- Trials with a EudraCT protocol (65)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
65 result(s) found for: Ajcc Staging System.
Displaying page 1 of 4.
EudraCT Number: 2022-002189-34 | Sponsor Protocol Number: HLX11-BC301 | Start Date*: 2022-10-26 | ||||||||||||||||
Sponsor Name:Shanghai Henlius Biotech, Inc. | ||||||||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Parallel-Controlled Phase III Clinical Study to Evaluate the Efficacy and Safety of Pertuzumab Biosimilar HLX11 vs. EU-Perjeta® in the Neoadjuvant Therapy o... | ||||||||||||||||||
Medical condition: HER2-Positive and HR-Negative Early-stage or Locally advanced Breast Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) BG (Prematurely Ended) HU (Prematurely Ended) PL (Prematurely Ended) CZ (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020965-26 | Sponsor Protocol Number: VEG113387 | Start Date*: 2010-10-28 | ||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
Full Title: A randomized, double-blind, placebo-controlled phase III study to evaluate the efficacy and safety of pazopanib as adjuvant therapy for subjects with localized or locally advanced RCC following nep... | ||||||||||||||||||
Medical condition: Renal Cell Carcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SK (Completed) DE (Completed) DK (Completed) IE (Completed) CZ (Completed) ES (Completed) BE (Completed) GR (Completed) GB (Completed) AT (Completed) PL (Completed) HU (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-001868-11 | Sponsor Protocol Number: PELICAN-IPC2015-016 | Start Date*: 2017-09-08 | |||||||||||
Sponsor Name:Institut Paoli Calmettes | |||||||||||||
Full Title: A prospective, multicentre, open-label, randomized, phase II study of Pembrolizumab in combination with neoadjuvante (F)EC-Paclitaxel regimen in HER2-negative inflammatory breast cancer. | |||||||||||||
Medical condition: Inflammatory breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006532-21 | Sponsor Protocol Number: 40054-22062 | Start Date*: 2008-10-27 | ||||||||||||||||
Sponsor Name:EORTC | ||||||||||||||||||
Full Title: Preoperative chemoradiotherapy and postoperative chemotherapy with capecitabine and oxaliplatin vs. capecitabine alone in locally advanced rectal cancer (PETACC-6) | ||||||||||||||||||
Medical condition: locally advanced rectal cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) GB (Completed) FR (Completed) DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-005367-10 | Sponsor Protocol Number: CRAF265A2101 | Start Date*: 2009-05-18 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A Phase I/II, open-label, dose escalation trial to evaluate the safety, pharmacokinetics, and pharmacodynamics of RAF265 (CHIR-265) administered orally to patients with locally advanced or metastat... | |||||||||||||
Medical condition: local advanced or metastatic melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004371-12 | Sponsor Protocol Number: U31287-A-U301 | Start Date*: 2014-08-04 | |||||||||||
Sponsor Name:Daiichi Sankyo Development Limited | |||||||||||||
Full Title: Phase 3, Randomized, Placebo-Controlled, Double-blind, Multi-Center, Two-Part Study of Patritumab (U3-1287) in Combination with Erlotinib in EGFR Wild-type Subjects with Locally Advanced or Metasta... | |||||||||||||
Medical condition: Non-Small Cell Lung Cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) GB (Prematurely Ended) IT (Completed) DE (Prematurely Ended) HU (Completed) ES (Prematurely Ended) CZ (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003583-12 | Sponsor Protocol Number: CA224-047 | Start Date*: 2018-05-30 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: A Randomized, Double-Blind Phase 2/3 Study of Relatlimab Combined with Nivolumab versus Nivolumab in Participants with Previously Untreated Metastatic or Unresectable Melanoma | ||||||||||||||||||
Medical condition: Previously Untreated Metastatic or Unresectable Melanoma | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Trial now transitioned) DE (Trial now transitioned) AT (Trial now transitioned) GB (GB - no longer in EU/EEA) SE (Trial now transitioned) DK (Trial now transitioned) FR (Trial now transitioned) ES (Ongoing) GR (Ongoing) FI (Trial now transitioned) PL (Trial now transitioned) Outside EU/EEA IT (Ongoing) RO (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000577-36 | Sponsor Protocol Number: S60379 | Start Date*: 2018-08-27 |
Sponsor Name:University Hospitals Leuven | ||
Full Title: Durvalumab (MEDI4736) plus tremelimumab in resectable, locally advanced squamous cell carcinoma of the oral cavity: a window of opportunity study | ||
Medical condition: resectable, locally advanced squamous cell carcinoma of the oral cavity | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-000601-27 | Sponsor Protocol Number: MERCURY | Start Date*: 2022-09-27 | |||||||||||
Sponsor Name:Fondazione GONO | |||||||||||||
Full Title: Window-of-opportunity study of chemo-immunotherapy in patients with resectable Merkel Cell Carcinoma prior to surgery: the MERCURY trial | |||||||||||||
Medical condition: The disease under clinical investigation is represented by resectable Merkel Cell Carcinoma (MCC), stage IIA-III (according to the AJCC staging system 8th edition). The study will include patients ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003718-16 | Sponsor Protocol Number: CA209-066 | Start Date*: 2013-04-04 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind Study of BMS-936558 vs Dacarbazine in Subjects with Previously Untreated Unresectable or Metastatic Melanoma Country specific Protocol Amendment 05, dated 09-... | |||||||||||||
Medical condition: Melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) SE (Completed) ES (Completed) DK (Completed) NO (Completed) IT (Completed) PL (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003306-32 | Sponsor Protocol Number: 030(Z)WO19247 | Start Date*: 2021-01-18 | |||||||||||
Sponsor Name:Angelini Pharma S.p.A. | |||||||||||||
Full Title: Phase IV study on the feasibility of a preventative/therapeutic approach with Benzydamine Oromucosal solution in radiation-induced Oral Mucositis (OM) in patients with head and neck cancer (HNC) | |||||||||||||
Medical condition: Oral Mucositis (OM) in patients with head and neck cancer (HNC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003239-36 | Sponsor Protocol Number: B9991010 | Start Date*: 2016-08-22 | |||||||||||
Sponsor Name:Pfizer Inc. | |||||||||||||
Full Title: A Randomized, Open-Label, Multicenter, Phase 3 Study to Evaluate the Efficacy and Safety of Avelumab (MSB0010718C) in Combination with and/or Following Chemotherapy in Patients with Previously Unt... | |||||||||||||
Medical condition: Epithelial ovarian cancer (EOC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: SK (Prematurely Ended) NL (Prematurely Ended) BG (Prematurely Ended) HU (Prematurely Ended) EE (Completed) IE (Prematurely Ended) GB (Prematurely Ended) LV (Prematurely Ended) DE (Completed) PL (Prematurely Ended) HR (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005025-11 | Sponsor Protocol Number: BAY43-9006/13162 | Start Date*: 2009-05-06 | |||||||||||
Sponsor Name:Bayer Healthcare AG, D-51368 Leverkusen, Germany | |||||||||||||
Full Title: A Phase 2b, Double Blind, Randomized Study Evaluating the Efficacy and Safety of Sorafenib Compared With Placebo When Administered in Combination With Chemotherapy (Modified FOLFOX6) for the Treatm... | |||||||||||||
Medical condition: The patient population includes patients with Stage IV metastatic colorectal cancer (mCRC), with Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1. Patients must have measurable ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002857-12 | Sponsor Protocol Number: GO40241 | Start Date*: 2018-04-26 | |||||||||||
Sponsor Name:F. Hoffman-La Roche Ltd. | |||||||||||||
Full Title: A PHASE III, DOUBLE-BLINDED, MULTICENTER, RANDOMIZED STUDY EVALUATING THE EFFICACY AND SAFETY OF NEOADJUVANT TREATMENT WITH ATEZOLIZUMAB OR PLACEBO IN COMBINATION WITH PLATINUM-BASED CHEMOTHERAPY I... | |||||||||||||
Medical condition: Early Stage Resectable Non-small cell lung cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) GB (GB - no longer in EU/EEA) SI (Ongoing) SE (Trial now transitioned) AT (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) HU (Completed) FR (Trial now transitioned) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002346-33 | Sponsor Protocol Number: MO43110 | Start Date*: 2022-05-17 |
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 IIIB, MULTINATIONAL, MULTICENTER, RANDOMIZED, OPEN-LABEL STUDY TO EVALUATE PATIENT PREFERENCE FOR HOME ADMINISTRATION OF FIXED-DOSE COMBINATION OF PERTUZUMAB AND TRASTUZUMAB FOR SUBCUTANEOU... | ||
Medical condition: Early or locally advanced/inflammatory HER2-positive (HER2+) breast cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) BG (Ongoing) HR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002202-20 | Sponsor Protocol Number: 213400 | Start Date*: 2020-12-07 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd. | ||||||||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study Comparing Niraparib Plus Pembrolizumab Versus Placebo Plus Pembrolizumab as Maintenance Therapy in Participants Whose Dise... | ||||||||||||||||||
Medical condition: Non-small Cell Lung Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Trial now transitioned) NL (Trial now transitioned) DE (Ongoing) NO (Trial now transitioned) BE (Trial now transitioned) GR (Trial now transitioned) HU (Ongoing) BG (Trial now transitioned) IT (Ongoing) PL (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-005007-14 | Sponsor Protocol Number: 20040122 | Start Date*: 2005-05-20 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled Study Evaluating the Efficacy and Safety of Palifermin (Recombinant Human Keratinocyte Growth Factor) for Reduction of Oral Mucositis in Subjects Wit... | |||||||||||||
Medical condition: Oral Mucositis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000194-12 | Sponsor Protocol Number: QUASAR-2014-001 | Start Date*: 2016-06-27 | ||||||||||||||||||||||||||
Sponsor Name:CONSORZIO ONCOTECH | ||||||||||||||||||||||||||||
Full Title: Isoquercetin as an adjunct therapy in patients with kidney cancer receiving first-line sunitinib: a phase I/II trial | ||||||||||||||||||||||||||||
Medical condition: Locally advanced or metastatic renal cell carcinoma of any histology (equivalent to Stage IV RCC according to AJCC staging) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018501-10 | Sponsor Protocol Number: BAY43-9006/12444 | Start Date*: 2011-03-23 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A Phase III Randomized, Double blind, Placebo-controlled Trial Comparing Capecitabine Plus Sorafenib Versus Capecitabine Plus Placebo in the Treatment of Locally Advanced or Metastatic HER2-Negativ... | |||||||||||||
Medical condition: Locally advanced or metastatic HER2-negative breast cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) GB (Completed) AT (Completed) CZ (Completed) IE (Completed) ES (Completed) HU (Completed) IT (Completed) GR (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018982-43 | Sponsor Protocol Number: AB08025 | Start Date*: 2010-06-18 | ||||||||||||||||
Sponsor Name:AB SCIENCE | ||||||||||||||||||
Full Title: A prospective, multicenter, open-label, uncontrolled, two-parallel group, phase 1/2 study to evaluate safety and efficacy of masitinib at 9 mg/kg/day in monotherapy and in combination with dacarbaz... | ||||||||||||||||||
Medical condition: Mélanome métastasé ou non-opérable stade 3 ou stade 4, ne portant pas de mutation dans le domaine juxta-membranaire de c-kit | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
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