- Trials with a EudraCT protocol (899)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
899 result(s) found for: Chemotherapy agent.
Displaying page 9 of 45.
EudraCT Number: 2022-001191-34 | Sponsor Protocol Number: ASND0029 | Start Date*: 2023-07-14 | |||||||||||
Sponsor Name:Ascendis Pharma Oncology Division A/S | |||||||||||||
Full Title: IL Believe: A Phase 1/2, Open-label, Dose Escalation and Dose Expansion Study to Investigate the Safety and Tolerability of TransCon IL-2 β/γ Alone or in Combination with Pembrolizumab, Standard of... | |||||||||||||
Medical condition: locally advanced or metastatic solid tumor malignancies, platinum resistant ovarian cancer, post-anti-pd-1 melanoma, second line or later cervical cancer, neoadjuvant melanoma and neoadjuvant non-s... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002552-16 | Sponsor Protocol Number: RRK4368 | Start Date*: 2012-11-29 | |||||||||||
Sponsor Name:University Hospitals Birmingham NHS Foundation Trust | |||||||||||||
Full Title: Cabazitaxel in platinum pre-treated patients with locally advanced or metastatic transitional cell carcinoma who developed disease progression within 12 months of platinum based chemotherapy. | |||||||||||||
Medical condition: Transitional cell carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004852-77 | Sponsor Protocol Number: GO29642 | Start Date*: 2015-05-27 | |||||||||||
Sponsor Name:Genentech, Inc | |||||||||||||
Full Title: AN OPEN-LABEL, PHASE I/IIA STUDY OF GDC-0810 IN POSTMENOPAUSAL WOMEN WITH LOCALLY ADVANCED OR METASTATIC ESTROGEN RECEPTOR POSITIVE BREAST CANCER | |||||||||||||
Medical condition: Patients with locally advanced or metastatic estrogen receptor (ER) positive breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001862-84 | Sponsor Protocol Number: ISO-CC-005 | Start Date*: 2014-07-24 | |||||||||||
Sponsor Name:Isofol Medical AB | |||||||||||||
Full Title: An Open-label, Multiple-site, Phase I/II Dose Cohort Trial of [6R] 5,10-Methylene Tetrahydrofolate (Modufolin®) in Combination with a Fixed Dose of 5-Fluorouracil (5-FU) alone or together with a Fi... | |||||||||||||
Medical condition: Advanced metastatic colorectal cancer (stage IV) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) NO (Prematurely Ended) DK (Prematurely Ended) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002453-38 | Sponsor Protocol Number: 15-102-14 | Start Date*: 2017-01-17 | ||||||||||||||||
Sponsor Name:Nektar Therapeutics | ||||||||||||||||||
Full Title: A Phase 3 Open-Label, Randomized, Multicenter Study of NKTR-102 versus Treatment of Physician’s Choice (TPC) in Patients with Metastatic Breast Cancer Who Have Stable Brain Metastases and Have Been... | ||||||||||||||||||
Medical condition: Metastatic breast cancer with stable brain metastases | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) ES (Prematurely Ended) CZ (Completed) BE (Completed) PT (Completed) FR (Completed) HU (Completed) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-003498-27 | Sponsor Protocol Number: JEVTCC-SOGUG-2011-04 | Start Date*: 2011-12-19 | |||||||||||
Sponsor Name:Grupo Español de Tratamiento de Tumores Genitourinarios (SOGUG)-Spanish Genitourinary Oncologic Group | |||||||||||||
Full Title: A phase II open label study of cabazitaxel in patients with advanced or metastatic transitional cell carcinoma of the urothelium who have progressed ?12 months after a previous platinum based chemo... | |||||||||||||
Medical condition: advanced or metastatic transitional cell carcinoma of the urothelium | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002326-24 | Sponsor Protocol Number: ALKS4230-007 | Start Date*: 2023-02-13 | |||||||||||||||||||||
Sponsor Name:Mural Oncology, Inc. | |||||||||||||||||||||||
