Pharmabiz
 

Cypralis receives funding of $524,000 from ADDF to develop new cyclophilin inhibitors for neurodegenerative diseases

Cambridge, UKFriday, March 3, 2017, 12:00 Hrs  [IST]

Cypralis, a life sciences company focussed on the discovery of therapeutics for the modulation of peptidyl-prolyl isomerases (PPIases), has been awarded funding of $524,000 by the Alzheimer’s Drug Discovery Foundation (ADDF). The ADDF funding will augment the existing collaboration, facilitated by Johnson & Johnson Innovation, between Cypralis and Janssen Pharmaceuticals, (Janssen) which aims to develop new cyclophilin inhibitors for neurodegenerative diseases.

Cyclophilin inhibitors on the market or in development are non-selective between the four commonly screened cyclophilin isoforms A, B, C and D. Cypralis and Janssen are currently undertaking a joint research programme to generate a new class of CNS penetrant, selective inhibitors of cyclophilin D applicable to targeting degenerative diseases including CNS degeneration. The ADDF funding will enable Cypralis to extend ‘hit-to-lead’ medicinal chemistry and broaden its library of novel brain-penetrant cyclophilin inhibitors, whilst continuing to participate in the joint research programme with Janssen.

Dr Michael Peel, CSO of Cypralis, commented ‘The ADDF funding opens an exciting pathway towards developing a novel class of cyclophilin D inhibitors for neurodegenerative diseases, including Alzheimer’s. Many previous publications have recognised the potential for cyclophilin D as a novel target for degenerative disease but no group has published on compounds which combine sub-type selectivity and brain penetration. If data from the ADDF funding is encouraging, Cypralis would expect to initiate a Lead Optimisation campaign in early 2018 with the goal of generating a novel pre-clinical candidate for this extremely challenging and devastating disease.’  

Dr Howard Fillit, CSO of the ADDF, added ‘With ADDF funding, Cypralis will use its extensive knowledge of cyclophilin inhibitors to explore their potential as a treatment for Alzheimer’s and other neurogenerative diseases. We are excited to support this first-in-class program.’

 
[Close]