- Trials with a EudraCT protocol (171)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
171 result(s) found for: Biological target.
Displaying page 4 of 9.
| EudraCT Number: 2016-005129-35 | Sponsor Protocol Number: FENET-2016 | Start Date*: 2018-02-22 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERO UNIVERSITARIA DI FERRARA | |||||||||||||
| Full Title: "Peptide Receptor Radionuclide Therapy (PRRT) with somatostatin analogs in tumors over-expressing somatostatin receptors" | |||||||||||||
| Medical condition: Tumors over-expressing somatostatin receptors | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-004201-33 | Sponsor Protocol Number: IMMU-132-09 | Start Date*: 2019-08-16 | |||||||||||||||||||||
| Sponsor Name:Immunomedics, Inc. | |||||||||||||||||||||||
| Full Title: Phase 3 Study of Sacituzumab Govitecan (IMMU-132) Versus Treatment of Physician's Choice (TPC) in subjects with Hormonal Receptor-Positive (HR+) Human Epidermal Growth Factor Receptor 2 (HER2) Nega... | |||||||||||||||||||||||
| Medical condition: Hormonal Receptor-Positive (HR+) Human Epidermal Growth Factor Receptor 2 (HER2) Negative Metastatic Breast Cancer (MBC) | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) DE (Completed) NL (Completed) ES (Ongoing) BE (Completed) IT (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2016-002817-22 | Sponsor Protocol Number: AAG-G-H-1624 | Start Date*: 2017-02-09 | |||||||||||||||||||||||||||||||
| Sponsor Name:TETEC Tissue Engineering Technologies - AG | |||||||||||||||||||||||||||||||||
| Full Title: Prospective, Multicenter, Single-arm Phase III Clinical Trial to Evaluate the Efficacy and Safety of NOVOCART® Inject plus in the Treatment of Cartilage Defects of the Knee | |||||||||||||||||||||||||||||||||
| Medical condition: Repair of cartilage defects of the knee (medial or lateral femoral condyle or tibial plateau, trochlea or patella) caused by traumatic events or osteochondritis dissecans (defect size is ≥ 4 and ≤... | |||||||||||||||||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: HU (Completed) CZ (Completed) DE (Completed) PL (Completed) LT (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2005-002241-39 | Sponsor Protocol Number: BO 18192 | Start Date*: 2005-11-09 |
| Sponsor Name:F. Hoffmann-La Roche Ltd | ||
| Full Title: A multicentre, double-blind randomised, phase III study to evaluate the efficacy of Tarceva or placebo following 4 cycles of platinum-based chemotherapy in patients with histologically documented a... | ||
| Medical condition: Advanced (stage IIIB or IV) NSCLC previously treated with 4 cycles of a platinum-based chemotherapy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: HU (Completed) ES (Completed) SI (Completed) GB (Completed) AT (Completed) LT (Completed) SK (Completed) PT (Prematurely Ended) DE (Completed) DK (Completed) CZ (Completed) IT (Completed) GR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-000120-33 | Sponsor Protocol Number: C-550-01 | Start Date*: 2018-11-19 | |||||||||||||||||||||
| Sponsor Name:Agenus Inc., | |||||||||||||||||||||||
| Full Title: A Phase 1/2, Open-Label, Multi-Arm Trial to Investigate the Safety, Tolerability, Pharmacokinetics, Biological, and Clinical Activity of AGEN1884 in Combination with AGEN2034 in Subjects with Metas... | |||||||||||||||||||||||
| Medical condition: Phase 1 – Part A dose escalation in patients with locally advanced, recurrent and/or metastatic solid tumor for which no standard therapy exists or standard therapy has failed. Phase 2 - Part B adv... | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
| Trial protocol: HU (Completed) PL (Completed) ES (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2012-005036-28 | Sponsor Protocol Number: 2012/41 | Start Date*: 2013-04-12 | |||||||||||
| Sponsor Name:CENTRE ANTOINE LACASSAGNE | |||||||||||||
| Full Title: Pharmacogenetic study in castration-resistant prostate cancer patients treated with abiraterone acetate | |||||||||||||
