Drug intelligence / Profile preview

INCB160058 + famotidine

Development stage
Unknown
Lead developer
Incyte
Modality
Small Molecules
Administration
Oral
01

Overview

INCB160058 + famotidine is a hypothetical combination of two distinct pharmaceutical agents: INCB160058, an investigational oral small molecule inhibitor of the JAK2V617F pseudokinase (JH2) domain developed for selective targeting of JAK2V617F-mutant myeloproliferative neoplasms, and famotidine, an oral H2-histamine receptor antagonist widely used to reduce gastric acid secretion. INCB160058 acts by binding with high specificity to the JAK2 JH2 domain, blocking cytokine-independent mutant JAK2 signaling while sparing normal cytokine-dependent activity, leading to elimination of JAK2V617F-positive malignant clones[4]. Famotidine acts as a competitive antagonist at the H2-receptor on gastric parietal cells, resulting in reduced acid secretion. There is no evidence or approved therapeutic product for a fixed-dose combination of these two agents, but both might be co-administered for investigator-initiated or off-label research—especially to address potential upper gastrointestinal adverse events related to JAK inhibitor therapy or in clinical trials where famotidine is used as supportive care.

02

Targets

JAK2 V617F (Janus kinase 2 V617F mutant)HRH2 (Histamine H2 Receptor)

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