Report
EUR 12.69 For Business Accounts Only

Increased risk weighs on KYOWA KIRIN, penalising its rating down to Neutral

The independent financial analyst theScreener just lowered the general evaluation of KYOWA KIRIN (JP), active in the Pharmaceuticals industry. As regards its fundamental valuation, the title still shows 1 out of 4 possible stars. Its market behaviour, however, has slightly deteriorated and will be qualified as moderately risky moving forward. theScreener considers that these new qualifications justify an overall rating downgrade to Neutral. As of the analysis date January 28, 2022, the closing price was JPY 2,865.00 and its target price was estimated at JPY 2,716.72.
Underlying
Kyowa Kirin Co. Ltd.

Kyowa Hakko Kirin is a pharmaceutical company mainly engaged in medical product and biochemical businesses. Co. operates in two business segments: medical product, and biochemical. Co. is engaged in the manufacture, sale and sales promotion of medical products for hospital use, the development of candidate substances for new drugs, the provision of technologies for antibody drug creation; the manufacture and sale of medical and industrial materials, mainly amino and nucleic acids, and health care products; the design and construction of facilities; the distribution, insurance agency and wholesale businesses.

Provider
TheScreener
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Other Reports on these Companies

協和キリン (Kyowa Kirin)、ロカチンリマブ (Rocatinlimab) の開発・商業化プログラムの管理権を再取得、アトピー性皮膚炎における高いアンメット・メディカル・ニーズへの強いコミットメントを示す

協和キリン (Kyowa Kirin)、ロカチンリマブ (Rocatinlimab) の開発・商業化プログラムの管理権を再取得、アトピー性皮膚炎における高いアンメット・メディカル・ニーズへの強いコミットメントを示す 協和キリンは、ロカチンリマブを、大きな市場潜在力を有する、人生を変え得る差別化された資産として開発することへのコミットメントを改めて表明。病原性T細胞に発現するOX40受容体を直接標的とする、開発中の新規T細胞リバランス療法としてのロカチンリマブのアプローチは、中等症から重症のアトピー性皮膚炎 (msAD) 患者において長期的な疾患コントロールをもたらす可能性を示している。規制当局への申請は2026年前半に予定されている。 東京およびニュージャージー州プリンストン発, Feb. 01, 2026 (GLOBE NEWSWIRE) -- 日本発のグローバルなスペシャリティ製薬企業である協和キリン株式会社 (Kyowa Kirin Co., Ltd.) (TSE:4151、協和キリン) は本日、ロカチンリマブの開発および商業化に関するアムジェン (Amgen) との現在の提携を終了することを発表した。 協和キリンは、規制当局への申請および将来の商業化を含むロカチンリマブのグローバルプログラムの管理権を再取得する。 本件の事業上の決定は、アムジェンによる戦略的ポー...

교와기린 (Kyowa Kirin), 로카틴리맙 (Rocatinlimab) 개발·상업화 프로그램 통제권 재확보하며 아토피 피부염 분야의 높은 미충족 의료 수요 해결에 대한 강력한 의지 재확인

교와기린 (Kyowa Kirin), 로카틴리맙 (Rocatinlimab) 개발·상업화 프로그램 통제권 재확보하며 아토피 피부염 분야의 높은 미충족 의료 수요 해결에 대한 강력한 의지 재확인 교와기린은 로카틴리맙을 차별화된 혁신 치료 자산이자 높은 시장 잠재력을 지닌 ‘삶을 변화시키는 치료제’로 개발하겠다는 의지를 재확인병원성 T세포에 발현되는 OX40 수용체를 직접 표적으로 하는 T세포 균형 조절 치료제로서의 로카틴리맙의 새로운 접근법은 중등도에서 중증 아토피 피부염(msAD) 환자에서 장기적인 질환 조절 효과를 제공할 잠재력을 보여줘규제 당국 제출은 2026년 상반기에 진행될 예정 도쿄 & 미국 뉴저지주 프린스턴, Feb. 01, 2026 (GLOBE NEWSWIRE) -- 일본에 본사를 둔 글로벌 전문 제약사 교와기린 주식회사(Kyowa Kirin Co., Ltd., TSE: 4151, 이하 교와기린)는 암젠(Amgen)과 진행해 온 로카틴리맙(rocatinlimab)의 개발 및 상업화 관련 기존 협력을 종료한다고 발표했다. 이에 따라 교와기린은 규제 당국 제출 자료와 향후 상업화를 포함한 글로벌 로카틴리맙 프로그램에 대한 통제권을 다시 확보하...

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