- Trials with a EudraCT protocol (427)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
427 result(s) found for: Cetuximab.
Displaying page 1 of 22.
EudraCT Number: 2011-006017-34 | Sponsor Protocol Number: CBYL719X2104 | Start Date*: 2013-03-05 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A phase Ib dose escalation/randomized phase II, multicenter, open-label study of BYL719 in combination with cetuximab in patients with recurrent or metastatic head and neck squamous cell carcinoma | ||
Medical condition: Head and Neck Carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-014440-10 | Sponsor Protocol Number: EMR200068-006 | Start Date*: 2009-12-03 | |||||||||||
Sponsor Name:Merck KGaA | |||||||||||||
Full Title: A Phase II, Open-label, 1:1 Randomized, Controlled Trial Exploring the Efficacy of EMD 1201081 in Combination with Cetuximab in Second-Line Cetuximab-Naïve Subjects with Recurrent or Metastatic Squ... | |||||||||||||
Medical condition: Recurrent/metastatic squamous cell cancer of the head and neck | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Prematurely Ended) CZ (Prematurely Ended) HU (Completed) FR (Completed) SK (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014041-81 | Sponsor Protocol Number: 2906 | Start Date*: 2009-11-13 |
Sponsor Name:GOIM GRUPPO ONCOLOGICO MERIDIONALE | ||
Full Title: Optimal strategy in K-ras wild type metastatic colorectal cancer patients: cetuximab plus FOLFIRI followed by FOLFOX+/- cetuximab (GOIM multicenter program) | ||
Medical condition: k-ras wild type metastatic colorectal cancer patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2008-008282-36 | Sponsor Protocol Number: GPICD–CR–0801 | Start Date*: 2010-05-07 |
Sponsor Name:Grupo de Investigação do Cancro Digestivo | ||
Full Title: Randomized, open-label phase II study evaluating the safety and efficacy of Cetuximab plus modified FOLFOX - 6 versus modified FOLFOX - 6 alone as 2nd line therapy after progression on the 1st line... | ||
Medical condition: Colorectal cancer KRAS wild-type | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2022-001527-32 | Sponsor Protocol Number: SC105(AURELIO-05) | Start Date*: 2022-10-21 |
Sponsor Name:SOTIO Biotech AG | ||
Full Title: A phase 2, open-label, single-arm, multicenter study to evaluate the efficacy and safety of SOT101 in combination with cetuximab in patients with RAS wild-type colorectal cancer (AURELIO-05) | ||
Medical condition: RAS wild-type colorectal cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) BE (Completed) IT (Prematurely Ended) FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000459-14 | Sponsor Protocol Number: VUB/MedOnc/05-001 | Start Date*: 2007-07-02 |
Sponsor Name:Oncologisch Centrum, Academisch Ziekenhuis Vrije Universiteit Brussel | ||
Full Title: A Stratified Phase II Study of Cetuximab (ErbituxTM) for the Treatment of Recurrent Glioblastoma Multiforme / Estudio de fase II estratificado de cetuximab para el tratamiento del glioblastoma mult... | ||
Medical condition: patients with a recurrent glioblastoma multiforme following preceding surgery, radiation therapy and chemotherapy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-002837-37 | Sponsor Protocol Number: CA225-045 | Start Date*: 2004-11-11 | |||||||||||
Sponsor Name:Merck Farma y Química, S.A. | |||||||||||||
Full Title: An exploratory pharmacogenomic study of cetuximab monotherapy in patients with metastatic EGFR-Positive colorectal carcinoma | |||||||||||||
Medical condition: Metastatic colorectal carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001742-13 | Sponsor Protocol Number: 06_RADIO_56 | Start Date*: 2006-10-04 |
Sponsor Name:Christie Hospital NHS Trust | ||
Full Title: Locally Advanced Pancreatic Cancer: Phase II study of cetuximab and 3-D conformal image-guided radiotherapy (PACER Study) | ||
Medical condition: Adenocarcinoma of the pancreas which is locally advanced/inoperable | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2012-001879-37 | Sponsor Protocol Number: ArtscanIII | Start Date*: 2013-03-05 | ||||||||||||||||
Sponsor Name:Department of Oncology, Skåne University Hospital Lund | ||||||||||||||||||
Full Title: A randomized multicenter phase III study of cisplatin plus radiotherapy compared to cetuximab plus radiotherapy in locally advanced head and neck cancer | ||||||||||||||||||
Medical condition: Stage III and IV head and neck squamous cell cancer (HNSCC) without radiographic signs of distant metastases aimed for radiotherapy with curative intent | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004639-31 | Sponsor Protocol Number: INN06 | Start Date*: 2007-01-18 |
Sponsor Name:TAKO | ||
Full Title: Multicenter phase II study evaluating docetaxel, CDDP, and cetuximab as induction regimen prior to surgery in chemonaive patients with NSCLC stage IB, II, and IIIA. | ||
