- Trials with a EudraCT protocol (294)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
294 result(s) found for: In situ hybridization.
Displaying page 7 of 15.
| EudraCT Number: 2019-002291-13 | Sponsor Protocol Number: KTE-C19-112 | Start Date*: 2020-02-07 | |||||||||||
| Sponsor Name:Kite Pharma, Inc | |||||||||||||
| Full Title: A Phase 2 Multicenter Study Evaluating the Efficacy and Safety of Axicabtagene Ciloleucel as First-Line Therapy in Subjects with High-Risk Large B-Cell Lymphoma (ZUMA-12) | |||||||||||||
| Medical condition: Adult subjects with high-risk large B-cell lymphoma, including either high-grade B-cell lymphoma (HGBL) with MYC and BCL2 and/or BCL6 translocations (double-hit or triple-hit lymphomas) or Internat... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000626-60 | Sponsor Protocol Number: UC-0130/1804 | Start Date*: 2019-01-08 |
| Sponsor Name:UNICANCER | ||
| Full Title: A multicenter, randomized, open label, phase II study evaluating the feasibility and tolerance of nivolumab neoadjuvant immunotherapy in high risk HPV driven Oropharynx Cancer. | ||
| Medical condition: High risk Human Papilloma Virus (HPV)-driven oropharynx cancer patients | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-003440-92 | Sponsor Protocol Number: INFINITY | Start Date*: 2020-12-22 | ||||||||||||||||
| Sponsor Name:G.O.N.O. - GRUPPO ONCOLOGICO DEL NORD OVEST | ||||||||||||||||||
| Full Title: TremelImumab aNd durvalumab combination For the non-operatIve management (NOM) of Microsatellite InstabiliTY (MSI)-high resectable gastric or gastroesophageal junction cancer: The multicentre, sing... | ||||||||||||||||||
| Medical condition: The disease under clinical investigation is represented by resectable gastric or gastroesophageal junction (Siewert II-III) adenocarcinoma staged as cT = 2, any cN, or any cT, cN1-3 (TNM classifica... | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2022-001780-27 | Sponsor Protocol Number: HTA-HG5-04 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Holostem Terapie Avanzate s.r.l. | |||||||||||||
| Full Title: OPEN-LABEL, UNCONTROLLED, CLINICAL TRIAL TO EVALUATE THE SAFETY AND EFFICACY OF AUTOLOGOUS FIBRIN-CULTURED EPIDERMAL GRAFTS CONTAINING EPIDERMAL STEM CELLS GENETICALLY MODIFIED FOR RESTORATION OF E... | |||||||||||||
| Medical condition: Inherited Epidermolysis Bullosa (EB) is a group of rare, devastating genetic disorders characterized by structural and mechanical fragility of skin and mucosal membranes, impairing the patient’s qu... | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-002493-13 | Sponsor Protocol Number: M16BRC | Start Date*: 2016-09-15 | |||||||||||
| Sponsor Name:NKI-AVL | |||||||||||||
| Full Title: Substantially improving the cure rate of high-risk BRCA1-like breast cancer patients with personalized therapy | |||||||||||||
| Medical condition: High risk breast cancer (stage III), BRCA1-like | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-001969-49 | Sponsor Protocol Number: N15TON | Start Date*: 2015-09-03 | |||||||||||
| Sponsor Name:NKI-AvL | |||||||||||||
| Full Title: Adaptive phase II randomized non-comparative trial of nivolumab after induction treatment in triple-negative breast cancer (TNBC) patients: TONIC-trial | |||||||||||||
| Medical condition: Triple negative breast cancer (TNBC) patients with metastatic disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-001027-40 | Sponsor Protocol Number: ERIBRAIN-IPC2017-014 | Start Date*: 2018-09-11 | |||||||||||
| Sponsor Name:Institut Paoli-Calmettes | |||||||||||||
| Full Title: ERIBRAIN - A phase II study of Eribulin in brain metastases from HER2-negative breast cancer pre-treated with anthracyclines and taxanes | |||||||||||||
