Drug intelligence / Profile preview

KP606

Development stage
Preclinical
Lead developer
Zevra Therapeutics
Modality
Small Molecules
Administration
Oral
01

Overview

KP606 is an investigational, first‑in‑class oral prodrug of oxycodone developed by KemPharm using its Ligand Activated Therapy (LAT) technology to create an abuse‑deterrent opioid analgesic for pain management.[1][3][7] In KP606, oxycodone is covalently linked to a ligand, rendering the molecule inactive until enzymatically cleaved in the body; this design aims to provide effective analgesia while reducing rapid oxycodone release associated with euphoria, limiting intranasal and intravenous abuse, and potentially reducing opioid‑induced constipation through altered pharmacokinetics.[1][3][7] The program has also included development of an immediate‑release formulation (KP606/IR) intended for acute pain, with tamper‑resistant physicochemical properties that make extraction or rapid activation of oxycodone difficult using common manipulation techniques employed by abusers.[4][6][14]

02

Targets

KOR (Kappa opioid receptor)MOR (Mu opioid receptor)DOR (Opioid Receptor Delta 1)

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