Biopharmaceutical company ImmuPharma PLC (LSE: IMM) announced on Monday that it has filed a new patent application covering its lead asset P140, described as the world's first 'Immunormalizer'. The filing, which provides up to 20 years of commercial exclusivity, discloses both a novel diagnostic test and a targeted treatment approach for patients with a newly identified Type M immune disorder.
The diagnostic enables rapid identification of "super-responders" to P140, which has shown potential to normalise immune function rather than suppress it. This mechanism offers a safer alternative to conventional immunosuppressants, avoiding risks such as infection and cancer, and supporting the possibility of full remission across up to 50 autoimmune diseases.
ImmuPharma said the test could accelerate diagnosis, improve patient selection and enhance clinical trial outcomes by reducing placebo effects and enabling earlier efficacy detection. This is expected to shorten development timelines and increase the probability of regulatory approval.
Autoimmune diseases affect over 400 million people globally, with a therapeutic market worth more than USD100bn annually and diagnostics valued above USD10bn. Management said the dual platform of P140 therapy and precision diagnostics positions the company to address significant unmet needs in both markets.
Research underpinning the filing was led by ImmuPharma Biotech, where teams have been expanding P140's scope beyond systemic lupus erythematosus to a wider spectrum of autoimmune disorders. The company described P140's mechanism as disease-modifying, with potential to deliver durable remission.
Natera submits Signatera CDx PMA to FDA for bladder cancer use
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
Frontage expands early phase clinical research capabilities across US and China
Summit Therapeutics' BLA for ivonescimab in EGFR-mutated NSCLC accepted by FDA
InSysBio agrees new collaborative project with BeOne Medicines
Physiomics secures new modelling contract with Numab Therapeutics
Mabwell reports first patient dosed with 7MW4911 in US trial
Atossa Therapeutics' founder and CEO named one of The Top 50 Healthcare Technology CEOs of 2025
Avacta secures FDA clearance for second pre|CISION oncology programme
Guardant Health and Merck enter multi-year oncology diagnostics collaboration
Akeso secures NMPA review acceptance for gumokimab in ankylosing spondylitis