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3426 : REG3A Polymorphism Is Associated with the Incidence of Extensive Chronic Gvhd after Allogeneic BMT

Researchers

Presenter

  • Daisuke Koyama

Principal Investigators

  • Makoto Murata

  • Ryo Hanajiri

  • Yukiyasu Ozawa

  • Koichi Miyamura

  • Seitaro Terakura

  • Tetsuya Nishida

  • Hitoshi Kiyoi

  • Shingo Okuno

  • Sonoko Kamoshita

  • Jakrawadee Julamanee

  • Erina Takagi

  • Kotaro Miyao

  • Reona Sakemura

  • Tatsunori Goto

  • Aika Seto

Medical Centers

  • Department of Pediatrics, Japanese Red Cross Nagoya First Hospital, Nagoya, Japan

  • Department of Pathologic Oncology, Mie University Graduate School of Medicine, Mie, Japan

Locations

  • Japan

Companies

  • N/A

Study Components

Therapeutic Area

  • Autoimmune (AI)

Disease

  • Paroxysmal nocturnal hemoglobinuria

  • Acute lymphoblastic leukemia

  • Alpha-thalassemia myelodysplasia syndrome

  • Chronic Myelogenous Leukemia

  • Acute myelocytic leukemia

  • Aplastic anemia

  • Anemia

  • Graft-versus-host disease

Biomarkers

  • Ph chromosome

  • Regenerating Family Member 3 Alpha

  • Apoptotic body index

Drug/Treatment

  • Cyclosporine eent

  • Methotrexate

Outcome

  • N/A

Study Design

  • N/A

Phase

  • NA

Study Id's

  • N/A

Sponsors

  • N/A

Result

  • Interim

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