Following this puts new work involving it at the top of your briefing, with a note saying why it is there. Links are taken from the source record, never inferred.
FDA supplemental approval of a Risk Evaluation and Mitigation Strategy (REMS) for pomalidomide; establishes regulatory requirements but does not report clinical efficacy or safety trial outcomes.
This is an FDA supplemental approval action for a labeling change to adagrasib; it documents an administrative decision, not clinical efficacy or safety data.