- Trials with a EudraCT protocol (741)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
741 result(s) found for: neuropathy.
Displaying page 19 of 38.
| EudraCT Number: 2011-002092-42 | Sponsor Protocol Number: KF6010/01 | Start Date*: 2011-11-04 | |||||||||||
| Sponsor Name:Grünenthal GmbH | |||||||||||||
| Full Title: Evaluation of the efficacy, tolerability, and safety of 7 days of treatment with GRT6010 or pregabalin in comparison to placebo in subjects with peripheral neuropathic pain. | |||||||||||||
| Medical condition: mononeuropathic pain due to post-herpetic neuralgia, post-operative neuropathic pain, or traumatic nerve injury | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) GB (Completed) DE (Completed) PL (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-004998-53 | Sponsor Protocol Number: OMB116024 | Start Date*: 2013-02-05 |
| Sponsor Name:National and Kapodistrian University of Athens | ||
| Full Title: A phase II study of the efficacy of the combination of ofatumumab with fludarabine and cyclophosphamide in patients with relapsed or refractory Waldenström’s Macroglobulinemia. | ||
| Medical condition: Relapsed or refractory Waldenström’s Macroglobulinemia. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GR (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-003657-24 | Sponsor Protocol Number: BRIL06 | Start Date*: 2006-09-06 | |||||||||||
| Sponsor Name:GIMURELL | |||||||||||||
| Full Title: A PHASE II MULTICENTER NON-RANDOMIZED STUDY TO ASSESS SAFETY, TOXICITY AND CLINICAL ACTIVITY OF THE ASSOCIATION OF BORTEZOMID VELCADE WITH RITUXIMAB IN RELAPSED/REFRACTORY INDOLENT NON FOLLICULAR... | |||||||||||||
| Medical condition: relapsed non follicular non-Hodgkin s Lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-001270-24 | Sponsor Protocol Number: A3671014 | Start Date*: 2007-02-13 | |||||||||||
| Sponsor Name:Pfizer Pharma GmbH | |||||||||||||
| Full Title: Phase 2, single arm study of ticilimumab in patients with refractory metastatic adenocarcinoma of the colon or rectum | |||||||||||||
| Medical condition: Refractory meatstatic adenocarcinoma of the colon or rectum | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-004562-40 | Sponsor Protocol Number: GOG-0146Q | Start Date*: 2008-01-14 | |||||||||||
| Sponsor Name:Gynecologic Oncology Group | |||||||||||||
| Full Title: A PHASE II EVALUATION OF TOPOTECAN ADMINISTERED WEEKLY IN THE TREATMENT OF RECURRENT PLATINUM-SENSITIVE OVARIAN, FALLOPIAN TUBE, OR PRIMARY PERITONEAL CANCER | |||||||||||||
| Medical condition: Patients with recurrent ovarian, fallopian tube, or primary peritoneal cancers. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-021016-41 | Sponsor Protocol Number: 10.05 | Start Date*: 2011-01-14 | |||||||||||
| Sponsor Name:Odense University Hospital | |||||||||||||
| Full Title: Dose determination of Taxotere®, Eloxatin® and Xeloda® (TEX) in combination with Herpectin® as first line treatment to patients with HER2-positive non-resectable esophagus, cardia or gastric cancer | |||||||||||||
| Medical condition: Esophagus, cardiac or ventricular cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-001074-15 | Sponsor Protocol Number: GEN701 | Start Date*: 2013-10-08 | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Genmab A/S | |||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: First-in-human, dose-escalating safety study of tissue factor specific antibody drug conjugate tisotumab vedotin (HuMax®-TF-ADC) in patients with locally advanced and/or metastatic solid tumors kno... | |||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Cancer of the ovary, cervix, endometrium, bladder, prostate (castration-resistant prostate cancer [CRPC]), head and neck (squamous cell carcinoma of the head and neck [SCCHN]), esophagus or lung (n... | |||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2007-002797-56 | Sponsor Protocol Number: C04-2 | Start Date*: 2007-08-28 | |||||||||||
| Sponsor Name:Gercor | |||||||||||||
| Full Title: Phase III study of an optimized chemotherapy + Avastin strategy +/- Tarceva in metastatic colorectal cancer. | |||||||||||||
| Medical condition: Metastatic Colorectal Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-002131-32 | Sponsor Protocol Number: SP001033 | Start Date*: 2008-04-17 | |||||||||||
| Sponsor Name:ASSOCIAZIONE ITALIANA PER LO STUDIO DEL DOLORE | |||||||||||||
| Full Title: A RANDOMIZED, OPEN COMPARISON BETWEEN PREGABALIN/TRANSDERMAL BUPRENORPHINE AND PREGABALIN/DICLOFENAC IN CHRONIC NEUROPATHIC PAIN PATIENTS | |||||||||||||
| Medical condition: PERIPHERAL NEUROPATHIC PAIN DUE TO POST-HERPETIC NEURALGIA OR DIABETIC POLYNEUROPATHY | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-002231-18 | Sponsor Protocol Number: RMHCAN1104 | Start Date*: 2015-12-01 | |||||||||||
| Sponsor Name:University Southampton Hospital NHS Foundation Trust | |||||||||||||
| Full Title: A Phase I/IIa Study of Targeted Radiotherapy alone for Stem Cell Transplant Conditioning in Systemic AL Amyloidosis | |||||||||||||
