- Trials with a EudraCT protocol (328)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
328 result(s) found for: Single cell protein.
Displaying page 1 of 17.
EudraCT Number: 2009-012136-33 | Sponsor Protocol Number: IPH2101-201 | Start Date*: 2009-07-08 | |||||||||||
Sponsor Name:Innate Pharma | |||||||||||||
Full Title: Open randomised phase II study evaluating the anti-tumour activity, safety and pharmacology of two different dose regimens of IPH 2101, a human monoclonal anti-KIR antibody, in patients with multip... | |||||||||||||
Medical condition: Multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003214-13 | Sponsor Protocol Number: I4X-MC-JFCL | Start Date*: 2013-07-19 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Randomized, Multicenter, Open-Label, Phase 2 Study of Paclitaxel-Carboplatin Chemotherapy Plus Necitumumab (IMC-11F8) Versus Paclitaxel-Carboplatin Chemotherapy Alone in the First-Line Treatme... | |||||||||||||
Medical condition: Stage IV Squamous Non-Small Cell Lung Cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001510-10 | Sponsor Protocol Number: 109661 | Start Date*: 2015-06-17 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase III, single group, open study to assess the immunogenicity, safety and reactogenicity of GlaxoSmithKline (GSK) Biologicals’ 10-valent pneumococcal conjugate vaccine in Mexico when co-admini... | ||
Medical condition: Healthy volunteers (Three dose primary vaccination against Streptococcus pneumoniae, diphtheria, tetanus, pertussis, hepatitis B, polio, Haemophilus influenzae type b diseases and a two dose primar... | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2006-005905-79 | Sponsor Protocol Number: OSI-774-203 | Start Date*: 2007-03-13 | |||||||||||
Sponsor Name:OSI Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2 Randomized Study of Tarceva® (erlotinib) as a Single Agent or Intercalated with Combination Chemotherapy in Patients with Newly Diagnosed Advanced Non-Small Cell Lung Cancer who have Tumo... | |||||||||||||
Medical condition: Non-small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001052-39 | Sponsor Protocol Number: ARRAY-520-311 | Start Date*: 2014-11-02 | |||||||||||
Sponsor Name:Array BioPharma Inc. | |||||||||||||
Full Title: The FACTOR Study (Filanesib and Carfilzomib Treatment of Relapsed/Refractory Multiple Myeloma): A Multinational, Randomized, Open-label Phase 3 Study of Filanesib (ARRY-520) + Carfilzomib Versus ... | |||||||||||||
Medical condition: Multiple Myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) AT (Completed) DE (Completed) CZ (Completed) GB (Completed) HU (Completed) ES (Completed) BE (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000665-36 | Sponsor Protocol Number: 20180015 | Start Date*: 2019-06-12 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Randomized, Open-label, Phase 3 Study Comparing Once-weekly vs Twice-weekly Carfilzomib in Combination with Lenalidomide and Dexamethasone in Subjects With Relapsed or Refractory Multiple Myeloma... | |||||||||||||
Medical condition: Relapsed or Refractory Multiple Myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) NL (Completed) ES (Ongoing) CZ (Completed) FR (Completed) BG (Completed) SK (Completed) FI (Completed) LT (Completed) AT (Completed) RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005229-95 | Sponsor Protocol Number: PBKR03-001 | Start Date*: 2021-08-23 | |||||||||||
Sponsor Name:Passage Bio, Inc. | |||||||||||||
Full Title: A Phase 1/2 Open-Label, Multicenter, Dose Ranging and Confirmatory Study to Assess the Safety, Tolerability and Efficacy of PBKR03 Administered to Pediatric Subjects with Early Infantile Krabbe Dis... | |||||||||||||
Medical condition: Krabbe disease (globoid cell leukodystrophy) is an autosomal recessive lysosomal storage disease (LSD) caused by mutations in the gene encoding the hydrolytic enzyme galactosylceramidase (galactoce... | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004018-33 | Sponsor Protocol Number: PH-F16IL2TAXO-03/12 | Start Date*: 2013-05-22 | |||||||||||
Sponsor Name:Philogen S.p.A. | |||||||||||||
Full Title: A Phase II study of the tumour-targeting human F16IL2 monoclonal antibody-cytokine fusion protein in combination with paclitaxel versus paclitaxel alone in patients with Merkel cell carcinoma. | |||||||||||||
Medical condition: Merkel cell carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) AT (Prematurely Ended) ES (Prematurely Ended) DK (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022029-13 | Sponsor Protocol Number: CBHQ880A2204 | Start Date*: 2011-08-11 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A single-arm, open-label, phase 2 clinical trial evaluating disease response following treatment with intravenous BHQ880, a fully human, anti-Dickkopf1 (DKK1) neutralizing antibody in previously un... | |||||||||||||
Medical condition: Adults diagnosed with high-risk Smoldering Multiple Myeloma (SMM) and who have not received any previous antimyeloma treatment. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001990-22 | Sponsor Protocol Number: 54767414LEU2002 | Start Date*: 2021-08-09 | |||||||||||
Sponsor Name:Hellenic Society of Haematology (HSH) | |||||||||||||
Full Title: An Investigator-Initiated, Phase II, Multicenter, Open-Label, Single-Arm, Prospective Clinical Trial to Evaluate the Efficacy and Safety of Alternating Bortezomib-Based Regimens in Combination with... | |||||||||||||
Medical condition: Primary plasma cell leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013787-39 | Sponsor Protocol Number: I2I-MC-JMMD | Start Date*: 2009-09-07 | ||||||||||||||||
