United States-based Resolve Therapeutics has revealed results from its phase two study of RSLV-132 intended for the treatment of primary Sjogren's syndrome (pSS), an autoimmune disease that primarily affects women, it was reported on Wednesday.
The leading rheumatology journal, Arthritis and Rheumatology (doi.org/10.1002/art.41489) has published the work.
The phase two study has indicated a clinically meaningful improvement in four separate, independent, validated measures of fatigue in the product group, but not the placebo group. The product is a novel, targeted biologic drug aimed at removing pro-inflammatory nucleic acids from the circulation of patients, which is the main reason for multiple pro-inflammatory cascades.
'Up to 75% of pSS patients report profound fatigue as the most debilitating aspect of pSS, so we are pleased that RSLV-132 was able to significantly improve fatigue in this study,' said James Posada, PhD, CEO of Resolve Therapeutics. 'These results represent a potential step forward in the treatment of Sjogren's syndrome, Resolve will confirm the finding in a large Phase 3 study starting in early 2021.'
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