| Medical condition: Prostate cancer metastatic | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-004057-71 | Sponsor Protocol Number: BC-P2-2020 | Start Date*: 2021-01-12 | |||||||||||
| Sponsor Name:FONDAZIONE DEL PIEMONTE PER L'ONCOLOGIA IRCCS | |||||||||||||
| Full Title: miRNA100 as predictor of response to anti-endocrine treatment in luminal-HER2 negative breast cancer. a prospective validation clinical trial | |||||||||||||
| Medical condition: HER2 NEGATIVE/LUMINAL BREAST CANCER | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-001837-10 | Sponsor Protocol Number: PRODIGE25 | Start Date*: 2016-09-27 | |||||||||||
| Sponsor Name:Fédération Francophone de Cancérologie Digestive | |||||||||||||
| Full Title: PHASE II RANDOMIZED TRIAL EVALUATING AFLIBERCEPT ASSOCIATED WITH SCHEME LV5FU2 AS FIRST LINE TREATMENT OF NON-RESECTABLE METASTATIC COLORECTAL CANCERS | |||||||||||||
| Medical condition: first line of treatment for metastatic colorectal cancer | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-004904-35 | Sponsor Protocol Number: Protocol2-55-52030-726 | Start Date*: 2006-08-14 | |||||||||||
| Sponsor Name:IPSEN PHARMA S.A.S. | |||||||||||||
| Full Title: Phase III, randomised, double-blind, stratified comparative, placebo controlled, parallel group, multicentre study to assess the effect of deep subcutaneous injections of lanreotide Autogel 120 mg ... | |||||||||||||
| Medical condition: Non functioning entero-pancreatic tumours | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) NL (Completed) BE (Completed) DK (Completed) CZ (Completed) GR (Completed) SE (Completed) DE (Completed) AT (Completed) IT (Completed) SK (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-001988-52 | Sponsor Protocol Number: 90101 | Start Date*: 2012-07-30 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:EORTC | ||||||||||||||||||||||||||||||||||||||
| Full Title: Cross-tumoral Phase 2 clinical trial exploring Crizotinib (PF-02341066) in patients with advanced tumours induced by causal alterations of either ALK or MET. | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Locally advanced and/or metastatic malignant tumor (anaplastic large cell lymphoma, inflammatory myofibroblastic tumor, papillary renal cell carcinoma type 1, alveolar soft part sarcoma, clear cell... | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: BE (Completed) DE (Completed) GB (GB - no longer in EU/EEA) AT (Completed) NL (Completed) FR (Completed) NO (Completed) SI (Prematurely Ended) IT (Completed) PL (Completed) DK (Prematurely Ended) SK (Completed) | ||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2013-002777-22 | Sponsor Protocol Number: HG/1096 | Start Date*: 2013-11-14 | |||||||||||
| Sponsor Name:University of Leeds, Division of Musculoskeletal Disease, Leeds Institute of Molecular Medicine | |||||||||||||
| Full Title: Targeted Ultrasound in Rheumatoid Arthritis (TURA) | |||||||||||||
| Medical condition: Rheumatoid Arthritis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) DE (Prematurely Ended) HU (Prematurely Ended) ES (Prematurely Ended) IT (Completed) DK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-004116-32 | Sponsor Protocol Number: Protocol WIL1-0609 | Start Date*: 2008-12-03 | |||||||||||
| Sponsor Name:LFB BIOTECHNOLOGIES | |||||||||||||
| Full Title: EFFICACY AND SAFETY STUDY OF WILFACTIN ADMINISTERED BY CONTINUOUS INFUSION IN PATIENTS WITH SEVERE VON WILLEBRAND DISEASE UNDERGOING MAJOR SURGICAL PROCEDURES | |||||||||||||
| Medical condition: Severe von Willebrand disease patients undergoing elective major surgery | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) BE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-001574-28 | Sponsor Protocol Number: AT13387-04 | Start Date*: 2012-10-09 | |||||||||||
| Sponsor Name:Astex Pharmaceuticals Inc | |||||||||||||
