- Trials with a EudraCT protocol (25)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (21)
25 result(s) found for: Nasopharyngeal carcinoma.
Displaying page 1 of 2.
EudraCT Number: 2007-001211-33 | Sponsor Protocol Number: EFC10339 | Start Date*: 2007-06-20 | |||||||||||
Sponsor Name:sanofi-aventis recherche & développement | |||||||||||||
Full Title: International randomized study to evaluate the addition of docetaxel to the combination of cisplatin-5-fluorouracil (TCF) vs. cisplatin-5-fluorouracil (CF) in the induction treatment of nasopharyng... | |||||||||||||
Medical condition: Children and adolescents newly diagnosed with NPC with measurable disease T2-T4 any NM, of <18 years of age at the time of diagnosis. ---------- Niños y adolescentes recien diagnosticados con CNF c... | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) GR (Prematurely Ended) FR (Completed) IT (Completed) DE (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001745-25 | Sponsor Protocol Number: CC-486-NPC-001 | Start Date*: 2015-01-22 | |||||||||||
Sponsor Name:Celgene Corporation | |||||||||||||
Full Title: A Phase 2, Multicenter, International, Single Arm Study to Assess the Safety and Efficacy of Single Agent CC-486 (Oral Azacitidine) in Previously Treated Subjects With Locally Advanced or Metastati... | |||||||||||||
Medical condition: Locally advanced or metastatic nasopharyngeal carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) GR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-005017-31 | Sponsor Protocol Number: DERN | Start Date*: 2019-01-29 | |||||||||||
Sponsor Name:G.O.N.O. - GRUPPO ONCOLOGICO DEL NORD OVEST | |||||||||||||
Full Title: DENOSUMAB IN EBV RELATED NASOPHARYNGEAL CARCINOMA (NPC) AS A MODEL FOR RANK-MEDIATED IMMUNOLOGIC MODULATION OF VIRUS-RELATED TUMOURS – DERN STUDY | |||||||||||||
Medical condition: advanced or metastatic Nose Pharynx Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004649-35 | Sponsor Protocol Number: POINT | Start Date*: 2021-12-14 | |||||||||||
Sponsor Name:Fondazione GONO | |||||||||||||
Full Title: Pembrolizumab and olaparib in recurrent/metastatic, platinum resistant nasopharyngeal cancer | |||||||||||||
Medical condition: Nasopharyngeal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000230-29 | Sponsor Protocol Number: CA209-358 | Start Date*: 2015-09-29 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||||||||||||||||||||||||||||||||
Full Title: Non-Comparative, Open-Label, Multiple Cohort, Phase 1/2 Study of Nivolumab and Nivolumab plus Ipilimumab in Subjects with Virus-Positive and Virus-Negative Solid Tumors | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Virus-associated tumors | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) DE (Completed) BE (Completed) GB (GB - no longer in EU/EEA) ES (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-004939-22 | Sponsor Protocol Number: HE 5/06 | Start Date*: 2006-05-02 |
Sponsor Name:Hellenic Cooperative Oncology Group (HeCOG) | ||
Full Title: A PHASE I/II EFFICACY AND SAFETY STUDY OF SU011248 IN PATIENTS WITH RECURRENT OR METASTATIC NON-NASOPHARYNGEAL HEAD AND NECK CANCER | ||
Medical condition: Recurrent or metastatic non-nasopharyngeal head and neck cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022444-20 | Sponsor Protocol Number: 40-41200-98-9069 | Start Date*: 2010-11-15 |
Sponsor Name:ZonMW | ||
Full Title: PHASE I-II STUDY OF GEMCITABINE AND VALPROIC ACID PLUS VALGANCICLOVIR IN PATIENTS WITH ADVANCED NASOPHARYNGEAL CARCINOMA | ||
Medical condition: Patient has histological confirmed residual, recurrent or metastatic EBV-positive Nasopharynx carcinoma that has failed conventional curative treatments and deemed incurable, or patient refuses fur... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-004188-25 | Sponsor Protocol Number: ASST_FARM_ONCO_P-ACC_2022 | Start Date*: 2023-03-03 | ||||||||||||||||||||||||||
Sponsor Name:AZIENDA SOCIO SANITARIA TERRITORIALE DEGLI SPEDALI CIVILI DI BRESCIA | ||||||||||||||||||||||||||||
Full Title: P-ACC Trial - Phase II, single arm, multicenter, open-label study of PARP inhibitors + cisplatin in Recurrent and/or Metastatic Adenoid Cystic Carcinoma | ||||||||||||||||||||||||||||
Medical condition: patients with recurrent and/or Metastatic Adenoid Cystic Carcinoma | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000454-38 | Sponsor Protocol Number: CPDR001X2201 | Start Date*: 2015-10-13 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A phase II, open-label, randomized controlled study of PDR001 in patients with moderately differentiated/undifferentiated locally advanced recurrent or metastatic nasopharyngeal carcinoma who progr... | ||
Medical condition: Moderately differentiated/undifferentiated locally advanced recurrent or metastatic nasopharyngeal carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-000066-22 | Sponsor Protocol Number: BAY 43-9006 | Start Date*: 2008-04-30 | ||||||||||||||||
Sponsor Name:Christie Hospital NHS Foundation Trust | ||||||||||||||||||
Full Title: A Phase 2 study of Sorafenib (BAY 43-9006) in patients with advanced salivary Adenoid Cystic Carcinoma | ||||||||||||||||||
