The patent application describes a method that uses biological information derived from a patient’s tumour to predict treatment response prior to therapy initiation. The technology focuses on combination regimens involving established cisplatin or carboplatin, used together with immune checkpoint inhibitors targeting the PD-1 or PD-L1 pathway.

These combination therapies remain cornerstones across multiple cancer indications, however patient response varies considerably. Many patients benefit but there are also too many patients experiencing limited or no benefit while being exposed to significant side effects, high treatment costs, and they may even be deprived of a potentially more effective treatment.

The patented method aims to address this challenge by supporting more informed treatment selection, reducing reliance on trial-and-error approaches in the clinical decision-making.

"This international patent application published under the PCT is a key step in building a globally relevant intellectual property position around patient selection for platinum and PD-(L)1 combination therapies," said CHOSA’s CEO, Peter Buhl Jensen "It strengthens our ability to pursue partnerships and commercial opportunities in global oncology markets." he further commented.

Following publication, CHOSA intends to continue the patent process in selected jurisdictions while advancing development and validation of the technology and engaging with potential partners across pharmaceuticals, diagnostics and healthcare.

For additional information, contact:

Peter Buhl Jensen, CEO

Peter@chosa.bio

+ 45 21 60 89 22

Background

Cisplatin and its sister molecule carboplatin have been cornerstones in lung cancer chemotherapy for decades. Despite advances in immunotherapy, platinum drugs remain critical in treatment regimens, including combinations with PD- 1/L1 inhibitors. While numerous efforts to predict cisplatin efficacy have failed, the Cisplatin-DRP, based on a 205-gene biomarker signature, has shown promising results in other settings, including adjuvant therapy in NSCLC and progression-free survival in breast cancer. As previously announced CHOSA is also exploring the predictive potential of the Cisplatin-DRP not only in cisplatin-treated patients but also in those treated with carboplatin in lung cancer. Data from the SPLENDOUR trial provides a unique opportunity to validate this tool in a large cohort, potentially confirming its utility across both drugs. Future research will aim to determine whether the Cisplatin-DRP can predict the effectiveness of combinations of platinum drugs with PD-1/L1 inhibitors.

CHOSA in short

CHOSA Oncology AB is an oncology biotechnology company led by a proven international team with veteran specialists in oncology; drug development; running clinical trials; regulatory expertise; and business development. CHOSA intends to enter into agreements for partnership or sublicensing of LiPlaCis® and the DRP®.

About Cisplatin-DRP, a test to predict if cisplatin treatment is likely to be successful

CHOSA is focused on late-stage clinical development of LiPlaCis® and its DRP® drug response predictor to which it has worldwide rights. The cisplatin DRP is the only proven test to foresee and thereby select who to treat and who will benefit from cisplatin. Breast: We have strong phase 2b data in metastatic breast cancer, demonstrating that patients selected by DRP® responded better to treatment; have longer progression-free survival; and maybe even an overall longer total survival than those patients who were identified as unlikely to respond well to the treatment. Lung: The cisplatin DRP has previously shown its ability to foresee the value of cisplatin therapy in lung cancer. Cisplatin therapy after surgery is a gold standard that increases lung cancer cure, but not always, and until now the doctors do not know who will benefit from cisplatin and who should have something else. This is where the cisplatin DRP is a potential game changer, especially in new neoadjuvant treatment where immunotherapy obtains high efficacy rates when combined with cisplatin doubles. Cisplatin DRP was validated in a blinded retrospective study in two lung cancer patient cohorts receiving cisplatin after surgery to kill remaining tumor cells. Thus, patients with the 10% highest scores had a 3-year survival of 90% whereas the patients with the lowest 10% score had much lower survival with only 40% surviving 3 years1.

Immunotherapy There is a new development that adds further value to our DRP. Cisplatin has often been shown to activate the immune system (making cold tumors hot), which makes tumors susceptible to PD1 inhibitors. This synergy is particularly important but not limited to the treatment of lung cancer, bladder cancer, and head and neck cancer. In the ever-growing PD1 inhibitor market, where competition is fierce, our company stands out with the ability to predict if cisplatin will provide synergy with PD1. This can give the PD1 selling companies a significant competitive advantage. 1) Buhl et al PLOS One doi: 10.1371/journal.pone0194609 DRP® is a registered trademark of Allarity Therapeutics, Inc., and is used under license granted to CHOSA. LiPlaCis is in-licensed from Allarity Therapeutics Ltd (previous Oncology Venture ApS) and LiPlasome Pharma ApS.