On April 8, 2022 Tachyon Therapeutics, Inc. ("Tachyon" or "the Company"), a private biotechnology company developing transformative cancer therapies against novel targets, reported preclinical data for TACH101, the Company’s first-in-class KDM4 inhibitor, at the American Association for Cancer Research (AACR) (Free AACR Whitepaper) ("AACR") Annual Meeting 2022 (Press release, Tachyon Therapeutics, APR 8, 2022, View Source [SID1234611762]). TACH101 is an investigational agent for the potential treatment of adult patients with diffuse large B-cell lymphoma (DLBCL).
Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:
Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing
Schedule Your 30 min Free Demo!
"These preclinical data on TACH101 highlight its anti-tumor activity in DLBCL, the most common and aggressive type of non-Hodgkin lymphoma," said Frank Perabo, M.D., Ph.D., CEO of Tachyon Therapuetics. "This work has increased our understanding of the potential for TACH101 in hematologic malignancies and also attests to its broad applicability in cancer, including solid tumors as was presented at AACR (Free AACR Whitepaper) previously. We look forward to advancing TACH101 into clinical study."
The data presented from both in vitro and in vivo preclinical studies demonstrated that targeting KDM4 with TACH101 resulted in significantly reduced growth of DLBCL cell lines representing the major DLBCL subtypes (GCB, ABC, and PMBL). Additionally, in vivo studies showed TACH101 treatment resulted in significant inhibition of tumor growth leading to complete remission in patient-derived xenograft models.
Highlights from the poster presentation (Poster #3720) are summarized below:
TACH101 showed potent anti-proliferative activity in DLBCL cell lines with IC50 as low as 0.01 µM.
Further evaluation demonstrated DLBCL cell lines were 100% sensitive to TACH101 treatment independent of their molecular subtype.
In vivo, TACH101 triggered effective tumor control (100%) in xenograft models of DLBCL (OCI-LY19).
TACH101 treatment caused downregulation of PNUTS gene expression. PNUTS is a direct target of KDM4 and can serve as a potential pharmacodynamic marker of TACH101 activity in clinical studies.
TACH101 demonstrated favorable pharmacologic and ADME profile without significant off-target activity and low probability of drug-drug interactions.
AACR 2022 is taking place both virtually and in-person at the Ernest N. Morial Convention Center in New Orleans from April 8-13, 2022. The poster presentation titled, "TACH101, a First-in-Class Inhibitor of KDM4 Histone Lysine Demethylase for Treatment of Diffuse Large B-Cell Lymphoma," will be available for viewing to registered attendees starting on Friday, April 8 at 1 pm ET through Wednesday, July 13 on the AACR (Free AACR Whitepaper) Annual Meeting 2022 website. The poster will be presented on April 13 from 10am to 1:30pm ET in the session: PO.MCB05.04 – Chromatin Modifiers: Mutations and Novel Therapeutics.