Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Menghis Bairu"'
Autor:
Reisa A. Sperling, Ron Keren, Gerald Crans, C H van Dyck, Susan Abushakra, Aleksandra Pastrak, G. Quinn, Jesse M. Cedarbaum, Menghis Bairu, Chito Hernandez, Earvin Liang, Pierre N. Tariot, Sid Gilman, Anton P. Porsteinsson, Stephen Salloway, Douglas L. Arnold
Publikováno v:
Neurology. 77:1253-1262
Objective: This randomized, double-blind, placebo-controlled, dose-ranging phase 2 study explored safety, efficacy, and biomarker effects of ELND005 (an oral amyloid anti-aggregation agent) in mild to moderate Alzheimer disease (AD). Methods: A total
Autor:
Menghis Bairu, Michael Weiner
Global Clinical Trials for Alzheimer's Disease is a handy one-stop reference for researchers and physicians planning and conducting global clinical trials in this area. This book addresses important considerations that may arise during the successful
Autor:
Menghis Bairu
Publikováno v:
Journal of Commercial Biotechnology. 21
Whether it’s willful counterfeiting, sloppy manufacturing processes, or neglectful handing of drugs in the global supply chain, recent studies suggest the problem of weakened, adulterated, and fake drugs is a growing global issue with deadly c
Publikováno v:
Alzheimer's & Dementia. 10
Background: In a 78-week study in Mild to Moderate AD patients (Study AD201, Salloway et al., Neurology, 2011), oral ELND005 (scyllo-inositol, a myo-inositol stereoisomer) led to beneficial trends on agitation/aggression (Abushakra et al. CTAD 2012),
Publikováno v:
Alzheimer's & Dementia. 10
Autor:
Patrick Kesslak, Matthias Kurth, Menghis Bairu, Constantine G. Lyketsos, Frank Fan, David Miller, Susan Abushakra
Publikováno v:
Alzheimer's & Dementia. 10
Publikováno v:
Alzheimer's & Dementia. 10
Autor:
Ricardo F. Allegri, H. Michael Arrighi, Pablo M. Bagnati, Menghis Bairu, Sonia Brucki, Tal Burt, Lorne Cheeseman, Richard Chin, Debbie N. Cote, Jeffrey Cummings, Stephanie Danandjaja, P. Murali Doraiswamy, Murat Emre, James (Dachao) Fan, Yoko Fujimoto, Michel Grothe, Ibrahim Hakan Gürvit, Spencer Guthrie, Harald Hampel, Lynne Hughes, Michael Hüll, Hilal İlbars, Takeshi Iwatsubo, Roy W. Jones, Nadina C. Jose, Amir Kalali, Seong Yoon Kim, Miia Kivipelto, Bernd J. Krause, Jens Kurth, Huafang Li, Francesca Mangialasche, Hans J. Möbius, Ricardo Nitrini, Tiia Ngandu, Muriel O’Byrne, Peter Schüler, Klaudius Siegfried, Sidney A. Spector, Stefan Teipel, Yağiz Üresin, Michael Weiner, Jing Yin, Xue (Kate) Zhong
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ddf95cb08be205d45de9a3c12a30420
https://doi.org/10.1016/b978-0-12-411464-7.00027-4
https://doi.org/10.1016/b978-0-12-411464-7.00027-4
Autor:
Muriel O’ Byrne, Menghis Bairu
Data from clinical trials in emerging markets are becoming a standard component of the regulatory package being provided to support pharmaceutical marketing authorizations including the FDA New Drug Application (NDA) and the EMA Marketing Authorizati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82e4abd0678f51f8093dcd1f9aa83306
https://doi.org/10.1016/b978-0-12-411464-7.00008-0
https://doi.org/10.1016/b978-0-12-411464-7.00008-0