- Trials with a EudraCT protocol (1,056)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (15)
1,056 result(s) found for: Malignant Solid Tumor.
Displaying page 26 of 53.
EudraCT Number: 2017-003935-12 | Sponsor Protocol Number: ATRiUM | Start Date*: 2019-06-13 | ||||||||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and the University of Cambridge | ||||||||||||||||||
Full Title: ATRiUM: A phase 1 trial to assess the safety, tolerability, pharmacokinetics and preliminary antitumor activity of ascending doses of combined therapy with ATR inhibitor AZD6738 and gemcitabine, Us... | ||||||||||||||||||
Medical condition: Locally advanced or metastatic solid tumour. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
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: 2007-006717-17 | Sponsor Protocol Number: CP12-0711 | Start Date*: 2008-12-01 | ||||||||||||||||
Sponsor Name:ImClone LLC | ||||||||||||||||||
Full Title: A Phase 2, Non-randomized, Open-label, Multicenter Study of IMC-1121B in the Treatment of Persistent or Recurrent Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Carcinoma | ||||||||||||||||||
Medical condition: Persistent or Recurrent Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Carcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-004952-14 | Sponsor Protocol Number: 0209-01 | Start Date*: 2021-07-07 |
Sponsor Name:Constellation Pharmaceuticals, Inc. | ||
Full Title: A Phase 1/2 Study of CPI-0209 Monotherapy and in Combination with Other Therapy in Patients with Advanced Tumors | ||
Medical condition: advanced, solid, relapsed tumors / advanced tumors: human lymphomas / solid human tumor indications (urothelial carcinoma, ovarian clear cell cancer, endometrial carcinoma, GCB-DLBCL, small cell lu... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) PL (Trial now transitioned) IT (Trial now transitioned) ES (Temporarily Halted) | ||
Trial results: (No results available) |
EudraCT Number: 2004-004533-34 | Sponsor Protocol Number: BIOV-221 | Start Date*: 2005-05-19 | |||||||||||
Sponsor Name:Bioenvision | |||||||||||||
Full Title: A Phase IV Non-randomised Study of Modrenal® (Trilostane) in Post-menopausal Women with Advanced, Oestrogen Receptor Positive Breast Cancer for whom Prior Endocrine Therapies have Failed, One of w... | |||||||||||||
Medical condition: Advanced, Oestrogen Receptor Positive Breast Cancer for whom Prior Endocrine Therapies have Failed, One of which was an Aromatase Inhibitor | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004966-33 | Sponsor Protocol Number: UZB-2013-001 | Start Date*: 2014-04-30 | |||||||||||||||||||||||||||||||
Sponsor Name:UZ Brussel | |||||||||||||||||||||||||||||||||
Full Title: A phase II clinical trial on the combination of dabrafenib and trametinib for BRAF-inhibitor pretreated patients with advanced BRAF V600 mutant melanoma | |||||||||||||||||||||||||||||||||
Medical condition: advanced BRAF V600 mutant melanoma | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000300-26 | Sponsor Protocol Number: E7080-A001-111 | Start Date*: 2017-10-20 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Eisai Ltd. | ||||||||||||||||||||||||||||||||||||||
Full Title: A Multicenter, Open-Label Phase 1b/2 Trial of Lenvatinib (E7080) Plus Pembrolizumab in Subjects With Selected Solid Tumors | ||||||||||||||||||||||||||||||||||||||
Medical condition: Non-small cell lung cancer, predominantly clear cell renal cell carcinoma, endometrial carcinoma, urothelial carcinoma, squamous cell carcinoma of the head and neck, or melanoma (excluding uveal me... | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) NO (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-004747-39 | Sponsor Protocol Number: MK3475_MPNST | Start Date*: Information not available in EudraCT |
Sponsor Name:Oslo University Hospital | ||
Full Title: A phase II study of pembrolizumab in patients with malignant peripheral nerve sheath tumor (MPNST), not eligible for curative surgery | ||
Medical condition: Malignant peripheral nerve sheath tumor (MPNST), not eligible for curative surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004693-27 | Sponsor Protocol Number: A6181064 | Start Date*: 2006-11-09 |
Sponsor Name:Pfizer Ltd. | ||
Full Title: A RANDOMISED, PHASE 3 STUDY OF DOCETAXEL IN COMBINATION WITH SUNITINIB VERSUS DOCETAXEL IN THE FIRST-LINE TREATMENT OF ADVANCED BREAST CANCER PATIENTS | ||
Medical condition: Advanced breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SK (Prematurely Ended) CZ (Prematurely Ended) NL (Prematurely Ended) GB (Prematurely Ended) DE (Prematurely Ended) PT (Prematurely Ended) BE (Completed) AT (Prematurely Ended) SE (Prematurely Ended) FI (Completed) FR (Completed) IT (Prematurely Ended) IE (Prematurely Ended) HU (Prematurely Ended) ES (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2020-001538-37 | Sponsor Protocol Number: CO-338-111 | Start Date*: 2021-05-25 | |||||||||||||||||||||||||||||||
Sponsor Name:Clovis Oncology, Inc. | |||||||||||||||||||||||||||||||||
Full Title: CATCH-R: A Rollover Study to Provide Continued Access to Clinical Therapy with Rucaparib | |||||||||||||||||||||||||||||||||
Medical condition: Multiple solid tumor types | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: CZ (Completed) HU (Completed) PL (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-003734-32 | Sponsor Protocol Number: BXCL701-201 | Start Date*: 2019-07-02 | |||||||||||
Sponsor Name:BioXcel Therapeutics, Inc | |||||||||||||
Full Title: A Phase 1b/2 Study of BXCL701, a Small Molecule Inhibitor of Dipeptidyl Peptidases (DPP), Administered in Combination with the Anti-Programmed Cell Death 1 (PD-1) Monoclonal Antibody Pembrolizumab ... | |||||||||||||
Medical condition: Small Cell Neuroendocrine Prostate Cancer | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000179-36 | Sponsor Protocol Number: MS200647_0054 | Start Date*: 2021-10-15 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Merck KGaA | ||||||||||||||||||||||||||||||||||||||
Full Title: An Open-label, Multicenter Follow-up Study to Collect Long-term Data on Participants from Multiple Bintrafusp alfa (M7824) Clinical Studies | ||||||||||||||||||||||||||||||||||||||
Medical condition: Non-small cell lung cancer (NSCLC), biliary tract cancer (BTC), cervical cancer, and triple-negative breast cancer (TNBC) | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: FR (Ongoing) BE (Completed) ES (Ongoing) IT (Completed) DE (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001773-26 | Sponsor Protocol Number: 100554 | Start Date*: 2005-05-03 | |||||||||||
Sponsor Name:Bayer HealthCare AG, D-51368 Leverkusen Germany | |||||||||||||
Full Title: A Phase III randomized, placebo-controlled study of sorafenib in patients with advanced hepatocellular carcinoma | |||||||||||||
Medical condition: Advanced hepatocellular carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) BE (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002285-23 | Sponsor Protocol Number: POETIG | Start Date*: 2017-01-18 | |||||||||||
Sponsor Name:Universitaetsklinikum Essen | |||||||||||||
Full Title: Phase 2 trial of ponatinib in patients with metastatic and/or unresectable gastrointestinal stromal tumor (GIST) following failure or intolerance of prior therapy with imatinib (POETIG trial – POna... | |||||||||||||
Medical condition: gastrointestinal stromal tumor (GIST) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001546-34 | Sponsor Protocol Number: EADO_VC_NEO_1 | Start Date*: 2014-10-02 | ||||||||||||||||
Sponsor Name:University Hospital Tübingen | ||||||||||||||||||
Full Title: Neoadjuvant treatment with the combination of Vemurafenib, Cobimetinib and Atezolizumab in limited metastasis of malignant melanoma (AJCC stage IIIC/IV) and integrated biomarker study: A single arm... | ||||||||||||||||||
Medical condition: Patients with hardly resectable/unresectable limited metastasis in malignant melanoma stages IIIC/IV (American Joint Committee on Cancer (AJCC) 2010) carrying the BRAF V600 mutation, in order to ac... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) AT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-004624-36 | Sponsor Protocol Number: A6181099 | Start Date*: 2007-03-19 | |||||||||||
Sponsor Name:Pfizer Inc - 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A RANDOMIZED, PHASE 3 STUDY OF SUNITINIB IN COMBINATION WITH CAPECITABINE COMPARED WITH CAPECITABINE IN PATIENTS WITH PREVIOUSLY TREATED BREAST CANCER | |||||||||||||
Medical condition: Advanced breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) FR (Completed) DK (Completed) DE (Prematurely Ended) AT (Prematurely Ended) GR (Prematurely Ended) CZ (Prematurely Ended) IT (Prematurely Ended) IE (Prematurely Ended) GB (Prematurely Ended) NL (Completed) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023428-26 | Sponsor Protocol Number: D4200C00088 | Start Date*: 2011-01-31 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Randomized, International, Open-Label, Multi-Centre, Phase III Study to Assess the Effect of a Patient Outreach Program on the Percentage of Time Patients with Locally Advanced or Metastatic Medu... | |||||||||||||
Medical condition: Locally advanced or metastatic medullary thyroid cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) IT (Completed) AT (Completed) GB (Completed) SE (Completed) FI (Completed) GR (Ongoing) DK (Completed) PL (Completed) NO (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002641-29 | Sponsor Protocol Number: INCB57643-101 | Start Date*: 2018-03-20 | |||||||||||
Sponsor Name:Incyte Corporation | |||||||||||||
Full Title: A Phase 1/2, Open-Label, Dose-Escalation/Dose-Expansion, Safety and Tolerability Study of INCB057643 in Subjects With Advanced Malignancies | |||||||||||||
Medical condition: Subjects with relapsed or refractory advanced or metastatic malignancies. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002331-25 | Sponsor Protocol Number: BP27836 | Start Date*: 2011-12-07 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd. | |||||||||||||
Full Title: An Open-Label, Randomized, Multicenter Phase IIa Study Evaluating Pertuzumab in Combination with Trastuzumab and Chemotherapy in Patients with HER2-Positive Advanced Gastric Cancer | |||||||||||||
Medical condition: HER2-positive adenocarcinoma of the stomach or gastroesophageal junction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) BE (Completed) CZ (Completed) NL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000210-29 | Sponsor Protocol Number: CMCS110Z2102 | Start Date*: 2016-06-14 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A Phase Ib/II, open label, multicenter study of MCS110 in combination with PDR001 in patients with advanced malignancies | |||||||||||||
Medical condition: advanced malignancies | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) DE (Completed) ES (Completed) FR (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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