CHMP recommends EU approval of Columvi combination for people with R/R DLBCL
“For patients with DLBCL who relapse after initial therapy, urgent and effective treatment is required to regain disease control,” said Levi Garraway, MD, PhD, Roche’s Chief Medical Officer and Head of Global Product Development. “As the first bispecific antibody to show improved survival in DLBCL in a randomised phase III study, Columvi could offer an additional treatment option that is immediately available for patients who relapse.”
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