- Trials with a EudraCT protocol (5,819)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
5,819 result(s) found for: Chemotherapy.
Displaying page 141 of 291.
| EudraCT Number: 2016-002509-21 | Sponsor Protocol Number: FIL-Rouge | Start Date*: 2017-07-17 | |||||||||||
| Sponsor Name:FONDAZIONE ITALIANA LINFOMI ONLUS | |||||||||||||
| Full Title: A randomized, open-label, multicenter, phase III, 2-arm study comparing efficacy and tolerability of the intensified variant ‘dose-dense/dose-intense ABVD’ (ABVD DD-DI) with an interim PET response... | |||||||||||||
| Medical condition: Advanced stage (IIB-IV) Hodgkin Lymphoma. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-002284-18 | Sponsor Protocol Number: UC-0140/1711 | Start Date*: 2017-12-02 |
| Sponsor Name:UNICANCER | ||
| Full Title: A randomized phase 2 study in patients with triple-negative, androgen receptor positive locally advanced (unresectable) or metastatic breast cancer treated with darolutamide or capecitabine | ||
| Medical condition: Triple-negative androgen receptor positive (molecular apocrine-like HER2-negative subtype) locally advanced (unresectable) or metastatic breast cancer. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: FR (Trial now transitioned) BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-004181-20 | Sponsor Protocol Number: IEO1360 | Start Date*: 2021-09-22 | |||||||||||||||||||||
| Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||||||||||||
| Full Title: Camidanlumab tesirine (ADCT-301) in older classical Hodgkin lymphoma (cHL) patients with relapsed or refractory disease after front-line treatment or at high risk of failure, defined by a positive ... | |||||||||||||||||||||||
| Medical condition: Relapsed or refractory Hodgkin's lymphoma after first-line chemotherapy or at high risk of failure, as defined by persistence of PET-positivity after the first two courses of first-line chemotherap... | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2013-000276-15 | Sponsor Protocol Number: OV-AP-ICG-IV | Start Date*: 2013-03-08 |
| Sponsor Name:Jules Bordet Institute | ||
| Full Title: Feasibility study of the (intravenously injected) Indocyanine green (ICG) imaging of tumoral implants in patients with peritoneal carcinomatosis from ovarian carcinoma | ||
| Medical condition: Peritoneal carcinomatosis from ovarian cancer | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-000559-15 | Sponsor Protocol Number: FB2012 | Start Date*: 2012-09-14 |
| Sponsor Name:FinnBladder | ||
| Full Title: TREATMENT OF Ta BLADDER CANCER WITH HIGH RISK OF RECURRENCE – FLUORESCENCE CYSTOSCOPY WITH OPTIMIZED ADJUVANT MITOMYCIN-C | ||
| Medical condition: bladder cancer (non-invasive Ta urothelial bladder cancer) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-020472-34 | Sponsor Protocol Number: IEO S542/310 | Start Date*: 2010-12-14 | |||||||||||
| Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
| Full Title: 18F-Fluorothymidine Positron Emission Tomography as an early predictor of response to neoadjuvant therapy in patients with locally advanced breast carcinoma | |||||||||||||
| Medical condition: Breast carcinoma classified as cT1b,c, T2, T3, or cT4 a-c, cN0-2, N3, M0 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2023-000169-14 | Sponsor Protocol Number: INES | Start Date*: 2023-05-03 | |||||||||||
| Sponsor Name:Fondazione Santobono Pausilipon ONLUS | |||||||||||||
| Full Title: Phase II Prospective Multicenter Study of High-Dose Treosulfan/Melphalan as Consolidation Treatment in Newly Diagnosed High-Risk and Very High-Risk Ewing Sarcoma | |||||||||||||
| Medical condition: Ewing Sarcoma | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-004675-31 | Sponsor Protocol Number: AMCmedonc17-010 | Start Date*: 2019-11-13 |
| Sponsor Name:Academic Medical Center | ||
| Full Title: A randomized Phase II study of second line treatment with liposomal irinotecan and S1 versus liposomal irinotecan and 5-fluorouracil in patients with metastatic pancreatic cancer who failed on firs... | ||
| Medical condition: pancreatic cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Ongoing) ES (Ongoing) IT (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-001777-19 | Sponsor Protocol Number: HOVON 81 AML | Start Date*: 2006-12-07 | |||||||||||
| Sponsor Name:HOVON foundation | |||||||||||||
| Full Title: A Phase II multicenter study to assess the tolerability and efficacy of the addition of Bevacizumab to standard induction therapy in AML and high risk MDS above 60 years. | |||||||||||||
| Medical condition: Acute myeloid leukaemia (AML), AML FAB M0-M2 or M4-M7; diagnosis with refractory anemia with excess of blasts (RAEB) or refractory anemia with excess of blasts in transformation (RAEB-T) with an IP... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-000653-42 | Sponsor Protocol Number: OC-AP-ICG-IV | Start Date*: 2013-03-20 |
| Sponsor Name:Jules Bordet Institute | ||
| Full Title: Feasibility study of the (intravenously injected) ICG imaging of tumoral implants in patients with peritoneal carcinomatosis from colorectal cancer | ||
