Kyowa Kirin International (KKI), a subsidiary of Japanese pharmaceutical company Kyowa Kirin Co Ltd (TSE:4151), and the University Hospitals Birmingham NHS Foundation Trust on Wednesday announced new real-world data from the global PROCLIPI registry showing meaningful overall survival benefits for patients with advanced mycosis fungoides (MF) and Sézary syndrome (SS), two rare conditions and subtypes of cutaneous T-cell lymphoma (CTCL), who were treated with POTELIGEO (mogamulizumab).
The results were presented at the European Organisation for Research and Treatment of Cancer Cutaneous Lymphoma Tumour Group (EORTC-CLTG) Annual Meeting in Athens, Greece.
In the analysis of 371 patients, those receiving mogamulizumab had a median overall survival of 64 months compared to 54 months for patients not receiving the therapy. Among patients with SS, median survival reached approximately 6.5 years with mogamulizumab versus 3 years for systemic treatment without it. These findings align with earlier studies indicating a survival advantage across risk groups.
The PROCLIPI study, spanning 19 countries and more than 2,000 patients, is one of the largest international registries for cutaneous T-cell lymphoma and aims to develop refined prognostic indices such as the new Cutaneous Lymphoma International Prognostic Index (CLIPI).
Kyowa Kirin stated that the results reinforce the value of global collaboration in advancing understanding of rare cancers and improving patient care outcomes in cutaneous T-cell lymphoma.
Relay Therapeutics wins FDA breakthrough status for zovegalisib in breast cancer treatment
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Valneva and Instituto Butantan launch pilot chikungunya vaccination campaign in Brazil
Lupin launches Dasatinib tablets in US market
WuXi Biologics enters into licence and research service agreement with Vertex Pharmaceuticals
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Astrazeneca Imfinzi perioperative regimen gains positive EU CHMP opinion in early gastric cancer
I Peace generates human iPS cells from NKT cells and offers them for research use
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
AstraZeneca agrees obesity and type 2 diabetes collaboration with CSPC
Ascletis Pharma Inc reports topline results from Phase III open-label study of denifanstat
Innovative Molecules GmbH completes Phase 1 clinical development programme for adibelivir
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA