Cited by 216Diabetes Treatment and ManagementDiabetes Management and ResearchPharmaceutical Economics and Policy

Finding New Treatments for Diabetes — How Many, How Fast . . . How Good?

Nathan, David M.·2007·New England Journal of Medicine

Abstract

Two modern-day epidemics, HIV–AIDS and type 2 diabetes mellitus, have inspired impassioned calls for more effective interventions. In the 1980s, the rapid spread of HIV, with its associated severe, acute illness and high mortality, prompted activist groups and others to call for the accelerated approval of medications that showed promise of efficacy. There was no treatment available, and people were dying quickly. More recently, pressure to develop new drugs for type 2 diabetes has been stimulated by the remarkable worldwide increase in the incidence of this disease (54% in the past 7 years in the United States1) and the . . .

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Crossref · 10.1056/nejmp068294

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References 4 · Cited by 216

Authors
Nathan, D. M.
Affiliations
Harvard University (US)
Corresponding author
Nathan, David M.
Venue
New England Journal of Medicine
Published
2007-02
Volume
356
Issue
5
Pages
437-440
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W2005038357
Cited by
216
References
4
Citations by year
2025: 3 · 2024: 3 · 2023: 4 · 2022: 6 · 2021: 3 · 2020: 5 · 2019: 7 · 2018: 6 · 2017: 7 · 2016: 7 · 2015: 8 · 2014: 3 · 2013: 13 · 2012: 8
FWCI
28.74
Type
journal article
Language
en
Open access
closed
Locations
  • New England Journal of Medicine (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
  • Social Sciences › Economics, Econometrics and Finance › Economics and Econometrics › Pharmaceutical Economics and Policy
Keywords
type 2 diabetes, drug development, new treatments, accelerated approval, HIV/AIDS, incidence trends, antidiabetic drugs
MeSH terms
Sitagliptin Phosphate, Clinical Trials as Topic, Diabetes Mellitus, Type 2, Glycoproteins, Humans, Hypoglycemic Agents, Peptide Fragments, Pyrazines, Triazoles, United States, United States Food and Drug Administration, Drug Approval, Dipeptidyl Peptidase 4, History, 20th Century, History, 21st Century, Glucagon-Like Peptide 1, Dipeptidyl-Peptidase IV Inhibitors, Adenosine Deaminase Inhibitors

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