-

Palleon Pharmaceuticals to Present Preclinical Data on Lead Program E-602 and Novel Bifunctional PD-L1-Targeted Sialidase at AACR Annual Meeting

WALTHAM, Mass.--(BUSINESS WIRE)--Palleon Pharmaceuticals, a company pioneering the field of glyco-immunology to treat cancer and inflammatory diseases, today announced two poster presentations at the American Association for Cancer Research Annual Meeting in New Orleans, La., from April 8-13, 2022.

Palleon will present an assessment of the safety, pharmacokinetics, and pharmacodynamics of E-602, the company’s first-in-class immuno-oncology drug candidate, in non-human primates. Those studies found that E-602 exhibits sustained, dose-dependent pharmacodynamic effects on desialylation of immune cells and a wide safety margin.

Additionally, Palleon will present data on the company’s novel bifunctional PD-L1-targeted sialidase. Studies performed in a transgenic mouse model of colon cancer expressing PD-L1 found that the bifunctional PD-L1-targeted sialidase exhibited enhanced efficacy compared to E-602 and to an anti-PD-L1 antibody, as well as dose-dependent tumor growth inhibition and modulation of immune cell infiltration.

Details of the poster presentations are as follows:

Title: Assessment of the safety, pharmacokinetics, and pharmacodynamics of a first-in-class cancer drug candidate E-602, a sialoglycan degrader, in non-human primates
Number: LB203
Timing: April 13, 2022, 9:00 a.m. – 12:30 p.m. CDT

Title: Development of PD-L1-targeted sialidase as a novel cancer immunotherapeutic approach
Number: LB221
Timing: April 13, 2022, 9:00 a.m. – 12:30 p.m. CDT

About Palleon Pharmaceuticals
Palleon Pharmaceuticals is the leading biotechnology company developing drugs that harness glyco-immunology to treat cancer and inflammatory diseases. The company’s proprietary platforms overcome scientific hurdles in the glycobiology field to create novel therapeutics for devastating diseases characterized by immune system dysfunction. Palleon’s lead program in oncology, E-602, is an enzymatic degrader of immunosuppressive sialoglycans on tumors and immune cells which is now being evaluated in a Phase 1/2 study (NCT05259696). www.palleonpharma.com

Contacts

Palleon Media
Thomas Stephenson
Ten Bridge Communications
thomas@tenbridgecommunications.com
(617) 448-1803

Palleon Pharmaceuticals


Release Versions

Contacts

Palleon Media
Thomas Stephenson
Ten Bridge Communications
thomas@tenbridgecommunications.com
(617) 448-1803

More News From Palleon Pharmaceuticals

Palleon Pharmaceuticals to Present on Development of HLX79/E-602 in Autoimmune Disease at the American College of Rheumatology Convergence Annual Meeting and the American Society of Nephrology Kidney Week

WALTHAM, Mass.--(BUSINESS WIRE)--Palleon Pharmaceuticals, a company developing sialoglycan degradation as a therapy to treat autoimmune diseases and cancer, today announced two upcoming poster presentations at key autoimmune disease medical conferences. Together, the presentations provide insight into HLX79/E-602, a first-in-class human sialidase enzyme therapeutic, and its application in addressing autoimmune diseases through targeting cell surface sugars. Details on Poster Presentations: Amer...

Palleon Pharmaceuticals Announces First Patient Dosed in Phase 2 Clinical Trial of E-602 (HLX79), a Potential First-In-Class Treatment for Active Glomerulonephritis

WALTHAM, Mass.--(BUSINESS WIRE)--Palleon Pharmaceuticals, a company pioneering glyco-immunology drug development to treat autoimmune diseases and cancer, today announced the first patient has been dosed in the Phase 2 clinical trial of Palleon’s potential first-in-class human sialidase enzyme therapeutic E-602 (HLX79) in combination with Henlius’ self-developed HANLIKANG (rituximab biosimilar) in patients with active glomerulonephritis, a form of autoimmune kidney disease that includes membrano...

Palleon Pharmaceuticals Announces NMPA IND Clearance to Proceed with Phase 2 Clinical Trial of E-602 (HLX79), a First-In-Class Treatment for Autoimmune Diseases

WALTHAM, Mass.--(BUSINESS WIRE)--Palleon Pharmaceuticals announces NMPA IND clearance to proceed with Phase 2 clinical trial of E-602 (HLX79) for autoimmune diseases...
Back to Newsroom