Oncopeptides AB (STO:ONCO), a pharmaceutical company focused on the development of targeted therapies for difficult-to-treat haematological diseases, announced on Friday the successful completion of enrolment in the pivotal phase 3 study OCEAN for the treatment of relapsed refractory multiple myeloma.
This study includes 450 patients from over 100 hospitals around the world. Top line results are expected to be presented later this year.
According to the company, OCEAN is a randomised, comparative study between melflufen and pomalidomide in patients with relapsed refractory multiple myeloma (RRMM). The patients have been treated with immunomodulatory inhibitors (IMiD) and proteasome inhibitors (PI), they have developed resistance to their last line of therapy and are refractory to lenalidomide (IMiD), the most commonly used drug for the treatment of multiple myeloma. The primary endpoint is Progression Free Survival (PFS).
Based on the pivotal phase 3 data, the company intends to submit a supplemental New Drug Application (sNDA) to the US FDA in the second quarter of 2021, followed by a submission of a Marketing Authorisation Application (MAA) in Europe.
Krystal Biotech receives FDA approval for updated VYJUVEK label
Renalytix signs collaboration agreement with Tempus AI to expand KidneyIntelX.dkd access
Biophytis secures Brazilian funding and partnerships for obesity Phase 2 trial
Zhimeng Biopharma's investigational drug gains Phase 2 epilepsy clinical trial approval in China
Sanofi's SAR402663 granted FDA fast track designation for wet AMD
Implantica produces 10,000 RefluxStop units ahead of planned US launch
Sobi's Biologics License Application for NASP in uncontrolled gout accepted by FDA