- Trials with a EudraCT protocol (644)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
644 result(s) found for: Phase III trials.
Displaying page 1 of 33.
EudraCT Number: 2010-021209-18 | Sponsor Protocol Number: TMC278-TiDP6-C222 | Start Date*: 2011-03-03 | |||||||||||
Sponsor Name:Janssen R&D Ireland | |||||||||||||
Full Title: An open-label trial with TMC278 25 mg q.d. in combination with a background regimen containing 2 nucleoside/nucleotide reverse transcriptase inhibitors in HIV-1 infected subjects, who participated ... | |||||||||||||
Medical condition: HIV-1 infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) GB (Completed) SE (Completed) ES (Completed) IT (Completed) DK (Completed) AT (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001659-32 | Sponsor Protocol Number: M14-360 | Start Date*: 2016-10-05 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Phase 1 Dose Escalation and Phase 2 Randomized, Placebo-Controlled Study of the Efficacy and Tolerability of Veliparib in Combination with Paclitaxel/Carboplatin-Based Chemoradiotherapy Followed ... | |||||||||||||
Medical condition: Stage III Non-Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) ES (Prematurely Ended) GR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001246-33 | Sponsor Protocol Number: TMC114-C208 | Start Date*: 2004-11-23 | |||||||||||
Sponsor Name:Tibotec Pharmaceuticals Limited Ireland | |||||||||||||
Full Title: An open label trial of TMC114/RTV in HIV-1 infected subjects who were randomized in the trials TMC114-C201, TMC114-C207 or in sponsor selected Phase I trials. | |||||||||||||
Medical condition: HIV-1 infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) GB (Completed) IT (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003708-21 | Sponsor Protocol Number: VUB 06-001 | Start Date*: 2006-10-31 | |||||||||||
Sponsor Name:AZ-VUB | |||||||||||||
Full Title: Concurrent helical tomotherapy with chemotherapy in unresectable stage III non-small cell lung cancer (NSCLC): a phase I/II trial of radiation dose escalation and fixed dose chemotherapy. | |||||||||||||
Medical condition: stage III locally advanced non small cell lung cancer (LA-NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003107-19 | Sponsor Protocol Number: 13-0288 | Start Date*: 2014-04-28 | |||||||||||
Sponsor Name:University of Birmingham [...] | |||||||||||||
Full Title: Phase II clinical trial investigating the use of epigallocatechin-3-gallate (Veregen) in the treatment of vulval intraepithelial neoplasia | |||||||||||||
Medical condition: Vulval intraepithelial neoplasia (VIN) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002762-33 | Sponsor Protocol Number: AX250-401 | Start Date*: 2022-12-12 | ||||||||||||||||
Sponsor Name:Allievex Corporation | ||||||||||||||||||
Full Title: A Phase 3B/4 Open-Label Multicenter Study Extension Study to Further Evaluate Safety, Tolerability and Efficacy of Intracerebroventricular AX 250 Treatment in Mucopolysaccharidosis Type IIIB (MPS I... | ||||||||||||||||||
Medical condition: Mucopolysaccharidosis Type IIIB (Sanfilippo Syndrome Type B, MPS IIIB) | ||||||||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000958-98 | Sponsor Protocol Number: 2017-1-39-007 | Start Date*: 2020-08-07 | |||||||||||
Sponsor Name:Centre Régional de lutte contre le Cancer Eugène Marquis | |||||||||||||
Full Title: A phase II trial evaluating conformational intensity modulated radiotherapy with concomitant nivolumab followeb by nivolumab for patients with locally advanced non-small cell lung cancer | |||||||||||||
Medical condition: Patient having locally Advanced Non-Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003083-13 | Sponsor Protocol Number: 250-202 | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:Allievex Corporation | ||||||||||||||||||
Full Title: A Multicenter, Multinational, Extension Study to Evaluate the Long-Term Safety and Efficacy of Intracerebroventricular AX 250 in Patients with Mucopolysaccharidosis Type IIIB (MPS IIIB, Sanfilippo ... | ||||||||||||||||||
Medical condition: Mucopolysaccharidosis Type IIIB (Sanfilippo Syndrome Type B, MPS IIIB) | ||||||||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) ES (Prematurely Ended) GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000004-42 | Sponsor Protocol Number: C0993 | Start Date*: 2019-01-16 | |||||||||||
Sponsor Name:The Clatterbridge Cancer Centre NHS Foundation Trust | |||||||||||||
Full Title: TACE-3: A two-arm multi-stage (TAMS) seamless phase II/III randomised trial of nivolumab in combination with TACE/TAE for patients with intermediate stage HCC | |||||||||||||
Medical condition: Intermediate stage Hepatocellular Carcinoma | |||||||||||||
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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: 2014-005164-15 | Sponsor Protocol Number: ALTERNATIVE | Start Date*: 2015-12-22 | |||||||||||||||||||||
Sponsor Name:Klinikum der Universität München, Medizinische Klinik und Poliklinik III | |||||||||||||||||||||||
Full Title: A prospective multicenter Phase 2 Study of the Chemotherapy-free Combination of the Bruton's Tyrosine Kinase Inhibitor, PCI-32765 (Ibrutinib) in Combination with Obinutuzumab (GA 101) in Patients... | |||||||||||||||||||||||
