- Trials with a EudraCT protocol (2,770)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
2,770 result(s) found for: cancer.
Displaying page 65 of 139.
| EudraCT Number: 2016-004484-39 | Sponsor Protocol Number: BAY1895344/18594 | Start Date*: 2017-07-18 | |||||||||||
| Sponsor Name:Bayer AG | |||||||||||||
| Full Title: An open-label, first-in-human, dose-escalation study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and maximum tolerated dose and / or recommended Phase II dose of the A... | |||||||||||||
| Medical condition: Part A+A.1: Histologically confirmed solid tumors or NHL Part A J-arm : Advanced solid tumors Part B: a) DDR deficient advanced solid tumors: i) CRPC; ii) HER2- negative BC (estrogen-receptor posit... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000995-14 | Sponsor Protocol Number: MIV-818-101/201 | Start Date*: 2018-08-10 | |||||||||||||||||||||
| Sponsor Name:Medivir AB | |||||||||||||||||||||||
| Full Title: A Phase 1/2a Study in 3 Parts (Phase 1a and Phase 1b - Dose Escalations and Phase 2a Expansion Cohorts) to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Antitumor Activity of... | |||||||||||||||||||||||
| Medical condition: hepatocellular carcinoma (HCC), intrahepatic cholangiocarcinoma (iCCA), or, metastatic liver disease | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) ES (Ongoing) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2021-001967-26 | Sponsor Protocol Number: ACT16444 | Start Date*: 2021-09-16 | ||||||||||||||||
| Sponsor Name:Sanofi aventis recherche & développement | ||||||||||||||||||
| Full Title: Open-label study of tusamitamab ravtansine (SAR408701) in combination with ramucirumab in participants previously treated for advanced gastric or gastroesophageal junction (GEJ) adenocarcinoma with... | ||||||||||||||||||
| Medical condition: Cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Completed) ES (Ongoing) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2019-000589-39 | Sponsor Protocol Number: ADP-0044-002 | Start Date*: 2020-02-13 | |||||||||||||||||||||
| Sponsor Name:Adaptimmune LLC | |||||||||||||||||||||||
| Full Title: A Phase 2 Single Arm Open-Label Clinical Trial of ADP-A2M4 SPEAR™ T cells in subjects with Advanced Synovial Sarcoma or Myxoid/Round Cell Liposarcoma | |||||||||||||||||||||||
| Medical condition: Advanced Synovial Sarcoma Myxoid/Round Cell Liposarcoma | |||||||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: FR (Trial now transitioned) GB (GB - no longer in EU/EEA) ES (Ongoing) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2018-004568-72 | Sponsor Protocol Number: ASTX029-01 | Start Date*: 2021-05-27 | ||||||||||||||||||||||||||
| Sponsor Name:Astex Pharmaceuticals, Inc. | ||||||||||||||||||||||||||||
| Full Title: A Phase 1-2 Study of the Safety, Pharmacokinetics, and Activity of ASTX029 in Subjects with Advanced Solid Tumors | ||||||||||||||||||||||||||||
| Medical condition: Advanced Solid Tumors | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: FR (Completed) ES (Ongoing) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2014-003190-42 | Sponsor Protocol Number: ANZUP1304 | Start Date*: 2014-10-17 | ||||||||||||||||
| Sponsor Name:Cancer Trials Ireland | ||||||||||||||||||
| Full Title: Randomised phase 3 trial of enzalutamide in first line androgen deprivation therapy for metastatic prostate cancer: ENZAMET | ||||||||||||||||||
| Medical condition: Metastatic Prostate Cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
| Trial protocol: IE (Trial now transitioned) GB (GB - no longer in EU/EEA) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2011-001790-41 | Sponsor Protocol Number: AB11002 | Start Date*: 2013-04-10 | |||||||||||
| Sponsor Name:AB Science | |||||||||||||
| Full Title: A prospective, multicenter, randomised, open-label, active-controlled, two-parallel groups, phase 3 study to compare the efficacy and safety of masitinib to sunitinib in patients with gastrointesti... | |||||||||||||
| Medical condition: Gastrointestinal stromal tumor resistant to imatinib | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) ES (Ongoing) NL (Ongoing) DE (Prohibited by CA) BE (Prematurely Ended) AT (Ongoing) GB (GB - no longer in EU/EEA) GR (Prematurely Ended) IT (Suspended by CA) CY (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-002893-11 | Sponsor Protocol Number: PASIPHAE | Start Date*: 2017-08-14 |
| Sponsor Name:Karolinska University Hospital | ||
| Full Title: A phase 2, international, multicenter, open-labeled, randomized trial of PAlbociclib and fulvestrant vs. Standard oral capecitabine In Patients with Hormone receptor positive/HER2 negative Advanced... | ||
| Medical condition: Hormone receptor positive/HER2 negative advanced breast cancer with endocrine resistance | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: SE (Prematurely Ended) GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-004424-38 | Sponsor Protocol Number: 011604QM | Start Date*: 2017-11-16 | |||||||||||
| Sponsor Name:Queen Mary University of London | |||||||||||||
| Full Title: A phase II study investigating preoperative combination strategies for immunotherapy in patients with untreated, operable ER+, HER2-negative primary breast cancer. | |||||||||||||
| Medical condition: Untreated, operable ER+, HER2-negative primary breast cancer. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003959-16 | Sponsor Protocol Number: CAAA405A12301 | Start Date*: 2021-04-27 | |||||||||||
| Sponsor Name:Novartis Pharma AG | |||||||||||||
| Full Title: Phase III study for evaluation of the diagnostic performance of [18F]CTT1057 PET imaging in patients with prostate cancer with rising PSA levels [biochemical recurrence (BCR)] (GuidePath) | |||||||||||||
| Medical condition: Prostate cancer with rising PSA levels [biochemical recurrence (BCR)] | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: FR (Completed) ES (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-002729-27 | Sponsor Protocol Number: MK-3475-A86 | Start Date*: 2021-09-16 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
| Full Title: A Randomized, Phase 3, Open-label Study to Investigate the Pharmacokinetics and Safety of Subcutaneous Pembrolizumab versus Intravenous Pembrolizumab, Administered with Platinum Doublet Chemotherap... | |||||||||||||
| Medical condition: Metastatic Squamous or Nonsquamous Non-Small-Cell Lung Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) HU (Trial now transitioned) PL (Trial now transitioned) ES (Ongoing) RO (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-002821-39 | Sponsor Protocol Number: MCLA-128-CL02 | Start Date*: 2017-11-13 | |||||||||||
| Sponsor Name:Merus N.V. | |||||||||||||
| Full Title: Phase 2 study of MCLA-128-based combinations in metastatic breast cancer (MBC): MCLA-128/trastuzumab/chemotherapy in HER2-positive MBC and MCLA-128/endocrine therapy in estrogen receptor positive a... | |||||||||||||
| Medical condition: Metastatic Breast Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: BE (Completed) PT (Completed) ES (Ongoing) GB (GB - no longer in EU/EEA) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004203-41 | Sponsor Protocol Number: 54767414MMY2040 | Start Date*: 2018-04-26 | |||||||||||
| Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
| Full Title: A Multicenter Phase 2 Study to Evaluate Subcutaneous Daratumumab in Combination with Standard Multiple Myeloma Treatment Regimens | |||||||||||||
| Medical condition: Multiple Myeloma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) CZ (Completed) ES (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000363-91 | Sponsor Protocol Number: CX-839-008 | Start Date*: 2018-08-10 |
| Sponsor Name:Calithera Biosciences Inc | ||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled Phase 2 Clinical Trial Comparing CB-839 in Combination with Cabozantinib (CB-Cabo) vs. Placebo with Cabozantinib (Pbo-Cabo) in Patients with Advanced ... | ||
| Medical condition: Advanced or metastatic clear-cell renal cell carcinoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) ES (Prematurely Ended) DE (Ongoing) IT (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2022-002234-14 | Sponsor Protocol Number: OR2805-101 | Start Date*: 2023-06-07 |
| Sponsor Name:OncoResponse, Inc. | ||
| Full Title: A Phase 1-2 Study of OR2805 Alone and in Combination with other Anti-cancer Agents in Subjects with Advanced Malignancies | ||
| Medical condition: Solid tumor cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) FR (Completed) | ||
| Trial results: (No results available) | ||
| 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: 2021-001789-39 | Sponsor Protocol Number: LAVA1207-001 | Start Date*: 2021-07-13 | |||||||||||
| Sponsor Name:LAVA Therapeutics N.V. | |||||||||||||
| Full Title: A Phase 1 and 2a open-label trial to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, immunogenicity, and antitumor activity of LAVA-1207, a PSMA-targeting bispecific γδ-T cel... | |||||||||||||
| Medical condition: Prostate Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: NL (Trial now transitioned) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-001300-35 | Sponsor Protocol Number: UCL11/0034 | Start Date*: 2012-01-31 | ||||||||||||||||||||||||||
| Sponsor Name:University College London | ||||||||||||||||||||||||||||
| Full Title: A phase III multicentre trial of weekly induction chemotherapy followed by standard chemoradiation versus standard chemoradiation alone in patients with locally advanced cervical cancer | ||||||||||||||||||||||||||||
| Medical condition: Locally advanced cervical cancer | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) IT (Completed) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2018-000339-28 | Sponsor Protocol Number: CA025-006 | Start Date*: 2018-10-01 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: A Phase 2 Study of Cabiralizumab (BMS-986227, FPA008) Administered in Combination with Nivolumab (BMS-936558) with and without chemotherapy in Patients with Advanced Pancreatic Cancer | |||||||||||||
| Medical condition: Advanced Pancreatic Cancer. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) ES (Ongoing) DK (Completed) DE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001485-29 | Sponsor Protocol Number: G1T38-02 | Start Date*: 2017-03-21 | |||||||||||
| Sponsor Name:G1 Therapeutics, Inc | |||||||||||||
| Full Title: Phase 1/2 Safety, Pharmacokinetic, and Antitumor Activity Study of G1T38 in Combination with Fulvestrant in Patients with Hormone Receptor-Positive, HER2 Negative Locally Advanced or Metastatic Bre... | |||||||||||||
| Medical condition: Hormone Receptor-Positive, HER2 Negative Metastatic Breast Cancer after Endocrine Failure | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) BG (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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