| Medical condition: HER2-negative breast cancer with brain metastases | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-005712-62 | Sponsor Protocol Number: CO43613 | Start Date*: 2022-06-17 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: A PHASE Ib/II, OPEN-LABEL, MULTICENTER, RANDOMIZED UMBRELLA STUDY EVALUATING THE EFFICACY AND SAFETY OF MULTIPLE TREATMENT COMBINATIONS IN PATIENTS WITH LOCALLY ADVANCED SQUAMOUS CELL CARCINOMA OF... | |||||||||||||
| Medical condition: Squamous cell carcinoma of the head and neck | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-003151-34 | Sponsor Protocol Number: ET17-093 | Start Date*: 2019-01-15 | |||||||||||
| Sponsor Name:Centre Léon Bérard | |||||||||||||
| Full Title: A multicenter, randomised, open-label Phase II study to evaluate the clinical benefit of a post-operative treatment associating radiotherapy + Nivolumab + Ipilimumab versus radiotherapy + Capecitab... | |||||||||||||
| Medical condition: Triple negative breast cancer patients with residual disease after neoadjuvant chemotherapy | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-002164-13 | Sponsor Protocol Number: UZBRU_VHH1_3 | Start Date*: 2017-01-05 |
| Sponsor Name:UZ Brussel | ||
| Full Title: Quantification of 68GaNOTA-Anti-HER2 VHH1 Uptake in metastasis of Breast carcinoma and cancer patients and Assessment of Repeatability – Pilot study | ||
| Medical condition: Breast cancer; salivary gland cancer; adenocarcinoma of the gastric body or gastro-esophageal junction; endometrial cancer; cancer of cervix uteri; Non-small cell lung cancer; biliary tract cancer;... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-005178-43 | Sponsor Protocol Number: OMB115991 | Start Date*: 2012-02-08 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
| Full Title: A Phase II, Multi-centre Study Investigating the Safety and Efficacy of Ofatumumab and Bendamustine Combination in Patients with Untreated or Relapsed Chronic Lymphocytic Leukaemia (CLL) | |||||||||||||
| Medical condition: Untreated or Relapsed Chronic Lymphocytic Leukaemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) DE (Prematurely Ended) BE (Completed) ES (Completed) PL (Completed) GR (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004865-28 | Sponsor Protocol Number: CLAG525B2101 | Start Date*: 2018-12-05 | |||||||||||
| Sponsor Name:Novartis Pharma AG | |||||||||||||
| Full Title: A phase II open-label, randomized, three-arm, multicenter study of LAG525 given in combination with spartalizumab (PDR001), or with spartalizumab and carboplatin, or with carboplatin, as first or s... | |||||||||||||
| Medical condition: triple negative breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) FR (Completed) DE (Completed) HU (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-003220-52 | Sponsor Protocol Number: CC-486-BRSTM-001 | Start Date*: 2015-03-21 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Celgene Corporation | ||||||||||||||||||||||||||||||||||||||
| Full Title: A Phase 2, Randomized, Open-Label, Two-arm Study to Assess the Efficacy and Safety of the Epigenetic Modifying Effects of CC-486 (Oral Azacitidine) in Combination With Fulvestrant in Postmenopausal... | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Postmenopausal female subjects with estrogen receptor positive (ER+), human epidermal growth factor receptor 2 negative (HER2-) metastatic breast cancer, who have progressed on an aromatase inhibi... | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: BE (Completed) ES (Completed) DE (Completed) FR (Completed) IT (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2006-000564-81 | Sponsor Protocol Number: EGF106903 | Start Date*: 2008-01-14 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research and Development Limited | |||||||||||||
| Full Title: A randomised, multicentre, open-label, phase III study of neoadjuvant lapatinib, trastuzumab, and their combination plus paclitaxel in women with HER2/ErbB2 positive primary breast cancer | |||||||||||||