Medical condition: Stage II - IV follicular lymphoma grade 1 - 3a and a high tumor burden not previously treated | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-002955-85 | Sponsor Protocol Number: AVICCI001 | Start Date*: 2016-01-21 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: A feasibility study to assess the effects of AntiretroViral Intensification with Cenicriviroc for the management of HIV-associated Cognitive Impairment. The AVICCI study | |||||||||||||
Medical condition: Human Immunodeficiency Virus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003501-10 | Sponsor Protocol Number: 3883 | Start Date*: 2013-04-24 | |||||||||||
Sponsor Name:Vall d'Hebron Institut de Recerca (VHIR) | |||||||||||||
Full Title: Efficacy of dual antiretroviral treatment with maraviroc plus ritonavir-boosted darunavir in early rescue therapy in patients with HIV-1 infection: pilot, multicenter, randomized, controlled and op... | |||||||||||||
Medical condition: Adult patients with HIV-1 infection that present virologic failure to first-line antiretroviral treatment. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004773-29 | Sponsor Protocol Number: GO41854 | Start Date*: 2020-08-31 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A PHASE III, OPEN-LABEL, RANDOMIZED STUDY OF ATEZOLIZUMAB AND TIRAGOLUMAB COMPARED WITH DURVALUMAB IN PATIENTS WITH LOCALLY ADVANCED, UNRESECTABLE STAGE III NON-SMALL CELL LUNG CANCER WHO HAVE NOT... | |||||||||||||
Medical condition: Non−small cell lung cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Trial now transitioned) GB (GB - no longer in EU/EEA) DE (Trial now transitioned) BE (Trial now transitioned) AT (Trial now transitioned) PL (Trial now transitioned) HU (Trial now transitioned) NL (Trial now transitioned) GR (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003408-33 | Sponsor Protocol Number: ESR-21-21536 | Start Date*: 2023-04-25 | |||||||||||
Sponsor Name:TheraOp gGmbH | |||||||||||||
Full Title: PACCELIO - FDG-PET based small volume accelerated immuno chemoradio-therapy in locally advanced NSCLC | |||||||||||||
Medical condition: Locally advanced, unresectable non-small-cell lung cancer (NSCLC) (Stage III) with a PD-L1-expression of ≥ 1% | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002695-40 | Sponsor Protocol Number: MO43156 | Start Date*: 2021-12-28 | |||||||||||
Sponsor Name:Roche Farma S. A. U. que realiza el ensayo en España y que actúa como representante F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A PHASE II, SINGLE-ARM STUDY OF ATEZOLIZUMAB IN PATIENTS WITH LOCALLY ADVANCED, UNRESECTABLE STAGE III NON-SMALL CELL LUNG CANCER WHO HAVE NOT PROGRESSED AFTER PLATINUM-BASED CONCURRENT CHEMORADIAT... | |||||||||||||
Medical condition: Non-Small Cell Lung Cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) SI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002208-15 | Sponsor Protocol Number: 208132 | Start Date*: 2019-03-04 | |||||||||||
Sponsor Name:ViiV Healthcare UK Limited | |||||||||||||
Full Title: A Randomized, Double-Blind (Sponsor-unblinded), Placebo-Controlled, Adaptive Trial to Investigate the Antiviral Effect, Safety, Tolerability and Pharmacokinetics of GSK3640254 in HIV-1 Infected Tre... | |||||||||||||
Medical condition: Treatment of human immunodeficiency virus-1 (HIV-1) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002295-41 | Sponsor Protocol Number: PR2100 | Start Date*: 2009-01-29 |
Sponsor Name:The University of Birmingham | ||
Full Title: A randomised phase II/III study of Docetaxel plus Prednisolone vs. Docetaxel plus Prednisolone plus Zoledronic acid vs. Docetaxel plus Prednisolone plus Strontium-89 vs. Docetaxel plus Prednisolo... | ||
Medical condition: Hormone refractory Prostate Cancer (HRPC) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004215-13 | Sponsor Protocol Number: CCC844 | Start Date*: 2017-12-29 | |||||||||||||||||||||
Sponsor Name:The Clatterbridge Cancer Centre NHS Foundation | |||||||||||||||||||||||
Full Title: Randomised Phase II Trial of Cediranib and Olaparib Maintenance in Advanced/Recurrent Cervical Cancer (COMICE) | |||||||||||||||||||||||
Medical condition: Advanced recurrent and metastatic cervical cancer. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015884-15 | Sponsor Protocol Number: IMPAACT-P1066 | Start Date*: 2011-06-30 | |||||||||||
Sponsor Name:The National Institute of Allergy and Infectious Diseases (NIAID) and The Eunice Kennedy Shriver NICHD | |||||||||||||
Full Title: A Phase I/II, Multicenter, Open-Label, Non comparative Study of the International Maternal, Pediatric, Adolescent AIDS Clinical Trials (IMPAACT) Group to Evaluate the Safety, Tolerability, Pharmac... | |||||||||||||
Medical condition: HIV | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017978-21 | Sponsor Protocol Number: EMR700568-012 | Start Date*: 2010-12-20 | |||||||||||
Sponsor Name:Merck Serono S.A. - Geneva | |||||||||||||
Full Title: Prospective observational long-term safety registry of Multiple Sclerosis patients who have participated in cladribine clinical trials (PREMIERE) | |||||||||||||
Medical condition: Multiple Sclerosis patients who have participated in cladribine tablets clinical trials | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) LT (Completed) AT (Completed) GR (Completed) CZ (Completed) GB (Completed) EE (Completed) LV (Completed) BE (Completed) SE (Completed) PT (Completed) DK (Completed) ES (Completed) IT (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
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