- Trials with a EudraCT protocol (303)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
303 result(s) found for: Base rate.
Displaying page 3 of 16.
EudraCT Number: 2018-001604-10 | Sponsor Protocol Number: TriDiTe2018 | Start Date*: 2018-09-05 | ||||||||||||||||
Sponsor Name:BIODRUG s.r.o. | ||||||||||||||||||
Full Title: A single blind, randomized comparative and multicentre clinical trial of the immunogenicity and safety of booster immunisation with bivalent vaccine against tetanus and diphtheria VACDITE (BIODRUG)... | ||||||||||||||||||
Medical condition: Verification of immune response after booster immunisation with one dose of vaccine against tetanus and diphtheriae | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: SK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-001816-27 | Sponsor Protocol Number: 62202-655 | Start Date*: 2005-07-28 |
Sponsor Name:Clinical Data Care Spain S.L. | ||
Full Title: Open label randomized phase II, multicentre, pilot study to evaluate safety and efficacy of the combination of cetuximab and concomitant-boost accelerated radiotherapy followed or not by a compleme... | ||
Medical condition: locally advanced oropharynx squamous cell carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-004812-81 | Sponsor Protocol Number: 2019-48 | Start Date*: 2021-03-05 |
Sponsor Name:ASSISTANCE PUBLIQUE HOPITAUX DE MARSEILLE | ||
Full Title: Ketamine Low dOse Evaluation on morphine consumption in traumatic patient : a prospective randomized controlled double-blind study | ||
Medical condition: Traumatism | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000949-77 | Sponsor Protocol Number: BC3-CT008 | Start Date*: 2014-05-12 | |||||||||||
Sponsor Name:Adocia | |||||||||||||
Full Title: A double-blinded, randomised, four -period crossover euglycemic clamp trial investigating the dose-response and dose-exposure relationship of BC222 insulin lispro in three different doses in subje... | |||||||||||||
Medical condition: Diabetes mellitus type 1 | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003144-12 | Sponsor Protocol Number: DBC-14LIPOINJ01 | Start Date*: 2014-09-15 | |||||||||||
Sponsor Name:Profil Institut für Stoffwechselforschung GmbH | |||||||||||||
Full Title: A trial to compare the pharmacokinetics and pharmacodynamics of insulin lispro administered s.c. into lipohypertrophic or normal abdominal adipose tissue in subjects with diabetes mellitus type 1 | |||||||||||||
Medical condition: Diabetes mellitus | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006009-18 | Sponsor Protocol Number: TMC278-TiDP15-C221 | Start Date*: 2009-04-17 | |||||||||||
Sponsor Name:Tibotec Pharmaceuticals | |||||||||||||
Full Title: An open-label, Proof-of-Concept trial in treatment-naïve HIV-1- infected subjects to evaluate the antiviral activity of a single intramuscular dosing of TMC278LA as monotherapy. | |||||||||||||
Medical condition: HIV-1 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Temporarily Halted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001548-21 | Sponsor Protocol Number: ICLA-08-CSI1 | Start Date*: 2005-06-21 | |||||||||||
Sponsor Name:Arpida AG | |||||||||||||
Full Title: Phase 3, Randomized, Investigator-Blind, Multi-Center Study to Evaluate Efficacy and Safety of Intravenous Iclaprim versus Intravenous Linezolid in Complicated Skin and Skin Structure Infections | |||||||||||||
Medical condition: Complicated skin and skin structure infections are predominantly caused by the following Gram-positive pathogens: Staphylococcus aureus, including methicillin-resistant strains, beta hemolytic stre... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004052-15 | Sponsor Protocol Number: 202000570 | Start Date*: 2021-11-24 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: ImmunoPET imaging with 89Zr-DFO-REGN3767 in patients with advanced solid cancer prior to and during treatment with cemiplimab with or without platinum-based chemotherapy | ||
Medical condition: Patients with metastatic solid tumors, where clinical data has shown a rationale for ICI therapy with or without platinum-based chemotherapy, will be included in this study. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001940-37 | Sponsor Protocol Number: EFC15246 | Start Date*: 2017-12-13 | |||||||||||
Sponsor Name:Sanofi-aventis recherche & développement | |||||||||||||
Full Title: Randomized, Open Label, Multicenter Study Assessing The Clinical Benefit Of Isatuximab Combined With Carfilzomib (Kyprolis®) And Dexamethasone Versus Carfilzomib With Dexamethasone In Patients Wit... | |||||||||||||
Medical condition: Plasma cell myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) CZ (Completed) HU (Completed) ES (Ongoing) FR (Completed) GR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002025-19 | Sponsor Protocol Number: RPC01-2201 | Start Date*: 2015-12-30 | |||||||||||||||||||||
Sponsor Name:Celgene International II Sarl (CISII) awholly owned subsidiary of Celgene Corporation | |||||||||||||||||||||||
Full Title: A Phase 2, Multi-Center, Open-Label Induction Trial with Extension Period to Assess Endoscopic Improvement and Changes in Intestinal and Serum Biomarkers in Patients with Moderately to Severely Act... | |||||||||||||||||||||||
