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OmniAb to Participate in Five Investor Conferences in May

OmniAb, Inc. (NASDAQ: OABI) today announced that management will be participating in five investor conferences during the month of May.

  • RBC Capital Markets Global Healthcare Conference, May 14-15 at the InterContinental Barclay Hotel in New York City. Management will participate in a fireside chat on Wednesday, May 15th at 11:30 a.m. Eastern time and will hold one-on-one meetings with investors. A live and archived webcast of the fireside chat will be available in the Investors section of OmniAb’s website.
  • H.C. Wainwright 2nd Annual BioConnect Investor Conference at Nasdaq, May 20 in New York City. Management will participate in a fireside chat on Monday, May 20th at 9:30 a.m. Eastern time and will hold one-on-one meetings with investors.
  • Benchmark 4th Annual Virtual Healthcare House Call 1x1 Investor Conference, May 21-22. Management will participate in a virtual call on Wednesday, May 22nd at 3:00 p.m. Eastern time and will hold one-on-one virtual meetings with investors.
  • Craig-Hallum 21st Annual Institutional Investor Conference, May 29 at The Depot Renaissance Minneapolis Hotel. Management will be holding one-on-one and small group meetings on Wednesday, May 29th with investors.
  • 2024 Leerink Partners Healthcare Crossroads Conference, May 28-30 at the Omni Barton Creek Resort & Spa in Austin, Texas. Management will participate in a fireside chat on Thursday, May 30th at 8:00 a.m. Central time and will hold one-on-one meetings with investors.

About OmniAb®

OmniAb licenses cutting edge discovery research technology to the pharmaceutical and biotech industry to enable the discovery of next-generation therapeutics. Our technology platform creates and screens diverse antibody repertoires and is designed to quickly identify optimal antibodies and other target-binding proteins for our partners’ drug development efforts. At the heart of the OmniAb platform is something we call Biological Intelligence™ (BI), which powers the immune systems of our proprietary, engineered transgenic animals to create optimized antibody candidates for human therapeutics.

We believe the OmniAb animals comprise the most diverse host systems available in the industry. Our suite of technologies and methods, including computational antigen design and immunization methods, paired with high-throughput single B cell phenotypic screening and mining of next-generation sequencing datasets with custom algorithms, are used to identify fully-human antibodies with exceptional performance and developability characteristics.

Our proprietary transgenic animals, including OmniRat®, OmniChicken® and OmniMouse® have been genetically modified to generate antibodies with human sequences to streamline the development of human therapeutic candidates. OmniFlic® and OmniClic® are fixed or common light-chain rats and chickens, respectively, designed to facilitate the discovery of bispecific antibodies. OmniTaur™ provides cow-inspired antibodies with unique structural characteristics for challenging targets. OmnidAb™, is an in vivo platform for the discovery of single domain antibodies based upon a human VH scaffold that affinity matures in a chicken host environment to provide a functionally diverse immune repertoire unavailable from mammalian systems. Our proprietary technologies are joined with and leverage OmniDeep™, which is a suite of in silico, AI and machine learning tools for therapeutic discovery and optimization that are woven throughout our various technologies and capabilities. Additionally, an established core competency focused on ion channels and transporters further differentiates OmniAb’s technology and creates opportunities in many important and emerging target classes.

OmniAb technologies can be leveraged for the discovery of a variety of next-generation antibody-based therapeutic modalities, including bi- and multi-specific biologics, antibody-drug conjugates, CAR-T therapies, targeted radiotherapeutics, and many others.

For more information, please visit www.omniab.com.

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