Vor to Present New Platform and Preclinical Data at ASH

Rhea-AI Summary

Vor Biopharma (Nasdaq: VOR) announced new data from its eHSC platform at the ASH 63rd Annual Meeting. The data includes the potential of CRISPR-Cas9 gene editing to knock out CD123 and CLL-1, enhancing treatment options for acute myeloid leukemia (AML) patients. Vor's research showcases multiplex genome editing of hematopoietic stem cells, promising safe and efficient gene editing for multiple blood cancer therapies. Presentations will occur from December 11-14, 2021, in Atlanta, Georgia, highlighting the advancements in CAR-T cell therapy and engraftment potential.

Positive

• Presentation of preclinical data at ASH highlighting the potential of the eHSC platform.
• Use of CRISPR-Cas9 gene editing may enhance AML treatment options.
• Multiplex genome editing could enable multiple targeted therapies.
• Demonstrated engraftment potential of edited hematopoietic stem cells.

Negative

• None.

• Knock out of CD123 or CLL-1 by CRISPR-Cas9 from Human Hematopoietic Stem Cells Maintains Hematopoietic Function and is Resistant to Targeted Therapies
• Multiplex Engineering of Human CD34+ HSPCs Enables Dual Gene Knock-out with High Engraftment Potential
• Dual-Mobilized Donor Derived CD33 CAR T-Cells as Potent and Effective AML Therapy in Preclinical Models
  

CAMBRIDGE, Mass., Nov. 04, 2021 (GLOBE NEWSWIRE) -- Vor Biopharma (Nasdaq: VOR), a clinical-stage cell and genome engineering company, today announced the upcoming presentation of new data from its novel engineered hematopoietic stem cell (eHSC) platform at the American Society of Hematology (ASH) 63^rd Annual Meeting, taking place in Atlanta, Georgia from December 11-14, 2021.

“The data being presented at ASH underscore the potential of our novel cell and genome engineering platform to change the standard of care for patients living with blood cancers,” said Tirtha Chakraborty, Ph.D., Vor’s Chief Scientific Officer. “By knocking out either CD123 or CLL-1 through CRISPR-Cas9 gene editing, we are exploring a promising new path to treating patients with acute myeloid leukemia with our novel eHSC platform. In addition, our research demonstrating multiplex genome editing of allogeneic hematopoietic stem cells represents another exciting strategy to efficiently and safely edit multiple genes in blood stem cells, potentially enabling the use of multiple targeted blood cancer therapies.”

“In total, we believe these preclinical data, including results showing that T cells derived from the same HSC transplant donor are suitable to become cancer-targeting CAR-T cells, will enable Vor’s development of efficient and safe cell therapies to treat AML patients and support the potential of our novel platform approach.”

ASH Annual Meeting Presentations

Poster Presentation

Title: Knock out of CD123 or CLL-1 By CRISPR-Cas9 Editing from Human Hematopoietic Stem Cell Transplants Provide New Possibilities for Increasing Therapeutic Index and Safety for AML Treatment
Abstract Number: 3818
Session Title: 701. Experimental Transplantation: Basic and Translational: Poster III
Presenting Author: Michelle Lin, Ph.D., Head of Preclinical Sciences and HSC Biology, Vor
Date: Monday, December 13, 2021
Time: 6:00pm ET - 8:00pm ET
Location: Georgia World Congress Center, Hall B5

Poster Presentation

Title: Multiplex Engineering of Human CD34+ HSPCs Enables Dual Gene Knock-out while Maintaining High Engraftment Potential and Safety
Abstract Number: 2939
Session Title: 801. Gene Therapies: Poster II
Presenting Author: Nipul Patel, Scientist, Vor
Date: Sunday, December 12, 2021
Time: 6:00pm ET - 8:00pm ET
Location: Georgia World Congress Center, Hall B5

Poster Presentation

Title: G-CSF/Plerixafor Dual-Mobilized Donor Derived CD33 CAR-T cells as Potent and Effective AML Therapy in Pre-Clinical Models
Abstract Number: 1716
Session Title: 703. Cellular Immunotherapies: Basic and Translational: Poster I
Presenting Author: Giacomo Canesin, Ph.D., Scientist, Vor
Date: Saturday, December 11, 2021
Time: 5:30 pm ET - 7:30pm ET
Location: Georgia World Congress Center, Hall B5

The posters from these presentations will be available on the Vor corporate website on Monday, December 13, 2021 at 9:00am ET at https://ir.vorbio.com/news-and-events/events-and-presentations.

About Vor Biopharma
Vor Biopharma is a clinical-stage cell and genome engineering company that aims to change the standard of care for patients with blood cancers by engineering hematopoietic stem cells to enable targeted therapies post-transplant. For more information, visit: www.vorbio.com.

Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. The words “aims,” “believe,” “continue,” “could,” “estimate,” “expect,” “intend,” “may,” “plan,” “potential,” “project,” “should,” “target,” “will,” “would,” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Forward-looking statements in this press release include Vor Biopharma’s statements regarding the potential efficacy of its platform and its therapies. Vor Biopharma may not actually achieve the plans, intentions, or expectations disclosed in these forward-looking statements, and you should not place undue reliance on these forward-looking statements. Actual results or events could differ materially from the plans, intentions and expectations disclosed in these forward-looking statements as a result of various factors, including: uncertainties inherent in the initiation and completion of preclinical studies and clinical trials and clinical development of Vor Biopharma’s product candidates; availability and timing of results from preclinical studies and clinical trials; whether interim results from a clinical trial will be predictive of the final results of the trial or the results of future trials; expectations for regulatory approvals to conduct trials or to market products; the impact of the COVID-19 pandemic on Vor Biopharma’s business, including its preclinical studies and clinical trials and availability of funding sufficient for its foreseeable and unforeseeable operating expenses and capital expenditure requirements. These and other risks are described in greater detail under the caption “Risk Factors” included in the Vor Biopharma’s most recent annual or quarterly report and in other reports it has filed or may file with the Securities and Exchange Commission. Any forward-looking statements contained in this press release speak only as of the date hereof, and Vor Biopharma expressly disclaims any obligation to update any forward-looking statements, whether because of new information, future events or otherwise, except as may be required by law.

Contacts:

Media:
Sarah Spencer
+1 857-242-6076
sspencer@vorbio.com

Investors:
Chris Brinzey
ICR Westwicke
+1 339-970-2843
chris.brinzey@westwicke.com

FAQ

What new data did Vor Biopharma present at the ASH Annual Meeting 2021?

Vor Biopharma presented preclinical data demonstrating the potential of its eHSC platform and CRISPR-Cas9 gene editing for AML treatment.

What is the significance of CD123 and CLL-1 knockouts by Vor using CRISPR-Cas9?

The knockouts of CD123 and CLL-1 may improve therapeutic outcomes for AML patients by enabling targeted therapies.

When and where will Vor Biopharma's presentations take place?

The presentations will occur from December 11-14, 2021, at the Georgia World Congress Center in Atlanta, Georgia.

What are the implications of Vor Biopharma's multiplex genome editing research?

The implications include the potential for safe and efficient editing of multiple genes, improving treatment options for blood cancers.

How does Vor Biopharma plan to change the standard of care for blood cancers?

Vor aims to engineer hematopoietic stem cells to enable targeted therapies post-transplant, potentially changing treatment protocols.