SBIR/STTR Research Award
A Novel Pharmacological Treatment for Neuropathic Pain
Award amount
$2,340,324Program and phase
SBIR · Phase II – Direct to Phase IIAward year
2016Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- Aptinyx Inc
- Proposal award date
- 2016-09-30
- Contract end date
- 2018-08-31
- UEI
- Not reported
- Solicitation number
- PAR14-088
- Topic code
- 105
Research abstract
PROJECT SUMMARY
Neuropathic pain NP conditions affect up to of the population while the annual costs of treatment
reach $ billion in the US Pain reduction is more difficult to achieve in NP since the mechanisms involved
are not the same as the mechanisms of normal nociceptive pain Current therapeutic approaches offer
limited pain relief and frequently produce side effects that outweigh the benefits More effective and better
tolerated NP treatments are urgently needed
Aptinyx is developing a new approach to addressing NP The company has developed a novel class of
non toxic orally bioavailable compounds that modulate the N methyl D aspartate receptor NMDAR within
the glutamatergic system The NMDAR is a major player in regulating synaptic plasticity which is involved
in the development and maintenance of NP Aptinyxandapos s NMDAR partial agonists presumably act to normalize
NMDAR activity by their ability to act as agonists or antagonists Our preliminary data show that the lead
compound JY displays a robust dose dependent analgesic effect in multiple models of NP
matching or surpassing that of current treatments Furthermore its activity is restricted to NP producing no
sedation and having no effect on nociceptive pain Initial pharmacological data show excellent safety and
bioavailability of JY making it an excellent candidate for further development NMDAR partial
agonists previously developed at Aptinyx that JY is based on are currently in clinical development
for major depression
The goal of this direct to Phase II project is to complete the remaining pre clinical studies required for JY
to advance to human trials for NP To this end the specific aims are
Aim Evaluate dosing of JY in Bennett model of NP
Aim Develop analytical techniques and obtain GMP material of Drug Substance and Drug
Product
Aim Conduct day general toxicology studies in the rat and the dog under GLPs
Aim Conduct pharmacokinetics safety pharmacology and genotoxicity studies under GLPs
The end product of the proposed Phase II project is a complete safety package that will be submitted to the
FDA as a part of an IND that will allow JY to enter clinical trials PROJECT NARRATIVE
Aptinyx is developing an orally bioavailable small molecule NMDA receptor partial agonist for the treatment
of neuropathic pain The compound offers safe robust and long lasting analgesia in neuropathic pain
conditions This Direct to Phase II project will generate data that will enable the lead compound to enter
human clinical trials for neuropathic pain
Technology keywords
Not reported
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