Addex and CHUV-UNIL Collaborators Awarded Swiss Grant to Advance Addex mGluR7 and mGluR4 Allosteric Modulators for Neurodegenerative and Psychiatric Diseases

Addex and CHUV-UNIL Collaborators Awarded Swiss Grant to Advance Addex mGluR7 and mGluR4 Allosteric Modulators for Neurodegenerative and Psychiatric Diseases

Geneva, Switzerland, 23 November 2015 – Addex Therapeutics (SIX: ADXN), a leading company pioneering allosteric modulation-based drug discovery and development announced today that it has been awarded a CHF666,240 grant from the Swiss Commission for Technology and Innovation (CTI) to advance the characterization of allosteric modulator therapeutics for neurodegenerative and psychiatric diseases. Addex will collaborate with the group of Prof. Ron Stoop at the Center for Psychiatric Neuroscience (CNP), part of Lausanne University Hospital (CHUV) and Lausanne University (UNIL).

The objective of the project is the characterization and optimization of potent and selective allosteric modulators targeting metabotropic glutamate receptors subtypes 4 and 7. Effect of drug candidates will be assessed in electrophysiological studies using optogenetic approaches, targeting specifically the thalamus-to-amygdala synapse, a connection central to fear learning and extinction. Data from the project will contribute to the understanding of the role played by these glutamate receptors in anxiety disorders and help the selection of the best candidate compounds for clinical development.

“We are thrilled to extend our collaboration with Addex, a world leader in allosteric modulator discovery, and to help advance these two exciting neuroscience programs" commented Prof. Ron Stoop, Center for Psychiatric Neurosciences. "Using our optogenetic approaches to test Addex proprietary compounds will generate essential information on their potential to affect neurotransmission in the amygdala, a structure of the limbic system involved in the processing of emotional responses and emotional memory. We expect to identify key mechanisms involving mGlu4 and mGlu7 receptors in these processes, which are imbalanced in an important number of psychiatric diseases.”

Addex has identified a number of novel, selective, orally available mGluR4 positive allosteric modulators (PAMs), which have demonstrated efficacy in several different rodent models of Parkinson’s disease, anxiety and most recently in the industry standard neuroinflammation model of multiple sclerosis, the Relapsing-Remitting Experimental Allergic Encephalomyelitis (RR-EAE) model. Similarly, the Company has identified unique mGluR7 negative allosteric modulators (NAMs) which have been shown to be efficacious in animal models of anxiety.

“We are delighted to receive this grant award from the Swiss Government. The use of allosteric modulators targeting mGlu4 and mGlu7 receptors offers a more precise way to regulate brain function in a number of disease areas where there is a high unmet medical need,” explained Dr. Robert Lütjens, Head of Discovery at Addex. “Accessing cutting edge technologies such as optogenetics by collaborating with the world class academic lab of Prof Ron Stoop (CHUV-UNIL) will significantly improve our scientific understanding and help advance our drug candidates.”

“Following the recent signing of an agreement with Pierre Fabre Pharmaceuticals to advance our mGluR3 program, this is an important step forward for our mGluR4 and mGluR7 programs,” commented Tim Dyer, CEO at Addex. “While we continue to focus on advancing dipraglurant in PD-LID and dystonia, the depth of Addex pipeline and its potential should not be forgotten.”

About mGluR4
The mGluR4 belongs to the Group III mGluRs (Class C G-Protein Coupled Receptor) and is negatively coupled to adenylate cyclase via activation of the Gαi/o protein. It is expressed primarily on presynaptic terminals, functioning as an autoreceptor or heteroceptor and its activation leads to decreases in neurotransmitter release from presynaptic terminals. The mGluR4 is uniquely distributed in key brain regions involved in multiple CNS disorders. In particular, mGluR4 is abundant in striato-pallidal synapses within the basal ganglia circuitry a key area implicated in movement disorders, like Parkinson’s disease. In the immune system mGluR4 has been found on dendritic cells (DCs). Emerging data implicate mGluR4 in multiple indications such as multiple sclerosis, Parkinson’s disease, anxiety, neuropathic and inflammatory pain, schizophrenia, autism and diabetes.

About mGluR7
The mGluR7 receptor is the most highly conserved of all mGluR subtypes, exhibiting the widest distribution in the brain. It is localized pre-synaptically at a broad range of glutamatergic and GABAergic synapses and is thought to be one of the most important mGluR subtypes in regulating CNS function. Preclinical data suggest that mGluR7 antagonism could alleviate stress-related anxiety and depressive symptoms and deficits in amygdala-dependent behaviors (fear response and conditioned taste aversion). These data are consistent with the abundant localization of mGluR7 in brain regions involved in the control of fear and emotion.

About Addex Therapeutics
Addex Therapeutics ( is a biopharmaceutical company focused on the development of novel, orally available, small molecule allosteric modulators for neurological disorders. Addex lead drug candidate, dipraglurant (mGluR5 negative allosteric modulator or NAM) has successfully completed a Phase IIa POC in Parkinson’s disease levodopa-induced dyskinesia (PD-LID), and is currently being evaluated in a PET receptor occupancy study as part of its preparation to enter a Phase III pivotal trial for PD-LID. In parallel, dipraglurant’s therapeutic use in dystonia is being investigated. Addex second clinical program, ADX71149 (mGluR2 positive allosteric modulator or PAM) is being developed in collaboration with Janssen Pharmaceuticals, Inc. Addex also has several preclinical programs including: ADX71441 (GABAB receptor PAM) which has received regulatory approval to start Phase I and is being investigated for therapeutic use in Charcot-Marie-Tooth (Type 1A) disease, alcohol use disorder and nicotine dependence; mGluR4PAM for drug abuse and dependence, Parkinson’s disease and other neurodegenerative diseases; mGluR2NAM for treatment resistant depression and cognitive deficits; mGluR7NAM for psychosomatic disorders, TrkBPAM for neurodegenerative disorders; and GLP1PAM for type 2 diabetes. Allosteric modulators are an emerging class of small molecule drugs which have the potential to be more specific and confer significant therapeutic advantages over conventional "orthosteric" small molecule or biological drugs. Addex allosteric modulator drug discovery platform targets receptors and other proteins that are recognized as essential for therapeutic intervention – the Addex pipeline was generated from this pioneering allosteric modulator drug discovery platform.

Press Contact:

Tim Dyer
Chief Executive Officer
Addex Therapeutics
Telephone: +41 22 884 15 61
Email: PR(at)

Disclaimer / Forward-looking statements: This communication does not constitute an offer or invitation to subscribe for or purchase any securities of Addex Therapeutics Ltd. This publication may contain certain forward-looking statements concerning the Company and its business. Such statements involve certain risks, uncertainties and other factors which could cause the actual results, financial condition, performance or achievements of the Company to be materially different from those expressed or implied by such statements. Readers should therefore not place undue reliance on these statements, particularly not in connection with any contract or investment decision. The Company disclaims any obligation to update these forward-looking statements.