Drug intelligence / Profile preview

zsp1601

Development stage
Phase 2
Lead developer
Raynovent Biotech
Modality
Small Molecules
Administration
Oral
01

Overview

ZSP1601 is a novel, first-in-class pan-phosphodiesterase (PDE) inhibitor developed primarily for the treatment of nonalcoholic steatohepatitis (NASH) and nonalcoholic fatty liver disease (NAFLD). It is a small-molecule drug that acts as a nonselective PDE inhibitor with highest affinity for type 2 cyclic nucleotide phosphodiesterase. Clinical studies have shown that ZSP1601 is well-tolerated and safe in both healthy volunteers and patients with NAFLD/NASH, demonstrating improvements in liver chemistries, liver fat content, and fibrosis. The drug has been evaluated in multiple phase 1 and phase 2 clinical trials involving oral administration. Common adverse events include mild to moderate headache and diarrhea[1][3][4][9].

02

Targets

PDE1A (Phosphodiesterase 1A)PDE4B (3',5'-cyclic-AMP phosphodiesterase 4B)PDE2 (Phosphodiesterase 2)PDE5 (Phosphodiesterase 5A)

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