Using Trademarks to Ensure Completion of Postapproval Trials
Bibliographic Data
| ID | 15809013 |
|---|---|
| Authors | Catherine S Hwang (0009-0004-0185-3256, VA Portland Health Care System), S Sean Tu (0000-0003-0391-8186, West Virginia University, corresponding author) |
| Year | 2025 |
| Volume | 6 |
| Issue | 2 |
| Pages | e250001-e250001 |
| Publication date | 2025-02-28 |
| Open Access | Yes |
| Type | ARTICLE |
| Venue | JAMA Health Forum (JOURNAL) |
| Journal identifiers | ISSN: 2689-0186 • E-ISSN: 2689-0186 |
| Publisher | American Medical Association (PUBLISHER • US) |
| DOI | 10.1001/jamahealthforum.2025.0001 |
| PMID | 40019740 |
| OpenAlex | W4408052194 |
| Language | EN |
| References cited | 7 |
This Viewpoint evaluates how using trademarks can support the US Food and Drug Administration’s mission to approve safe and effective medications
Administration (probate law · Business · Food and drug administration · Political science · Risk analysis (engineering · Biomedical Ethics and Regulation · Health Systems, Economic Evaluations, Quality of Life · Law · Science, Research, and Medicine
Medicare Spending on Drugs With Accelerated Approval, 2015-2019
Timing of Confirmatory Trials for Drugs Granted Accelerated Approval Based on Surrogate Measures From 2012 to 2021
Spending by the Centers for Medicare & Medicaid Services Before and After Confirmation of Benefit for Drugs Granted US Food and Drug Administration Accelerated Approval, 2012 to 2017
| Highly cited | No |
|---|