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  • Will Roche¡¯s lymphoma drug Columvi be discussed for reimb?
  • by Eo, Yun-Ho | translator Alice Kang | Oct 28, 2024 05:53am
Industry eyes are on whether Columvi¡¯s reimbursement agenda will be reviewed by the CDDC in November
The first bispecific antibody treatment option for lymphoma
Company promptly reapplied for reimbursement after failing to be deliberated by CDDC in July
Will Columvi, the first bispecific antibody treatment option for lymphoma, enter the first step to its reimbursement within the year?

Roche Korea¡¯s CD20-CD3 bispecific antibody for diffuse large B-cell lymphoma (DLBCL), Columvi (glofitamab), may likely be redeliberated by the Health Insurance Review and Assessment Service's Cancer Disease Deliberation Committee meeting set to be held in November.

Originally, there were hopes for its discussions in October, supported by strong requests from patient groups. The agenda was reviewed by CDDC in July but failed to set reimbursement standards at the time. Therefore, industry eyes are on whether Columvi can break through the barrier this time.

Columvi was approved
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