| Medical condition: AL-Amyloidosis | |||||||||||||
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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: 2018-004348-47 | Sponsor Protocol Number: SOGUG-2017-A-IEC(VEJ)-4 | Start Date*: 2019-07-10 | |||||||||||
| Sponsor Name:Grupo Español de Oncología Genitourinaria (SOGUG) | |||||||||||||
| Full Title: EFFICACY OF ATEZOLIZUMAB CONCURRENT WITH RADIOTHERAPY IN PATIENTS WITH MUSCLE-INVASIVE BLADDER CANCER | |||||||||||||
| Medical condition: MUSCLE-INVASIVE BLADDER CANCER | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-004963-68 | Sponsor Protocol Number: 26866138-LUC-2006 | Start Date*: 2007-10-16 | |||||||||||
| Sponsor Name:Prof Vassilis Georgoulias | |||||||||||||
| Full Title: A Phase II, Open-Label Trial of Bortezomib (Velcade®) in Combination with Gemcitabine and Cisplatin in Patients with Locally Advanced or Metastatic Non-Small Cell Lung Cancer. | |||||||||||||
| Medical condition: First Line treatment for Locally Advanced or Metastatic Non-Small Cell Lung Cancer. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-005090-22 | Sponsor Protocol Number: 001 | Start Date*: 2012-02-28 | |||||||||||
| Sponsor Name:Southend Hospital | |||||||||||||
| Full Title: A study of efficacy and safety of delayed release prednisone in newly diagnosed cases of Giant Cell Arteritis | |||||||||||||
| Medical condition: Giant Cell Arteritis | |||||||||||||
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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: 2011-003201-14 | Sponsor Protocol Number: ERTUSO | Start Date*: 2012-03-02 | |||||||||||
| Sponsor Name: Krankenhaus Nordwest GmbH | |||||||||||||
| Full Title: Phase I/II, Open Label, Dose Escalating Study To Investigate Safety, Tolerability, And Preliminary Efficacy Of The Trifunctional Anti-HER-2/neu x Anti-CD3 Antibody Ertumaxomab In Patients With HER-... | |||||||||||||
| Medical condition: Patients with HER2/neu (1+/SISH positive, 2+ and 3+) expressing solid tumors that are progressing after standard therapy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-014336-38 | Sponsor Protocol Number: 2009-02-SUN-Case | Start Date*: 2009-10-09 | ||||||||||||||||
| Sponsor Name:Universitätsmedizin der Johannes Gutenberg-University Mainz | ||||||||||||||||||
| Full Title: A randomized, placebo-controlled phase II trial investigating SUNITINIB versus placebo in patients with chemorefractory advanced adenocarcinoma of the stomach or lower esophagus treated with chemot... | ||||||||||||||||||
| Medical condition: Chemo-refractory advanced or metastatic adenocarcinoma of stomach or lower esophagus | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2013-000236-94 | Sponsor Protocol Number: TTD-13-01 | Start Date*: 2013-06-05 | |||||||||||
| Sponsor Name:Grupo de Tratamiento de los Tumores Digestivos (TTD) | |||||||||||||
| Full Title: Phase II study of Regorafenib as a single agent for first-line treatment of patients with metastatic colorectal cancer (MCRC) who are fragile and/or not candidates for polychemotherapy | |||||||||||||
| Medical condition: Metastatic colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-002267-15 | Sponsor Protocol Number: GluST1_vers4_2014 | Start Date*: 2014-07-31 | |||||||||||
| Sponsor Name:Hvidovre Hospital | |||||||||||||
| Full Title: Treatment of hypoglycemia with glucagon among patients with type 1 diabetes mellitus | |||||||||||||
| Medical condition: Patients with type 1 diabetes mellitus | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-000530-30 | Sponsor Protocol Number: GY1508 | Start Date*: 2015-06-08 | |||||||||||
| Sponsor Name:Center for Cancer Immune Therapy | |||||||||||||
| Full Title: T cell therapy for patients with advanced Ovarian Cancer | |||||||||||||
| Medical condition: Advanced Ovarian Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-000234-57 | Sponsor Protocol Number: allo-APZ2-DFU-II-01 | Start Date*: 2017-08-07 | |||||||||||
| Sponsor Name:RHEACELL GmbH & Co. KG | |||||||||||||
| Full Title: An interventional, multicenter, single arm, phase I/IIa clinical trial to investigate the efficacy and safety of allo-APZ2-DFU on wound healing of diabetic neuropathic ulcer (DFU). | |||||||||||||
| Medical condition: Diabetic neuropathic ulcer (DFU) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-002826-70 | Sponsor Protocol Number: A3671008 | Start Date*: 2005-11-28 | |||||||||||
| Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, 10017, USA | |||||||||||||
| Full Title: A Phase 2, open label, single arm study to evaluate the efficacy, safety, tolerability and pharmacokinetics of ticilimumab in patients with advanced refractory and/or relapsed melanoma | |||||||||||||
| Medical condition: Malignant Melanoma | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) ES (Completed) DE (Prematurely Ended) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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