Sponsor Name:Eli Lilly and company | ||||||||||||||||||
Full Title: A Phase 2 Study to Evaluate LY2603618 in Combination with Pemetrexed in Patients with Advanced or Metastatic Non-small Cell Lung Cancer | ||||||||||||||||||
Medical condition: Advanced or metastatic non-squamous second-line Non-small cell lung cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-001904-36 | Sponsor Protocol Number: C0328T06 | Start Date*: 2006-09-07 | |||||||||||
Sponsor Name:Centocor B.V. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-blind, Placebo-controlled Study Comparing the Combination of CNTO 328 (Anti-IL-6 Monoclonal Antibody) and Velcade® versus Velcade alone in Subjects with Relapsed or Re... | |||||||||||||
Medical condition: relapsed or refractory multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) BE (Completed) FR (Completed) GB (Completed) CZ (Completed) PT (Completed) DE (Completed) GR (Completed) BG (Completed) SK (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006359-11 | Sponsor Protocol Number: BO20571 | Start Date*: 2007-09-14 | ||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche | ||||||||||||||||||
Full Title: A Phase II study of Tarceva® in Combination with Avastin® versus chemotherapy plus Avastin® in 1st line advanced NSCLC patients | ||||||||||||||||||
Medical condition: Advanced Non-Small-Cell-Lung-Cancer (Stage IIIb and IV) 1st line | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) FR (Completed) GB (Completed) NL (Completed) ES (Completed) LT (Completed) PL (Completed) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-007802-12 | Sponsor Protocol Number: 3129K5-2005-WW | Start Date*: 2009-07-23 | |||||||||||
Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc., A Pfizer Company | |||||||||||||
Full Title: An Open-label, Single-Arm, Phase 2 Study of Inotuzumab Ozogamicin Plus Rituximab in Subjects With Relapsed/Refractory CD22-Positive Diffuse Large B-Cell Lymphoma, Eligible for Autologous Stem Cell ... | |||||||||||||
Medical condition: Diffuse large B-cell Non-Hodgkin's lymphoma (DLBCL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000830-68 | Sponsor Protocol Number: BO39813 | Start Date*: 2018-03-19 | |||||||||||
Sponsor Name:F. Hoffman-La Roche Ltd. | |||||||||||||
Full Title: A PHASE IB/II STUDY OF COBIMETINIB ADMINISTERED AS SINGLE AGENT AND IN COMBINATION WITH VENETOCLAX, WITH OR WITHOUT ATEZOLIZUMAB, IN PATIENTS WITH RELAPSED AND REFRACTORY MULTIPLE MYELOMA | |||||||||||||
Medical condition: Multiple Myeloma (MM) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DK (Completed) SE (Completed) DE (Completed) CZ (Completed) ES (Completed) FR (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003715-38 | Sponsor Protocol Number: D4190C00006 | Start Date*: 2016-05-12 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:MedImmune LLC | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 1b Open-label Study to Evaluate the Safety and Tolerability of MEDI4736 in Combination with Tremelimumab in Subjects with Advanced Non-small Cell Lung Cancer | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Locally advanced or metastatic squamous or nonsquamous non- small cell lung cancer (NSCLC) | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) ES (Completed) DE (Completed) GB (Completed) FR (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-003829-16 | Sponsor Protocol Number: RV-MM-DSMM-0279 | Start Date*: 2009-09-15 | |||||||||||
Sponsor Name:GMIHO - Gesellschaft für medizinische Innovation Hämatologie und Onkologie mbH | |||||||||||||
Full Title: An open, randomized clinical phase I/II trial to investigate maximum tolerated dose, efficacy, and safety of lenalidomide/low-dose dexamethasone in combination with continuous oral cyclophosphamide... | |||||||||||||
Medical condition: relapsed multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-004151-16 | Sponsor Protocol Number: 209628 | Start Date*: 2021-11-22 | |||||||||||
Sponsor Name:GlaxoSmithKline, S.A. | |||||||||||||
Full Title: A Phase 2, Randomized, Parallel, Open-Label Study to Investigate the Safety, Efficacy, and Pharmacokinetics of Various Dosing Regimens of Single-Agent Belantamab Mafodotin (GSK2857916) in Participa... | |||||||||||||
Medical condition: Multiple myeloma = cancer of blood cells in the bone marrow | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) FR (Trial now transitioned) DE (Trial now transitioned) PL (Trial now transitioned) IT (Trial now transitioned) IE (Trial now transitioned) GR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002667-13 | Sponsor Protocol Number: PREST | Start Date*: 2008-09-15 | |||||||||||
Sponsor Name:University Clinic of Heidelberg | |||||||||||||
Full Title: A single-center controlled pilot study to investigate pre- and perioperative therapy with Sorafenib (Nexavar®) in patients who are candidates for a curative surgery of renal cell cancer (PREST = pr... | |||||||||||||
Medical condition: non metastatic renal tumors (RCC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005425-30 | Sponsor Protocol Number: AURA-6202-011 | Start Date*: 2008-04-17 | |||||||||||
Sponsor Name:Nerviano Medical Sciences S.r.l. | |||||||||||||
Full Title: An Exploratory Phase II Study of PHA-739358 in Patients with Multiple Myeloma Harbouring the t (4;14) translocation with or without FGFR3 Expression | |||||||||||||
Medical condition: Multiple Myeloma Harbouring the t (4;14) translocation with or without FGFR3 Expression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
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