- Trials with a EudraCT protocol (859)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
859 result(s) found for: Neoadjuvant chemotherapy.
Displaying page 1 of 43.
EudraCT Number: 2011-001856-12 | Sponsor Protocol Number: NT-12331-5 | Start Date*: 2011-08-11 |
Sponsor Name:The Motol University Hospital | ||
Full Title: Early assessment of effectivness of neoadjuvant chemotherapy for carcinoma of the esophagus and esophago-gastric junction using FDG-PET/CT. | ||
Medical condition: adenocarcinoma of the esophagus and esophago-gastric junction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002435-15 | Sponsor Protocol Number: FiHM003 | Start Date*: 2017-08-10 |
Sponsor Name:Fundación de Investigación HM Hospitales | ||
Full Title: Pilot study to assess physical exercise intervention in neoadjuvant treatment with nab-paclitaxel in patients with triple negative breast cancer | ||
Medical condition: Supervised exercise regimen given during neoadjuvant chemotherapy for triple negative breast cancer patients. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004796-12 | Sponsor Protocol Number: AIO-PAK-0113 | Start Date*: 2014-07-02 | |||||||||||
Sponsor Name:AIO-Studien-gGmbH | |||||||||||||
Full Title: Prospective Randomized Multicenter Phase II Trial to Investigate Intensified Neoadjuvant Chemotherapy in Locally Advanced Pancreatic Cancer | |||||||||||||
Medical condition: Locally advanced pancreatic cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002833-39 | Sponsor Protocol Number: CHUBX2017/52 | Start Date*: 2018-12-12 |
Sponsor Name:CHU DE BORDEAUX | ||
Full Title: A phase III randomized trial evaluating chemotherapy followed by pelvic reirradiation versus chemotherapy alone as pre-operative treatment for locally recurrent rectal cancer (GRECCAR – PRODIGE ... | ||
Medical condition: Recurrent rectal cancer after local excision | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002469-37 | Sponsor Protocol Number: CA209-7FL | Start Date*: 2020-01-29 | |||||||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||||||||||||
Full Title: A Randomized, Multicenter, Double-blind, Placebo-controlled Phase 3 Study of Nivolumab Versus Placebo in Combination With Neoadjuvant Chemotherapy and Adjuvant Endocrine Therapy in Patients With Hi... | |||||||||||||||||||||||
Medical condition: Patients With High-risk, Estrogen Receptor-Positive (ER+), Human Epidermal Growth Factor Receptor 2-Negative (HER2-) Primary Breast Cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: AT (Completed) DE (Completed) CZ (Completed) FR (Completed) PL (Completed) NL (Completed) BE (Completed) DK (Completed) FI (Completed) IE (Completed) ES (Ongoing) PT (Completed) GB (GB - no longer in EU/EEA) IT (Completed) RO (Ongoing) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-003808-39 | Sponsor Protocol Number: MK-3475-866 | Start Date*: 2019-07-01 | |||||||||||
Sponsor Name:Merck Sharp & Dohme LLC | |||||||||||||
Full Title: A Phase 3, Randomized Double Blind Study to Evaluate Peri-operative Pembrolizumab (MK-3475) + Neoadjuvant Chemotherapy versus Perioperative Placebo + Neoadjuvant Chemotherapy in Cisplatin-Eligible ... | |||||||||||||
Medical condition: Muscle Invasive Bladder Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) IE (Trial now transitioned) DE (Trial now transitioned) GB (GB - no longer in EU/EEA) DK (Trial now transitioned) BE (Trial now transitioned) HU (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003104-12 | Sponsor Protocol Number: M19VLC | Start Date*: 2020-01-14 | |||||||||||
Sponsor Name:NKI-AVL | |||||||||||||
Full Title: Treatment of locally advanced VULvar CArcinoma in a Neoadjuvant setting with Carboplatin and Paclitaxel chemotherapy | |||||||||||||
Medical condition: vulvar carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004692-31 | Sponsor Protocol Number: CA017-078 | Start Date*: 2019-03-18 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: A Phase 3, Randomized, Study of Neoadjuvant Chemotherapy alone versus Neoadjuvant Chemotherapy plus Nivolumab or Nivolumab and BMS-986205, Followed by Continued Post- Surgery Therapy with Nivolumab... | ||||||||||||||||||
Medical condition: Bladder Cancer Muscle-Invasive Bladder Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) AT (Trial now transitioned) FR (Trial now transitioned) BE (Trial now transitioned) NO (Trial now transitioned) NL (Trial now transitioned) FI (Trial now transitioned) GR (Trial now transitioned) ES (Ongoing) PT (Completed) IT (Trial now transitioned) RO (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000658-39 | Sponsor Protocol Number: AkupresSNP | Start Date*: 2016-07-11 |
Sponsor Name:Region Jönköpings län | ||
Full Title: Randomized multicenter study of Acupressure combined with personalized antiemetics based on genetic variations (SNPs) in women undergoing neoadjuvant or adjuvant chemotherapy EC / FEC against breas... | ||
Medical condition: Nausea in conjuction with neoadjuvant or adjuvant chemotherapy (FEC/EC) for patients with breast cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-003565-10 | Sponsor Protocol Number: SAKK06/17 | Start Date*: 2018-12-03 | |||||||||||
Sponsor Name:Swiss Group for Clinical Cancer Research | |||||||||||||
Full Title: Neoadjuvant and adjuvant durvalumab in combination with neoadjuvant chemotherapy in patients with operable urothelial cancer. A multicenter, single-arm phase II Trial. | |||||||||||||
