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Kissei Pharmaceutical Co., Ltd.

Kissei Pharmaceutical Co., Ltd. researches, develops, manufactures, and sells pharmaceutical products primarily in Japan. The company offers Calogra tablets, for the treatment of ulcerative colitis; Tabneos capsules for the treatment of microscopic polyangiitis and granulomatous polyangiitis; Minirin Melt OD tablets; Corsuba Intravenous Dialysis Syringe for the treatment of chronic idiopathic thrombocytopenic purpura; Beova tablets for the treatment of overactive bladder treatment; and Darbepoetin Alfa BS injection JCR for the treatment of renal anemia. Its products in pipeline include CG0070, which is in Phase III clinical trial to treat non-muscle-invasive bladder cancer; Linzagolix, which is in Phase III clinical trial for the treatment of uterine fibroids and endometriosis; KDT-3594, which is in Phase II clinical trial to treat Parkinson's disease; KSP-0243 that is in Phase II clinical trial to treat Ulcerative colitis; and Difelikefalin, which is in Phase III clinical trial to treat uremic pruritus in dialysis patients. The company is also developing Silodosin for dysuria associated with benign prostatic hyperplasia; and Fostamatinib for tyrosine kinase inhibitor. In addition, it develops and sells protein controlled and energy supply food; and purchases and sells related materials, as well as offers system development and information processing, construction contracting, facility and equipment management, and information gathering and development support services. Further, the company engages in the information equipment rentals; insurance agency business; manufactures and sells noodles; and undertakes construction of factories, research institutes, offices, etc., as well as computer system design and development, and cloud services. Kissei Pharmaceutical Co., Ltd. was formerly known as Kissei Yakuhin Kogyo Co., Ltd. and changed its name to Kissei Pharmaceutical Co., Ltd. in October 1964. The company was incorporated in 1946 and is based in Matsumoto, Japan.

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Biotech & Genomic Medicine

リゲル・ファーマシューティカルズ、2026年の売上高見通しを上方修正、乳がん治療薬VEPPANUを8月中旬に発売へ

リゲル・ファーマシューティカルズは2026年第2四半期の総収益を7870万ドルと発表し、契約収益の見通し引き上げにより、通期の売上高ガイダンスを2億8500万ドルから2億9500万ドルの範囲に引き上げた。純製品売上高は6700万ドルに達し、前年同期比14%増となった。内訳は、TAVALISSEが18%増の4740万ドル、REZLIDHIAが27%増の890万ドルと好調だった一方、GAVRETOは10%減の1070万ドルとなった。また、契約収益として1170万ドルを計上し、これにはキッセイ薬品工業からの400万ドルの規制マイルストンが含まれている。リゲルは、特定の乳がん変異を対象とする初の承認済みPROTACであるVEPPANUのライセンス導入を完了し、2026年8月中旬の商業化を見込んでいる。純利益は1730万ドル(1株当たり0.93ドル)で、前年同期の5960万ドルには一時的な非現金収益項目が含まれていた。現金および投資残高は9530万ドルで、2025年末の1億5500万ドルから減少したが、これはVEPPANUのライセンス導入に伴う7000万ドルの前払い金によるものである。経営陣はまた、低リスク骨髄異形成症候群を対象としたR289の用量拡大試験の進捗を強調し、年末までに主要データが得られる見通しを示した。
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