Medical condition: advanced salivary adenoid cystic carcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-001437-40 | Sponsor Protocol Number: KO-TIP-007 | Start Date*: 2019-03-08 | |||||||||||
Sponsor Name:Kura Oncology, Inc. | |||||||||||||
Full Title: The AIM-HN and SEQ-HN Study: A 2 Cohort, Non-comparative, Pivotal Study Evaluating the Efficacy of Tipifarnib in Patients with Head and Neck Squamous Cell Carcinoma (HNSCC) with HRAS Mutations (AIM... | |||||||||||||
Medical condition: Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma (HNSCC) with HRAS Mutations | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) DE (Completed) GB (GB - no longer in EU/EEA) NO (Completed) BE (Completed) AT (Completed) NL (Completed) GR (Completed) DK (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000309-64 | Sponsor Protocol Number: AL-ACC-01 | Start Date*: 2019-10-24 | |||||||||||
Sponsor Name:Ayala Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2, Open-Label, Multi-Center Study of AL101 in Patients With Adenoid Cystic Carcinoma (ACC) Bearing Activating Notch Mutations | |||||||||||||
Medical condition: Adenoid cystic carcinoma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002841-17 | Sponsor Protocol Number: ASST-FARM_ONCO_TEPMEETCET-2022 | Start Date*: 2023-04-07 | |||||||||||
Sponsor Name:AZIENDA SOCIO SANITARIA TERRITORIALE DEGLI SPEDALI CIVILI DI BRESCIA | |||||||||||||
Full Title: Phase 2, open-label, multicentre, single-arm study to evaluate the activity of the combination of EGFR inhibitors and c-MET inhibitors in patients with platinum-resistant head and neck squamous cel... | |||||||||||||
Medical condition: in patients with platinum-resistant head and neck squamous cell carcinoma after relapse to immunotherapy “ | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002206-52 | Sponsor Protocol Number: CD-ON-MEDI4736-1108 | Start Date*: 2012-12-05 |
Sponsor Name:MedImmune | ||
Full Title: A Phase 1/2 Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of MEDI4736 in Subjects with Advanced Solid Tumors | ||
Medical condition: Advanced Solid Tumors | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) GB (Completed) DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-006410-15 | Sponsor Protocol Number: CRSV604A2201 | Start Date*: 2007-05-18 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multi-center, randomized, double-blinded, placebo-controlled, multiple dose study to assess the efficacy of intravenously administered RSV604 in immunocompromised adults with evidence of RSV infe... | |||||||||||||
Medical condition: Respiratory Syncytial Virus (RSV) infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001523-69 | Sponsor Protocol Number: V-CHANCE | Start Date*: 2014-07-28 | |||||||||||
Sponsor Name: Istituto Nazionale Tumori di Napoli - Fondazione "G. Pascale" | |||||||||||||
Full Title: Preclinical and clinical study of valproic acid plus cisplatin and cetuximab in recurrent and/or metastatic squamous cell carcinoma of head and neck | |||||||||||||
Medical condition: Recurrent and/or metastatic squamous cell carcinoma of head and neck | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000461-23 | Sponsor Protocol Number: CA209-627 | Start Date*: 2017-03-07 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: An Open-label Phase 2 Multi-cohort Trial of Nivolumab in Advanced or Metastatic Malignancies | ||||||||||||||||||
Medical condition: Advanced/Metastatic malignancies | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-001860-12 | Sponsor Protocol Number: CMAK683X2101 | Start Date*: 2017-01-26 | ||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
Full Title: A phase I/II, multicenter, open-label study of MAK683 in adult patients with advanced malignancies | ||||||||||||||||||
Medical condition: Advanced malignancies | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) FR (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001534-13 | Sponsor Protocol Number: JAN13004-30 | Start Date*: 2015-10-02 | |||||||||||
Sponsor Name:SPHERIUM BIOMED S.L. | |||||||||||||
Full Title: Phase IB-II clinical trial of melatonin oral gel for the prevention and treatment of oral mucositis in patients with head and neck cancer undergoing chemoradiation. | |||||||||||||
Medical condition: Oral mucositis in patients with head and neck cancer undergoing chemoradiation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006804-34 | Sponsor Protocol Number: CYP003 | Start Date*: 2022-09-27 | |||||||||||||||||||||
Sponsor Name:Cytovation ASA | |||||||||||||||||||||||
Full Title: A Phase 1b/2a, Open-Label, Multi-Center Study of CyPep-1 in Combination With Pembrolizumab to Evaluate the Efficacy and Safety of CyPep-1 in Patients With Advanced or Metastatic Head and Neck Squam... | |||||||||||||||||||||||
Medical condition: Advanced or metastatic: -Head and Neck Squamous Cell Carcinoma (HNSCC); -Melanoma; -Triple-Negative Breast Cancer (TNBC); | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) NL (Completed) IT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
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