Synonyms: Lu AE58054, SGS 518
Chemical Name: 2-(6-fluoro-1H-indol-3-yl)-ethyl]-[3-(2,2,3,3-tetrafluoropropoxy)-benzyl]-amine
Therapy Type: Small Molecule (timeline)
Target Type: Other Neurotransmitters (timeline)
Condition(s): Alzheimer's Disease, Schizophrenia
U.S. FDA Status: Alzheimer's Disease (Phase 3), Schizophrenia (Inactive)
Company: H. Lundbeck, Otsuka Pharmaceutical Co., Ltd.
This orally available drug is an antagonist of the serotonin 6 (5-HT6) receptor. This receptor subtype is expressed primarily in the brain, particularly in the cerebral cortex and hippocampus, where it has been proposed to play a role in cognitive impairments associated with schizophrenia and Alzheimer's disease. The 5-HT6 receptor antagonists are thought to enhance cholinergic, glutamatergic, noradrenergic, and dopaminergic neurotransmission. Apart from some affinity for adrenergic receptors, Lu AE58054 has been reported to be highly selective over other G-protein coupled receptors. The compound enters the brain and was able to dose-dependently reverse deficits in a rat model of cognitive impairment (Upton et al., 2008; Arnt et al., 2010).
Lu AE58054 is being developed as a symptomatic adjunct to cholinesterase inhibitor treatment in Alzheimer's disease. Lu AE58054 was originally discovered by Lilly, which licensed it to the biotechnology company Saegis for clinical development in cognitive impairment in thinking disorders such as schizophrenia. In 2006, Saegis was acquired by Lundbeck, which in October 2013 launched a global Phase 3 program in AD. This program consists of four trials planned to enroll a total of about 3,000 patients (see company press release).
No Phase 1 trials on this drug are listed in publicly available databases. In 2005, Saegis conducted a Phase 2a trial in 20 schizophrenia patients in the United States, evaluating the safety, tolerability, pharmacokinetics, and pharmacodynamics of giving this drug as an add-on to Risperidone (see company press release). In 2009 and 2010, Lundbeck conducted a Phase 2 trial in Europe and Asia to evaluate the compound as an adjunct to Risperidone for its effect on cognitive deficits in 124 patients with schizophrenia. Results were not published in the peer-reviewed literature, but development of Lu AE58054 for cognitive deficits in schizophrenia appears to have ended.
In 2010 and 2011, Lundbeck evaluated Lu AE58054 in a Phase 2 study in 278 patients with probable Alzheimer's disease. Conducted in Australia, Canada, and Europe, the trial compared the effects of a six-month course of 90 mg/day of Lu AE58054 with 10 mg/day of Donepezil to the same dose of placebo. In June 2012, the company announced that the trial had met its primary cognition endpoint as measured by the ADAS-cog. On secondary endpoints, such as measures of global status and activities of daily living, Lu AE58054 treatment showed trends for a benefit but fell short of achieving statistical significance. Elevated liver enzymes in the treatment group, and higher dropout than in the placebo group, were also noted in this trial (see Jun 2012 news).
In October 2013, the first of four Phase 3 studies began, called STARSHINE. All Phase 3 trials in this program are enrolling patients with mild to moderate Alzheimer's disease who are already taking a stable dose of 10 mg/day of an acetylcholinesterase inhibitor; two studies require that patients be on donepezil, one allows any of the three available drugs of that mechanism, the fourth is an extension study. This first Phase 3 trial compares a six-month, adjunct course of a lower dose than in Phase 2, i.e., once-daily 30 or 60 mg capsules of idalopirdine, to placebo in 930 participants for added benefit on cognition as measured by the ADAS-cog. No functional co-primary endpoint is listed. Secondary outcomes will assess various aspects of global clinical function and behavior. No biomarkers are embedded in this development program.
