Glycine Transporter Type I (GlyT1) Inhibitor, Bitopertin: A Journey from Lab to Patient

Authors

  • Emmanuel Pinard Roche Pharmaceutical Research and Early Development (pRED) Roche Innovation Center Basel Medicinal Chemistry Department 124 Grenzacherstrasse, B 92 /6.30 CH-4070 Basel, Switzerland. emmanuel.pinard@roche.com
  • Edilio Borroni Roche Pharmaceutical Research and Early Development (pRED) Roche Innovation Center Basel Medicinal Chemistry Department 124 Grenzacherstrasse, B 92 /6.30 CH-4070 Basel, Switzerland
  • Annette Koerner Roche Pharmaceutical Research and Early Development (pRED) Roche Innovation Center Basel Medicinal Chemistry Department 124 Grenzacherstrasse, B 92 /6.30 CH-4070 Basel, Switzerland
  • Daniel Umbricht Roche Pharmaceutical Research and Early Development (pRED) Roche Innovation Center Basel Medicinal Chemistry Department 124 Grenzacherstrasse, B 92 /6.30 CH-4070 Basel, Switzerland
  • Daniela Alberati Roche Pharmaceutical Research and Early Development (pRED) Roche Innovation Center Basel Medicinal Chemistry Department 124 Grenzacherstrasse, B 92 /6.30 CH-4070 Basel, Switzerland

DOI:

https://doi.org/10.2533/chimia.2018.477

Keywords:

Beta-thalassemia, Glyt1, Medicinal chemistry, Pet, Schizophrenia, Transporter

Abstract

Glycine transporter-1 (GlyT1) inhibition has been extensively studied both in pharmaceutical companies and academic institutions primarily as a potential new approach to treat schizophrenia, a severe and chronic mental illness. More recently, preclinical results have suggested that this approach could also have therapeutic potential for CNS disorders beyond schizophrenia as well as for non-CNS indications. Over the past 17 years, Roche has been a key player in the GlyT1 field with the discovery and development of bitopertin, the most advanced GlyT1 inhibitor to date and the only one which completed Phase III clinical studies for schizophrenia. In this article, we relate the eventful journey of the discovery and development of bitopertin, from project initiation in 2001 to its evaluation today in patients suffering from beta-thalassemia, a monogenic hereditary haematological disorder.

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Published

2018-08-22

How to Cite

[1]
E. Pinard, E. Borroni, A. Koerner, D. Umbricht, D. Alberati, Chimia 2018, 72, 477, DOI: 10.2533/chimia.2018.477.