PMID- 31894029 OWN - NLM STAT- MEDLINE DCOM- 20200701 LR - 20200701 IS - 1011-601X (Print) IS - 1011-601X (Linking) VI - 32 IP - 5(Special) DP - 2019 Sep TI - Efficacy and safety of NAD+ ADP-ribosyltransferase 1 agonist versus Donepezil in elderly Chinese patients with Alzheimer disease: A novel target for effective therapy. PG - 2427-2432 AB - This pilot study designed to evaluate the efficacy and safety of NAD+ ADP-ribosyl transferase 1 (NART) agonist in comparison with Donepezil (DNP) in elderly Chinese patients with Alzheimer disease (AD). In the present clinical trial, Chinese elderly patients aged >65 years with a confirmed diagnosis of AD were enrolled. The patients received NART agonist (test, DAG-structured PKC blockers (GF109203X)) or DNP 10mg daily (reference) for 6 months. The efficacy and safety data were collected from 120 patients (60 patients in each group) every 3 weeks until 6 months. The primary endpoints were to assess the change in cognitive score from baseline in both the treatment group. The result of the present study showed that the patients treated with DNP and NART agonist have similar efficacy and safety profile. Considering the clinical benefit, improvement in sign and symptoms of was numerically greater in DNP-treated patients as compared to NART agonist. However, a statistical difference in terms of clinical benefit was similar between both the treatment groups. Overall, both the study drugs were found comparable in relieving the symptoms of AD. This indicates that NART is a potential target for the treatment of AD in China. The results of the present study may help to design a large clinical trial to evaluate the efficacy and safety of NART agonist in comparison with DNP in AD patients. FAU - Wang, Jianhong AU - Wang J AD - Department of Neurology, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, China. FAU - Yang, Shu AU - Yang S AD - Department of Neurology, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, China. FAU - Hu, Zicheng AU - Hu Z AD - Department of Neurology, Daping Hospital, Third Military Medical University, Chongqing, China. FAU - Yang, Haimei AU - Yang H AD - Department of Neurology, Daping Hospital, Third Military Medical University, Chongqing, China. FAU - Wei, Dong AU - Wei D AD - Department of Neurology, The People's Hospital of Lezhi, Ziyang, Sichuan, China. FAU - Wang, Duozi AU - Wang D AD - Department of Neurology, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, China. FAU - Guo, Fuqiang AU - Guo F AD - Department of Neurology, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, China. LA - eng PT - Journal Article PT - Randomized Controlled Trial PL - Pakistan TA - Pak J Pharm Sci JT - Pakistan journal of pharmaceutical sciences JID - 9426356 RN - 0 (Amyloid beta-Peptides) RN - 0 (Cholinesterase Inhibitors) RN - 0 (Enzyme Inhibitors) RN - 0 (Indoles) RN - 0 (Maleimides) RN - 8SSC91326P (Donepezil) RN - L79H6N0V6C (bisindolylmaleimide I) SB - IM MH - Aged MH - Amyloid beta-Peptides MH - China MH - Cholinesterase Inhibitors/*therapeutic use MH - Donepezil/*therapeutic use MH - Enzyme Inhibitors/*therapeutic use MH - Female MH - Humans MH - Indoles/*therapeutic use MH - Male MH - Maleimides/*therapeutic use EDAT- 2020/01/03 06:00 MHDA- 2020/07/02 06:00 CRDT- 2020/01/03 06:00 PHST- 2020/01/03 06:00 [entrez] PHST- 2020/01/03 06:00 [pubmed] PHST- 2020/07/02 06:00 [medline] PST - ppublish SO - Pak J Pharm Sci. 2019 Sep;32(5(Special)):2427-2432.