2,187 results on '"Kesselheim, Aaron"'
Search Results
2. Trends in Use and Evidence of Adherence to Risk Evaluation and Mitigation Strategy Pregnancy Testing Requirements for Thalidomide, Lenalidomide, and Pomalidomide in the USA, 2000–2020
3. Availability and Cost of Expensive and Common Generic Prescription Drugs: A Cross-sectional Analysis of Direct-to-Consumer Pharmacies
4. Measuring and Understanding Market Exclusivity Length for New Prescription Drugs in France, Australia, and the USA
5. The cost of drug patent expiration date errors
6. Biologic patent challenges under the America Invents Act
7. Independent Advice on Drug Approvals: an Investigation of EMA Practices
8. Approval and therapeutic value of gene therapies in the US and Europe
9. The prevalence of drug patent term extensions in the United States, 2000–2018
10. Complicated regulatory decision-making following inconsistent trial results: the issue with ibrutinib for mantle cell lymphoma
11. Clinical Benefit and Revenues of Drugs Affected by Rare Pediatric Disease Priority Review Vouchers, 2017-2023
12. How health technology assessment can help to address challenges in drug repurposing: a conceptual framework
13. Rates and costs of drug testing practices for private payors in the outpatient setting in the United States, 2015–2019
14. Market dynamics of authorized generics in Medicaid from 2014 to 2020
15. Ethical issues in new drug prescribing
16. Persistence of resistance: a panel data analysis of the effect of antibiotic usage on the prevalence of resistance
17. Sales Revenues for New Therapeutic Agents Approved by the United States Food and Drug Administration From 1995 to 2014
18. Infections following bispecific antibodies in myeloma: a systematic review and meta-analysis
19. Alternatives to the quality-adjusted life year: How well do they address common criticisms?
20. Coverage of New Drugs in Medicare Part D
21. Patents and regulatory exclusivities on FDA-approved insulin products: A longitudinal database study, 1986-2019
22. Overcoming Challenges to Implementing New Evidence for Low-Dose Anticoagulant Use in Peripheral Artery Disease
23. Patenting Strategies on Inhaler Delivery Devices
24. Getting the Price Right: Lessons for Medicare Price Negotiation from Peer Countries
25. Experts’ Views on FDA Regulatory Standards for Drug and High-Risk Medical Devices: Implications for Patient Care
26. Pursuing Value-Based Prices for Drugs : A Comprehensive Comparison of State Prescription Drug–Pricing Boards
27. Using Multiple Authorized Generics to Maintain High Prices: The Example of Entacapone
28. Brand-name market exclusivity for nebulizer therapy to treat asthma and COPD
29. Medicaid Expenditures and Estimated Rebates on Line Extension Drugs, 2010–2018
30. New Drug Postmarketing Requirements and Commitments in the US: A Systematic Review of the Evidence
31. State Laws and Generic Substitution in the Year After New Generic Competition
32. Price changes and within-class competition of cancer drugs in the USA and Europe: a comparative analysis
33. The characteristics of patents impacting availability of biosimilars
34. Why France Spends Less Than the United States on Drugs : A Comparative Study of Drug Pricing and Pricing Regulation
35. Patient perspectives on evidence supporting drug safety and effectiveness: "What does it mean for me?".
36. Commercial markups on pediatric oncology drugs at 340B pediatric hospitals.
37. Clinical value of guideline recommended molecular targets and genome targeted cancer therapies: cross sectional study.
38. Trust in the Food and Drug Administration: A National Survey Study.
39. Patent Portfolios Protecting 10 Top-Selling Prescription Drugs.
40. Producing and using timely comparative evidence on drugs : lessons from clinical trials for covid-19
41. Association between FDA and EMA expedited approval programs and therapeutic value of new medicines : retrospective cohort study
42. Accounting for US public funding in drug development : how can we better balance access, affordability, and innovation?
43. Characteristics of US Patients and Prescribers Using Hydroxychloroquine During the COVID-19 Pandemic
44. Recent Orange and Purple Book legislation suggests a need to bridge drug and biologic patent regimes
45. Reconsidering the scope of US state laws allowing pharmacist substitution of generic drugs
46. Reimagining Pharmaceutical Market Exclusivities: Should the Duration of Guaranteed Monopoly Periods Be Value Based?
47. A Multi-modal Approach to Evaluate the Impact of Risk Evaluation and Mitigation Strategy (REMS) Programs
48. Analysis of risk evaluation and mitigation strategies for teratogenic drugs: Variation in primary and secondary prevention measures
49. Public sector financial support for late stage discovery of new drugs in the United States : cohort study
50. Clinical Benefit and Expedited Approval of Cancer Drugs in the United States, European Union, Switzerland, Japan, Canada, and Australia
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.