Tallac Therapeutics Presents New Data on Toll-like Receptor Agonist Antibody Conjugate, TAC-001, at the 2021 Virtual Annual Meeting of the American Association for Cancer Research (AACR)
— TAC-001, Tallac’s lead candidate from novel Toll-like Receptor Agonist Antibody Conjugate (TRAAC) platform, induces innate and adaptive immune responses that generate potent anti-tumor activity in preclinical study —
BURLINGAME, CA–(BUSINESS WIRE)–April 10, 2021 — Tallac Therapeutics, Inc., a privately held biopharmaceutical company harnessing the power of innate and adaptive immunity to fight cancer, today announced the first presentation of preclinical data demonstrating potent single-agent anti-tumor activity in preclinical cancer models with systemically administered TAC-001, the company’s lead clinical candidate from its novel Toll-like Receptor Agonist Antibody Conjugate (TRAAC) platform. The data will be presented today as part of the Immunomodulatory Agents and Interventions Session at Week I of the American Association of Cancer Research’s (AACR) 2021 Virtual Annual Meeting (#AACR21) taking place April 10-15, 2021.
Toll-like receptor (TLR) agonists are a novel class of immunotherapy that generate both an innate and
adaptive immune response which may produce more robust and durable anti-cancer immunity to help
overcome resistance to standard-of-care oncology treatments. TLR9 is a key intracellular TLR present in
broad immune cell populations such as B lymphocytes and myeloid cells. Recent studies have shown that
the likelihood of patients responding to immune checkpoint inhibitor therapy may depend on B cells in
the tumor.i B cells play pivotal roles in the immune defense system, which bridge the innate and the
adaptive immunities against cancers.ii In preclinical studies, the activation of TLR9 in human and mouse
models drives B cell proliferation and differentiation.iii
“The results presented today at AACR elucidate the unique properties of TAC-001 responsible for
integrating B cells and TLR9 activation which trigger innate and adaptive immune responses to create
potent, systemically delivered anti-tumor immunity across solid tumor types,” said Dr. Hong I. Wan,
president, CEO and co-founder of Tallac Therapeutics. “The emerging data on TAC-001 continues to
strengthen our understanding of the roles that B cells and TLR9 activation play in eliciting anti-tumor
immunity in checkpoint inhibitor resistant and refractory settings and will help guide our clinical
In the e-poster, titled “TAC-001, a toll-like receptor 9 (TLR9) agonist antibody conjugate targeting B cells,
promotes anti-tumor immunity and favorable safety profile following systemic administration in
preclinical models,” investigators present data providing evidence that in vitro targeted delivery of TAC001 leads to superior TLR9 activation in B cells, increased expression of co-stimulatory molecules and
cross-presentation leading to T cell proliferation. In vivo, TAC-001 demonstrated robust, curative and
durable single agent anti-tumor activity in checkpoint inhibitor resistant and refractory tumor models.
Additionally, the systemic administration of TAC-001 was shown to trigger both innate and adaptive
immunity by increasing B cell infiltration, T effector cell functions and modulation in suppressive myeloid
cells within the tumor microenvironment. These results support the development of TAC-001 for a broad
range of solid tumor malignancies.
AACR Poster Presentation Details:
- Title: TAC-001, a toll-like receptor 9 (TLR9) agonist antibody conjugate targeting B cells, promotes antitumor immunity and favorable safety profile following systemic administration in preclinical models
- Session Type: E-Poster Session
- Session Category: Immunology
- Session Title: Immunomodulatory Agents and Interventions
- Track: Immunology, Clinical Research Excluding Trials
- Permanent Abstract Number: 1721
TAC-001 is a Toll-like Receptor Agonist Antibody Conjugate (TRAAC) comprised of a potent Toll-like
Receptor 9 agonist (T-CpG) conjugated to an anti-CD22 antibody, a receptor restricted to B cells.
TAC-001 is designed to systemically deliver T-CpG to B cells by binding to CD22, leading to internalization
of TAC-001, TLR9 signaling, B cell activation and a cascade of immune reactions. Preclinical studies
demonstrate that the innate and adaptive immune responses triggered by TAC-001 leads to potent antitumor activity. TAC-001 is being developed to systemically deliver targeted immune activation in solid
About Tallac Therapeutics, Inc.
Tallac Therapeutics is a privately held biopharmaceutical company harnessing the power of innate and
adaptive immunity to fight cancer. Tallac’s pipeline of immunotherapy candidates are derived from the
company’s novel Toll-like Receptor Agonist Antibody Conjugate (TRAAC) platform to deliver a potent Tolllike receptor (TLR9) agonist (T-CpG) for targeted immune activation via systemic administration. Several
TRAAC molecules are in various stages of discovery and preclinical development. For more information,
please visit www.tallactherapeutics.com.
Tallac Media Contact:
The Grace Communication Group
i Helmink, B.A., Reddy, S.M., Gao, J. et al. B cells and tertiary lymphoid structures promote immunotherapy response. Nature 577, 549–555
ii Yanqiu, L., Shala, Y., Jiushen, D. Harnessing B Cells for Cancer Immunotherapy. Journal of Medical Oncology and Therapeutics Volume 1, Issue 1 (2016). https://doi.org/10.35841/medical-oncology.1.1.8-13
iii Kuo, T.C., et al. TAC-001, a toll-like receptor 9 (TLR9) agonist antibody conjugate targeting B cells, promotes anti-tumor immunity and favorable safety profile following systemic administration in preclinical models. AACR Annual Meeting 2021 Online Proceedings (Abstract 1721)