Europe Neoantigen Summit

On March 22, 2023 Anocca reported that it will attend 6th Annual Neoantigen Summit Europe (Press release, Anocca, MAR 22, 2023, View Source [SID1234629152]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

Reagan Jarvis, our CEO, is presenting ‘Showcasing Individualised Neoantigen Discovery Platform’ at the TCR-Based Therapies for Solid Tumours, where he talks about understanding HLA-restricted neoantigen target complexity with cell-based assays, validating neoantigen targets with T-cell Receptor reagents derived by rapid
multiplex discovery and considering TCR potency and safety trade-off for HLA-restricted neoantigens.

2023 Cell & Gene Meeting on the Med

On March 22, 2023 Anocca reported it wil attend 2023 Cell & Gene Meeting on the Med (Press release, Anocca, MAR 22, 2023, View Source [SID1234629151]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

We are delighted to be one of the sponsors of this year’s 2023 Cell & Gene Meeting on the Med, with Reagan Jarvis, our CEO and Brian McGee, our CBO presenting Anocca, our technology platforms and our pipeline of novel T-cell therapies.

TCR-Based Therapies for Solid Tumours

On March 22, 2023 Anocca reported that it will attend TCR-Based Therapies for Solid Tumours summit (Press release, Anocca, MAR 22, 2023, View Source [SID1234629150]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

Reagan Jarvis, our CEO, is presenting ‘Systematic Isolation & Characterization of Clinical TCR Candidates’ at the TCR-Based Therapies for Solid Tumours, where he discusses native and optimized TCR frameworks, TCR cross-reactivity including insights and practical benchmarks and preventing TCR allo-reactivity.

ImmuneOnco Biopharmaceuticals’ IMM47, IMM40H, IMM2520, and IMM2902 projects debut at the 2023 American Association for Cancer Research (AACR) Annual Meeting

On March 21, 2023 ImmuneOnco Biopharmaceuticals (Shanghai) Inc. (hereinafter referred to as "ImmuneOnco") reported that the company will present the preclinical research data of IMM47 (CD24 antibody), IMM40H (CD70 antibody), IMM2520 (CD47×PD-L1), and IMM2902 (CD47×Her2) in the form of posters at the 2023 American Association for Cancer Research (AACR) (Free AACR Whitepaper) (AACR 2023) Annual Meeting in Orlando, Florida from April 14th to 19th (Press release, ImmuneOnco Biopharma, MAR 21, 2023, View Source [SID1234655687]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!


HLB Life, Phase 3 Clinical Trial Plan for ‘Pyrotinib’ for Breast Cancer Approved

On March 21, 2023 HLB Life Science reported that it received approval from the Ministry of Food and Drug Safety for a phase 3 clinical trial plan for the anticancer drug ‘Pyrotinib’ (Press release, HLB Life Science, MAR 21, 2023, View Source;word=&page=1&v=381 [SID1234649274]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

The title of the clinical trial is ‘A randomized, active-controlled, open-label, multi-center phase 3 clinical trial to evaluate the efficacy and safety of Pyrotinib + Capecitabine combination compared to Lapatinib + Capecitabine combination in patients with HER2-positive metastatic or recurrent breast cancer’. The clinical trial will be conducted on 204 patients in 11 hospitals in Korea (total of 12 hospitals) excluding Seoul National University Hospital. (Clinical period: 36 months from the date of approval by the Institutional Review Board)

The company plans to confirm the progression-free survival period (PFS, primary endpoint) through this clinical trial.

Pyrotinib is a small molecule compound independently developed by Hengrui Pharmaceutical of China, and is an oral targeted anticancer drug targeting EGFR/HER2/HER4. In 2020, it received official approval in China as a second-line treatment for HER2 metastatic breast cancer. In

2020, HLB Life Science signed an exclusive licensing agreement for Pyrotinib in Korea with Hangseo Pharmaceutical, and has exclusive rights to the clinical development and sales of Pyrotinib as a treatment for various cancers, including breast cancer and lung cancer, in Korea.

HLB Life Science applied for the clinical trial to the Ministry of Food and Drug Safety on July 29, 2022.