Medical condition: muscle invasive urothelial cancer (MIUC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003503-39 | Sponsor Protocol Number: 2006-6 | Start Date*: 2006-09-08 |
Sponsor Name:Jens Benn Sorensen, Dept. oncology, Finsen Centre/National University Hospital | ||
Full Title: Multicenter fase III undersøgelse af effekten af præoperativ (neoadjuverende) kemoterapi inden operation med efterfølgende adjuverende kemoterapi ved operabel NSCLC stadie IB, IIA; IIB, og IIIA/T3. | ||
Medical condition: operable NSCLC. Pts are randomized to receive or not receive two courses of neoadjuvant chemotherapy before surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001199-23 | Sponsor Protocol Number: ICR-CTSU/2014/10048 | Start Date*: 2016-10-11 | |||||||||||
Sponsor Name:The Institute of Cancer Research | |||||||||||||
Full Title: InPACT - International Penile Advanced Cancer Trial (International Rare Cancer Initiative) | |||||||||||||
Medical condition: Locally advanced squamous carcinoma of the penis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005850-27 | Sponsor Protocol Number: NAPEER | Start Date*: 2022-05-31 |
Sponsor Name:Oslo University Hospital | ||
Full Title: An open label phase II trial in hormone receptor positive breast cancer patients randomized to neoadjuvant chamotherapy with or without bevacizumab (if ViRP signature positive) followed by endocrin... | ||
Medical condition: Hormone receptor positive primary breast cancer with tumor measuring > 2.0 cm that will be recommended chemotherapy and antihormone therapy according to the treatment guidelines for curative breast... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002520-17 | Sponsor Protocol Number: GOGER-01 | Start Date*: 2013-11-27 | |||||||||||||||||||||||||||||||
Sponsor Name:AOU di Bologna, Policlinico S.Orsola-Malpighi | |||||||||||||||||||||||||||||||||
Full Title: Randomized phase II study of 3 vs 6 courses of neoadjuvant carboplatin-paclitaxel chemotherapy in stage IIIC or IV epithelial ovarian cancer, fallopian tube carcinoma or primary peritoneal carcinoma | |||||||||||||||||||||||||||||||||
Medical condition: neoadjuvant carboplatin-paclitaxel chemotherapy in stage IIIC or IV epithelial ovarian cancer, fallopian tube carcinoma or primary peritoneal carcinoma | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004045-16 | Sponsor Protocol Number: ET18-272 | Start Date*: 2019-03-14 |
Sponsor Name:Centre Léon Bérard | ||
Full Title: REGOSTA – A randomized, placebo-controlled, double-blinded, multicentre study evaluating the efficacy and safety of regorafenib as maintenance therapy after first-line treatment in patients with bo... | ||
Medical condition: Patients with bone sarcomas other than Ewing sarcoma or chondrosarcoma or chordoma, who have no residual disease after neoadjuvant chemotherapy, surgery and/or adjuvant chemotherapy. | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004123-19 | Sponsor Protocol Number: MUN-391-LOR-0050-I | Start Date*: 2006-01-24 |
Sponsor Name:Klinikum rechts der Isar der Technischen Universitaet Muenchen | ||
Full Title: Metabolic Response Evaluation for an Individualization of Neoadjuvant Chemo- and Radiotherapy in Esophageal Adenocarcinoma | ||
Medical condition: This study will test an optimized therapy for patients with chemotherapy-resistent locally advanced adenocarcinomas at the gastro-esophageal junction. According to the protocol, patients should re... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004526-41 | Sponsor Protocol Number: ONCOGHdC2015-02 | Start Date*: 2017-03-23 |
Sponsor Name:Grand hôpital de Charleroi | ||
Full Title: A PHASE Ib/II STUDY TO EVALUATE SAFETY AND EFFICACY OF ATEZOLIZUMAB COMBINED WITH RADIO-CHEMOTHERAPY IN A PREOPERATIVE SETTING FOR PATIENTS WITH LOCALIZED RECTAL CANCER (R-IMMUNE) | ||
Medical condition: Rectum cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-015238-31 | Sponsor Protocol Number: M09TNM | Start Date*: 2009-12-16 | |||||||||||
Sponsor Name:NKI-AVL | |||||||||||||
Full Title: RANDOMIZED PHASE II/III STUDY OF INDIVIDUALIZED NEOADJUVANT CHEMOTHERAPY IN ‘TRIPLE-NEGATIVE’ BREAST TUMORS | |||||||||||||
Medical condition: Triple negative breast cancer treated with neoadjuvant chemotherapy | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012019-17 | Sponsor Protocol Number: BO22280 | Start Date*: 2009-09-02 | |||||||||||
Sponsor Name:F. Hoffmann - La Roche Ltd | |||||||||||||
Full Title: A randomised, multicentre, multinational Phase II study to evaluate pertuzumab in combination with trastuzumab given either concomitantly or sequentially with standard anthracycline based chemother... | |||||||||||||
Medical condition: Locally advanced, inflammatory or early stage HER2-positive breast cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) GB (Completed) PT (Completed) GR (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001850-24 | Sponsor Protocol Number: ABCSG_P02 | Start Date*: 2012-08-10 |
Sponsor Name:ABCSG (Austrian Breast & Colorectal Cancer Study Group) | ||
Full Title: A prospective randomized phase II trial of FOLFIRINOX alone versus FOLFIRINOX followed by radiochemotherapy in patients with locally advanced, primarily inoperable pancreatic cancer | ||
Medical condition: locally advanced, primarily inoperable pancreatic carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: (No results available) |
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