Overview

NCI Definition [1]:
An orally bioavailable activator of pyruvate kinase M2 isoform (PKM2), with potential immunomodulating and antineoplastic activities. Upon oral administration, PKM2 activator TP-1454 locks PKM2 into the active tetrameric form. This may prevent the production of glycolytic intermediates by the less active dimer form of PKM2, depleting the supply of glycolytic intermediates which are needed for tumor cell growth. This may also inhibit immune suppression mediated by the dimer form of PKM2. Altogether, this may slow tumor cell growth and enhance anti-tumor immune responses, thereby inhibiting tumor cell proliferation. PKM2, the predominant PK isoform found in tumor cells, is responsible for catalyzing the last step of glycolysis. PKM2 plays a critical role in the metabolic changes observed in cancer and immune cells and establishes a metabolic advantage for tumor cells over the tumor immune microenvironment.

Tp-1454 has been investigated in 1 clinical trial, of which 1 is open and 0 are closed. Of the trial investigating tp-1454, 1 is phase 1 (1 open).

EGFR A763_Y764insFQEA, EGFR Codon 719 Missense, and EGFR Exon 19 Deletion are the most frequent biomarker inclusion criteria for tp-1454 clinical trials.

Malignant solid tumor is the most common disease being investigated in tp-1454 clinical trials [2].

Top Biomarker Inclusion Criteria for Open Clinical Trials Investigating Tp-1454
This graph displays the 20 most frequently occurring biomarkers curated on clinical trials investigating tp-1454 and the cancer types associated with these biomarkers. These numbers are derived from a set of 5,956 clinical trials for which biomarker status defines treatment.

Drug Details

Synonyms [2]:
tp 1454, pkm2 activator tp-1454, pyruvate kinase m2 isoform activator tp-1454, tp1454
NCIT ID [1]:
C175380

References

1. National Cancer Institute. NCI Thesaurus Version 18.11d. https://ncit.nci.nih.gov/ncitbrowser/. [2018-07-30] [2018-08-02].

2. All assertions and clinical trial landscape data are curated from primary sources. You can read more about the curation process here.