Full Title: A Phase 3, Multicenter, Open-Label, Randomized Study of Nemvaleukin Alfa in Combination With Pembrolizumab Versus Investigator’s Choice Chemotherapy in Patients With Platinum-Resistant Epithelial O... | |||||||||||||||||||||||
Medical condition: Patients with Platinum-Resistant Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) ES (Ongoing) PL (Prematurely Ended) IT (Trial now transitioned) NO (Trial now transitioned) AT (Ongoing) LT (Trial now transitioned) BE (Trial now transitioned) DK (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019121-34 | Sponsor Protocol Number: E-3810-I-01 | Start Date*: 2011-03-28 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: An Open-Label, Dose-escalation, Phase I/IIa Study to Determine the Maximum Tolerated Dose, Recommended Dose, Efficacy, Pharmacokinetics, and Pharmacodynamics of the dual VEGFR-FGFR Tyrosine Kinase ... | |||||||||||||
Medical condition: Dose escalation: solid tumors failing standard therapy. Dose-expansion: solid tumors A) with FGFR1 amplification and for breast cancer ? 1 prior endocrine therapy if ER+ or ? 1 chemotherapy otherwi... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002074-22 | Sponsor Protocol Number: UM2005/00201/00 | Start Date*: 2006-10-18 |
Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||
Full Title: A Randomized, Phase III, Open-Label Study of Oral Topotecan Plus Whole-Brain Radiation Therapy (WBRT) Compared with WBRT Alone in Patients with Brain Metastases from Non-Small Cell Lung Cancer. | ||
Medical condition: Brain metastases from primary non-small cell lung cancer (NSCLC). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-003855-11 | Sponsor Protocol Number: 025/05 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Klinikum Großhadern, University of Munich / Medical Director: Prof. Dr. med. Burkhard Götze | |||||||||||||
Full Title: Gemcitabine and cisplatin in combination with hyperthermia in patients with locally advanced or metastatic pancreatic cancer as second-line therapy after adjuvant or first-line chemotherapy with Ge... | |||||||||||||
Medical condition: Combination of standard chemotherapy with Gemcitabine and Cisplatin and regional hyperthermia in patients with locally advanced or metastatic pancreatic cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Restarted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002808-28 | Sponsor Protocol Number: OZM-061 | Start Date*: 2017-12-29 | |||||||||||
Sponsor Name:Princess Margaret Cancer Centre | |||||||||||||
Full Title: Olala Trial: A Retrospective/Prospective Analysis of Characterization of the Long-Term Responders on Olaparib in Solid Tumours | |||||||||||||
Medical condition: epithelial ovarian cancer (including fallopian tube or peritoneal cancer) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003098-17 | Sponsor Protocol Number: SOLTI-1402 | Start Date*: 2017-03-29 |
Sponsor Name:SOLTI | ||
Full Title: CORALLEEN: A Phase 2 Clinical Trial of multi-agent Chemotherapy or letrozole plus Ribociclib (LEE001) as neoadjuvant treatment for postmenopausal patients with Luminal B/HER2-negative breast cancer. | ||
Medical condition: Luminal B/HER2-negative breast cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-001319-36 | Sponsor Protocol Number: FIERCE-21(B-701-U21) | Start Date*: 2017-08-23 | |||||||||||
Sponsor Name:BioClin Therapeutics, Inc. | |||||||||||||
Full Title: A Dose Escalation, Expansion Study of Vofatamab (B 701) Alone, Plus Docetaxel, or Versus Docetaxel in Subjects with Locally Advanced or Metastatic Urothelial Cell Carcinoma who have Relapsed After,... | |||||||||||||
Medical condition: Treatment of progressed or refractory metastatic UCC | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) ES (Prematurely Ended) GB (Prematurely Ended) CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005085-19 | Sponsor Protocol Number: CBGJ398X2204 | Start Date*: 2014-06-30 | |||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | |||||||||||||
