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cGVHD has a high unmet need beyond 2L, as current treatments inadequately address diverse manifestations such as fibrosis and do not support long-term use, resulting in rapid disease progression.1

Guidelines clearly state that there are no standard therapies for SR patients1,2,4,6, limiting these patients to the following available therapies:

Currently, there is no consensus on the optimal choice of agents for 3L or further lines of therapy as per the major guidelines1

The need to investigate novel therapies to address the fibrotic manifestations of cGVHD in 2L and 3L has been recognized7, 10

cGVHD progression is a key reason to modify or discontinue cGVHD therapy7

1L

2L

3L

3 to 7 months3 to 4 months4 to 5 months
96%771%747%7

Abbreviations

1L: First Line; 2L: Second Line; 3L: Third Line; SR: Steroid-resistant; NCCN : National Comprehensive Cancer Network; ASH: American Society of Hematology; ANZTCT: Australia and New Zealand Transplant & Cellular Therapies; EBMT: European Society for Blood and Marrow Transplantation; ECP: Extracorporeal photopheresis; cGVHD: Chronic graft-versus-host disease.

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