.css-1n63hu8{box-sizing:border-box;margin:0;min-width:0;display:inline;}Cara is developing a proprietary class of product candidates that target the body's peripheral nervous system and have demonstrated initial efficacy in patients with moderate-to-severe pain and pruritus (itch) without inducing many of the side effects typically associated with other pain and itch therapeutics. by Neethu Shaji Saji. [10] The drug was originally developed as an analgesic in surgery, but while effective in animal models of nociception,[11] it was repurposed as an antipruritic at lower treatment doses due to an apparently unacceptable incidence of sedative effects in humans. %���� [15] The drug is a 4,5-epoxymorphinan derivative, and is structurally unique relative to other KOR agonists. An injectible version of Korsuva is ready for commercialization, while the oral version for Puritus CKD and Pruritus CLD are in Phase 3 and Phase 2 of clinical studies respectively. , has been formulated both as an IV and oral formulation. 1 0 obj [18] However, in vivo, nalfurafine has shown no indications of MOR agonism or antagonism in animals or humans, including no evidence of rewarding or reinforcing effects or physical dependence. Cara Therapeutics is a publicly held .css-1n63hu8{box-sizing:border-box;margin:0;min-width:0;display:inline;}biotechnology company based in .css-1n63hu8{box-sizing:border-box;margin:0;min-width:0;display:inline;}Stamford, Connecticut that was founded in 2004 by Derek Chalmers, Frederique Menzaghi, and Michael E. Lewis.

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D-Argininamide, D-phenylalanyl-D-phenylalanyl-D-norleucyl-N-(4-pyridinylmethyl)- | C36H49N9O4 | CID 25030387 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more. An injectible version of Korsuva is ready for commercialization, while the oral version for Puritus CKD and Pruritus CLD are in Phase 3 and Phase 2 of clinical studies respectively. Nalfurafine (INN, USAN)[3] (brand name Remitch; former developmental code names TRK-820, AC-820, MT-9938) is an antipruritic (anti-itch drug) that is marketed in Japan for the treatment of uremic pruritus in individuals with chronic kidney disease undergoing hemodialysis. [2][4] It acts as a potent, selective, centrally-penetrant κ-opioid receptor (KOR) agonist,[5] and is the first and currently the only selective KOR agonist to have been approved for clinical use.

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