- Trials with a EudraCT protocol (270)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
270 result(s) found for: Amylase.
Displaying page 8 of 14.
EudraCT Number: 2018-002374-46 | Sponsor Protocol Number: UC-0110/1807 | Start Date*: 2018-11-09 |
Sponsor Name:UNICANCER | ||
Full Title: A randomised phase II trial assessing REGorafenib combined with IRInotecan as second-line treatment in patients with metastatic gastro-oesophageal adenocarcinomas. | ||
Medical condition: Patients aged ≥18 years old with metastatic gastro-oesophageal adenocarcinomas after failure of a first-line fluoropyrimidine and platinum-based chemotherapies. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2020-001493-29 | Sponsor Protocol Number: CVC-for-COVID-19 | Start Date*: 2020-05-11 |
Sponsor Name:Charité - Universitaetsmedizin Berlin | ||
Full Title: Charité trial of Cenicriviroc (CVC) treatment for COVID-19 patients | ||
Medical condition: SARS-CoV-2 infection | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2012-005626-30 | Sponsor Protocol Number: REACHIN | Start Date*: 2014-01-23 |
Sponsor Name:CUB Erasme Hospital | ||
Full Title: Regorafenib after failure of gemcitabine and platinum-based chemotherapy for locally advanced (non resectable) and metastatic cholangiocarcinoma: a randomized double-blinded phase II trial. | ||
Medical condition: Locally advanced (non resectable) and metastatic histologically proven intra-hepatic or hilum cholangiocarcinoma + histologically proven metastatic extra-hepatic cholangiocarcinoma (common bile duc... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002231-24 | Sponsor Protocol Number: PROICM2018-01NEX | Start Date*: 2018-08-06 | |||||||||||
Sponsor Name:Institut régional du Cancer de Montpellier | |||||||||||||
Full Title: A randomized phase III trial assessing a regorafenib-irinotecan combination (REGIRI) versus regorafenib alone in metastatic colorectal cancer patients after failure of standard therapies, according... | |||||||||||||
Medical condition: Metastatic colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-006106-23 | Sponsor Protocol Number: 2020/3210 | Start Date*: 2021-07-21 | |||||||||||
Sponsor Name:Gustave Roussy | |||||||||||||
Full Title: Short-term Pre-OPerative Durvalumab (MEDI 4736) in early small triple negative breast cancer patients | |||||||||||||
Medical condition: Untreated operable small triple negative breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002612-31 | Sponsor Protocol Number: MANTICO | Start Date*: 2021-05-25 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA INTEGRATA VERONA | |||||||||||||
Full Title: Adaptive, randomized, placebo-controlled trial to evaluate the efficacy of monoclonal antibodies in outpatients with mild or moderate COVID-19 (MANTICO) | |||||||||||||
Medical condition: COVID-19 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000355-40 | Sponsor Protocol Number: SOLARIS | Start Date*: 2021-09-20 | |||||||||||
Sponsor Name:Frankfurter Institut für Klinische Krebsforschung IKF GmbH at Krankenhaus Nordwest | |||||||||||||
Full Title: SOLARIS – A phase-II open-label study of pembrolizumab and lenvatinib in patients with advanced stage hepatocellular carcinoma who are refractory to atezolizumab and bevacizumab/ IO-based therapy | |||||||||||||
Medical condition: advanced stage hepatocellular carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004760-37 | Sponsor Protocol Number: NA | Start Date*: 2015-12-23 | |||||||||||
Sponsor Name:Riitta Veijola | |||||||||||||
Full Title: Incretin-based therapy in non-symptomatic, early diagnosed type 1 diabetics | |||||||||||||
Medical condition: Type 1 diabetes | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000358-11 | Sponsor Protocol Number: CAMN107DDE06 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: An open-label, multi-center, single-arm study to evaluate the efficacy of nilotinib in adult patients with metastatic or unresectable gastrointestinal stromal tumors in first line treatment | |||||||||||||
Medical condition: metastatic or unresectable gastrointestinal stromal tumor | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Ongoing) FI (Completed) IT (Completed) FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003166-39 | Sponsor Protocol Number: ChImDLP-2 | Start Date*: 2022-08-08 | |||||||||||
Sponsor Name:UAB Froceth | |||||||||||||
Full Title: A study of the safety of chemoimmunotherapy with autologous Dendritic Cell Preparations in patients with stage III ovarian cancer | |||||||||||||
Medical condition: Stage III of high malignancy Ovarian serous adenocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: LT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000417-31 | Sponsor Protocol Number: IM101-473 | Start Date*: 2014-07-01 | |||||||||||
Sponsor Name:University Medical Center Groningen | |||||||||||||
Full Title: Randomized, double-blind, placebo-controlled phase III study (ASAP III study) to assess the efficacy and safety of Abatacept treatment in patients with primary Sjögren’s syndrome (ASAP III study = ... | |||||||||||||
Medical condition: Primary Sjögren's syndrome (pSS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000845-42 | Sponsor Protocol Number: CBYL719A0HR01T | Start Date*: 2022-04-04 |
Sponsor Name:CCGCRO | ||
