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Immunoprecise Antibodies Ltd IPA

ImmunoPrecise Antibodies Ltd. is a biotechnology company that leverages multi-omics modeling and complex artificial intelligence through a series of proprietary and patented technologies. The Company owns an integrated end-to-end suite of capabilities to support the development of therapeutic antibodies. It has several subsidiaries in North America and Europe including entities, such as Talem Therapeutics LLC, BioStrand BV, ImmunoPrecise Antibodies (Canada) Ltd. and ImmunoPrecise Antibodies (Europe) B.V. (collectively, the IPA Family). Its Contract Research Organizations (CRO) services include B cell Select; Phage Display; DeepDisplay; Abthena Bispecifics; LucinaTech Humanization; Affinity Maturation; Immunization, hybridoma, sequencing; rPEx protein manufacturing, and Cell line development. The Company utilizes custom antigen modeling, target analysis using Natural Language Processing and the HYFTTM analysis to lay the groundwork for the subsequent experimental phases.


NDAQ:IPA - Post by User

Post by GoldenArmon Sep 15, 2022 9:37am
293 Views
Post# 34964058

WOW! Now in NIH and NIAID - Fauciland

WOW! Now in NIH and NIAID - FaucilandThis is MEGA HUGE acknowledgement by NIH in regards to Covid on the efficacy of TATX-03

This NIAID-conducted pseudovirus-based study has reconfirmed the neutralizing activity of TATX-03 against the European variant (D614G mutant) of the parental virus and several previously tested variants, including Delta (B.1.617.2), and Omicron sublineages (BA.2, BA.4/5). Importantly, TATX-03 has now demonstrated its neutralizing activity against the currently spreading BA.2.75 variant. Maintained neutralizing potency was also confirmed for the Omicron sublineage BA.2.12.1, SARS-Co-V-2 variant that had not yet been screened in virus neutralization studies.

IPA’s Chief Scientific Officer (CSO), Dr. Ilse Roodink, stated: “We appreciate that our interactions with the FDA resulted in this collaboration with the NIAID. This division of the NIH is continuously screening clinical-stage antibody therapeutics for neutralizing potency towards emerging variants. We highly value this independent validation of the resilience of our PolyTope® TATX-03 product, further strengthening our position as we progress into clinical trials in humans.”


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