The oral proteasome inhibitor ixazomib is approved in the United States, European Union and other countries, in combination with oral lenalidomide and dexamethasone (Rd), for the treatment of patients with multiple myeloma...
Takeda announced that a New Drug Application (NDA) has been submitted to the FDA for ixazomib, an investigational oral proteasome...
The National Institute for Health and Care Excellence (NICE), in a draft recommendation, has rejected Ninlaro (ixazomib) combination with lenalidomide...
Takeda Pharmaceutical Company Limited announced the results from the TOURMALINE-MM2 study designed to evaluate the addition of Ninlaro (ixazomib) to lenalidomide and dexamethasone in newly diagnosed transplant ineligible multiple myeloma patients.
Takeda Pharmaceutical Company Limited has announced that the FDA has approved Ninlaro (ixazomib) capsules, the first and only oral proteasome...
Takeda Pharmaceutical has announced that the European Commission has granted conditional marketing authorization for Ninlaro (ixazomib) capsules, indicated in combination...
Takeda and Millennium Oncology have begun a Phase III development programme for ixazomib citrate (MLN 9708), the first oral proteasome...
Takeda has announced results from the TOURMALINE-MM1, an international, randomized, double-blind, placebo-controlled Phase III clinical trial, showing that treatment with...
Takeda Pharmaceutical Company Limited announced that the European Medicines Agency (EMA) has accepted the Marketing Authorization Application (MAA) for ixazomib,...
Takeda Pharmaceutical Company Limited announced that the randomized, double-blind, placebo-controlled TOURMALINE-MM1 pivotal Phase III trial evaluating the safety and efficacy...