Medical condition: Moderately to Severely Active Crohn's Disease | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: HU (Completed) PL (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-001418-13 | Sponsor Protocol Number: TED10893 | Start Date*: 2014-11-04 | |||||||||||
Sponsor Name:Sanofi-aventis recherche & développement | |||||||||||||
Full Title: A Phase I Dose Escalation Safety and Pharmacokinetic Study of Multiple Intravenous Administrations of a Humanized Monoclonal Antibody (SAR650984) Against CD38 In Patients with Selected CD38+ Hemat... | |||||||||||||
Medical condition: Haematological malignancy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) GR (Completed) GB (GB - no longer in EU/EEA) FI (Completed) BE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005153-22 | Sponsor Protocol Number: CA180-043 | Start Date*: 2006-07-24 |
Sponsor Name:Bristol-Myers Squibb International Corporation | ||
Full Title: An open-label, randomized study of dasatinib vs. high-dose (800 mg) imatinib in the treatment of subjects with chronic phase chronic myeloid leukemia who have had a suboptimal response after at lea... | ||
Medical condition: Subjects with Ph+ chronic phase Chronic Myeloid leukemia (CML) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) FI (Completed) DK (Prematurely Ended) PT (Completed) BE (Completed) DE (Completed) GB (Completed) IT (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-005314-12 | Sponsor Protocol Number: WX/60-004 | Start Date*: 2007-01-05 | |||||||||||
Sponsor Name:Wilex AG | |||||||||||||
Full Title: A randomised, open label, Phase II Proof of Concept study of WX-671 in combination with gemcitabine vs gemcitabine in patients with locally advanced, non-resectable pancreatic cancer in order to ev... | |||||||||||||
Medical condition: Locally advanced, non-resectable pancreatic adenocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) ES (Ongoing) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000968-42 | Sponsor Protocol Number: PRPZDSKIN | Start Date*: 2016-06-23 |
Sponsor Name:INSTITUTO DE INVESTIGACION SANITARIA LA FE | ||
Full Title: Study on the healing of the partial skin graft donor site in burn patients after application of platelet-rich plasma (PRP) or plasma rich in growth factors versus usual therapeutical practice. | ||
Medical condition: Study on healing the graft donor skin on burn patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-001775-35 | Sponsor Protocol Number: MC-BCG.4/HBCA | Start Date*: 2007-07-12 | |||||||||||
Sponsor Name:medac GmbH | |||||||||||||
Full Title: Intravesical instillation of BCG strain RIVM versus TICE for prevention of recurrenec in patients with high-risk papillary superficial carcinomas of the urinary bladder. A randomised phase II clini... | |||||||||||||
Medical condition: immunostimulating adjuvant therapy of superficial carcinomas of the urinary bladder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003671-17 | Sponsor Protocol Number: NANOPRO | Start Date*: 2021-02-15 | |||||||||||
Sponsor Name:Centre François Baclesse | |||||||||||||
Full Title: Nanoparticle reirradiation and hypofractionated protontherapy of pan-tumor relapse: non-randomized phase II study. | |||||||||||||
Medical condition: recurrent tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000134-18 | Sponsor Protocol Number: RenoMet | Start Date*: 2019-08-26 |
Sponsor Name:University of Antwerp | ||
Full Title: Metformin as RenoProtector in Non-Diabetic Patients with Progressive Chronic Kidney Disease (CKD stages 2, 3A and 3B): a multi-centre, practice-oriented, repurposing, double-blind, placebo-contro... | ||
Medical condition: Chronic Kidney Disease (CKD stage 2, 3A, 3B) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004349-29 | Sponsor Protocol Number: 01-10-2014 | Start Date*: 2015-04-01 | ||||||||||||||||
Sponsor Name:Rigshospitalet | ||||||||||||||||||
Full Title: Mesenchymal stem cells for radiation-induced xerostomia (MESRIX) in previous HPV-positive oropharyngeal head and neck cancer patients | ||||||||||||||||||
Medical condition: The study will include participants with xerostomi (International Classification of Diseases-10: DQ 838A) and oropharyngeal cancer (DC 10). | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-002767-30 | Sponsor Protocol Number: ACT17453 | Start Date*: 2023-02-23 | |||||||||||
Sponsor Name:Sanofi-aventis recherche & developpement | |||||||||||||
Full Title: A randomized, Phase 2, open label study evaluating subcutaneous administration of isatuximab in combination with carfilzomib and dexamethasone in adult participants with relapsed and/or refractory ... | |||||||||||||
Medical condition: Relapsed/refractory multiple myeloma (RRMM) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Trial now transitioned) GR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002717-35 | Sponsor Protocol Number: P170920J | Start Date*: 2018-12-13 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HÔPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Non inferiority multicenter phase III randomized trial comparing preoperative chemotherapy only to chemoradiotherapy for locally advanced resectable rectal cancer (intergroup FRENCH-GRECCAR- PRODIGE) | |||||||||||||
Medical condition: Adults ≥ 18 years with middle or low locally advanced resectable rectal carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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