- Trials with a EudraCT protocol (2,612)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (42)
2,612 result(s) found for: Combination chemotherapy.
Displaying page 1 of 131.
EudraCT Number: 2016-002349-50 | Sponsor Protocol Number: M16TGA | Start Date*: 2017-09-29 |
Sponsor Name:Netherlands Cancer Institute- Antoni van Leeuwenhoek Hospital (NKI-AVL) | ||
Full Title: Phase I/II study with galunisertib (LY2157299) combined with capecitabine in patients with advanced chemotherapy resistant colorectal cancer and an activated TGF-β signature | ||
Medical condition: colorectal carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) BE (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003981-42 | Sponsor Protocol Number: 209227 | Start Date*: 2020-09-04 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A Randomized, Double-Blind, Adaptive, Phase II/III Study of GSK3359609 in Combination with Pembrolizumab and 5FU-Platinum Chemotherapy versus Placebo in Combination with Pembrolizumab plus 5FU-Plat... | |||||||||||||
Medical condition: Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) SE (Completed) DK (Completed) DE (Completed) BE (Completed) GB (GB - no longer in EU/EEA) HU (Prematurely Ended) PL (Completed) GR (Completed) IT (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000296-36 | Sponsor Protocol Number: ZWI-ZW25-301 | Start Date*: 2021-11-17 | ||||||||||||||||
Sponsor Name:Zymeworks Inc. | ||||||||||||||||||
Full Title: A Randomized, Multicenter, Phase 3 Study of Zanidatamab in Combination with Chemotherapy with or without Tislelizumab in Subjects with HER2-positive Unresectable Locally Advanced or Metastatic Gast... | ||||||||||||||||||
Medical condition: Gastroesophageal Adenocarcinoma (GEA) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) PT (Trial now transitioned) BE (Trial now transitioned) ES (Ongoing) NL (Trial now transitioned) IE (Trial now transitioned) IT (Trial now transitioned) EE (Trial now transitioned) RO (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000250-35 | Sponsor Protocol Number: WO30070 | Start Date*: 2016-06-16 | |||||||||||
Sponsor Name:Roche Farma, S.A., que representa en España a F. Hoffmann-La Roche Ltd. | |||||||||||||
Full Title: A PHASE III, MULTICENTER, RANDOMIZED, PLACEBO-CONTROLLED, DOUBLE-BLIND STUDY OF ATEZOLIZUMAB (ANTI?PD-L1 ANTIBODY) IN COMBINATION WITH GEMCITABINE/CARBOPLATIN VERSUS GEMCITABINE/CARBOPLATIN ALONE I... | |||||||||||||
Medical condition: Urothelial Carcinoma, locally advanced or metastatic | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) CZ (Completed) EE (Completed) GR (Completed) PL (Completed) SI (Completed) GB (GB - no longer in EU/EEA) FI (Completed) NL (Completed) PT (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004682-40 | Sponsor Protocol Number: CBYL719K12301 | Start Date*: 2021-06-16 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: EPIK-O: A Phase III, multi-center, randomized (1:1), open-label, active-controlled study to assess the efficacy and safety of alpelisib (BYL719) in combination with olaparib as compared to single a... | |||||||||||||
Medical condition: Platinum-resistant or refractory, high-grade serous ovarian cancer with no germline BRCA mutation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) PT (Completed) FI (Trial now transitioned) CZ (Completed) DK (Completed) SK (Completed) FR (Completed) NL (Completed) ES (Ongoing) DE (Trial now transitioned) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001664-22 | Sponsor Protocol Number: 2011-001664-22 | Start Date*: 2011-12-22 |
Sponsor Name:Medizinische Universität Wien - Universitätsklinik für Frauenheilkunde | ||
Full Title: A prospective, randomized, multicenter study to evaluate the impact of Darbepoetin alfa in combination with Ferric(III)-Carboxymaltose in comparison to Darbepoetin alfa and Ferric(III)-Carboxymalto... | ||
Medical condition: This is a prospective, multicenter, randomized, comparative, parallel group, phase IV study to assess the efficacy and safety of FCM 800mg or Darbepoetin alfa 500µg or the combination of FCM 800mg ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-000682-32 | Sponsor Protocol Number: PAUF-I | Start Date*: 2022-02-16 |
Sponsor Name:Prestige Biopharma Limited | ||
Full Title: A First in human, Phase 1/2a, Multicentre, Open-label Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Efficacy of PBP1510 in Patients with Advanced/Metastatic Pancreatic Cancer | ||
Medical condition: Advanced and/or metastatic pancreatic adenocarcinoma. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002417-36 | Sponsor Protocol Number: CAPTEM | Start Date*: 2014-08-28 | ||||||||||||||||
Sponsor Name:Fondazione IRCCS Istituto Nazionale dei Tumori | ||||||||||||||||||
Full Title: An open-label, randomized, multicenter, phase II trial designed to estimate the activity of CAPTEM combination versus FOLFIRI as second line treatment in patients who have progressed on or after fi... | ||||||||||||||||||
Medical condition: colorectal cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-001075-17 | Sponsor Protocol Number: AdvanTIG-205 | Start Date*: 2022-05-26 | |||||||||||
