FDA Approves Easier-to-Swallow Imbruvica Formulation
An oral suspension formula of Imbruvica received the green light from the Food and Drug Administration to be used in all approved indications.
Source: curetoday.com
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FDA Approves Label Expansion for Oral Ibrutinib Suspension in All Current Indications
The FDA has approved a label expansion for ibrutinib with an oral suspension formulation in all current indications.
Source: onclive.com
J&J Broadens Scope in Multiple Myeloma, Winning FDA Approval for New Drug
Johnson & Johnson’s stable of multiple myeloma drugs has grown to five products with the FDA approval of Talvey. The bispecific antibody is the first in a new class of new drugs designed to go after the novel multiple myeloma target GPRC5D.
Source: medcitynews.com
Janssen Presents Efficacy and Subgroup Analyses from MAIA Study Showing Long-Term Results of DARZALEX® (daratumumab)-based Regimen in Newly Diagnosed, Transplant-Ineligible Multiple Myeloma
/PRNewswire/ -- The Janssen Pharmaceutical Companies of Johnson & Johnson today announced new analyses from the Phase 3 MAIA study of DARZALEX® (daratumumab)...
Source: prnewswire.com