With mandatory clinical trial registration now in place for most novel therapeutic interventions, key questions remain on how to maximize the potential benefits of the enhanced transparency that ...

Why do clinical trials need to be registered at ClinicalTrials.gov? Section 801 of the Food and Drug Administration Amendments Act (FDAAA 801) requires registration of all clinical trials and ...

Investigators should be aware that studies that meet the definition of clinical trial may be subject to additional regulatory and/or policy requirements, such as posting of consent forms on federal ...

Learn more about the FDA definition of an "applicable clinical trial." The site uses a web-based data entry system called the Protocol Registration and Results System (PRS) to register clinical ...

Registration on ClinicalTrials.gov is a requirement for all National Institutes of Health (NIH)-funded clinical trials and all Food and Drug Administration (FDA) “Applicable Clinical Trials." This ...

Moleculin Biotech, Inc., (Nasdaq: MBRX) ("Moleculin" or the "Company"), a late-stage pharmaceutical company with a broad portfolio of drug candidates targeting hard-to-treat tumors and viruses, today ...

SMi Group are proud to announce the 11th annual Adaptive Designs in Clinical Trials conference and exhibition will return to London from the 1st – 2nd April 2019. With the growing popularity in ...

(Headquarters: Chuo-ku, Tokyo; "Renalys Pharma") announced today that it has completed patient enrollment for its registrational Phase III clinical trial of sparsentan for the treatment of IgA ...