Sponsor Name:BeiGene, Ltd. | |||||||||||||
Full Title: AdvanTIG-205: A Phase 2, Randomized, Double-blind Study of Ociperlimab (BGB-A1217) and Tislelizumab With Chemotherapy in Patients With Metastatic Non-Small Cell Lung Cancer (NSCLC) Without Sensitiz... | |||||||||||||
Medical condition: Metastatic non-small cell lung cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) AT (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002040-78 | Sponsor Protocol Number: D8151C00001 | Start Date*: 2021-11-02 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase II Study to Evaluate the Safety, Pharmacokinetics, and Clinical Activity of AZD0171 in Combination with Durvalumab and Chemotherapy in Participants with Locally Advanced or Metastatic Solid... | |||||||||||||
Medical condition: Pancreatic ductal adenocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001028-21 | Sponsor Protocol Number: D6070C00005 | Start Date*: 2018-09-19 | |||||||||||
Sponsor Name:MedImmune, LLC | |||||||||||||
Full Title: A Phase 1b/2 Study to Evaluate the Safety, Pharmacokinetics, and Clinical Activity of Oleclumab (MEDI9447) with or without Durvalumab in Combination with Chemotherapy in Subjects with Metastatic Pa... | |||||||||||||
Medical condition: Pancreatic Ductal Adenocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) ES (Ongoing) | |||||||||||||
Trial results: View results |
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: 2020-005182-14 | Sponsor Protocol Number: A-20-1013-C-03 | Start Date*: 2021-02-25 | |||||||||||
Sponsor Name:Alligator Bioscience AB | |||||||||||||
Full Title: An open-label phase 1b/2 study assessing the safety and efficacy of mitazalimab in combination with chemotherapy in patients with metastatic pancreatic ductal adenocarcinoma | |||||||||||||
Medical condition: Metastatic Pancreatic Ductal Adenocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000124-34 | Sponsor Protocol Number: PFO-CTC | Start Date*: 2013-03-27 |
Sponsor Name:PD Dr. Maria De Santis | ||
Full Title: Circulating Tumor cells in urothelial cancer patients relapsing after or refractory to platinum based first line chemotherapy | ||
Medical condition: Circulating tumor cells in urothelial cancer patients relapsing after or refractory to platinum based first line chemotherapy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000587-28 | Sponsor Protocol Number: BGB-A317-306 | Start Date*: 2019-06-06 | |||||||||||
Sponsor Name:BeiGene, Ltd., c/o BeiGene USA, Inc. | |||||||||||||
Full Title: A Randomized, Placebo-Controlled, Double-Blind Phase 3 Study to Evaluate the Efficacy and Safety of Tislelizumab (BGB-A317) in Combination with Chemotherapy as First-Line Treatment in Patients with... | |||||||||||||
Medical condition: Unresectable, locally advanced recurrent or metastatic esophageal squamous cell carcinoma (ESCC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) FR (Completed) BE (Completed) ES (Completed) PL (Completed) CZ (Completed) IT (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
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: 2017-001741-27 | Sponsor Protocol Number: B9991023 | Start Date*: 2018-03-28 | |||||||||||
Sponsor Name:Pfizer Inc. | |||||||||||||
Full Title: A MULTICENTER, OPEN-LABEL, PHASE 1B/2 STUDY TO EVALUATE SAFETY AND EFFICACY OF AVELUMAB (MSB0010718C) IN COMBINATION WITH CHEMOTHERAPY WITH OR WITHOUT OTHER ANTI-CANCER IMMUNOTHERAPIES AS FIRST-LIN... | |||||||||||||
Medical condition: Advanced malignances in the first-line treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) ES (Ongoing) HU (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002738-55 | Sponsor Protocol Number: 69HCL16-0134 | Start Date*: 2017-01-06 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: Safety of Intraperitoneal (IP) OXAliplatin (OXA) in Association With Systemic FOLFIRI Bevacizumab Chemotherapy in Patients With Peritoneal Carcinosis ( IPOXA ) | |||||||||||||
Medical condition: Patients with peritoneal carcinosis of colorectal origin and uncertain resectability with an indication for systemic chemotherapy compatible with the FOLFIRI + bevacizumab combination. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001020-20 | Sponsor Protocol Number: NKV101983 | Start Date*: 2005-01-25 |
Sponsor Name:GlaxoSmithKline Group of Companies | ||
Full Title: | ||
Medical condition: Chemotherapy Induced Nausea and Vomiting (CINV) 0 Moderately Emetogenic Chemotherapy (MEC) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) IE (Completed) SK (Completed) HU (Completed) AT (Completed) GB (Completed) DE (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-003739-30 | Sponsor Protocol Number: AMLSG 05-04 | Start Date*: 2005-11-02 |
Sponsor Name:Universitätsklinikum Ulm / University Clinical Center Ulm | ||
Full Title: Phase II Study on Gemtuzumab Ozogamicin in Combination with All-trans-Retinoic Acid, high-dose Cytarabine and Mitoxantrone in Patients with primary refractory acute myeloid leukemia [GO-A-HAM] | ||
Medical condition: primary refractory patients with acute myeloid leukemia | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
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