- Trials with a EudraCT protocol (1,057)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (15)
1,057 result(s) found for: Malignant Solid Tumor.
Displaying page 14 of 53.
EudraCT Number: 2007-007734-19 | Sponsor Protocol Number: P53SLP01/01 | Start Date*: 2008-07-03 | |||||||||||
Sponsor Name:University Medical Center Groningen, UMCG-Department of Gynaecologic Oncology | |||||||||||||
Full Title: p53 synthetic long peptides vaccine with cyclophosphamide for ovarian cancer, a phase II trial. | |||||||||||||
Medical condition: This is an uncontrolled, mono-centre, phase II single dose trial for patients with ovarian cancer, who have a rising serum tumor marker CA-125 after previous treatment (surgery and platinum based c... | |||||||||||||
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Population Age: | Gender: Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-005076-26 | Sponsor Protocol Number: SGNTV-001 | Start Date*: 2019-04-16 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Seagen, Inc. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Open Label Phase 2 Study of Tisotumab Vedotin for Locally Advanced or Metastatic Disease in Solid Tumors | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Locally Advanced or Metastatic Disease in Solid Tumors | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) GB (GB - no longer in EU/EEA) FR (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004826-32 | Sponsor Protocol Number: 3121001 | Start Date*: 2016-10-24 | |||||||||||
Sponsor Name:Orion Corporation Orion Pharma | |||||||||||||
Full Title: Safety and pharmacokinetics of ODM-207 in patients with selected advanced solid tumours: an open-label, non-randomised, uncontrolled, multicentre, first-in-human study with cohort expansion | |||||||||||||
Medical condition: Advanced Solid Tumours | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FI (Completed) ES (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004750-15 | Sponsor Protocol Number: AIO-STS-0415 | Start Date*: 2017-10-06 | ||||||||||||||||
Sponsor Name:AIO-Studien-gGmbH | ||||||||||||||||||
Full Title: A randomized phase II study of Durvalumab (MEDI4736) and Tremelimumab compared to doxorubicin in patients with advanced or metastatic soft tissue sarcoma. | ||||||||||||||||||
Medical condition: advanced or metastatic soft tissue sarcoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-004630-42 | Sponsor Protocol Number: TAS-120-301 | Start Date*: 2021-01-25 | |||||||||||
Sponsor Name:Taiho Oncology Inc | |||||||||||||
Full Title: A Phase 3, Open-Label, Randomized Study of Futibatinib Versus Gemcitabine-Cisplatin Chemotherapy as First-Line Treatment of Patients with Advanced Cholangiocarcinoma Harboring FGFR2 Gene Rearrangem... | |||||||||||||
Medical condition: Advanced solid tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) PT (Prematurely Ended) DE (Prematurely Ended) PL (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003126-25 | Sponsor Protocol Number: MS201923-0001 | Start Date*: 2012-09-27 | |||||||||||
Sponsor Name:Merck KGaA | |||||||||||||
Full Title: An Open-Label, First-in-Human Study of the Safety, Tolerability, and Pharmacokinetics of VX-970/M6620 in Combination With Cytotoxic Chemotherapy in Participants With Advanced Solid Tumors | |||||||||||||
Medical condition: cancer (malignant solid tumors) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002929-35 | Sponsor Protocol Number: CFGF401X2101 | Start Date*: 2015-01-02 | ||||||||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | ||||||||||||||||||
Full Title: A phase I/II, multicenter, open-label study of oral FGF401 in adult patients with hepatocellular carcinoma or solid malignancies characterized by positive FGFR4 and KLB expression | ||||||||||||||||||
Medical condition: Hepatocellular carcinoma or other solid tumors characterized by positive FGFR4 and KLB expression | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) DE (Prematurely Ended) FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-001796-21 | Sponsor Protocol Number: 2102-ONC-102 | Start Date*: 2019-02-21 | |||||||||||||||||||||||||||||||
Sponsor Name:Forma Therapeutics, Inc. | |||||||||||||||||||||||||||||||||
Full Title: A Phase 1b/2 Study of FT-2102 in Patients with Advanced Solid Tumors and Gliomas with an IDH1 Mutation | |||||||||||||||||||||||||||||||||
Medical condition: Advanced Solid Tumors and Gliomas with an IDH1 Mutation | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) ES (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001249-15 | Sponsor Protocol Number: 314-12-401 | Start Date*: 2013-11-07 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Otsuka Novel Products GmbH | ||||||||||||||||||||||||||||||||||||||
Full Title: A Two-Part Phase 1/2a, Open-Label, Dose-Escalation Study to Evaluate the Tolerability and Preliminary Antitumour Activity of OPB-111001 in Patients with Advanced Cancers that are Poorly Responsive ... | ||||||||||||||||||||||||||||||||||||||
Medical condition: • Advanced prostate cancer • Advanced epithelial ovarian cancer, advanced squamous cell carcinoma of the cervix, advanced breast cancer, endometrial cancer, and salivary gland cancer that are p... | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-003593-17 | Sponsor Protocol Number: BNT411-01 | Start Date*: 2021-02-18 | ||||||||||||||||
Sponsor Name:BioNTech SE | ||||||||||||||||||
Full Title: Phase 1/2a, first-in-human, open-label, dose-escalation trial with expansion cohorts to evaluate safety, pharmacokinetics, pharmacodynamics, and preliminary efficacy of BNT411 as a monotherapy in p... | ||||||||||||||||||
