Pharmaceutical Business review

Nuformix announces UK MHRA approval to start NXP001 human pharmacokinetics studies

Image: Nuformix has announced MHRA approval to commence NXP001 human pharmacokinetics studies. Photo: courtesy of poommy105 / FreeDigitalPhotos.net.

The approval allows Nuformix to initiate the first dosing of NXP001 in an open-label study to compare the bioavailability of NXP001 to Merck’s EMEND  in healthy subjects.

Nuformix is developing NXP001 as a treatment for chemotherapy-induced nausea and vomiting (CINV).

CINV is a large, under-exploited and growing market, which in demographic terms comprises one third of global cancer patients. The primary objective of the study is to investigate the pharmacokinetics and bioavailability of single oral doses of NXP001. Dosing will commence in March 2019, with results expected by end H1 2019.

Dr Dan Gooding, CEO, Nuformix plc, said: “Although expected, receiving approval to advance our first programme into human studies is a major step forward for our Company and our pipeline. The MHRA’s decision validates the speed to clinic of our cocrystal approach without the need for further safety data and sets a precedent for our broader pipeline.

“ Completion of these studies will allow us to rapidly progress NXP001 as a cancer supportive care treatment. In addition to triggering the payment of the final £2m milestone by our China market partner and advancing product registration in China, the approval and successful completion of the study will significantly increase Nuformix’s ability to secure further commercial partnerships in other territories, with discussions on-going with multiple parties.”

Market Abuse Regulation (MAR) Disclosure. Certain information contained in this announcement would have been deemed inside information for the purposes of Article 7 of Regulation (EU) No 596/2014 until the publication of this announcement via a Regulatory Information Service and accordingly, this inside information is now considered to be in the public domain.

Nuformix is a pharmaceutical development company using cocrystal technology to unlock the therapeutic potential of approved small molecule drugs. Nuformix’s risk-mitigated development strategy has resulted in a pipeline of discoveries through which it has developed and patented novel cocrystal forms of approved small molecules.

Source: Company Press Release