Eudract study search
WebCTIS. FAQs . Transitional trials from EudraCT to CTIS . Training Programme – Module 23 . Version 1.3 – January 2024. What you will find • Answers to general questions regarding Transitional trials . • Answers to questions regarding how to create and submit Transitional trials . • Answers to questions regarding how to submit notifications and clinical trial WebSearch in the EU Clinical Trials Register Transition period By 31 January 2025, any ongoing trials approved under the Clinical Trials Directive will fall under the Clinical Trials Regulation. Read more about the transition period EMA news and events Find EMA news and events related to clinical trials in the EU and the EEA.
Eudract study search
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WebThe European Union Clinical Trials Register allows you to search for protocol and results information on: interventional clinical trials that were approved in the European Union … WebThe EU Clinical Trials Register currently displays 43259 clinical trials with a EudraCT protocol, of which 7159 are clinical trials conducted with subjects less than 18 years old. The register also displays information on 18700 older paediatric trials (in scope of Article 45 of the Paediatric Regulation (EC) No 1901/2006).
WebTrial category What is in scope of EudraCT Composition of results Timing of posting5 Non-paediatric trials • Non-paediatric trials conducted in at least one EEA country, and not included in an agreed PIP, ended before 21 July 2013 Summary attachment(s) mandatory; full data set optional Trials ended between 21 July 2013 and 21 July 2014: WebResult-related information for interventional clinical trials in children and/or adults included in an agreed PIP has to be posted directly to the EudraCT database using the full EudraCT data set. For more information, see Paediatric clinical trials Related documents Better medicines for children (PDF/247.68 KB) First published: 24/02/2009
WebDec 22, 2024 · The past. Prior to 1 January 2024, details of UK clinical trials of investigational medicinal products (‘CTIMP’s) took a circuitous route to public disclosure. The trial applicant would create an application form according to a structured data set in the European database (EudraCT), convert this to an Extensible Markup Language ‘XML ... WebApr 6, 2024 · ISRCTN: ISRCTN79334891. Registered 07 June 2024. EudraCT: 2024-001268-40. Registered 13 September 2024. Clinicaltrials.gov: NCT04316494. ... The HAVEN study—hydroxychloroquine in ANCA vasculitis evaluation—a multicentre, randomised, double-blind, placebo-controlled trial: study protocol and statistical analysis …
WebNov 13, 2013 · Search PMC Full-Text Archive Search in PMC. ... (SHARP) and the Asia-Pacific trials because of the different characteristics of the study populations. Results of the SHARP and Asia-Pacific trials were not available when our trial was designed. ... EudraCT 2008-002299-92 Sponsor(s): Azienda Ospedaliera di Bologna Policlinico Sant'Orsola …
WebJan 31, 2024 · EudraCT (European Union Drug Regulating Authorities Clinical Trials Database) is the database for all interventional clinical trials on medicinal products … EudraCT step-by-step guide: For a trial conducted in the European Economic … Your search for returned result(s). Create Profile Username * Email Address * … Welcome to EudraCT As of 31 January 2024, creation and submission of new … EudraCT Results Legislation: Commission guideline , Joint letter signed by EC, … a summary attachment (e.g. pdf file), if the end of trial date of your trial is before … Create a EudraCT Number. Below are the steps necessary to get a EudraCT … You have logged out or your session has been closed due to inactivity. Click here … The below specific instructions are linked in the EudraCT step-by-step guide and in … Those Commission guidance documents had been further detailed by two … EudraCT statistics (archived - zip) 2024 statistics; 2024 statistics; 2024 statistics; … 原付バイク 乗り方 手順WebApr 7, 2024 · Search Results; Study Record Detail; Saved Studies. Save this study . Warning. You have reached the maximum number of saved studies (100). ... LLC ) 2024-004144-22 ( EudraCT Number ) First Posted: April 7, 2024 Key Record Dates: Last Update Posted: March 24, 2024 Last Verified: March 2024 Individual Participant Data (IPD) … 原付バイク 乗れなくなるWebJan 24, 2024 · Study Description Go to Brief Summary: This study aims to compare treatment with Imipenem/Cilastatin-XNW4107 (IMI-XNW4107) with imipenem/cilastatin/relebactam (IMI/REL) in participants with hospital-acquired or ventilator-associated bacterial pneumonia (HABP or VAPB, respectively). 原付バイク 保険 ファミリーバイク特約WebApr 6, 2024 · The study is designed as an international, multicenter, open-label, two-arm, prospective phase III study to compare the treatment of polatuzumab vedotin plus rituximab, ifosfamide, carboplatin and etoposide (Pola-R-ICE) with the combination of rituximab, ifosfamide, carboplatin and etoposide (R-ICE) alone as salvage therapy in patients with … benq mobiuz ex2710u ファームウェアWebSearching for clinical trials. Processing of personal data. The Clinical Trials Information System (CTIS) supports the flow of information between clinical trial sponsors, European Union (EU) Member States, European Economic Area (EEA) countries and the European Commission. CTIS went live with a searchable public website on 31 January 2024. 原付バイク 住所変更WebEudraCT A database that includes information on clinical trials taking place in the European Union and clinical studies conducted worldwide in accordance with a paediatric … 原付バイク 安く買う方法WebEudraCT (European Union Drug Regulating Authorities Clinical Trials) is the European Clinical Trials Database of all clinical trials of investigational medicinal products with at … benq mobiuz ex2710u アップデート