- Trials with a EudraCT protocol (187)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
187 result(s) found for: Kaplan-Meier method.
Displaying page 4 of 10.
| EudraCT Number: 2018-000452-18 | Sponsor Protocol Number: ETB115J2411 | Start Date*: 2018-09-26 | ||||||||||||||||
| Sponsor Name:Novartis Pharma AG | ||||||||||||||||||
| Full Title: A phase II, open-label, prospective, single-arm, study to assess ability of eltrombopag to induce sustained remission in subjects with ITP who are refractory or relapsed after first-line steroids (... | ||||||||||||||||||
| Medical condition: immune thrombocytopenia | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: AT (Completed) GR (Completed) ES (Ongoing) GB (GB - no longer in EU/EEA) IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2018-002944-10 | Sponsor Protocol Number: c16174 | Start Date*: 2019-02-27 |
| Sponsor Name:Memorial Sloan Kettering Cancer Center | ||
| Full Title: Phase III Trial of Docetaxel vs. Docetaxel and Radium-223 for Metastatic Castration-Resistant Prostate Cancer (mCRPC) | ||
| Medical condition: Patients with histological or cytological proof of Metastatic Castration-Resistant Prostate Cancer (mCRPC) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: NL (Trial now transitioned) ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-003494-25 | Sponsor Protocol Number: CAEB071A2203 | Start Date*: 2006-08-30 |
| Sponsor Name:Novartis Pharma Services AG | ||
| Full Title: 12-month open label, randomized, multicenter study evaluating efficacy, safety and tolerability of oral AEB071 plus tacrolimus (converted to myfortic after 3 months), vs. myfortic plus tacrolimus i... | ||
| Medical condition: First evaluation of the efficacy and safety of AEB071 in its target indication: prevention of rejection in solid organ tranplantation. The study population will consist of a representative group of... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-003184-62 | Sponsor Protocol Number: J1369 | Start Date*: 2014-04-23 | |||||||||||
| Sponsor Name:Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins | |||||||||||||
| Full Title: A phase I study of SGI-110 combined with irinotecan followed by a randomized phase II study of SGI-110 combined with irinotecan versus regorafenib in previously treated metastatic colorectal cancer... | |||||||||||||
| Medical condition: Previously treated metastatic colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-003497-14 | Sponsor Protocol Number: BLU-285-1303 | Start Date*: 2018-04-23 | ||||||||||||||||
| Sponsor Name:Blueprint Medicines Corporation | ||||||||||||||||||
| Full Title: An International, Multicenter, Open-label, Randomized, Phase 3 Study of BLU-285 vs Regorafenib in Patients with Locally Advanced Unresectable or Metastatic Gastrointestinal Stromal Tumor (GIST) | ||||||||||||||||||
| Medical condition: Locally Advanced Unresectable or Metastatic Gastrointestinal Stromal Tumor (GIST) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) SE (Completed) HU (Completed) DE (Completed) NL (Completed) AT (Completed) ES (Completed) BE (Completed) CZ (Completed) IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2019-004084-49 | Sponsor Protocol Number: TAS-120-202 | Start Date*: 2020-06-22 | |||||||||||
| Sponsor Name:Taiho Oncology Inc. | |||||||||||||
| Full Title: A PHASE 2 STUDY OF FUTIBATINIB IN PATIENTS WITH SPECIFIC FGFR ABERRATIONS | |||||||||||||
| Medical condition: Fibroblast growth factor receptor (FGFR) aberrations | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) GB (GB - no longer in EU/EEA) NL (Completed) FR (Completed) BE (Completed) PT (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-004997-41 | Sponsor Protocol Number: H7T-MC-TACW | Start Date*: Information not available in EudraCT |
| Sponsor Name:Eli Lilly and Company | ||
| Full Title: Effectiveness of Prasugrel versus Clopidogrel in Subjects with High Platelet Reactivity on Clopidogrel Following Elective Percutaneous Coronary Intervention with Implantation of Drug-Eluting Stent | ||
| Medical condition: Reduction of composite cardio-vascular end-point in patients who have successfully undergone elective percutaneous coronary intervention with placement of at least one drug-eluting stent. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-003993-24 | Sponsor Protocol Number: CA186006 | Start Date*: 2008-05-29 | ||||||||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
| Full Title: A Randomized, Multi-Dose, Open-Label, Phase II Study of BMS-663513 as a Second-Line Monotherapy in Subjects with Previously Treated Unresectable Stage III or Stage IV Melanoma. Revised Protocol 0... | ||||||||||||||||||
| Medical condition: MELANOMA | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) FR (Completed) IT (Prematurely Ended) DK (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2016-004879-46 | Sponsor Protocol Number: RG_16-123 | Start Date*: 2017-06-15 | |||||||||||
| Sponsor Name:University of Birmingham | |||||||||||||
| Full Title: AVAIL-T: A Phase 2a trial of Avelumab, an anti-PDL1 antibody, in relapsed and refractory peripheral T-cell lymphoma (PTCL) | |||||||||||||
| Medical condition: Relapsed and refractory T-cell lymphoma | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-019033-98 | Sponsor Protocol Number: BMS-TUE-01 | Start Date*: 2011-10-27 | |||||||||||