Full Title: Impact of time of alpelisib administration, concomitant fasting and low carbohydrate diet on alpelisib toxicity and efficacy; a pilot randomized controlled phase IIb trial - ITACA | ||
Medical condition: metastatic breast cancer HER2- HR+ PIK3CA+ | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HR (Suspended by CA) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000516-25 | Sponsor Protocol Number: GS-US-292-0112 | Start Date*: 2013-06-04 | |||||||||||
Sponsor Name:Gilead Sciences Inc. | |||||||||||||
Full Title: A Phase 3 Open-label Safety Study of Elvitegravir/Cobicistat/Emtricitabine/Tenofovir Alafenamide Single-Tablet Regimen in HIV-1 Positive Patients with Mild to Moderate Renal Impairment | |||||||||||||
Medical condition: Human Immunodeficiency Virus (HIV-1) Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) GB (Completed) DE (Completed) IT (Completed) BE (Completed) NL (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002379-40 | Sponsor Protocol Number: CAFQ056B2278 | Start Date*: 2012-01-09 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: An open-label study to evaluate the long-term safety and tolerability of AFQ056 in adolescent patients with Fragile X Syndrome | |||||||||||||
Medical condition: Fragile X syndrome | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) DE (Prematurely Ended) Outside EU/EEA GB (Prematurely Ended) ES (Temporarily Halted) DK (Prematurely Ended) IT (Completed) FR (Completed) NL (Prematurely Ended) BE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024007-27 | Sponsor Protocol Number: GS-US-264-0110 | Start Date*: 2011-06-01 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: A Phase 3B, Randomized, Open-label Study to Evaluate the Safety and Efficacy of a Single Tablet Regimen of Emtricitabine/Rilpivirine/Tenofovir Disoproxil Fumarate Compared with a Single Tablet Reg... | |||||||||||||
Medical condition: Human Immunodeficiency Virus (Type 1) Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) PT (Completed) BE (Completed) ES (Completed) AT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000571-85 | Sponsor Protocol Number: AN-EPI3333 | Start Date*: 2017-06-15 |
Sponsor Name:ANTHERA Pharmaceuticals, Inc. | ||
Full Title: A Phase 3, Randomized, Open-Label, Assessor-Blind, Non-Inferiority, Active-Comparator Study Evaluating the Efficacy and Safety of Liprotamase in Subjects with Cystic Fibrosis-Related Exocrine Pancr... | ||
Medical condition: Pancreatic Exocrine Insufficiency due to Cystic Fibrosis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: HU (Prematurely Ended) ES (Prematurely Ended) PL (Prematurely Ended) GB (Prematurely Ended) LT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2009-015514-21 | Sponsor Protocol Number: CAMN107B2301 | Start Date*: 2010-04-16 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: The TEAM Trial (Tasigna Efficacy in Advanced Melanoma): A randomized, phase III, open label, multi-center, two-arm study to compare the efficacy of Tasigna ® versus dacarbazine (DTIC) in the treatm... | |||||||||||||
Medical condition: treatment of patients with metastatic and/or inoperable melanoma harboring a c-Kit mutation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) SE (Completed) DE (Completed) NL (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000311-25 | Sponsor Protocol Number: BAY86-9766/16553 | Start Date*: 2013-10-17 |
Sponsor Name:Bayer Healthcare AG | ||
Full Title: A prospective, single-arm, multicenter, uncontrolled, open-label Phase II trial of refametinib (BAY 86-9766) in patients with RAS mutant Hepatocellular Carcinoma (HCC) | ||
Medical condition: KRAS or NRAS mutant unresectable or metastatic Hepatocellular carcinoma (HCC) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) BE (Completed) AT (Completed) GB (Completed) DE (Completed) HU (Completed) ES (Completed) IT (Completed) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-003650-88 | Sponsor Protocol Number: BAY94-9343/15743 | Start Date*: 2015-11-25 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: A randomized, open-label, active-controlled, Phase II study of intravenous anetumab ravtansine (BAY 94-9343) or vinorelbine in patients with advanced or metastatic malignant pleural mesothelioma ov... | |||||||||||||
Medical condition: Patients with advanced or metastatic malignant pleural mesothelioma overexpressing mesothelin | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) DE (Completed) BE (Completed) GB (Completed) ES (Completed) NL (Completed) PL (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002446-76 | Sponsor Protocol Number: DCC-2618-03-001 | Start Date*: 2018-03-29 |
Sponsor Name:Deciphera Pharmaceuticals, LLC | ||
Full Title: A Phase 3, INterVentional, Double-Blind, Placebo-Controlled Study to Assess the Safety and Efficacy of DCC-2618 In Patients with AdvanCed Gastrointestinal Stromal TUmorS who have Received Treatment... | ||
Medical condition: Patients with AdvanCed Gastrointestinal Stromal TUmorS | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) FR (Completed) NL (Prematurely Ended) BE (Completed) ES (Prematurely Ended) PL (Prematurely Ended) FI (Completed) IT (Completed) | ||
Trial results: View results |
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