- Trials with a EudraCT protocol (55)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
55 result(s) found for: Negative therapeutic reaction.
Displaying page 1 of 3.
EudraCT Number: 2007-000789-19 | Sponsor Protocol Number: MiniCept | Start Date*: 2007-05-30 | |||||||||||||||||||||
Sponsor Name:CHU de Liège, Domaine Universitaire du Sart Tilman | |||||||||||||||||||||||
Full Title: Withdrawal of Calcineurin Inhibitors (CNIs) during administration of Mycophenolate Mofetil (MMF) in liver transplant patients suffering adverse effects from CNIs: Study of the reduction in rejectio... | |||||||||||||||||||||||
Medical condition: liver transplant patients suffering adverse effects from treatment with calcineurin inhibitors | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-001218-24 | Sponsor Protocol Number: TDL-CS-001 | Start Date*: 2014-06-05 | |||||||||||
Sponsor Name:Trichocare Diagnostics Ltd | |||||||||||||
Full Title: An open label, intra-subject, controlled multi-centre study to assess the concordance (specificity and sensitivity) between Colourstart® Test 73 mcg Cutaneous Patch and Finn Chamber in the detectio... | |||||||||||||
Medical condition: Para-Phenylenediamine allergy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002073-26 | Sponsor Protocol Number: 1125-ECIR | Start Date*: Information not available in EudraCT | |||||||||||||||||||||
Sponsor Name:Medical Center - University of Freiburg | |||||||||||||||||||||||
Full Title: Phase 1/2 Trial to determine the safety and efficacy of Extracorporeal photopheresis as treatment for steroid-refractory immune related adverse events after immune checkpoint inhibitor therapy | |||||||||||||||||||||||
Medical condition: Immune related adverse events induced by treatment with immune checkpoint inhibitors (monoclocanl antibodies against PD-1, PD-L1 or CTLA-4) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001935-21 | Sponsor Protocol Number: 8-55-52133-010 | Start Date*: 2011-08-30 | |||||||||||
Sponsor Name:IPSEN PHARMA SAS | |||||||||||||
Full Title: An interventional non-therapeutic study to assess ex vivo basophil activation in response to various preparations of taspoglutide and related items in blood samples from subjects who previously rec... | |||||||||||||
Medical condition: Diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003248-36 | Sponsor Protocol Number: 61383082 | Start Date*: 2011-09-30 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Central Military Hospital | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: The clinical significance of epigenetic factors research to refine the diagnosis, estimate prognosis and risk of recurrence after curative pancreatic cancer resection. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: The aim of the study to estimate frequence of epigenetics changes in pancreatic cancer and to assess the signidicance of apllication of the intravenous contrast agent during endosonography to bette... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002644-24 | Sponsor Protocol Number: DIA-STA--11-01-19 | Start Date*: 2020-03-11 | |||||||||||
Sponsor Name:Diater, Laboratorio de Diagnóstico y Aplicaciones Terapéuticas S.A. | |||||||||||||
Full Title: Biological standarization of allergic extracts of will grasses: Phleum pratense, Lolium perenne, Poa pratensis y Dactylis glomerata and its mixture to determinate their biological activity, the In ... | |||||||||||||
Medical condition: Biological standarization for allergenic extracts in patients with hipersensibility to extract | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003828-21 | Sponsor Protocol Number: 71617 | Start Date*: 2020-02-10 |
Sponsor Name:St Antonius Hospital | ||
Full Title: Identification of sentinel lymph nodes in breast cancer patients through non-invasively and percutaneously fluorescent imaging using indocyanine green | ||
Medical condition: Axillar staging in breast cancer patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003270-28 | Sponsor Protocol Number: VB-02-DFLOP | Start Date*: 2014-01-27 | |||||||||||
Sponsor Name:Instituto de Inmunología y Alergia INMUNAL S.A..U. | |||||||||||||
Full Title: Biological standardization of allergenic extracts of Dermatophagoides farinae and Lolium perenne. Open label. Single Center. Phase II Study. | |||||||||||||
Medical condition: Biological standardization for allergenic extracts in patients with hipersensibility to extracts. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001347-66 | Sponsor Protocol Number: A0081092 | Start Date*: 2006-08-18 | |||||||||||
Sponsor Name:Pfizer España | |||||||||||||
Full Title: A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY OF PREGABALIN IN SUBJECTS WITH GENERALIZED ANXIETY DISORDER (GAD) SWITCHING FROM BENZODIAZEPINE THERAPY Estudio multicéntrico, alea... | |||||||||||||
Medical condition: Generalized Anxiety Disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000588-53 | Sponsor Protocol Number: SNIPER | Start Date*: 2023-02-07 | |||||||||||
Sponsor Name:RIGENERAND Srl | |||||||||||||
Full Title: RR001 in combination with chemotherapy for patients with locally advanced pancreatic adenocarcinoma: open-label, non-randomized dose escalation phase I/IIa study | |||||||||||||
Medical condition: Locally advanced pancreatic adenocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003932-26 | Sponsor Protocol Number: Ga-68-CCK2R | Start Date*: 2021-01-20 |
Sponsor Name:Medizinische Universität Innsbruck | ||
Full Title: Phase I/IIa study to evaluate the safety, tolerability, whole-body distribution, and preliminary diagnostic performance of a novel 68Ga-labelled minigastrin analogue in patients with advanced neuro... | ||
Medical condition: Advanced neuroendocrine tumours (NET), including medullary thyroid carcinoma (MTC), as well as gastroenteropancreatic and bronchopulmonary NET | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003516-31 | Sponsor Protocol Number: NEOPACHI-001 | Start Date*: 2012-11-29 |
Sponsor Name:CUB Erasme Hospital | ||
Full Title: Evaluation of tumoral perfusion modification by dynamic imaging after neoadjuvant chemotherapy combining gemcitabine and a Hedgehog inhibitor (Vismodegib) in patients with resectable pancreatic ade... | ||
Medical condition: Potentially resectable pancreatic ductal adenocarcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004504-35 | Sponsor Protocol Number: RF-2010-2311148 | Start Date*: 2013-02-26 | |||||||||||
Sponsor Name:IRCCS CENTRO SAN GIOVANNI DI DIO FATEBENEFRATELLI | |||||||||||||
Full Title: The use of Oxytocin as adjunctive therapy for the treatment of schizophrenia: a randomized, double blind trial | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002311-26 | Sponsor Protocol Number: INMUNOCELL | Start Date*: 2021-12-09 | |||||||||||||||||||||||||||||||
Sponsor Name:IDIVAL | |||||||||||||||||||||||||||||||||
Full Title: PROPHYLAXIS OF CYTOMEGALOVIRUS INFECTION IN haploidentical PROGENITORS HEMATOPOIETIC TRANSPLANTATIONWITH ADOPTIVE CELL IMMUNOTHERAPY. | |||||||||||||||||||||||||||||||||
Medical condition: Primary prophylaxis of CMV infection in haploidentical transplantation of hematopoietic progenitors. | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005362-35 | Sponsor Protocol Number: VB-01-DPHLOLEG | Start Date*: 2013-04-09 | |||||||||||
Sponsor Name:Instituto de Inmunología y Alergia INMUNAL SAU | |||||||||||||
Full Title: Biological standardization of pollen of Phleum pratense, Olea europaea, mite extract Dermatophagoides pteronyssinus and animal allergen Felis domesticus. Open label, single center, phase II study. | |||||||||||||
Medical condition: Biological standardization for allergenic extracts in patients with hipersensibility to extracts | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002255-15 | Sponsor Protocol Number: ST3073-ST3074-DM-12-002 | Start Date*: 2014-11-04 |
Sponsor Name:Sigma-Tau Industrie Farmaceutiche Riunite S.p.A. | ||
Full Title: A phase II, open-label, multicentre, pharmacokinetic, pharmacodynamics and safety study of a new paediatric eurartesim dispersible formulation and crushed film coated eurartesim tablet, in infant p... | ||
Medical condition: Uncomplicated Plasmodium falciparum malaria | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2013-003892-36 | Sponsor Protocol Number: VB-03-PASKCHAV | Start Date*: 2015-07-22 | |||||||||||
Sponsor Name:INMUNAL SAU | |||||||||||||
Full Title: Biological standardization of allergenic extracts of Platanus acerifolia, Salsola kali, Chenopodium album y Artemisia vulgaris . Open label. Multicenter. Phase II Study. | |||||||||||||
Medical condition: Biological standardization for allergenic extracts in patients with hipersensibility to extracts. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002271-36 | Sponsor Protocol Number: MEPIC | Start Date*: 2021-03-09 |
Sponsor Name:Danderyd Hospital | ||
Full Title: Mepivacaine for pain relief at insertion of intrauterine contraception (MEPIC) – a triple-blind randomized controlled trial. | ||
Medical condition: Insertion of intrauterine contraception | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002096-42 | Sponsor Protocol Number: 6057-PR-PRI-188 | Start Date*: 2012-09-18 | |||||||||||
Sponsor Name:LETI Pharma GmbH | |||||||||||||
Full Title: Biological Standardization of Ambrosia elatior Allergen Extract Determination of the Biological Activity in HEP units. An Open Monocenter Study. | |||||||||||||
Medical condition: Allergy to Ambrosia elatior (ragweed) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004616-19 | Sponsor Protocol Number: ABT-gpCPT001 | Start Date*: 2018-09-12 | |||||||||||
Sponsor Name:ASIT biotech S.A. | |||||||||||||
Full Title: A dose-ranging clinical study to determine the range of grass pollen allergen (gpCPT+) concentrations to be used in a conjunctival provocation test to grade moderate to severe grass pollen allergic... | |||||||||||||
Medical condition: This clinical trial aims to evaluate a conjunctival provocation test (CPT) with the IMP gpCPT+ for the assessment and grading of grass pollen allergic rhinoconjunctivitis. Thus, a diagnostic solu... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
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