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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

Rigel Pharmaceuticals raises 2026 revenue guidance, prepares mid-August launch of breast cancer drug VEPPANU

Rigel Pharmaceuticals reported second-quarter 2026 total revenue of $78.7 million and raised its full-year revenue guidance to a range of $285 million to $295 million, driven by higher contract revenue expectations. Net product sales reached $67.0 million, a 14% year-over-year increase, led by TAVALISSE sales of $47.4 million, up 18%, and REZLIDHIA sales of $8.9 million, up 27%, while GAVRETO sales declined 10% to $10.7 million. The company also recorded $11.7 million in contract revenues, including a $4 million regulatory milestone from Kissei Pharmaceutical. Rigel completed the in-license of VEPPANU, the first approved PROTAC for certain breast cancer mutations, and expects commercial availability in mid-August 2026. The company reported net income of $17.3 million, or $0.93 per basic share, compared to $59.6 million in the prior-year quarter, which included a one-time non-cash revenue item. Cash and investments stood at $95.3 million, down from $155.0 million at year-end 2025 following a $70 million upfront licensing payment for VEPPANU. Management also highlighted progress in the R289 dose expansion trial in lower-risk MDS, with top-line data expected by year-end.
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