| Full Title: A Phase 2 Study of Hsp90 Inhibitor AT13387 Alone or in Combination with Abiraterone Acetate in the Treatment of Castration-Resistant Prostate Cancer (CRPC) no Longer Responding to Abiraterone | |||||||||||||
| Medical condition: Castration-Resistant Prostate Cancer (CRPC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: GB (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-003063-21 | Sponsor Protocol Number: HLX10-005-SCLC301 | Start Date*: 2020-06-17 | |||||||||||
| Sponsor Name:Shanghai Henlius Biotech, Inc. | |||||||||||||
| Full Title: A Randomized, Double-Blind, Multicenter, Phase III Study to Compare Clinical Efficacy and Safety of HLX10 (Recombinant Humanized Anti-PD-1 Monoclonal Antibody Injection) in Combination with Chemoth... | |||||||||||||
| Medical condition: Extensive Stage Small Cell Lung Cancer (ES-SCLC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) BG (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002167-23 | Sponsor Protocol Number: IPC_2011-001 | Start Date*: 2013-06-12 | |||||||||||
| Sponsor Name:Institut Paoli-Calmettes | |||||||||||||
| Full Title: A phase Ib/II open-label study evaluating safety and efficacy of oral BKM120 in combination with lapatinib in HER2+/PI3K-activated, trastuzumab-resistant locally advanced, recurrent and metastatic ... | |||||||||||||
| Medical condition: locally advanced, recurrent and metastatic breast cancer. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-002540-67 | Sponsor Protocol Number: 2019-06 | Start Date*: 2022-04-08 | |||||||||||
| Sponsor Name:Centre Oscar Lambret | |||||||||||||
| Full Title: Phase 2 trial evaluating metronomic chemotherapy in patients with relapsed or refractory Wilms tumor | |||||||||||||
| Medical condition: Wilms tumor | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-001931-27 | Sponsor Protocol Number: STARS-trial | Start Date*: 2019-02-28 | |||||||||||
| Sponsor Name:IRCCS Istituto Giannina Gaslini | |||||||||||||
| Full Title: Comparison of STep-up and step-down therapeutic strategies in childhood ARthritiS | |||||||||||||
| Medical condition: Juvenile idiopathic arthritis (JIA) is an umbrella term that encompasses a heterogeneous group of disorders characterised by prolonged synovial inflammation that may cause destructive damage to joi... | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-005968-90 | Sponsor Protocol Number: TORCH | Start Date*: 2007-02-26 | |||||||||||
| Sponsor Name:ISTITUTO NAZIONALE PER LO STUDIO E LA CURA DEI TUMORI - FONDAZIONE G. PASCALE | |||||||||||||
| Full Title: An international multicenter randomized phase III study of first-line Erlotinib followed by second-line Cisplatin Gemcitabine versus first-line Cisplatin Gemcitabine followed by second-line Er... | |||||||||||||
| Medical condition: advanced non small cell lung cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-000424-10 | Sponsor Protocol Number: UC-0130/1703 | Start Date*: 2017-06-16 |
| Sponsor Name:UNICANCER | ||
| Full Title: A Safety study of Nivolumab in Patients with Recurrent and/or Metastatic Platinum-refractory Squamous Cell Carcinoma of the Head and Neck (SCCHN). | ||
| Medical condition: Patients with recurrent and/or metastatic platinum refractory Squamous Cell Carcinoma of the Head and Neck (SCCHN), with poor prognosis and no effective chemotherapy options. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-000394-23 | Sponsor Protocol Number: SOLTI-1007 | Start Date*: 2012-08-06 |
| Sponsor Name:SOLTI | ||
| Full Title: A Phase II, open-label, single-arm, exploratory pharmacogenomic study of single agent eribulin (HALAVEN®) as neoadjuvant treatment for operable Stage I-II HER2 non-overexpressing breast cancer | ||
| Medical condition: Patients at Stage I-II HER2-negative breast cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) DE (Completed) PT (Completed) | ||
| Trial results: (No results available) | ||
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