On May 14, 2020, the U.S. Food and Drug Administration (FDA) approved pomalidomide (Pomalyst^®, Bristol Myers Squibb) capsules for the treatment of adult patients with AIDS-related Kaposi sarcoma (KS) after failure of highly active antiretroviral therapy (HAART) or in patients with KS who are HIV-negative. This indication is approved under accelerated approval based on overall response rate. 

Read corporate announcement.


Posted 5/26/2020