Poseida Therapeutics Presents Encouraging Preclinical Data Across its CAR-T and Gene Therapy Programs at the American Society of Gene and Cell Therapy 2021 Virtual Annual Meeting

On May 11, 2021 Poseida Therapeutics, Inc. (Nasdaq: PSTX), a clinical-stage biopharmaceutical company utilizing proprietary genetic engineering platform technologies to create cell and gene therapeutics with the capacity to cure, reported that it will give multiple oral and poster presentations at the American Society of Gene and Cell Therapy 2021 Virtual Annual Meeting being held May 11-14, 2021 (Press release, Poseida Therapeutics, MAY 11, 2021, View Source [SID1234579726]).

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 Company’s oral presentation will highlight new data demonstrating the potential of its proprietary piggyBac DNA Delivery System for the treatment of genetic liver disorders in children and infants. Two additional presentations will highlight preclinical data supporting Poseida’s first allogeneic CAR-T product candidate, P-BCMA-ALLO1 for R/R multiple myeloma, as well as preclinical data supporting the Company’s anti-c-kit CAR-T program as a potentially safer preconditioning regimen for hematopoietic stem cell transplantation in patients with AML.

"At Poseida, we are applying our proprietary technology platforms to develop the next wave of cell and gene therapies to not only treat severe cancers but to also unlock the potential of single treatment cures," said Eric Ostertag, M.D., Ph.D., Chief Executive Officer. "The preclinical data being presented today further validate our CAR-T approach in multiple myeloma and in preconditioning for patients with AML, as well as demonstrate the exciting potential of our liver directed gene therapies, particularly in juvenile patients."

Presentation Highlights:

Oral Presentation: "Preclinical Evaluation of Combined Adeno-Associated Virus and Nanoparticle Delivery of piggyBac Transposon System for Durable Transgene Expression in the Growing Neonatal Murine Liver"
Session Date/Time: Tuesday, May 11, 2021, 5:45pm – 6:00pm ET
Abstract Number: 30

In a preclinical study, Poseida evaluated concomitant delivery of recombinant adeno-associated virus (rAAV) vectors and novel nanoparticle (NP) vectors using its piggyBac and "Super" piggyBac (SPB) technologies in order to deliver transposon and transposase in a growing neonatal mouse model. Data demonstrated that the piggyBac DNA Delivery System was effective in using both rAAV and NP vectors to introduce edited genes into targeted hepatocyte genomes. Poseida also found that SPB, a hyperactive form of the transposase, produced stable vector integration into the hepatocyte genome for more than three months, compared to transpose alone. Similarly, delivery of a novel NP formulation using SPB produced efficient delivery of mRNA to the liver hepatocytes, with similarly high levels of durability in the transgene expression. Taken together, these preclinical findings suggest the potential of piggyBac and SPB technology for gene therapies that treat congenital liver disease in infants and young children.

Poster Presentation: "P-BCMA-ALL01: A Fully Allogeneic Stem Cell Memory T Cell (TSCM) CAR-T Therapy Targeting BCMA for the Treatment of Multiple Myeloma Shows Potent Anti-Tumor Activity"
Session Date/Time: Tuesday, May 11, 2021, 8:00am – 10:00am ET
Abstract Number: 789

P-BCMA-ALLO1 is Poseida’s first fully allogenic product candidate targeting B-cell maturation antigen (BCMA) for the treatment of relapsed/refractory multiple myeloma. In in vitro and in vivo preclinical studies, P-BCMA-ALL01 showed effective, targeted cancer cell killing and cytokine secretion, with similar or superior performance in anti-tumor efficacy compared to an autologous CAR-T therapy. Inclusion of a proprietary "booster molecule" in the allogeneic manufacturing process further improved expansion of gene-edited cells and enabled production of hundreds of patient doses from a single manufacturing run, thereby reducing the manufacturing cost per dose into the same range as that of a monoclonal antibody.

Poster Presentation: "Anti-c-kit CAR-T Cells Afford Effective Eradication of Human AML and Normal Hematopoietic Cells in a Preclinical Model of Safer Non-Genotoxic Stem Cell Transplant Conditioning"
Session Date/Time: Tuesday, May 11, 2021, 8:00am – 10:00am ET
Abstract Number: 715

Poseida is investigating its anti-c-kit CAR-T program, which leverages its proprietary piggyBac DNA Delivery System in preclinical studies as a potentially safer precursor conditioning therapy to the transplantation of hematopoietic stem cells (HSC) for patients suffering from AML. The piggyBac delivery vectors under investigation include a transposon that generates pure CAR+ product as well as a safety switch that allows rapid clearance of the reactive CAR-T cells prior to donor transplant of hematopoietic stem cells. Preclinical data to be presented in the poster showed that the lead CAR-T cells that express the anti-c-kit binder (CAR 1) deplete up to 92% of human CD34+ stem and progenitor cells in bone marrow within 48 hours. Additionally, an enhanced anti-c-kit CAR-T product, CAR 2, killed an estimated >99% of leukemia cells, exceeding the killing ability of a single dose of 30 mg/kg dose of busulfan. These encouraging data suggest that stem cell-directed CAR-T cells may be a safer preconditioning regimen compared to the current standard of care and may expand access to treatment for acute myeloid leukemia patients needing HSC transplant.

Imvax to present at UBS Global Healthcare Virtual Conference

On May 11, 2021 Imvax, a clinical stage immuno-oncology company driven to transform patient treatment and outcomes with its novel technology platform, reported that John Furey, chief executive officer, will present at the UBS Global Healthcare Virtual Conference at 1 p.m. EDT Wednesday, May 26, 2021 (Press release, Imvax, MAY 11, 2021, View Source [SID1234579725]).

