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A case study of foliglurax, the first clinical mGluR4 PAM for symptomatic treatment of Parkinson's disease: translational gaps or a failing industry innovation model?

AbstractINTRODUCTION:
Approximately 40% of Parkinson's disease (PD) patients that take mostly dopamine receptor agonists for motor fluctuations, experience the return of symptoms between regular doses. This is a phenomenon known as 'OFF periods.' Positive allosteric modulators (PAMs) of metabotropic glutamate receptor 4 (mGluR4) are a promising non-dopaminergic mechanism with potential to address the unmet need of patients suffering from OFF periods. Foliglurax is the first mGluR4 PAM that has advanced into clinical testing in PD patients.
AREAS COVERED:
We summarize the chemistry, pharmacokinetics, and preclinical pharmacology of foliglurax. Translational PET imaging studies, clinical efficacy data, and a competitive landscape analysis of available therapies are presented to the readers. In this Perspective article, foliglurax is used as a case study to illustrate the inherent R&D challenges that companies face when developing drugs. These challenges include the delivery of drugs acting through novel mechanisms, long-term scientific investment, and commercial success and shorter-term positive financial returns.
EXPERT OPINION:
Failure to meet the primary and secondary endpoints in a Phase 2 study led Lundbeck to discontinue the development of foliglurax. Understanding the evidence supporting compound progression into Phase 2 will enable the proper assessment of the therapeutic potential of mGluR4 PAMs.
AuthorsDario Doller, Anton Bespalov, Rob Miller, Malgorzata Pietraszek, Mikhail Kalinichev
JournalExpert opinion on investigational drugs (Expert Opin Investig Drugs) Vol. 29 Issue 12 Pg. 1323-1338 (Dec 2020) ISSN: 1744-7658 [Electronic] England
PMID33074728 (Publication Type: Journal Article, Review)
Chemical References
  • Antiparkinson Agents
  • Receptors, Metabotropic Glutamate
  • metabotropic glutamate receptor 4
Topics
  • Allosteric Regulation (drug effects)
  • Animals
  • Antiparkinson Agents (administration & dosage, pharmacokinetics, pharmacology)
  • Drug Delivery Systems
  • Humans
  • Parkinson Disease (drug therapy, physiopathology)
  • Receptors, Metabotropic Glutamate (drug effects, metabolism)

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