Medical condition: Neoadjuvant treatment of non-small lung cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-005805-35 | Sponsor Protocol Number: ARRAY-818-302 | Start Date*: 2016-11-28 | |||||||||||
Sponsor Name:Array BioPharma Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Open-label, 3-Arm Phase 3 Study of Encorafenib + Cetuximab Plus or Minus Binimetinib vs. Irinotecan/Cetuximab or Infusional 5-Fluorouracil (5-FU)/Folinic Acid (FA) /Irino... | |||||||||||||
Medical condition: BRAF V600E-mutant Metastatic Colorectal Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) HU (Completed) BE (Completed) AT (Completed) NL (Completed) CZ (Completed) DK (Completed) ES (Ongoing) NO (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001126-15 | Sponsor Protocol Number: CRICKET | Start Date*: 2014-10-03 | |||||||||||
Sponsor Name:G.O.N.O. (Gruppo Oncologico Nord Ovest) | |||||||||||||
Full Title: A phase II single-arm study of cetuximab plus irinotecan as rechallenge 3rd-line treatment of kras, nras and braf wild-type irinotecan-pretreated metastatic colorectal cancer patients progressing... | |||||||||||||
Medical condition: metastatic colonrectal cancer KRAS, NRAS and BRAF wild type. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
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: 2019-004770-25 | Sponsor Protocol Number: D7310C00001 | Start Date*: 2020-12-11 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase 3 Randomized, Double-blind, Multicenter, Global Study of Monalizumab or Placebo in Combination with Cetuximab in Patients with Recurrent or Metastatic Squamous Cell Carcinoma of the Head an... | |||||||||||||
Medical condition: Patients With Recurrent or Metastatic Squamous Cell Carcinoma of the Head and Neck Previously Treated With an Immune Checkpoint Inhibitor | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) NL (Completed) GR (Completed) DE (Trial now transitioned) BE (Completed) AT (Completed) BG (Completed) PL (Completed) FR (Completed) PT (Completed) IT (Completed) RO (Ongoing) | |||||||||||||
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 |
EudraCT Number: 2014-004299-41 | Sponsor Protocol Number: ERMES | Start Date*: 2014-12-24 | |||||||||||
Sponsor Name:Dipartimento di Scienze Mediche Oncologia Medica Policlinico Gemelli | |||||||||||||
Full Title: ERbitux MEtastatic colorectal cancer Strategy Study: A phase III randomized two arm study with FOLFIRI + Cetuximab until disease progression compared to FOLFIRI + Cetuximab for 8 cycles followed by... | |||||||||||||
Medical condition: Patients with unresectable RAS and BRAF wild-type metastatic colorectal cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004593-56 | Sponsor Protocol Number: CAVE-2 | Start Date*: 2022-05-19 | |||||||||||
Sponsor Name:GRUPPO ONCOLOGICO DELL'ITALIA MERIDIONALE | |||||||||||||
Full Title: A phase II randomized clinical study of the combination of avelumab plus cetuximab as rechallenge strategy in pre-treated RAS/BRAF wild type metastatic colorectal cancer patients | |||||||||||||
Medical condition: Pre-treated RAS/BRAF wild type metastatic colorectal cancer patients. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002177-25 | Sponsor Protocol Number: 19-255-03 | Start Date*: 2021-11-08 | ||||||||||||||||||||||||||
Sponsor Name:Nektar Therapeutics | ||||||||||||||||||||||||||||
Full Title: A Phase 1b/2, Open-label, Multicenter, Dose Escalation and Dose Expansion Study of NKTR-255 in Combination with Cetuximab as a Salvage Regimen for Solid Tumors | ||||||||||||||||||||||||||||
Medical condition: Relapsed or refractory (R/R) head and neck squamous cell carcinoma (HNSCC) or colorectal carcinoma (CRC) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-002826-11 | Sponsor Protocol Number: CWNT974X2102C | Start Date*: 2014-12-18 | |||||||||||
Sponsor Name:Array BioPharma Inc. | |||||||||||||
Full Title: A phase Ib/II multi-center, open label, dose escalation study of WNT974, LGX818 and cetuximab in patients with BRAFV600-mutant metastatic colorectal cancer harboring Wnt pathway mutations | |||||||||||||
Medical condition: colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) ES (Completed) NL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019885-10 | Sponsor Protocol Number: Dermatux | Start Date*: 2011-01-05 | |||||||||||
Sponsor Name:Universitätsmedizin Mainz (vertreten durch den wissenschaftlichen Vorstand) | |||||||||||||
Full Title: Non-randomized phase-IV-study to investigate the efficacy of FOLFIRI in combination with cetuximab in the first-line treatment of metastatic colorectal cancer inculding a regular dermal prophylaxis... | |||||||||||||
Medical condition: metastatic colorectal cancer (mCRC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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