Full Title: A phase II multicenter, single arm study of oral BGJ398 in adult patients with advanced or metastatic cholangiocarcinoma with FGFR2 gene fusions or other FGFR genetic alterations who failed or are ... | |||||||||||||
Medical condition: advanced or metastatic cholangiocarcinoma FGFR2 gene fusion, FGFR genetic alteration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) BE (Completed) IT (Completed) DE (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002990-24 | Sponsor Protocol Number: RAD1901-308 | Start Date*: 2019-05-29 | |||||||||||
Sponsor Name:Stemline Therapeutics, Inc. | |||||||||||||
Full Title: Elacestrant Monotherapy vs. Standard of Care for the Treatment of Patients with ER+/HER2- Advanced Breast Cancer Following CDK4/6 Inhibitor Therapy: A Phase 3 Randomized, Open-Label, Active-Control... | |||||||||||||
Medical condition: Advanced breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FR (Ongoing) HU (Completed) AT (Completed) GR (Completed) IE (Completed) PT (Completed) DK (Completed) ES (Ongoing) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002705-10 | Sponsor Protocol Number: SENS-401-202 | Start Date*: 2022-03-04 |
Sponsor Name:SENSORION PHARMA | ||
Full Title: An Exploratory, Phase IIa, Multicenter, Randomized, Controlled, Open label Study to Evaluate the Efficacy of SENS-401 to Prevent or Treat the Ototoxicity due to Cisplatin in Adult Subjects with a N... | ||
Medical condition: Cisplatin-induced hearing loss | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2021-001206-29 | Sponsor Protocol Number: ShorTrip | Start Date*: 2021-07-22 | |||||||||||
Sponsor Name:Fondazione GONO | |||||||||||||
Full Title: ShorTrip study - Phase II study of Short-course radiotherapy followed by consolidation chemotherapy with the Triplet FOLFOXIRI as total neoadjuvant therapy for locally advanced rectal cancer. | |||||||||||||
Medical condition: Locally advanced rectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001628-37 | Sponsor Protocol Number: MO28231 | Start Date*: 2012-11-22 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A TWO-COHORT, OPEN-LABEL, MULTICENTER, STUDY OF TRASTUZUMAB EMTANSINE (T-DM1) IN HER2-POSITIVE LOCALLY ADVANCED OR METASTATIC BREAST CANCER PATIENTS WHO HAVE RECEIVED PRIOR ANTI-HER2 AND CHEMOTHERA... | |||||||||||||
Medical condition: HER2 positive metastatic breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) ES (Completed) SE (Completed) GB (Completed) DK (Completed) HU (Completed) PT (Completed) NO (Completed) AT (Completed) FI (Completed) IT (Completed) GR (Completed) IE (Completed) SI (Completed) BG (Completed) NL (Completed) EE (Completed) IS (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001111-36 | Sponsor Protocol Number: CAN04CLIN001 | Start Date*: 2018-01-25 |
Sponsor Name:Cantargia AB | ||
Full Title: An open label, dose escalation followed by dose expansion, safety and tolerability trial of CAN04, a fully humanized monoclonal antibody against IL1RAP, in subjects with solid malignant tumors | ||
Medical condition: Solid malignant tumors, in the following two indications; Non-Small Cell Lung Cancer (NSCLC) and Pancreatic Ductal Adenocarcinoma (PDAC), | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) NO (Completed) DK (Completed) NL (Completed) DE (Completed) AT (Completed) EE (Completed) ES (Ongoing) LT (Completed) LV (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004916-23 | Sponsor Protocol Number: MORE | Start Date*: 2014-04-28 | |||||||||||
Sponsor Name:Ospedale San Raffaele | |||||||||||||
Full Title: Monotherapy with Ofatumumab for RElapsed/refractory Splenic B-cell marginal zone lymphoma (MORE) | |||||||||||||
Medical condition: Splenic B-cell marginal zone lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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