Drug intelligence / Profile preview

celecoxib + reboxetine

Development stage
Preclinical
Lead developer
Pfizer
Modality
Small Molecules
Administration
Oral
01

Overview

Celecoxib + reboxetine is a combination of two small molecule drugs, each with distinct mechanisms of action. Celecoxib is a selective cyclooxygenase-2 (COX-2) inhibitor that reduces the production of pro-inflammatory prostaglandins, thereby decreasing pain and inflammation. Reboxetine is a selective noradrenaline reuptake inhibitor (NaRI) used primarily as an antidepressant; it increases synaptic concentrations of noradrenaline by inhibiting its transporter. This combination has been investigated for its potential to enhance antidepressant efficacy in major depressive disorder (MDD), particularly in treatment-resistant cases where inflammatory processes may play a role. Preclinical studies suggest that celecoxib can potentiate the effects of reboxetine on cortical noradrenaline output, supporting the rationale for combining anti-inflammatory and monoaminergic agents in mood disorders[1][3].

02

Targets

PTGS2 (Prostaglandin-Endoperoxide Synthase 2)PGHS-1 (Prostaglandin G/H Synthase 1)HTR2C (5-hydroxytryptamine 2C receptor)NET (Norepinephrine Transporter)SERT (Sodium-dependent serotonin transporter)HRH1 (Histamine H1 Receptor)

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