Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
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.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on dexamethasone + diphenhydramine + ranitidine.