Drug intelligence / Profile preview

dexamethasone + diphenhydramine + ranitidine

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

Overview

This premedication regimen is a specific combination of dexamethasone, diphenhydramine, and an H2 blocker (such as ranitidine) utilized in a Columbia University Phase 2 clinical trial (NCT02013440) for patients with newly diagnosed stage II-III breast cancer. The regimen is administered 30-60 minutes prior to each paclitaxel infusion to prevent hypersensitivity reactions and mitigate side effects associated with taxane-based chemotherapy. Dexamethasone acts as a corticosteroid to reduce inflammation and immune response, diphenhydramine is an H1-antagonist used to prevent allergic reactions, and ranitidine (or an equivalent H2 blocker) provides additional prophylaxis against histamine-mediated reactions. This supportive care regimen was used alongside the investigational drug propranolol and standard neoadjuvant chemotherapy.

Brand names
DecadronBenadrylZantac
Other names
Premedicationpaclitaxel premedicationpremedication-Columbia University-breast cancer
02

Targets

GR (Glucocorticoid receptor)HRH1 (Histamine H1 Receptor)HRH2 (Histamine H2 Receptor)

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