In spring 2014, Lundbeck started up three additional Phase 3 studies. STARBEAM is comparing a lower dose of 10 mg to 30 mg once daily for six months in 840 patients, STARBRIGHT is a worldwide study comparing 30 to 60 mg once daily for six months in 720 patients. The third is an open-label study to enroll 1,770 patients who have completed one of the two trials comparing the higher two doses; it will assess safety, cognition, clinical, and psychiatric measures for another seven months. These studies are set to end between November 2015 and August 2016.
In 2013 and 2014, Phase 1 studies evaluating pharmacokinetics of single and multiple ascending doses in healthy volunteers and in people with liver impairment were added.
In 2015, Lundbeck conducted four additional Phase 1 trials in France, Germany, and the United Kingdom. One evaluates the bioequivalence of two different formulations, the others investigate idalopirdine's effect on kidney function, excretion, and heart repolarization.
In July 2016, Idalopirdine received Fast Track designation by the FDAl; however in September, Lundbeck announced that topline results showed weak efficacy: none of the two doses in the STARSHINE phase 3 trial reached the primary endpoint (see 30 Sept news).
Clinical Trial Timeline
- Phase 2
- Phase 3
- Study completed / Planned end date
- Planned end date unavailable
- Study aborted
- Upton N, Chuang TT, Hunter AJ, Virley DJ. 5-HT6 receptor antagonists as novel cognitive enhancing agents for Alzheimer's disease. Neurotherapeutics. 2008 Jul;5(3):458-69. PubMed.
- Arnt J, Bang-Andersen B, Grayson B, Bymaster FP, Cohen MP, DeLapp NW, Giethlen B, Kreilgaard M, McKinzie DL, Neill JC, Nelson DL, Nielsen SM, Poulsen MN, Schaus JM, Witten LM. Lu AE58054, a 5-HT6 antagonist, reverses cognitive impairment induced by subchronic phencyclidine in a novel object recognition test in rats. Int J Neuropsychopharmacol. 2010 Sep;13(8):1021-33. Epub 2010 Jun 23 PubMed.
- Maher-Edwards G, Zvartau-Hind M, Hunter AJ, Gold M, Hopton G, Jacobs G, Davy M, Williams P. Double-blind, controlled phase II study of a 5-HT6 receptor antagonist, SB-742457, in Alzheimer's disease. Curr Alzheimer Res. 2010 Aug;7(5):374-85. PubMed.
- Yun HM, Rhim H. The serotonin-6 receptor as a novel therapeutic target. Exp Neurobiol. 2011 Dec;20(4):159-68. PubMed.
- Brodney MA, Johnson DE, Sawant-Basak A, Coffman KJ, Drummond EM, Hudson EL, Fisher KE, Noguchi H, Waizumi N, McDowell LL, Papanikolaou A, Pettersen BA, Schmidt AW, Tseng E, Stutzman-Engwall K, Rubitski DM, Vanase-Frawley MA, Grimwood S. Identification of Multiple 5-HT(4) Partial Agonist Clinical Candidates for the Treatment of Alzheimer's Disease. J Med Chem. 2012 Nov 8;55(21):9240-54. PubMed.
- Cirrito JR, Disabato BM, Restivo JL, Verges DK, Goebel WD, Sathyan A, Hayreh D, D'Angelo G, Benzinger T, Yoon H, Kim J, Morris JC, Mintun MA, Sheline YI. Serotonin signaling is associated with lower amyloid-β levels and plaques in transgenic mice and humans. Proc Natl Acad Sci U S A. 2011 Sep 6;108(36):14968-73. PubMed.
- Wilkinson D, Windfeld K, Colding-Jørgensen E. Safety and efficacy of idalopirdine, a 5-HT6 receptor antagonist, in patients with moderate Alzheimer's disease (LADDER): a randomised, double-blind, placebo-controlled phase 2 trial. Lancet Neurol. 2014 Nov;13(11):1092-9. Epub 2014 Oct 5 PubMed.