| Medical condition: Women with primary ErbB2 overexpressing and/or gene amplified breast cancer > 2 cm diameter who have not undergone previous treatment for invasive breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: FR (Completed) DE (Completed) BE (Completed) GB (Completed) LT (Completed) GR (Prematurely Ended) HU (Completed) ES (Completed) IT (Completed) SE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003874-29 | Sponsor Protocol Number: E-3810-II-02 | Start Date*: 2014-01-20 | |||||||||||
| Sponsor Name:EOS S.p.A. | |||||||||||||
| Full Title: A single arm, open-label, phase II study to assess the efficacy of the dual VEGFR-FGFR tyrosine kinase inhibitor, lucitanib, given orally as a single agent to patients with FGFR1-driven lung cancer | |||||||||||||
| Medical condition: FGFR1-amplified squamous non-small cell lung cancer (NSCLC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) DE (Prematurely Ended) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-006109-19 | Sponsor Protocol Number: STM01-102 | Start Date*: 2006-09-08 | |||||||||||
| Sponsor Name:Sopherion Therapeutics, Inc. | |||||||||||||
| Full Title: A Phase III Randomized, Controlled Trial of Myocet, Trastuzumab and Paclitaxel versus Trastuzumab and Paclitaxel for First line Therapy of Metastatic Breast Cancer | |||||||||||||
| Medical condition: HER2+ Metastatic Breast Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: PT (Completed) DE (Completed) ES (Prematurely Ended) GB (Completed) IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-000565-76 | Sponsor Protocol Number: MM-121-02-02-10 | Start Date*: 2018-04-05 | |||||||||||
| Sponsor Name:Merrimack Pharmaceuticals, Inc. | |||||||||||||
| Full Title: SHERBOC: A Double-blind, Placebo-controlled, Phase 2 trial of Seribantumab Plus Fulvestrant in Postmenopausal Women with Hormone Receptor-positive, Heregulin Positive (HRG+), HER2 Negative Metastat... | |||||||||||||
| Medical condition: Hormone Receptor-positive, Heregulin Positive (HRG+), HER2 Negative Metastatic Breast Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) ES (Prematurely Ended) AT (Prematurely Ended) BE (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-005127-29 | Sponsor Protocol Number: TAX_GMA_302 | Start Date*: 2001-05-21 | |||||||||||
| Sponsor Name:SANOFI-AVENTIS | |||||||||||||
| Full Title: MULTICENTER PHASE III RANDOMIZED TRIAL COMPARING DOXORUBICIN AND CYCLOPHOSPHAMIDE FOLLOWED BY DOCETAXEL (AC->T) WITH DOXORUBICIN AND CYCLOPHOSPHAMIDE FOLLOWED BY DOCETAXEL AND TRASTUZUMAB (HERCEPTI... | |||||||||||||
| Medical condition: node positive and high risk node negative patients with operable breast cancer containing the the HER2 alteration. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: HU (Completed) SK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-008697-31 | Sponsor Protocol Number: CRAD001W2301 | Start Date*: 2009-11-12 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A randomized Phase III, double-blind, placebo-controlled multicenter trial of daily everolimus in combination with trastuzumab and vinorelbine, in pretreated women with HER2/neu over-expressing loc... | |||||||||||||
| Medical condition: HER2-neu overexpressing metastatic breast cancer after previous trastuzumab use | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) GR (Completed) BE (Completed) IT (Completed) ES (Completed) FR (Completed) CZ (Completed) GB (Completed) HU (Completed) SK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-009885-15 | Sponsor Protocol Number: LAP112620 | Start Date*: 2009-08-27 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
| Full Title: A Phase II, Randomised, Multi-Centre Study Evaluating Lapatinib in Combination with Vinorelbine or Capecitabine in Women with ErbB2 Overexpressing Metastatic Breast Cancer | |||||||||||||
| Medical condition: Breast Cancer (with ErbB2 Overexpressing Metastatic Breast Cancer) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) FR (Completed) ES (Completed) IT (Completed) GR (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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