Overall Conclusions - HORIZON Poster Presentation
· Patients in the HORIZON study had a median of five prior lines of therapy, 71% of patients were triple-class refractory, 97% were refractory to the last line of treatment, and 32% suffered from extramedullary disease (EMD).
· In the ITT population (n=125), the overall response rate (ORR) was 29% and the clinical benefit rate (CBR) was 37%.
· In patients with triple-class refractory disease (n=97), the ORR was 24% with a median progression-free survival (PFS) of 4.0 months, a median duration of response (DOR) of 7.5 months and a median overall survival (OS) of 11.3 months.
· In patients with EMD (n=42), the ORR was 24% with a median PFS of 3.0 months, a median DOR of 5.1 months and a median OS of 8.1 months.
· Grade 3 and 4 Adverse Events (AE) were primarily hematologic and the incidence of non-hematologic AEs was low.
"These data from our pivotal HORIZON study confirm that melflufen is efficacious in this late stage patient population where currently available treatment options may not be sufficient. In particular, the ORR of 24% with a DOR or 7.5 months in patients with triple-class refractory disease is impressive. The responses seen in patients with EMD are also very encouraging as no other available single agent has shown similar efficacy in this very difficult-to-treat patient population. Taken together with a relatively clean safety profile from a patient perspective, these data lead us to believe that melflufen has the potential to play an important role in the treatment of patients with relapsed/refractory multiple myeloma. Consultations with regulatory bodies are ongoing and we are planning to submit an NDA in the first half of 2020. This represents a slight change compared to previously communicated timelines after regulatory interactions have resulted in minor changes to the planned submission package."
The posters are available on the company webpage under:
www.oncopeptides.com / Investor Relations / Presentations / ASH 2019 (https://oncopeptides.se/en/ash-2019/)
For more information, please contact:
E-mail: jakob.lindberg@oncopeptides.com
Telephone: +46 8 615 20 40
E-mail: rein.piir@oncopeptides.com
Cell phone: +46 70 853 72 92
The information in the press release is information that
About the OP-106 HORIZON study
Patient recruitment in the pivotal Phase 2 HORIZON study is completed with 157 patients enrolled. The efficacy population (n=125) reflects patients dosed on or before
About melflufen
Melflufen is a novel peptide-drug conjugate that rapidly delivers a cytotoxic payload into tumor cells. Melflufen is rapidly taken up by myeloma cells due to its high lipophilicity and is immediately cleaved by peptidases to deliver an entrapped hydrophilic alkylator payload. Peptidases play a key role in protein homeostasis and feature in cellular processes such as cell-cycle progression and programmed cell death. In vitro, melflufen is 50-fold more potent in myeloma cells than the alkylator payload itself due to the increased intracellular alkylator concentration. Melflufen displays cytotoxic activity against myeloma cell lines resistant to other treatments, including alkylators, and has also demonstrated inhibition of DNA repair induction and angiogenesis in preclinical studies.
About
More information is available on www.oncopeptides.com.
https://news.cision.com/oncopeptides-ab/r/oncopeptides-presents-updated-efficacy-and-safety-data-from-pivotal-phase-2-horizon-study-in-patient,c2985301
https://mb.cision.com/Main/15404/2985301/1157745.pdf
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