Drug intelligence / Profile preview

Esarin Gel

Development stage
Phase 4
Lead developer
Sun Pharmaceutical Industries
Modality
Small Molecules
Administration
Topical
01

Overview

**Esarin Gel** is a topical fixed-dose combination marketed in Taiwan for supportive improvement of chronic venous insufficiency and relief of post-traumatic pain. Each gram contains diethylamine salicylate 50 mg, escin 10 mg, and heparinoid 10 mg, specified as sodium polyanhydromannuronic acid sulfate. The heparinoid component supports local antithrombin-mediated anticoagulant activity, escin is a venotonic and capillary-permeability-modulating triterpene saponin, and diethylamine salicylate provides local salicylate-mediated analgesic and anti-inflammatory effects. A completed open-label Phase 4 study evaluated twice-daily Esarin Gel for 28 days in chronic venous insufficiency, varicose veins, and superficial vein thrombophlebitis. ([web-reg-server.803.org.tw](https://web-reg-server.803.org.tw/PhC/PharmaBooks/Keyword_Detail/xhzhegXOzgaK0br_hW5j0rHD3cByTmL3GhCIXv9cbXp7fkfkdobKplfGzlUHabwx))

Brand names
Esarin Gel
Other names
diethylamine salicylate + escin + sodium polyanhydromannuronic acid sulfate礙沙凝膠
02

Targets

ATIII (Antithrombin III)HYAL (Hyaluronidase family (HYAL))PGHS-1 (Prostaglandin G/H Synthase 1)PTGS2 (Prostaglandin-Endoperoxide Synthase 2)

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