Celegene said the U.S. Food and Drug Administration (FDA) approved Revlimid in combination with a rituximab product for the treatment of adult patients with previously treated follicular lymphoma or marginal zone lymphoma.
Celgene said this is the first FDA-approved combination treatment regimen for patients with these indolent forms of non-Hodgkin’s lymphoma that doesn’t include chemotherapy.
Approval was based on a Phase 3 study which showed the combination significantly improved median progression-free survival versus rituximab monotherapy, the company said.
No comments:
Post a Comment
Note: Only a member of this blog may post a comment.