- Trials with a EudraCT protocol (257)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
257 result(s) found for: Head and Neck Neoplasms.
Displaying page 3 of 13.
EudraCT Number: 2017-001628-23 | Sponsor Protocol Number: 2017/2558 | Start Date*: 2017-10-17 | ||||||||||||||||
Sponsor Name:Gustave Roussy | ||||||||||||||||||
Full Title: Phase II multicentric study: efficacy evaluation of neo-adjuvant treatment associated with maintenance therapy by anti-PD1 immunotherapy on disease-free-survival (DFS) in patients with resectable h... | ||||||||||||||||||
Medical condition: Resectable head and neck mucosal melanoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000391-34 | Sponsor Protocol Number: 1200.43 | Start Date*: 2011-10-25 | |||||||||||
Sponsor Name:Boehringer Ingelheim | |||||||||||||
Full Title: LUX-Head & Neck 1 A randomised, open-label, phase III study to evaluate the efficacy and safety of oral afatinib (BIBW 2992) versus intravenous methotrexate in patients with recurrent and/or metas... | |||||||||||||
Medical condition: Recurrent and/or metastatic head and neck squamous cell carcinoma in patients who have progessed after platinum based therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DK (Completed) FR (Completed) DE (Completed) GR (Completed) ES (Completed) AT (Completed) CZ (Completed) SE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001976-39 | Sponsor Protocol Number: GORTEC-2018-02 | Start Date*: 2018-12-14 | |||||||||||
Sponsor Name:GORTEC | |||||||||||||
Full Title: A phase II trial of radiotherapy-durvalumab without prophylactic neck irradiation in squamous cell carcinoma of the head and neck | |||||||||||||
Medical condition: Untreated Squamous cell carcinoma : Oral cavity, oropharynx, hypopharynx or larynx | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005188-34 | Sponsor Protocol Number: GORTEC2014-03 | Start Date*: 2015-04-20 | |||||||||||
Sponsor Name:GORTEC | |||||||||||||
Full Title: Phase III trial of laryngeal preservation comparating Induction chemotherapy with cisplatin, 5-fluorouracil and docetaxel (TPF) followed by radiotherapy and concomitant administration of radiother... | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002403-18 | Sponsor Protocol Number: ET12-034 | Start Date*: 2013-01-17 | |||||||||||
Sponsor Name:Centre Léon Berard | |||||||||||||
Full Title: PIK-ORL: A Phase II, multicenter trial aiming to evaluate BKM120 in monotherapy in patients with metastatic head and neck cancer recurrent or progressive under platin and cetuximab-based chemotherapy | |||||||||||||
Medical condition: Patients with metastatic or relapsed head and neck cancer and documented progression or relapse after platin and cetuximab-based chemotherapy (combination or sequential treatment) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002017-37 | Sponsor Protocol Number: EFC5512 | Start Date*: 2005-03-23 | |||||||||||
Sponsor Name:Sanofi-Synthelabo Research | |||||||||||||
Full Title: Phase III randomized trial of concomitant radiation, cisplatin, and tirapazamine (SR259075) versus concomitant radiation and cisplatin in patients with advanced head and neck cancer | |||||||||||||
Medical condition: Oncology: Advanced Head and Neck cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) IT (Prematurely Ended) BE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002163-22 | Sponsor Protocol Number: NANORAY-312 | Start Date*: 2022-07-13 | |||||||||||
Sponsor Name:Nanobiotix SA | |||||||||||||
Full Title: A Phase 3 (Pivotal Stage) Study of NBTXR3 Activated by Investigator’s Choice of Radiotherapy Alone or Radiotherapy in Combination with Cetuximab for platinum-based Chemotherapy-ineligible Elderly P... | |||||||||||||
Medical condition: Locally Advanced Head & Neck Squamous Cell Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) IT (Prematurely Ended) CZ (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003589-10 | Sponsor Protocol Number: D419LC00001 | Start Date*: 2015-12-11 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase III Randomized, Open-label, Multi-center, Global Study of MEDI4736 Alone or in Combination with Tremelimumab versus Standard of Care in the Treatment of First-line Recurrent or Metastatic S... | |||||||||||||
Medical condition: Adult patients with recurrent or metastatic squamous cell carcinoma of the head and neck (SCCHN) who have not received prior systemic chemotherapy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) GR (Completed) DE (Completed) GB (GB - no longer in EU/EEA) ES (Completed) BE (Completed) PL (Completed) AT (Completed) RO (Completed) FR (Completed) PT (Completed) BG (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004093-21 | Sponsor Protocol Number: AT148003 | Start Date*: 2021-12-14 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:ALX Oncology Inc. | ||||||||||||||||||||||||||||||||||||||
Full Title: A PHASE 2 STUDY OF ALX148 IN COMBINATION WITH PEMBROLIZUMAB IN PATIENTS WITH ADVANCED HEAD AND NECK SQUAMOUS CELL CARCINOMA (ASPEN-03) | ||||||||||||||||||||||||||||||||||||||
Medical condition: Patients with metastatic or unresectable, recurrent HNSCC who have not yet been treated for their advanced disease | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Trial now transitioned) BE (Trial now transitioned) ES (Ongoing) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003786-13 | Sponsor Protocol Number: 20050251 | Start Date*: 2007-03-30 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Phase 3 Randomized Trial of Chemotherapy With or Without Panitumumab in Patients with Metastatic and/or Recurrent Squamous Cell Carcinoma of the Head and Neck | |||||||||||||
