Orum Therapeutics Announces Formation Of Scientific Advisory Board

BOSTON, US & DAEJEON, South Korea, April 4, 2022 -- Orum Therapeutics, a biotechnology company pioneering the development of tumor-directed targeted protein degraders to treat cancer, today announced the formation of its scientific advisory board (SAB). The SAB is comprised of a distinguished group of academic and industry experts who will advise the Orum Therapeutics team on the development of Orum’s novel targeted protein degraders (TPD) that use Orum’s TPD²™ approach, which combines the power of protein degradation with the precise tumor cell delivery mechanism of an antibody.

“We are proud to have experienced leaders in drug discovery and clinical development joining our SAB,” said Peter U. Park, Ph.D., Chief Scientific Officer of Orum Therapeutics. “We look forward to meeting regularly and fully leveraging the team’s diverse breadth of experiences as we progress the first molecule from our Antibody neoDegrader Conjugate platform, ORM-5029, into the clinic and continue to expand our pipeline in dual-precision protein degradation and broader protein homeostasis. With our scientific advisors’ guidance, we believe that we can bring first-in-class, dual-precision therapeutics to cancer patients quickly.”

Appointed members of the newly formed Orum Therapeutics SAB include the following:

  • Julie M. Cherrington Ph.D., is an experienced life science executive with extensive insight in bringing drugs into the clinic and through to commercialization. She has been a key contributor to the successful development of multiple FDA-approved products, including SUTENT®, PALLADIA®, VISTIDE®, VIREAD®, and HEPSERA®. Dr. Cherrington previously served as President and CEO of several oncology companies and currently serves on the Board of Directors for Mirati Therapeutics, Vaxart, Syncona Ltd., MycRx, Kisoji Biotechnology, and Sardona Therapeutics.

  • Sara Hurvitz, M.D., is Professor of Medicine at the University of California, Los Angeles (UCLA), Co-director of the Santa Monica-UCLA Outpatient Oncology Practice, Medical Director of the Clinical Research Unit of the Jonsson Comprehensive Cancer Center at UCLA, and Director of Breast Oncology. She has an active clinical practice specializing in the treatment of women with breast cancer. In addition, Dr. Hurvitz is a leader of multiple clinical trials testing new targeted therapies, including ENHERTU® for HER2 breast cancer, and preclinical evaluation of novel breast cancer targets.

  • Maria Koehler, M.D., Ph.D., is Chief Medical Officer of Repare Therapeutics and has more than 20 years of experience in both large, multinational pharmaceutical and biotechnology companies. Dr. Koehler served as an independent Board Member for Celyad Oncology and now serves as Board of Director for IKENA and Silverback Therapeutics. Her industry experience includes leading the development of IBRANCE®

  • Zoran Rankovic, Ph.D., is Director, Chemistry Centers at Jude Children’s Research Hospital. Prior to joining St. Jude, he served as director in medicinal chemistry at large pharmaceutical companies, where he led teams that delivered clinical candidates over a range of therapeutic areas. At St. Jude, Dr. Rankovic directs a multidisciplinary team that focuses on targeted protein degradation. He has published over 90 scientific papers, patents, and book chapters on drug discovery topics.

  • Roland B. Walter, M.D., Ph.D., M.S., is Professor at the Fred Hutchinson Cancer Center and a Professor of Medicine at the University of Washington. Dr. Walter specializes in treating acute myeloid leukemia (AML). His research seeks to develop new and improved antibody-based therapies in the laboratory that effectively kill AML cells, including treatments that eradicate the AML stem cells, and then to bring these therapies to patients.

About Orum Therapeutics

Orum Therapeutics is pioneering the development of tumor-directed targeted protein degraders by leveraging its TPD²™ approach to provide dual precision, antibody-enabled targeted protein degraders for cell-specific delivery. The Company’s proprietary platforms generated using the TPD² approach includes the Antibody neoDegrader Conjugate (AnDC™) platform, which generates first-in-class antibody drug conjugates. The first therapeutic candidates from the AnDC platform are in development for the treatment of solid tumors and hematologic cancers. Orum is located in Cambridge, Massachusetts, and Daejeon, South Korea. For more information, visit www.orumrx.com.

Contacts

Corporate: Kyuri Kim Ph.D., Senior Manager, Business Development, Orum Therapeutics, contact@orumrx.com

Media: Jessica Yingling, Ph.D., President, Little Dog Communications Inc., +1-858-344-8091, jessica@litldog.com 

 

 

Forward-looking Statements

This press release contains forward-looking statements that are based on the current expectations and beliefs of Orum Therapeutics, Inc. (“Orum”). Statements in this release regarding matters that are not historical facts, including, but not limited to, statements relating to the successful development and clinical benefits of novel targeted protein degraders, the frequency of SAB meetings, the commencement of first-in-human studies, the potential for development of other product candidates, the speed with which such candidates are brought to market, and the preferability of Orum products to others available are forward looking statements. These forward-looking statements are based on management’s expectations and assumptions as of the date of this release and are subject to numerous risks and uncertainties, which could cause actual results to differ materially from those expressed or implied by such statements. These risks and uncertainties include, without limitation, the uncertain and continually changing impacts and expected duration of the COVID-19 pandemic; the uncertainty of success in research and development activities; risks related to clinical trials, including potential delays, safety issues, or negative results; competition from alternative therapies; the risk that Orum may not be able to maintain and enforce its intellectual property; the risk that product candidates may not be successfully commercialized or adopted; the availability of financing; and risks related to the recruitment and retention of key employees, fluctuating markets and economic conditions, health care reform, prices, and reimbursement rates. The forward-looking statements in this presentation speak only as of the date of this release, and Orum undertakes no obligation to update or revise any of the statements. Orum cautions investors not to place considerable reliance on the forward-looking statements contained in this release.

Previous
Previous

­Orum Therapeutics Presents Preclinical Data At AACR 2022 Highlighting Novel Dual-Precision Targeted Protein Degrader, ORM-5029, Degrading GSPT1

Next
Next

Orum Therapeutics To Present Preclinical Data For ORM-5029, A Novel Antibody Neodegrader Conjugate, At The AACR Annual Meeting 2022