Abstract 5797: PK/PD and preclinical ADME characterization of TB-008, a first-in-class CDK9 degrader in xenograft models

Abstract Targeted protein degradation (TPD) offers a promising therapeutic strategy by removing, rather than inhibiting, disease-driving proteins. Cyclin-dependent kinase 9 (CDK9) is a key oncogenic regulator implicated in multiple hematologic and solid tumors. TB008 is a rationally designed CDK9-targeting PROTAC developed using an AI-driven degrader platform to achieve high affinity, selectivity, and favorable pharmacologic properties. Preclinical studies have demonstrated potent, selective CDK9 degradation with downstream suppression of oncogenic targets such as c-MYC and MCL-1. TB008 has shown robust antiproliferative and pro-apoptotic activity across cancer cell lines and strong tumor growth inhibition >95% in triple negative breast cancer xenograft model which support further development of TB008 as a CDK9-directed therapeutic candidate. Pharmacokinetics in Balb/c-nude mice (efficacy study species) has shown that TB-008 is rapidly absorbed following an intraperitoneal dose with ∼90% bioavailability and a half-life of 1 hr. Interestingly, in-silico PK and bioavailability analysis does predict that there is a 90% decrease in drug concentration in mouse plasma within the first hour after administration. Furthermore, also based on in-silico evaluation, it is also predicted that higher drug concentration will be in the GI tract, lungs, plasma, spleen and portal vein. Even with the relatively short half-life, the high tumor growth inhibition observed in xenograft studies confirms the potency and fast kinetics of TB-008 in effecting the degradation of the tumor CDK9. We have initiated studies in mouse xenograft models to better understand the PK/PD and design optimal dosing regimens. Also, we will report the efficacy of TB-008 in additional xenograft models. Additional preclinical ADME data and PK in higher nonclinical species will be reported. Citation Format: Narayana Narasimhan, Mahesh Koirala, Isabelle Dussault, Lindy Yan, Oscar Kashala, Zoser Mohamed, Mario DiPaola, . PK/PD and preclinical ADME characterization of TB-008, a first-in-class CDK9 degrader in xenograft models [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 5797.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-5797
Primary Topic
Protein Degradation and Inhibitors
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article
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article

Abstract 5797: PK/PD and preclinical ADME characterization of TB-008, a first-in-class CDK9 degrader in xenograft models

Oscar Kashala, Mario DiPaola, Mahesh Koirala, Narayana I. Narasimhan et al.
Cancer Research
Protein Degradation and Inhibitors
article

Abstract 5797: PK/PD and preclinical ADME characterization of TB-008, a first-in-class CDK9 degrader in xenograft models

Oscar Kashala, Mario DiPaola, Mahesh Koirala, Narayana I. Narasimhan, Isabelle Dussault, Lindy Yan, Zoser Mohamed
article en

Abstract

Abstract Targeted protein degradation (TPD) offers a promising therapeutic strategy by removing, rather than inhibiting, disease-driving proteins. Cyclin-dependent kinase 9 (CDK9) is a key oncogenic regulator implicated in multiple hematologic and solid tumors. TB008 is a rationally designed CDK9-targeting PROTAC developed using an AI-driven degrader platform to achieve high affinity, selectivity, and favorable pharmacologic properties. Preclinical studies have demonstrated potent, selective CDK9 degradation with downstream suppression of oncogenic targets such as c-MYC and MCL-1. TB008 has shown robust antiproliferative and pro-apoptotic activity across cancer cell lines and strong tumor growth inhibition >95% in triple negative breast cancer xenograft model which support further development of TB008 as a CDK9-directed therapeutic candidate. Pharmacokinetics in Balb/c-nude mice (efficacy study species) has shown that TB-008 is rapidly absorbed following an intraperitoneal dose with ∼90% bioavailability and a half-life of 1 hr. Interestingly, in-silico PK and bioavailability analysis does predict that there is a 90% decrease in drug concentration in mouse plasma within the first hour after administration. Furthermore, also based on in-silico evaluation, it is also predicted that higher drug concentration will be in the GI tract, lungs, plasma, spleen and portal vein. Even with the relatively short half-life, the high tumor growth inhibition observed in xenograft studies confirms the potency and fast kinetics of TB-008 in effecting the degradation of the tumor CDK9. We have initiated studies in mouse xenograft models to better understand the PK/PD and design optimal dosing regimens. Also, we will report the efficacy of TB-008 in additional xenograft models. Additional preclinical ADME data and PK in higher nonclinical species will be reported. Citation Format: Narayana Narasimhan, Mahesh Koirala, Isabelle Dussault, Lindy Yan, Oscar Kashala, Zoser Mohamed, Mario DiPaola, . PK/PD and preclinical ADME characterization of TB-008, a first-in-class CDK9 degrader in xenograft models [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 5797.

Cancer ResearchVol. 86(7_Supplement)
Norwood Hospital (US), Spectra Solutions (United States) (US)
Openalex Percentile: Top 9%
Protein Degradation and Inhibitors
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