Drug intelligence / Profile preview

PK101

Development stage
Phase 3
Lead developer
iGATE
Modality
Small Molecules
Administration
Oral
01

Overview

**PK101** is an oral fixed-dose combination of celecoxib and PG201, a 12-herb ethanol soft extract used for osteoarthritis. The product contains 100 mg celecoxib and 405.4 mg PG201 per tablet. Celecoxib selectively inhibits cyclooxygenase-2 to reduce inflammatory prostaglandin production, while PG201 has been reported to suppress inflammatory cytokine pathways including interleukin-1 beta and tumor necrosis factor alpha. PK101 was developed by PMG Pharm for symptomatic knee osteoarthritis, evaluated in Phase 3, and subsequently marketed in South Korea as Layla DS. ([cnu.elsevierpure.com](https://cnu.elsevierpure.com/en/publications/comparison-of-a-fixed-dose-combination-of-celecoxibpg201-laylasup/))

Brand names
Layla DS
Other names
celecoxib + PG201celecoxib/PG201
02

Targets

PTGS2 (Prostaglandin-Endoperoxide Synthase 2)IL1B (Interleukin-1 beta)TNFA (Tumor necrosis factor alpha (soluble))

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