| Sponsor Name:University Clinical Center of Tuebingen | |||||||||||||
| Full Title: A phase II study to evaluate safety and efficacy of combined treatment with ipilimumab and intratumoral interleukin-2 in pretreated patients with stage IV melanoma | |||||||||||||
| Medical condition: Stage IV Melanoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-002512-49 | Sponsor Protocol Number: PRS-343-PCS_09_20 | Start Date*: 2022-06-13 |
| Sponsor Name:Pieris Pharmaceuticals, Inc. | ||
| Full Title: A Phase 2, Multi-Center, Open-Label Study of Cinrebafusp Alfa (PRS-343) in Combination with Ramucirumab and Paclitaxel in Patients with HER2-Positive Gastric or Gastroesophageal Junction (GEJ) Aden... | ||
| Medical condition: HER2-Positive Gastric or Gastroesophageal Junction (GEJ) Adenocarcinoma and in HER2 Low Gastric or Gastroesophageal Junction (GEJ) Adenocarcinoma | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-002231-24 | Sponsor Protocol Number: PROICM2018-01NEX | Start Date*: 2018-08-06 | |||||||||||
| Sponsor Name:Institut régional du Cancer de Montpellier | |||||||||||||
| Full Title: A randomized phase III trial assessing a regorafenib-irinotecan combination (REGIRI) versus regorafenib alone in metastatic colorectal cancer patients after failure of standard therapies, according... | |||||||||||||
| Medical condition: Metastatic colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-003022-92 | Sponsor Protocol Number: 9785-CL-0403 | Start Date*: 2014-04-29 | |||||||||||
| Sponsor Name:Astellas Pharma Global Development, Inc. | |||||||||||||
| Full Title: A Multicenter, Single-Arm, Open-Label, Post-Marketing Safety Study to Evaluate the Risk of Seizure Among Subjects with Metastatic Castration-Resistant Prostate Cancer (mCRPC) Treated with Enzalutam... | |||||||||||||
| Medical condition: Medical condition: metastatic castration-resistant prostate cancer (mCRPC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: SE (Completed) DE (Completed) HU (Completed) GB (Completed) BE (Completed) FI (Completed) IT (Completed) CZ (Completed) GR (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000454-22 | Sponsor Protocol Number: CCR4825 | Start Date*: 2019-02-01 |
| Sponsor Name:The Royal Marsden NHS Foundation Trust | ||
| Full Title: A translational phase II study of single agent Olaparib in the treatment of advanced oesophagogastric cancer | ||
| Medical condition: Advanced Oesophago-gastric cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-004831-30 | Sponsor Protocol Number: UC-0101/1104 | Start Date*: 2012-09-21 | |||||||||||
| Sponsor Name:UNICANCER | |||||||||||||
| Full Title: Safety and efficacy of radiotherapy combined with a 6-month LH-RH agonist and abiraterone hormone therapy treatment in biochemically-relapsing prostate cancer following surgery. | |||||||||||||
| Medical condition: Biochemically-relapsing prostate adenocarcinoma following radical prostatectomy. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-001804-39 | Sponsor Protocol Number: GLLC-EARLY | Start Date*: 2019-09-24 | |||||||||||
| Sponsor Name:Fundación PETHEMA | |||||||||||||
| Full Title: Phase III Randomized Study to Investigate the Use of Acalabrutinib in the Treatment of Patients With Early Stage CLL With High Risk of Early Disease Progression | |||||||||||||
| Medical condition: Early Stage CLL With High Risk of Early Disease Progression | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-002345-39 | Sponsor Protocol Number: Göteborg University | Start Date*: 2006-02-16 |
| Sponsor Name:NOPHO NHL-group | ||
| Full Title: B-NHL BFM 04 | ||
| Medical condition: B-cell lymphoma or B-ALL in children up to 18 years of age | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-000227-24 | Sponsor Protocol Number: RG_13-320 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:University of Birmingham | |||||||||||||
| Full Title: A Study of Thiotepa, Ifosphamide, Etoposide and Rituximab for the treatment of relapsed or refractory primary central nervous system lymphoma | |||||||||||||
| Medical condition: Relapsed or refractory primary central neurvous system lymphoma. | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-003993-16 | Sponsor Protocol Number: IM-T-hPAM4-02 | Start Date*: 2009-04-03 | ||||||||||||||||
| Sponsor Name:Immunomedics, Inc. | ||||||||||||||||||
| Full Title: A Phase Ib/II Study of Fractionated 90-Y-hPAM4 Plus Gemcitabine in Patients with Previously Untreated Advanced Pancreatic Cancer | ||||||||||||||||||
| Medical condition: This is a phase Ib, open-label, dose exploration study of 90-Y-hPAM4 administered as one or more treatment cycles of fractionated radioimmunotherapy in combination with radiosensitizing gemcitabine... | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2007-005396-34 | Sponsor Protocol Number: RG_10-040 | Start Date*: 2004-09-22 | |||||||||||
| Sponsor Name:University of Birmingham | |||||||||||||
| Full Title: Treatment Protocol for T-Cell and B-Precursor Cell Lymphoblastic Lymphoma of the European Inter-group Co-operation on Childhood Non-Hodgkin-Lymphoma (EICNHL) | |||||||||||||
| Medical condition: lymphoblastic lymphoma | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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