Drug intelligence / Profile preview

rovadicitinib

Development stage
Phase 3
Lead developer
Chia Tai-Tianqing Pharmaceutical Group
Modality
Small Molecules
Administration
Oral
01

Overview

Rovadicitinib is a novel, oral small molecule drug that acts as a dual inhibitor of Janus kinase 1 and 2 (JAK1/2) and Rho-associated protein kinase 1 and 2 (ROCK1/2). This first-in-class agent targets both inflammatory and fibrotic pathways, making it particularly promising for diseases with these components. Rovadicitinib is being developed primarily for the treatment of chronic graft-versus-host disease (cGVHD), especially in patients who are glucocorticoid-refractory or -dependent. It has also been investigated in myelofibrosis and hemophagocytic lymphohistiocytosis. Clinical trials have shown high response rates, good tolerability, and significant steroid-sparing effects in cGVHD patients[1][5][7][8].

Brand names
Rovadicitinib
Other names
rovadicitinib1948242-59-8(3R)-3-[3-amino-4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrazol-1-yl]-3-cyclopentylpropanenitrile
02

Targets

JAK2 (Janus kinase 2)JAK1 (Janus kinase 1)ROCK1 (Rho-associated coiled-coil containing protein kinase 1)ROCK2 (Rho-associated coiled-coil containing protein kinase 2)

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