Medical condition: Metastatic and/or Recurrent Squamous Cell Carcinoma of the Head and Neck | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) GB (Completed) DE (Completed) HU (Completed) BE (Completed) FR (Completed) SE (Completed) PT (Completed) IT (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022924-57 | Sponsor Protocol Number: 17176 | Start Date*: 2011-08-17 |
Sponsor Name:Radiumhemmet Karolinska University Hospital [...] | ||
Full Title: Randomised phase II study with cetuximab (Erbitux®) in combination with 5-FU and cisplatin or carboplatin versus cetuximab (Erbitux®) in combination with paclitaxel and carboplatin for treatment of... | ||
Medical condition: Patients with relapsed or metastatic squamous cell carcinoma of the head and neck Previously not treated for relapsed or metastatic SCCHN. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-005014-12 | Sponsor Protocol Number: 1122P1811 | Start Date*: 2012-06-13 | |||||||||||
Sponsor Name:Shionogi & Co., Ltd. | |||||||||||||
Full Title: A Phase 1/2 Study to Evaluate the Safety, Tolerability, Immune Response, and Clinical Efficacy of Cancer Peptide Vaccine S-488210 in Patients with Unresectable Locoregionally Recurrent and/or Metas... | |||||||||||||
Medical condition: Head and Neck Squamous Cell Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005910-17 | Sponsor Protocol Number: KKSH176 | Start Date*: 2021-06-01 | |||||||||||
Sponsor Name:Martin-Luther-Universität Halle-Wittenberg | |||||||||||||
Full Title: Phase 2 multicenter study investigating the tolerability and efficacy of UV1 vaccine in patients with recurrent or metastatic PD-L1 positive (CPS≥1) head and neck squamous cell carcinoma planned fo... | |||||||||||||
Medical condition: Recurrent or metastatic Head and Neck Squamous Cell Carcinoma (HNSCC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002546-74 | Sponsor Protocol Number: ADRISK | Start Date*: 2018-06-21 | |||||||||||
Sponsor Name:University Leipzig | |||||||||||||
Full Title: Postoperative adjuvant radiochemotherapy (aRCH) with Cisplatin (C) versus aRCH with C and Pembrolizumab (P) in locally advanced head and neck squamous cell carcinoma (HNSCC); multicenter randomized... | |||||||||||||
Medical condition: Advanced primary resectable stage III, IVA/B head and neck squamous cell carcinoma (HNSCC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001144-18 | Sponsor Protocol Number: MS202359_0002 | Start Date*: 2022-09-29 | |||||||||||
Sponsor Name:MERCK HEALTHCARE KGaA | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, 2-arm Phase III study to assess efficacy and safety of xevinapant and radiotherapy compared to placebo and radiotherapy for demonstrating improvement... | |||||||||||||
Medical condition: Resected squamous cell carcinoma of the head and neck | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) ES (Trial now transitioned) BE (Trial now transitioned) PT (Trial now transitioned) NL (Trial now transitioned) CZ (Trial now transitioned) GR (Trial now transitioned) AT (Trial now transitioned) FR (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000773-31 | Sponsor Protocol Number: E7050-702 | Start Date*: 2011-12-20 | |||||||||||
Sponsor Name:Eisai Inc. | |||||||||||||
Full Title: An Open-Label, Multicenter, Randomized, Phase Ib/II Study of E7050 in Combination with Cetuximab versus Cetuximab Alone in the Treatment of Platinum-Resistant Squamous Cell Carcinoma of the Head an... | |||||||||||||
Medical condition: Squamous Cell Carcinoma of the Head and Neck | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004655-31 | Sponsor Protocol Number: 1143-SCCHN-202 | Start Date*: 2015-03-25 | |||||||||||
Sponsor Name:Debiopharm International S.A. | |||||||||||||
Full Title: Preoperative window-of-opportunity (WoO) study of Debio 1143 with or without cisplatin (CDDP) in patients with resectable squamous cell carcinoma of the head and neck. | |||||||||||||
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: 2016-003934-25 | Sponsor Protocol Number: 3475-412 | Start Date*: 2017-03-20 | |||||||||||
Sponsor Name:Merck Sharp & Dohme LLC | |||||||||||||
Full Title: A Randomized Phase III study of pembrolizumab given concomitantly with chemoradiation and as maintenance therapy versus chemoradiation alone in subjects with locally advanced head and neck squamous... | |||||||||||||
Medical condition: Locally advanced head and neck squamous cell carcinoma (LA HNSCC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) ES (Completed) NL (Completed) AT (Completed) PL (Completed) CZ (Completed) BE (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004662-19 | Sponsor Protocol Number: AT148004 | Start Date*: 2022-01-05 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:ALX Oncology Inc. | ||||||||||||||||||||||||||||||||||||||
Full Title: A PHASE 2 STUDY OF ALX148 IN COMBINATION WITH PEMBROLIZUMAB AND CHEMOTHERAPY IN PATIENTS WITH ADVANCED HEAD AND NECK SQUAMOUS CELL CARCINOMA (ASPEN-04) | ||||||||||||||||||||||||||||||||||||||
Medical condition: Patients with metastatic or unresectable, recurrent HNSCC who have not yet been treated for their advanced disease | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Trial now transitioned) BE (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000579-20 | Sponsor Protocol Number: CINC280X2104 | Start Date*: 2014-07-24 | ||||||||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | ||||||||||||||||||
Full Title: A phase Ib, open-label, multicenter, dose escalation and expansion study, to evaluate the safety, pharmacokinetics and activity of INC280 in combination with cetuximab in c-MET positive CRC and HNS... | ||||||||||||||||||
Medical condition: Head and neck squamous cell carcinoma. Colorectal cancer. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Temporarily Halted) IT (Completed) DE (Completed) BE (Completed) | ||||||||||||||||||
Trial results: View results |
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