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!

Mr. Furey, Dr. David Andrews, chief medical officer, and Dr. Mark Exley, chief scientific officer, will also participate in one-on-one investor meetings during the conference.

The presentation will be webcast live and will be available for replay for 30 days following the event at https://bit.ly/3gPPF8U.

CNS Pharmaceuticals to Present at the Q2 Virtual Investor Summit

On May 11, 2021 CNS Pharmaceuticals, Inc. (NASDAQ: CNSP) ("CNS" or the "Company"), a biopharmaceutical company specializing in the development of novel treatments for primary and metastatic cancers of the brain and central nervous system, reported that John Climaco, Chief Executive Officer of CNS Pharmaceuticals, will present at the Q2 Virtual Investor Summit on Tuesday, May 18th at 12:30 PM ET (Press release, CNS Pharmaceuticals, MAY 11, 2021, View Source [SID1234579724]).

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!

In addition to the presentation, management will be available to participate in virtual one-on-one meetings with qualified members of the investor community who are registered to attend the conference. For more information about the conference, please visit the conference website.

A live video webcast will be accessible on the Events page in the Investors section of the Company’s website (www.cnspharma.com) and will be archived for 90 days following the event.

Heligenics & The Jackson Laboratory Announce New Collaboration on ERBB2 Breast Cancer Gene

On May 11, 2021 Heligenics, Inc. reported a new collaboration with The Jackson Laboratory (JAX) (Press release, Heligenics, MAY 11, 2021, View Source;the-jackson-laboratory-announce-new-collaboration-on-erbb2-breast-cancer-gene-301288500.html [SID1234579723]). This joint project will make available the functional output of Variants of Unknown Significance (VUS) throughout key portion of the ERBB2 gene through the JAX Clinical Knowledgebase (CKB), a digital resource that connects clinicians and researchers around the globe in order to interpret complex cancer genomic profiles.

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!

"This is a fabulous partnership that will help modernize and expand variant interpretation for key cancer genes," says Dr. Martin R. Schiller, CEO at Heligenics. "JAX is bringing a lot to the table and is a valued partner."

Heligenics’ proprietary GigaAssay process measures causal functional impact of all mutants in a gene in 4 to 5 months while it takes other technologies decades to identify just a single marker. This collaboration will lead to future clinical trials, research grants, and publications to advance the fight against cancers, offering patients hope by identifying actionable ERBB2 variants for potential treatment.

CKB currently provides extensive information relevant to interpretation of cancer-related genomic data, including thousands of genevariant descriptions, therapies, as well as evidence of therapeutic efficacy, accessbile through a web-based application.

JAX-CKB can help increase clinician confidence in completeness and accuracy of the information related to the patient’s tumor genomic profile. For translational and clinical researchers, JAX-CKB provides thousands of literature citations, FDA drug labels, and clinical trials relative to a tumor’s genomic mutational profile, resulting in a clear and up-to-date picture of discoveries and active developments for a variety of biomarkers.

"Heligenics’ GigaAssay technology has the potential to advance genomic interpretation, and we are excited for the opportunity to provide large scale interpretation of previously unknown genomic variants to our users, with the hope of connecting patients to relevant treatment options that otherwise may not have been identified," says Sara Patterson, Ph.D. manager, clinical analytics and curation at JAX.

The benefits of this new collaboration include:

Identifying the impact of thousands of poorly understood ERBB2 mutations
Enhancing the understanding of how ERBB2 mutations cause various types of breast and other cancers, including gastric cancer
Testing of 95% of possible mutants being tested for functional impact in 5 months – a dramatic improvement over today’s less than 8% of possible ERBB2 mutants characterized after more than 25 years of study
Analyzing, retrospectively, how the gene mutation/function library data can improve patient outcomes
Providing additional insight into breast and other cancers caused by these genetic mutations through a collaboration of research and publications
"This collaboration with Heligenics will allow us to define new therapeutic targets for cancer patients," said Jens Rueter, M.D., medical director at JAX’s Maine Cancer Genomics Initiative (MCGI). "Ultimately, this has the potential to lead to new treatment options for cancer patients, including the many patients and families affected by cancer in Maine."

Cannabics Pharmaceuticals Files a PCT Patent Application for Proprietary Cancer Treatment Formulations

On May 11, 2021 Cannabics Pharmaceuticals Inc. (OTCQB: CNBX), a global leader in the development of cancer related cannabinoid-based medicine, reported that it had filed a patent application under the Patent Cooperation Treaty (PCT) for novel formulations developed for treatment of various cancer types (Press release, Cannabics Pharmaceuticals, MAY 11, 2021, View Source [SID1234579722]).

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!

Said patent application includes ample preclinical supporting data collected from in-vitro experiments performed in the company’s in-house drug discovery facilities in Israel, as well as from in-vivo experiments performed on mice.

Gabriel Yariv, Cannabics Pharmaceuticals President and COO: "After a rigorous process of screening, testing and analyzing a variety of unique molecular compounds, and their effect on human biopsies and cancer cell lines, we have identified specific formulations that stand out in terms of their performance. These formulations are detailed in the current PCT application, and we plan to turn them into new drug candidates for specific cancer treatments in the near future".

This news follows the company’s announcement from last week concerning "Notice of Allowance" received by the company from The Mexican Patent and Trademark Office (IMPI) on a separate patent application.