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PR Newswire
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Cantargia reports first patient treated with CAN04 in a US phase I study investigating combination with pembrolizumab

STOCKHOLM, Oct. 2, 2020 /PRNewswire/ -- Cantargia AB today announced that the first patient has started treatment with the antibody CAN04 and pembrolizumab in a phase I clinical trial in USA. The trial continues according to the clinical protocol and will include up to 18 patients.

Cantargia develops antibody-based pharmaceuticals against interleukin-1 receptor accessory protein (IL1RAP). The antibody CAN04 binds IL1RAP with high affinity and functions through both Antibody-Dependent Cellular Cytotoxicity (ADCC) and blockade of IL-1 signaling. A new phase Ib clinical trial investigates CAN04 in combination with pembrolizumab which targets PD-1 (https://clinicaltrials.gov/ct2/show/NCT04452214). A second ongoing trial investigates CAN04 in combination with two different chemotherapy regimens.

The first patient has now been dosed with CAN04 in combination with pembrolizumab, the latter a standard immune therapy for several different cancer forms. The trial will be performed at three different centres in the US with the goal to investigate this combination in up to 18 patients with non-small cell lung cancer, head and neck cancer, bladder cancer or malignant melanoma who progressed on previous therapy with pembrolizumab. Recruitment timelines are estimated to be 9-12 months.

In addition to exploring CAN04 in the context of cancer progression after pembrolizumab therapy, the data generated will be used to potentially expand the use of CAN04. The results from this trial, together with the data generated on CAN04 in combination with platinum-based chemotherapy, will be the basis for studies of CAN04 in combination with pembrolizumab and chemotherapy.

"Immune therapy has now become a cornerstone in the treatment of many types of cancer and we are very pleased to start the clinical investigation of CAN04 in that setting. This trial is the starting point to explore the opportunities for new groups of patients to receive CAN04", says Göran Forsberg, CEO of Cantargia.

"Patients progressing on PD-1 based therapies still have very few useful immune therapy treatment options. The concept of counteracting immune suppressive signals to allow additional beneficial treatment with immune therapy beyond the PD-1/PDL-1 antibodies is very appealing. I look forward to taking part in this trial investigating the addition of one of these novel immune therapeutics to pembrolizumab" says Prof Roger Cohen, coordinating investigator at Abramson Cancer Center and the Perelman School of Medicine at the University of Pennsylvania

For further information, please contact
Göran Forsberg, CEO
Telephone: +46 (0)46-275 62 60
E-mail: goran.forsberg@cantargia.com

This is information that Cantargia AB is obliged to make public pursuant to the EU Market Abuse Regulation. The information was submitted for publication, through the agency of the contact person set out above, at 17.10 CET on 2 October 2020.

About Cantargia

Cantargia AB (publ), reg. no. 556791-6019, is a biotechnology company that develops antibody-based treatments for life-threatening diseases. The basis for this is the protein IL1RAP that is involved in a number of diseases and where Cantargia has established a platform. The main project, the antibody CAN04, is being studied in the clinical phase I/IIa CANFOUR study with a primary focus on non-small cell lung cancer and pancreatic cancer. The study is focused on combination therapies, but also includes a monotherapy arm. Positive interim data from the combination therapies were presented in December 2019. Cantargia's second project, the antibody CAN10, addresses treatment of serious autoimmune/inflammatory diseases, with initial focus on systemic sclerosis and myocarditis.

This information was brought to you by Cision http://news.cision.com

https://news.cision.com/cantargia-ab/r/cantargia-reports-first-patient-treated-with-can04-in-a-us-phase-i-study-investigating-combination-w,c3209746

The following files are available for download:

https://mb.cision.com/Main/7470/3209746/1314426.pdf

Release

© 2020 PR Newswire
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