Medical condition: Chemotherapy-naïve extensive-stage small cell lung cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) ES (Prematurely Ended) GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-003657-30 | Sponsor Protocol Number: DAY101-001 | Start Date*: Information not available in EudraCT |
Sponsor Name:DOT Therapeutics-1 Inc. (Day One) | ||
Full Title: A Phase 2, Open-Label, Multicenter Study to Evaluate the Safety and Efficacy of the Oral Pan-RAF Inhibitor DAY101 in Pediatric Patients with BRAF-Altered, Recurrent or Progressive Low-Grade Glioma | ||
Medical condition: BRAF-Altered, Recurrent or Progressive Low-Grade Glioma in pediatric patients | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) DE (Restarted) DK (Trial now transitioned) NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000084-16 | Sponsor Protocol Number: NC-6004-004A | Start Date*: 2016-11-24 | |||||||||||||||||||||
Sponsor Name:NanoCarrier Co, Ltd | |||||||||||||||||||||||
Full Title: A Phase 1b/2 Dose Escalation and Expansion Trial of NC-6004 (Nanoparticle Cisplatin) plus Gemcitabine in Patients with Advanced Solid Tumors or Squamous Non-Small Cell Lung, Biliary Tract, and Blad... | |||||||||||||||||||||||
Medical condition: Advanced solid tumors and first-line metastatic squamous NSCLC; first-line metastatic or locally advanced cholangiocarcinoma, gallbladder cancer, or ampullary cancer (biliary tract cancer); and fir... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BG (Completed) PL (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004745-24 | Sponsor Protocol Number: MCLA-158-CL01 | Start Date*: 2018-02-22 | ||||||||||||||||
Sponsor Name:Merus N.V. | ||||||||||||||||||
Full Title: Phase 1/2 dose escalation and cohort expansion study evaluating MCLA-158 (Petosemtamab) as single agent or in combination in advanced solid tumors | ||||||||||||||||||
Medical condition: Metastatic colorectal cancer Advanced solid tumors | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Trial now transitioned) NL (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000528-39 | Sponsor Protocol Number: TAK-676-1002 | Start Date*: 2023-03-20 | |||||||||||
Sponsor Name:Takeda Development Center Americas, Inc. (TDC Americas) | |||||||||||||
Full Title: An Open-label, Dose Escalation, Phase 1/2 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of TAK-676 as a Single Agent and in Combination With Pembrolizumab in Ad... | |||||||||||||
Medical condition: Solid Neoplasms | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Trial now transitioned) PL (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-005068-33 | Sponsor Protocol Number: D4191C00068 | Start Date*: 2017-08-28 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: An Open-Label, Multi-Centre, Safety Study of Fixed-Dose Durvalumab + Tremelimumab Combination Therapy or Durvalumab Monotherapy in Advanced Solid Malignancies | |||||||||||||
Medical condition: The target patient population of the protocol includes patients with advanced solid tumors who meet the overall and tumor specific inclusion and exclusion criteria as outlined in each protocol Modu... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004103-20 | Sponsor Protocol Number: INO-VT-464-CL-001 | Start Date*: 2011-10-13 | |||||||||||
Sponsor Name:Innocrin Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 1/2 Open-Label Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of Seviteronel in Subjects with Castration-Resistant Prostate Cancer | |||||||||||||
Medical condition: Castration-resistant prostate cancer (CRPC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002113-19 | Sponsor Protocol Number: 42756493CAN2002 | Start Date*: 2019-10-31 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 2 Study of Erdafitinib in Subjects with Advanced Solid Tumors and FGFR Gene Alterations | |||||||||||||
Medical condition: Advanced solid tumors (other than Urothelial tumors), and FGFR gene alterations. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) PL (Completed) FR (Completed) DE (Trial now transitioned) ES (Ongoing) BE (Completed) IT (Completed) Outside EU/EEA SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000347-41 | Sponsor Protocol Number: N17DEX | Start Date*: 2017-04-19 | |||||||||||
Sponsor Name:Modra Pharmaceuticals BV | |||||||||||||
Full Title: Safety of extended use of the weekly oral docetaxel formulation ModraDoc006/r in patients with advanced solid tumours | |||||||||||||
Medical condition: Advanced solid malignancies | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001329-29 | Sponsor Protocol Number: TIG-006 | Start Date*: 2021-07-15 |
Sponsor Name:iTeos Belgium SA | ||
Full Title: A Multicenter, Open-Label, Phase I/II Study of EOS884448 in combination with standard of care and/or investigational therapies in participants with advanced solid tumors | ||
Medical condition: Advanced solid tumors | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) IT (Trial now transitioned) ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005718-12 | Sponsor Protocol Number: AP26113-11-101 | Start Date*: 2012-07-12 | |||||||||||||||||||||||||||||||
Sponsor Name:ARIAD Pharmaceuticals, Inc. | |||||||||||||||||||||||||||||||||
Full Title: A Phase 1/2 Study of the Safety, Tolerability, Pharmacokinetics and Preliminary Anti-Tumor Activity of the Oral ALK/EGFR Inhibitor AP26113 | |||||||||||||||||||||||||||||||||
Medical condition: Dose Escalation Phase: Histologically confirmed advanced malignancies. All histologies except leukaemia. Dose Expansion Phase: Non-small cell lung cancer (NSCLC) | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: ES (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
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