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FDA and CPMP rulings on subgroup analyses.
Maggioni AP, Darne B, Atar D, Abadie E, Pitt B, Zannad F; 5th Cardiovascular Clinical Trialists Workshop. Maggioni AP, et al. Among authors: abadie e. Cardiology. 2007;107(2):97-102. doi: 10.1159/000094508. Epub 2006 Jul 13. Cardiology. 2007. PMID: 16847375
Pharmacogenomics in cardiovascular clinical trials.
Shah R, Darne B, Atar D, Abadie E, Adams KF, Zannad F; 5th Cardiovascular Clinical Trialists Workshop. Shah R, et al. Among authors: abadie e. Fundam Clin Pharmacol. 2004 Dec;18(6):705-8. doi: 10.1111/j.1472-8206.2004.00289.x. Fundam Clin Pharmacol. 2004. PMID: 15548243
Vascular dementia: European perspectives.
Orgogozo JM, Abadie E. Orgogozo JM, et al. Among authors: abadie e. Alzheimer Dis Assoc Disord. 1999 Oct-Dec;13 Suppl 3:S192-200. doi: 10.1097/00002093-199912003-00027. Alzheimer Dis Assoc Disord. 1999. PMID: 10609700
Clinical trials of new drugs for the treatment of rheumatoid arthritis: focus on early disease.
Smolen JS, Collaud Basset S, Boers M, Breedveld F, Edwards CJ, Kvien TK, Miossec P, Sokka-Isler T, van Vollenhoven RF, Abadie EC, Bruyère O, Cooper C, Mäkinen H, Thomas T, Tugwell P, Reginster JY; European Society for Clinical and Economic Aspects of Osteoporosis, Osteoarthritis and Musculoskeletal Diseases (ESCEO). Smolen JS, et al. Ann Rheum Dis. 2016 Jul;75(7):1268-71. doi: 10.1136/annrheumdis-2016-209429. Epub 2016 Apr 1. Ann Rheum Dis. 2016. PMID: 27037326 Free PMC article. Review.
The use of placebo-controlled and non-inferiority trials for the evaluation of new drugs in the treatment of postmenopausal osteoporosis.
Delmas PD, Calvo G, Boers M, Abadie E, Avouac B, Kahan A, Kaufman JM, Laslop A, Lekkerkerker JF, Nilsson P, Van Zwieten-Boot B, Kreutz G, Reginster JY; Group for the Respect of Ethics and Excellence in Science (GREES). Delmas PD, et al. Among authors: abadie e. Osteoporos Int. 2002 Jan;13(1):1-5. doi: 10.1007/s198-002-8331-3. Osteoporos Int. 2002. PMID: 11878450 Review.
Where is industry getting it wrong? A review of quality concerns raised at Day 120 by the Committee For Medicinal Products for Human Use during European Centralised Marketing Authorisation Submissions for Chemical Entity Medicinal Products.
Borg JJ, Robert JL, Wade G, Aislaitner G, Pirozynski M, Abadie E, Salmonson T, Vella Bonanno P. Borg JJ, et al. Among authors: abadie e. J Pharm Pharm Sci. 2009;12(2):181-98. doi: 10.18433/j3fw2q. J Pharm Pharm Sci. 2009. PMID: 19732496 Free article.
124 results