
Ozmosi | SHP-639 Drug Profile
Aug 7, 2019 · TAK-639 is a topical, nine-amino acid, synthetic, C-type natriuretic peptide analog in Phase 1 development for the treatment of ocular hypertension (OHT) and primary open-angle …
SHP-639 - Drug Targets, Indications, Patents - Synapse
SHP-639: a CNP modulators Drug, Initially developed by Shire Pharmaceuticals Services Ltd., Now, its global highest R&D status is Pending, Mechanism: CNP modulators(2',3'-cyclic …
Full article: Randomized, Double-Masked, Placebo-Controlled …
Nov 21, 2022 · TAK-639 is postulated to lower intraocular pressure (IOP) through a novel mechanism of action (MOA) that increases trabecular meshwork outflow. We investigated the …
Stanton SHP639 Tonearm Assembly (Without Cartridge) For …
By continuing, I agree to the and authorize you to charge my payment method at the prices, frequency and dates listed on this page until my order is fulfilled or I cancel, if permitted. Tone …
Study of SHP639 Eye Drops in Adults With High Eye Pressure or …
Safety and tolerability of three different concentrations (0.1%, 03%, 0.6%) of the investigational SHP639 eye drops will be evaluated in participants with high eye pressure or primary open …
(PDF) Randomized, Double-Masked, Placebo-Controlled Dose …
Mar 1, 2020 · TAK-639 is postulated to lower intraocular pressure (IOP) through a novel mechanism of action (MOA) that increases trabecular meshwork outflow. We investigated the …
Shire initiates phase I study of SHP-639 in intraocular …
Shire initiates phase I study of SHP-639 in intraocular hypertension and primary open-angle glaucoma
TAK 639 - AdisInsight
TAK 639 (also designated as SHP 639), a 9-amino acid, synthetic, C-type natriuretic peptide analog, is being developed by Takeda (previously Shire) for the
SHP-639 (SHP-639) - 药物靶点:CNP_专利_临床_研发
TAK-639 is a topical, 9-amino acid, synthetic, C-type natriuretic peptide analog in development for the treatment of primary open-angle glaucoma and ocular hypertension.
SHP-639-靶点: NPR3_适应症-临床_专利_批准
SHP-639是由Shire Pharmaceuticals研发的一种合成多肽,是一种NPR3激动剂。 目前该药物最高研发阶段为无进展,用于治疗高眼压和开角型青光眼。