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Global Top > Research and Development > Antibody Engineering Technology > Antibody Pipeline

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Antibody Pipeline

While making full use of our unique technological achievements in fully human antibody production, POTELLIGENTR® and COMPLEGENT® technologies, Kyowa Hakko Kirin continues to make new advances in research and development on therapeutic antibodies.

Antibody Pipeline (January 2012)

Therapeutic Areas Code Name Country / Stage Indication Remarks
Oncology KW-0761 Japan
Filed (April 2011)
Cancer
(Adult T-cell leukemia-lymphoma)
  • Utilizing the POTELLIGENT® technology
  • Humanized monoclonal antibody
Japan
Phase 2
Cancer
(Adult T-cell leukemia-lymphoma, add-on therapy)
Japan
Phase 2
Cancer
(Peripheral T/NK-cell Lymphoma)
U.S.
Phase 1/2a
Cancer
(Peripheral T-cell lymphoma and cutaneous T-cell lymphoma)
KRN330 U.S.
Phase 1/2a
Cancer
  • Utilizing the KM-Mouse technology
  • Fully human monoclonal antibody
BIW-8962 U.S.
Phase 1/2a
Cancer
  • Utilizing the POTELLIGENT® technology
  • Humanized monoclonal antibody
KHK2866 U.S.
Phase 1
Cancer
  • Utilizing the POTELLIGENT® technology
  • Humanized monoclonal antibody
CEP-37250/KHK2804 U.S.
Phase 1
Cancer
KHK2898 Singapore
Phase 1
Cancer
  • Utilizing the POTELLIGENT® technology
  • Utilizing the KM-Mouse technology
  • Fully human monoclonal antibody
Immunology/Allergy ASKP1240 Japan
Phase 1
Organ Transplant Rejection
  • Utilizing the KM-Mouse technology
  • Fully human monoclonal antibody
  • Developing with Astellas
U.S.
Phase 2
KHK4563 Japan/Korea
Phase 2
Asthma
  • Utilizing the POTELLIGENT® technology
  • Humanized monoclonal antibody
KHK4827 Japan
Phase 1
Psoriasis
  • Fully human monoclonal antibody
  • Licensed from Kirin-Amgen
Other KRN23 U.S./Canada
Phase 1/2
X-linked hypophosphatemic rickets/osteomalacia (XLH)
  • Utilizing the KM-Mouse technology
  • Fully human monoclonal antibody

Outlicensed Antibodies

KW-0761 [Anti-CCR4 humanized monoclonal antibody, utilizing the POTELLIGENT® technology platform]

CCR4 is a chemokine receptor that binds specifically to its ligands TARC and MDC, and participates in the control of T cell migration. CCR4 is expressed mainly on Th2-type helper T cells and regulatory T cells in normal conditions. CCR4+ T cells are implicated in the pathology of asthma and other inflammatory diseases and T-cell malignancies.
KW-0761 is a humanized monoclonal antibody targeting CCR4 utilizing the POTELLIGENT® technology platform for the development of therapies for CCR4+ T cell-related diseases.

  • News Release; March 6, 2008

“KYOWA HAKKO AND AMGEN ENTER LICENSING AGREEMENT FOR ANTI-CCR4 HUMANIZED MONOCLONAL ANTIBODY- KW-0761 Studies Underway in Inflammation and Oncology -”

KHK4563 [BIW-8405 : Anti-IL5R humanized monoclonal antibody, utilizing the POTELLIGENT® technology platform]

KHK4563 targeting asthma is outlicensed to MedImmune, Inc. (USA) on December 19th, 2006.
KHK4563 is a humanized afucosylated IgG1 anti-IL-5R alpha chain monoclonal antibody. It neutralizes IL-5 activity and depletes tissue eosinophils which are believed to play a key role in the pathogenesis of asthma in pre-clinical models with an acceptable toxicology profile.

KW-2871 [Anti-GD3 chimeric monoclonal antibody]

KW-2871 is a chimeric monoclonal antibody specifically binding to the ganglioside antigen, GD3, expressed on the surface of malignant melanoma cells and is expected to treat mallignant melanoma by antibody-dependent cellular cytotoxicity (ADCC), and complement-dependent cytotoxicity (CDC).

  • News Release; March 6, 2007

“Kyowa Hakko Kogyo Co., Ltd. licenses its in-house developed antibody KW-2871 targeting malignant melanoma to Life Science Pharmaceuticals in the US. ”

Anti LIGHT fully human monoclonal antibody

LIGHT molecule was discovered by La Jolla Institute for Allergy and Immunology (LIAI), is a key mediator of inflammation, and enhances several immune cells. The antibody against LIGHT was created by both Kyowa Hakko Kirin California, a wholly-owned subsidiary of Kyowa Hakko Kirin, and LIAI. It could become an immune-regulatory agent with a novel mode of action, and expected to be the first in class in Ulcerative Colitis and in Crohn's disease. The development could be pursued in further indications such as Rheumatoid Arthritis.


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