Clinical Trial Data Access Request

Diurnal is committed to public disclosure and transparency of our clinical study data. Diurnal is committed to transparency in clinical trials and publishes the protocols and results of its clinical trials on the website www.clinicaltrials.gov

Qualified scientific and medical researchers may request clinical trial data. Diurnal agrees to share patient- and study-level data and protocols from clinical trials in patients, for medicines and indications approved by national regulatory authorities. Diurnal will consider requests for study data or full Clinical Study Reports (CSRs) received via our Contact Us page. Requests will be forwarded to the Chief Medical Officer (CMO) for review of validity and Diurnal will request a formal research proposal to evaluate a data request. The Review will be focussed on: The Review will be focussed on:

  • patient informed consent

  • patient confidentiality and anonymity

  • data being requested

  • the hypothesis to be tested

  • the rationale for the proposed research

  • analysis plan

  • publication plan

  • qualifications and experience of the proposed research team

  • any potential conflicts of interest, including potential competitive use of

  • the data

  • the source of any research funding.

Diurnal reserves the right to refuse or delay data requests that are inconsistent with existing data publication obligations for a study, for example, as contained in site/investigator agreements. Diurnal reserves the right to refuse data requests for commercial purposes or from commercial competitors.

Diurnal Limited (Company Number: 05237326) is registered in England & Wales. Registered office: Cardiff Medicentre, Heath Park, Cardiff CF14 4UJ, UK.