| Medical condition: Peritoneal carcinomatosis from colon Cancer. | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-005050-20 | Sponsor Protocol Number: NURE-Combo | Start Date*: 2021-10-13 | |||||||||||
| Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
| Full Title: An open label, single-arm, phase 2 study od neoadjuvant nivolumab and nab-paclitaxel before cystectomy for patients with muscle-invasive bladder cancer | |||||||||||||
| Medical condition: muscle-invasive bladder cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-000035-50 | Sponsor Protocol Number: ACT16146 | Start Date*: 2020-08-07 | |||||||||||
| Sponsor Name:Sanofi aventis recherche & développement | |||||||||||||
| Full Title: Randomized, open-label, Phase 2 study of SAR408701 combined with pembrolizumab and pembrolizumab alone in patients with CEACAM5 and PD-L1 positive advanced/metastatic non-squamous non–small-cell lu... | |||||||||||||
| Medical condition: Non-squamous non–small-cell lung cancer (NSQ NSCLC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) HU (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-001103-21 | Sponsor Protocol Number: ONC-MANILA12 | Start Date*: 2012-12-05 | ||||||||||||||||
| Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | ||||||||||||||||||
| Full Title: MANTAINANCE METRONOMIC PER OS NAVELBINE IN ADVANCED NSCLC PATIENTS AFTER PREVIOUS PLATINUM BASED CHEMOTHERAPY: A MULTICENTER RANDOMIZED BEST SUPPORTIVE CARE CONTROLLED PHASE II STUDY: MA.NI.LA. TRIAL. | ||||||||||||||||||
| Medical condition: Advanced non small cell lung cancer (NSCLC) (Inoperable Stage III - IV). | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2018-004853-26 | Sponsor Protocol Number: T315/2018 | Start Date*: 2019-03-25 | ||||||||||||||||
| Sponsor Name:Turku University Hospital | ||||||||||||||||||
| Full Title: The effect of androgen deprivation therapy on the expression of prostate specific membrane antigen (PSMA) in treatment naive metastatic prostate cancer | ||||||||||||||||||
| Medical condition: Metastatic prostate cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
| Trial protocol: FI (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2022-002134-14 | Sponsor Protocol Number: 1.0 | Start Date*: 2022-09-02 |
| Sponsor Name:Catharina Hospital Eindhoven | ||
| Full Title: Intraperitoneal irinotecan with concomitant FOLFOX and bevacizumab for patients with unresectable colorectal peritoneal metastases – a phase II study | ||
| Medical condition: Patients with peritoneal carcinomatosis of colorectal origin | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-003645-41 | Sponsor Protocol Number: STARDUST | Start Date*: 2019-09-13 | ||||||||||||||||
| Sponsor Name:FONDAZIONE RICERCA TRASLAZIONALE | ||||||||||||||||||
| Full Title: Phase II trial evaluating the efficacy of durvalumab (MEDI4736) as second-line therapy in Non- Small-Cell Lung Cancer patients receiving concomitant steroids | ||||||||||||||||||
| Medical condition: Non- Small-Cell Lung Cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2011-001557-85 | Sponsor Protocol Number: 5.0 | Start Date*: 2011-08-22 | |||||||||||
| Sponsor Name:Nordic Lymphoma Group | |||||||||||||
| Full Title: NLG-MCL5 (MARiT) Rituximab, High Dose Ara-C and Dexamethasone Followed by BEAM in Mantle Cell Lymphoma Patients <66 years A Nordic Lymphoma Group and British Lymphoma Group Phase-II Trial | |||||||||||||
| Medical condition: Mantle cell lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Temporarily Halted) DK (Prematurely Ended) FI (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-000317-78 | Sponsor Protocol Number: PV-10-MM-31 | Start Date*: 2017-02-24 | |||||||||||
| Sponsor Name:PROVECTUS BIOPHARMACEUTICALS, INC. | |||||||||||||
| Full Title: PV-10 Intralesional Injection vs Systemic Chemotherapy or Intralesional Oncolytic Viral Therapy for Treatment of Locally Advanced Cutaneous Melanoma | |||||||||||||
| Medical condition: Locally Advanced Cutaneous Melanoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-003888-10 | Sponsor Protocol Number: PANDA | Start Date*: 2016-05-23 | |||||||||||
| Sponsor Name:Fondazione GONO | |||||||||||||
| Full Title: The PANDA STUDY: RANDOMIZED PHASE II STUDY OF FIRST-LINE FOLFOX PLUS PANITUMUMAB versus 5FU PLUS PANITUMUMAB IN RAS AND BRAF WILD-TYPE METASTATIC COLORECTAL CANCER ELDERLY PATIENTS | |||||||||||||
| Medical condition: Metastatic Colorectal Cancer | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-006030-40 | Sponsor Protocol Number: Pola_R | Start Date*: 2022-05-31 |
| Sponsor Name:Med. Univ. Wien, Klinik f. Innere Med I, Onkologie | ||
| Full Title: EFFICACY OF POLATUZUMAB, BENDAMUSTINE AND RITUXIMAB IN PATIENTS WITH RELAPSED/ REFRACTORY MANTLE CELL LYMPHOMA – A SINGLE CENTER PHASE II TRIAL | ||
| Medical condition: MANTLE CELL LYMPHOMA | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Trial now transitioned) | ||
| Trial results: (No results available) | ||
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