Drug intelligence / Profile preview

ondansetron + meloxicam

Development stage
Unknown
Lead developer
GSK
Modality
Small Molecules
Administration
Oral, Intravenous
01

Overview

**Ondansetron + meloxicam** is a fixed-dose combination of two small-molecule pharmaceuticals: ondansetron, a selective serotonin 5-HT3 receptor antagonist that prevents nausea and vomiting by blocking serotonin effects in the gut and central nervous system, primarily used for chemotherapy-, radiotherapy-, and postoperative-induced emesis; and meloxicam, a nonsteroidal anti-inflammatory drug (NSAID) that inhibits cyclooxygenase-2 (COX-2) preferentially over COX-1 to reduce inflammation, pain, and fever. This combination lacks a unique brand name and is not a standard marketed product but may be used empirically for multimodal symptom control, such as postoperative pain with nausea or chemotherapy-related symptoms, leveraging ondansetron's antiemetic action and meloxicam's analgesic/anti-inflammatory effects. No specific developers or primary indications are established for this pairing, and interactions between the components are unlikely based on their metabolic profiles.[1][2][7]

02

Targets

HTR3A (5-hydroxytryptamine receptor 3A)PTGS2 (Prostaglandin-Endoperoxide Synthase 2)PGHS-1 (Prostaglandin G/H Synthase 1)

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