Antengene Corporation Limited announced that the Malaysian National Pharmaceutical Regulatory Agency has approved a supplemental New Drug Application (sNDA) for XPOVIO® (selinexor) for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) after at least two lines of systemic therapy, who are ineligible for autologous stem cell transplant. This regulatory approval marks a new indication for XPOVIO® in Malaysia. No other organizations were mentioned as recipients of this regulatory approval.
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