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https://www.nih.gov/news-events/news-releases/drug-delivery-technology-leads-sustained-hiv-antibody-production-nih-study
Mar 09, 2020 · A new approach to direct the body to make a specific antibody against HIV led to sustained production of that antibody for more than a year among participants in a National Institutes of Health clinical trial. This drug-delivery technology uses a …
https://www.drugdeliverybusiness.com/category/clinical-trials/
The EluNIR drug-eluting stent made by Medinol performed just as well as the Resolute Integrity or Resolute Onyx stents from Medtronic (NYSE:MDT), according to new clinical study results from an international team of researchers.
https://grants.nih.gov/grants/guide/pa-files/PAR-18-252.html
NIH Funding Opportunities and Notices in the NIH Guide for Grants and Contracts: Image-guided Drug Delivery (R01 Clinical Trial Optional) PAR-18-252. NCI
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867146/
A proposal to expand the clinical trial registry to include results of these trials 9 may provide insights on the impact of drug delivery systems and clinical trial designs to help sponsors and regulators in optimizing dosing or drug delivery strategies that improve drug efficacy and safety.Author: Jenny Y. Chien, Rodney J.Y. Ho
https://www.news-medical.net/news/20200226/Renishaw-Announces-Completion-of-the-Main-Part-of-a-Multi-Centre-Clinical-Trial-Jointly-Undertaken-with-Herantis-Pharma-plc-for-the-Treatment-of-Parkinsons-Disease-Patients.aspx
Feb 26, 2020 · Rupert Jones, Managing Director of Renishaw Medical, said, “The results of this trial and the performance of Renishaw's drug delivery system are …
https://clinicaltrials.gov/ct2/show/NCT03798912
A First-in-Human Study of Enteral Drug Delivery Device (RANIFIM) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government.
https://www.meddeviceonline.com/doc/a-primer-on-investigational-drug-delivery-device-regulatory-requirements-0001
Nov 16, 2015 · Let’s review, in detail, each of the variables that device regulators will assess in your combination drug/delivery device submission: DHF device. In most cases, a drug delivery device using the NDA pathway will have to be evaluated just like a drug …
https://markets.businessinsider.com/news/stocks/global-controlled-release-drug-delivery-market-opportunity-clinical-trial-outlook-2025-1028889946
Feb 10, 2020 · NEW YORK, Feb. 10, 2020 /PRNewswire/ --'Global Controlled Release Drug Delivery Market Opportunity & Clinical Trial Outlook 2025' Report Highlight...
https://clinicaltrials.gov/ct2/show/NCT01321073
Mar 23, 2011 · DelIVery for Pulmonary Arterial Hypertension (PAH) (DelIVery) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government.
https://www.drugs.com/clinical_trials.html
Clinical Trial News. This section provides information about recently completed clinical trials. If you cannot find information about a particular clinical trial, you should note that results may not be available even after the trial ends. Some trials end before completion and results are never published. Get news by email or subscribe to our ...
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