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08 Monoclonal Antibody Facility

$5,456P30FY2019CANIH

University Of Tx Md Anderson Can Ctr, Houston TX

Investigators

Linked publications, trials & patents

Trial NCT07407920Trial NCT07349641Trial NCT06651580Trial NCT05681026Trial NCT05223036Trial NCT05078866Trial NCT05057312Trial NCT05054296Trial NCT05044546Trial NCT05023967Trial NCT05011045Trial NCT04875728Trial NCT04870645Trial NCT04810091Trial NCT04751422Trial NCT04740164Trial NCT04668300Trial NCT04615013Trial NCT04505267Trial NCT04484909Trial NCT04483349Trial NCT04481204Trial NCT04474301Trial NCT04458610Trial NCT04447222Trial NCT04435691Trial NCT04430725Trial NCT04407247Trial NCT04373720Trial NCT04317781Trial NCT04311723Trial NCT04310826Trial NCT04310397Trial NCT04265430Trial NCT04257045Trial NCT04256941Trial NCT04239989Trial NCT04239976Trial NCT04239157Trial NCT04236882Trial NCT04228042Trial NCT04220827Trial NCT04220775Trial NCT04220008Trial NCT04219969Trial NCT04219904Trial NCT04216732Trial NCT04216563Trial NCT04216524Trial NCT04216472Trial NCT04215029Trial NCT04200534Trial NCT04199026Trial NCT04196972Trial NCT04189783Trial NCT04189770Trial NCT04189757Trial NCT04188418Trial NCT04188405Trial NCT04186884Trial NCT04186832Trial NCT04185337Trial NCT04181463Trial NCT04171622Trial NCT04171219Trial NCT04171037Trial NCT04169763Trial NCT04169737Trial NCT04169542Trial NCT04160052Trial NCT04151082Trial NCT04150939Trial NCT04140487Trial NCT04135326Trial NCT04134208Trial NCT04132843Trial NCT04132505Trial NCT04132440Trial NCT04129138Trial NCT04128748Trial NCT04128501Trial NCT04127721Trial NCT04125914Trial NCT04119037Trial NCT04106843Trial NCT04106245Trial NCT04090619Trial NCT04090567Trial NCT04087057Trial NCT04083378Trial NCT04082572Trial NCT04074746Trial NCT04066894Trial NCT04062305Trial NCT04062266Trial NCT04058964Trial NCT04054245Trial NCT04054167Trial NCT04054154Trial NCT04053517

Abstract

PROJECT SUMMARY: MONOCLONAL ANTIBODY FACILITY (MAF) The importance of immunotherapy research to advancing the field of cancer biology and improving clinical outcomes has surged in recent years, prompting Science magazine to name cancer immunotherapy its 2013 Breakthrough of the Year. Recognition of the power of immunotherapy has heightened interest in and demand for rapid, affordable monoclonal antibody (MAb) services, and improved technologies are needed to provide cutting-edge, high-quality molecules required for today's science. The Monoclonal Antibody Facility (MAF) at MD Anderson is actively participating in this endeavor. The mission of the MAF is to produce de novo MAbs against newly discovered or existing antigens, and to purify unique high-quality custom MAbs in a timely and effective manner, with the value added of scientific advice and competitive prices. Dr. Laura Bover has directed the MAF since 2007, and in 2016 hired a senior research scientist, Dr. Roberto Rangel, who is bringing additional new technologies to the core. The number of MAbs produced in grant Yr42 has tripled when compared with the average of the previous grant period (48 in Yr42 and 16 on average for the previous grant period). Four MAF- generated MAbs have been licensed to pharmaceutical companies for clinical development, and additional MAbs have been licensed to biotechnology companies for in vitro use. In addition, the MAb anti-OX40, generated in 2012, has progressed to a phase I clinical trial. In the past 6-year period, the MAF has supported the research of 72 MD Anderson center members, representing all 16 CCSG programs, in contrast to 40 investigators in the previous grant period. MD Anderson has provided an additional $717,769 in capital equipment funds. MD Anderson members with peer-reviewed funding accounted for 90% of the usage, and 35% ($128,415) support is requested from the CCSG in Yr44. MAF supported 57 publications, with 35 publications (61%) in journals with an IF of >5 and 10 publications (18%) in journals with an IF of >10. The MAF Specific Aims are: 1) To produce, in a timely, effective manner at competitive prices, unique high-affinity, high-quality custom MAbs that are suitable for diverse applications that meet the cancer center users' requirements. 2) To provide consultation and assistance, including: a) selection and generation of appropriate antigen formats (peptides, proteins, or cells expressing the target); b) troubleshooting any antigen- or screening-related issues; c) characterization of the produced antibodies (PK, affinity, avidity, and competition); d) assay development for the particular applications and users' goals, including imaging, immunohistochemistry, diagnostic assays, crystallography, and preclinical and future therapeutic use; e) advice for IND filing and patent requirements; f) training and assistance on the subsequent screening (in users' hands) of the positive candidates selected by the MAF for the particular desired application.

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