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6 Studies presented in AACR Abstract! Simcere Researchers will Make Oral Presentations at 2022 AACR Annual Conference

发布时间:2022-03-09

On March 9 Beijing Time (March 8 Eastern Time), the world's leading cancer research organization, the America Association for Cancer Research(AACR)has disclosed the abstract of AACR annual meeting 2022.

 

6 studies by Simcere researcher were presented in the abstract (including two oral presentations during AACR annual meeting from April 8 to 13, 2022), involving preclinical data on small-molecule targeted drugs, bispecific antibodies and multi-functional T cell engagers independently developed by Simcere. These might bring new insights to cancer scientists, clinicians, patients, and other attendees around the world and raise opportunities for further collaborations.

 

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n  A bispecific antibody that synergistically enhances both NK and T cell functions

Session OPO.CL06.01 - Immuno-oncology(E-Poster)

5203 - Discovery and development of SLD2435, a novel humanized IgG1 bispecific antibody simultaneously targeting human TIGIT and PVRIG for cancer immunotherapy

Presenter:Dr. Xiaofeng Zhao



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n  A targeted therapy with potentially much lower hematologic toxicity

Session MS.ET06.02 - Emerging New Anticancer Agents

2157 - SCR-6277, a potent and high selective arginine methyltransferase 5 (PRMT5) inhibitor with high tumor/plasma distribution ratio demonstrated robust anti-tumor activities and decreased hematological toxicities

Presenter:Dr. Feng Zhou


 

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n  A novel multi-specific bivalent T cell engager with strong anti-tumor efficacy

Session PO.IM02.10 - Therapeutic Antibodies 2

2897 / 12 - A multispecific T cell engager binding to both membrane proximal and membrane distal epitopes of MSLN with low affinity CD3 for the treatment of AML and solid tumors

Presenter:Dr. Renhong Tang



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n  A Highly selective MAT2A inhibitor that addresses off-targeted side effects

Session OPO.ET06.01 - Small Molecule Therapeutic Agents(E-Poster)

5434 - Discovery of SCR-7952, a novel, potent and high selective MAT2A inhibitor shows robust anti-tumor activities and better safety profile

Presenter:Dr. Feng Zhou



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n  A RAD51 inhibitor that significantly enhances anticancer effect of chemo/targeted therapy

Session OPO.ET06.01 - Small Molecule Therapeutic Agents(E-Poster)

5441 - Discovery of a novel RAD51 inhibitor SCR-6992 targeting homologous recombination pathways in cancer

Presenter:Dr. Wenqing Yang



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n  A novel CDK2/4/6 inhibitor that overcomes drug resistance

Session OPO.MCB06.01 - Cell Cycle (E-Poster)

5642 - Discovery of SCR-8079, a novel and selective CDK2/4/6 inhibitor overcomes the resistance to CDK4/6 inhibition and demonstrates broad anti-tumor activities in breast cancers

Presenter:Dr. Feng Zhou



About Simcere 

Simcere Pharmaceutical Group (2096.HK) is rapidly transitioning to an innovation and R&D-driven pharmaceutical company, with a mission of “providing today’s patients with medicines of the future.” It has established a national key laboratory of translational medicine and innovative pharmaceuticals. Simcere focuses on oncology, central nervous system disease and autoimmune disease therapeutic areas, with a diversified product portfolio and industry-leading capabilities. Its vigorous in-house R&D efforts and extensive R&D collaborations have made it a strategic cooperation partner with world leading pharmaceutical companies and biotechnology companies, in an effort to bring more global life science breakthroughs to China. For more information, please visit www.simcere.com.