Last reviewed · How we verify
Myelodysplastic Syndromes (MDS)
Approved treatments
Clinical guidelines
- FDA label — 1L|2L|3L+
Lenalidomide is indicated for the treatment of adult patients with transfusion-dependent anemia due to low- or intermediate-1-risk myelodysplastic syndromes associated with a deletion 5q cytogenetic abnormality with or without additional cytogenetic abnormalities. - FDA label — 3L+
Lenalidomide is indicated for the treatment of adult patients with mantle cell lymphoma whose disease has relapsed or progressed after two prior therapies, one of which included bortezomib.
Competitive intelligence
For the full treatment-landscape CI brief — marketed leaders side-by-side, pipeline by phase, recent regulatory actions, sponsor landscape: