EMA accepts MAA for multiple myeloma drug ixazomib
Posted: 21 August 2015 |
Takeda has announced that the EMA has accepted is Marketing Authorisation Application for ixazomib for the treatment of patients with multiple myeloma…
The European Medicines Agency (EMA) has accepted the Marketing Authorisation Application (MAA) for Takeda’s ixazomib, an investigational oral proteasome inhibitor for the treatment of patients with relapsed and/or refractory multiple myeloma.
On 23 July, ixazomib was granted accelerated assessment by the Committee for Medicinal Products for Human Use (CHMP) of the EMA, a designation reserved for those medicines deemed to be of major public health interest and, in particular, therapeutic innovation.
“The ixazomib applications in Europe and the United States are the first of several that we anticipate submitting by the end of this fiscal year,” said Melody Brown, Vice President of Regulatory Affairs, Takeda. “By filing in many regions in rapid succession, we hope to bring ixazomib to as many people living with relapsed/refractory multiple myeloma as soon as possible. We express our thanks to the patients and physicians participating in the TOURMALINE clinical trial programme globally as their support has been critical in making these filings possible.”
Takeda have filed a New Drug Application for ixazomib in the US
The MAA submission was primarily based on the results of the first pre-specified interim analysis of the pivotal Phase 3 trial TOURMALINE-MM1, an international, randomised, double-blind, placebo controlled clinical trial of 722 patients designed to evaluate the superiority of ixazomib plus lenalidomide and dexamethasone over placebo plus lenalidomide and dexamethasone in adult patients with relapsed and/or refractory multiple myeloma. Patients continue to be treated to progression in this trial and will be evaluated for long-term outcomes.
In addition to the ixazomib MAA submission with the EMA, a New Drug Application for ixazomib was filed with the US Food and Drug Administration (FDA). Additional filings in other countries are planned to begin later this fiscal year.