||||
Full Title: A Randomized, Open-label, Phase 3 Study in Subjects with Relapsed and Refractory Multiple Myeloma Receiving Carfilzomib in Combination with Dexamethasone, Comparing Once-weekly versus Twice-weekly ... | |||||||||||||
Medical condition: Multiple Myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) IT (Completed) HU (Completed) BE (Completed) DK (Completed) ES (Completed) PL (Completed) GR (Completed) SE (Completed) FI (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000941-10 | Sponsor Protocol Number: CLI24-001 | Start Date*: 2020-07-02 |
Sponsor Name:Menarini Ricerche S.p.A | ||
Full Title: A Phase I/II Study of SEL24 in Patients with Acute Myeloid Leukemia | ||
Medical condition: Acute Myeloid Leukemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PL (Completed) ES (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-003947-27 | Sponsor Protocol Number: TAK-981-1002 | Start Date*: 2021-07-04 | |||||||||||
Sponsor Name:Takeda Development Center Americas, Inc. | |||||||||||||
Full Title: An Open Label, Dose-Escalation, Phase 1/2 Study to Evaluate the Safety, Tolerability, Preliminary Efficacy, and Pharmacokinetics of TAK-981 in Adult Patients With Advanced or Metastatic Solid Tumor... | |||||||||||||
Medical condition: Advanced or Metastatic Solid Tumors or Relapsed/Refractory Hematologic Malignancies | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) ES (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005008-32 | Sponsor Protocol Number: ICORG13-17 | Start Date*: 2014-07-16 |
Sponsor Name:Cancer Trials Ireland | ||
Full Title: A phase II Study of the Efficacy and Safety of lenalidomide, subcutaneous bortezomib, and dexamethasone combination therapy for patients with newly diagnosed multiple myeloma | ||
Medical condition: Newly diagnosed multiple myeloma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001933-16 | Sponsor Protocol Number: 26866138PCR2002 | Start Date*: 2007-03-13 |
Sponsor Name:Christos N. Papandreou | ||
Full Title: "A Phase II, Open-Label study of Velcade(Bortezomib)for patients with Androgen-Independent Prostate Carcinoma who progressed on or after prior chemotherapy" | ||
Medical condition: Treatment of patients with Androgen-Independent Prostate Carcinoma who progressed on or after prior chemotherapy. | ||
Disease: | ||
Population Age: | Gender: Male | |
Trial protocol: GR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-004418-32 | Sponsor Protocol Number: U31402-A-U202 | Start Date*: 2020-10-30 | |||||||||||
Sponsor Name:DAIICHI SANKYO, INC | |||||||||||||
Full Title: A MULTI-CENTER, OPEN-LABEL, PHASE 2 STUDY TO EVALUATE SAFETY AND EFFICACY OF U3-1402 IN SUBJECTS WITH ADVANCED OR METASTATIC COLORECTAL CANCER (CRC) | |||||||||||||
Medical condition: Advanced or metastatic colorectal cancer (CRC) which is resistant, refractory, or intolerant to at least 2 prior lines of therapy, that must include all of the following agents: fluoropyrimidine, i... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) PL (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000820-20 | Sponsor Protocol Number: NVG111-101 | Start Date*: 2020-10-30 | ||||||||||||||||
Sponsor Name:NovalGen Ltd | ||||||||||||||||||
Full Title: AN OPEN-LABEL, PHASE 1/2, FIRST IN HUMAN STUDY INVESTIGATING THE SAFETY, TOLERABILITY, PHARMACOKINETICS AND EFFICACY OF NVG-111 IN SUBJECTS WITH RELAPSED/REFRACTORY CHRONIC LYMPHOCYTIC LEUKAEMIA ... | ||||||||||||||||||
Medical condition: RELAPSED/REFRACTORY CHRONIC LYMPHOCYTIC LEUKAEMIA AND MANTLE CELL LYMPHOMA | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003684-35 | Sponsor Protocol Number: R2810-ONC-1763 | Start Date*: 2018-07-10 | |||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Open-Label Study of Combinations of Standard and High Dose REGN2810 (Cemiplimab; Anti-PD-1 Antibody) and Ipilimumab (Anti-CTLA-4 Antibody) in the Second-Line Treatment of Patients wit... | |||||||||||||
Medical condition: Non-Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) GB (GB - no longer in EU/EEA) FR (Completed) PL (Completed) ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001698-89 | Sponsor Protocol Number: Monet | Start Date*: 2006-06-08 |
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust | ||
Full Title: Molecular profiling of postmenopausal women with breast cancer on neoadjuvant exemestane or tamoxifen | ||
Medical condition: Early or locally advanced breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-003743-30 | Sponsor Protocol Number: BEVPAC | Start Date*: 2012-11-20 |
Sponsor Name:Karolinska University Hospital | ||
Full Title: A prospective randomized Phase II study to identify predictive biomarkers and mechanisms of therapy resistance in patients with HER2-negative metastatic breast cancer (MBC) treated with the combina... | ||
Medical condition: Advanced breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000661-19 | Sponsor Protocol Number: CFEM345EGB07 | Start Date*: 2005-11-04 |
Sponsor Name:Novartis Pharmaceuticals UK Ltd | ||
Full Title: Neoadjuvant hormone therapy for postmenopausal women with ER and/or PgR positive primary breast cancer: A multi-center study to determine the optimum length of treatment with Femara (letrozole 2.5m... | ||
Medical condition: Postmenopausal women with ER and/or PgR positive primary breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2008-000524-82 | Sponsor Protocol Number: RMH CCR No 3107 | Start Date*: 2008-10-09 | |||||||||||
Sponsor Name:Royal Marsden Hospital | |||||||||||||
Full Title: MESH: A Non-Randomised Phase II Trial of Methotrexate in Metastatic Colorectal Cancer with MSH2 Deficiency | |||||||||||||
Medical condition: Metastatic colorectal cancer resistanct to standard chemotherapy with evidence of deficiency of the mismatch repair gene MSH2, either on immunohistochemistry of tumour histology or on testing of pe... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000306-70 | Sponsor Protocol Number: 2009/07 | Start Date*: 2008-01-29 | |||||||||||
Sponsor Name:University of Dundee | |||||||||||||
Full Title: The effect of metformin on biomarker activity in primary breast cancer | |||||||||||||
Medical condition: Women with histologically proven operable primary, invasive breast cancer of ≥ 1cm in size. The study will involve women from the east of Scotland. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005018-47 | Sponsor Protocol Number: 008-IRCC-10IIS-14 | Start Date*: 2015-04-08 | |||||||||||
Sponsor Name:FONDAZIONE DEL PIEMONTE PER L'ONCOLOGIA IRCCS | |||||||||||||
Full Title: A PHASE II, RANDOMIZED, MULTICENTER STUDY TO ASSESS THE EFFICACY OF NAB-PACLITAXEL-BASED DOUBLET AS FIRST LINE THERAPY IN PATIENTS WITH CANCER OF UNKNOWN PRIMARY (CUP): the AGNOSTOS trial | |||||||||||||
Medical condition: Cancers of Unknown Primary (CUP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003483-32 | Sponsor Protocol Number: FILO | Start Date*: 2019-04-25 |
Sponsor Name:FILO | ||
Full Title: BLINAtumomab after R-CHOP debulking therapy for patients with Richter Transformation. | ||
Medical condition: Richter transformation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-003328-22 | Sponsor Protocol Number: 56022473MDS2002 | Start Date*: 2017-02-13 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 2 Proof-of-Concept Study to Separately Evaluate the Activity of Talacotuzumab (JNJ-56022473) or Daratumumab in Transfusion-Dependent Subjects with Low or Intermediate-1 Risk Myelodysplast... | |||||||||||||
Medical condition: Transfusion-Dependent Subjects with Low or Intermediate-1 Risk Myelodysplastic Syndromes (MDS) who are Relapsed or Refractory to Erythropoiesis-Stimulating Agent (ESA) Treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) NL (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004985-27 | Sponsor Protocol Number: HO139 | Start Date*: 2016-09-29 | |||||||||||
Sponsor Name:HOVON Foundation | |||||||||||||
Full Title: A prospective, open-label, multicenter randomized phase-II trial to evaluate the efficacy and safety of a sequential regimen of obinutuzumab (Gazyvaro) followed by obinutuzumab and venetoclax, foll... | |||||||||||||
Medical condition: Chronic Lymphocytic Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014445-80 | Sponsor Protocol Number: CP4055-306 | Start Date*: 2010-06-23 | |||||||||||
Sponsor Name:Clavis Pharma | |||||||||||||
Full Title: A Randomised Phase III Study of Elacytarabine vs. Investigator’s Choice in Patients with Late Stage Acute Myeloid Leukaemia | |||||||||||||
Medical condition: Late Stage Acute Myeloid Leukaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) DE (Completed) ES (Ongoing) BE (Completed) PL (Completed) IT (Ongoing) GB (Completed) IE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000033-36 | Sponsor Protocol Number: LYMRIT-37-01 | Start Date*: 2012-10-18 | |||||||||||
Sponsor Name:Nordic Nanovector ASA | |||||||||||||
Full Title: A phase I/II study of lutetium (177Lu)-lilotomab satetraxetan (Betalutin®) antibody-radionuclide-conjugate for treatment of relapsed non-Hodgkin lymphoma. | |||||||||||||
Medical condition: Non-Hodgkin B-cell lymphoma Part A: Relapsed indolent Non-Hodgkin B-cell lymphoma Part B: Relapsed follicular lymphoma Part C: Relapsed indolent Non-Hodgkin B-cell lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) GB (GB - no longer in EU/EEA) IT (Prematurely Ended) CZ (Prematurely Ended) AT (Completed) FR (Prematurely Ended) ES (Prematurely Ended) HR (Completed) HU (Completed) IE (Completed) DK (Prematurely Ended) FI (Completed) DE (Completed) NL (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
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