RecruitingPhase 1NCT06853496

Study of a Tankyrase Inhibitor RK-582 for Patients With Unresectable Metastatic Colorectal Cancer

Investigator-initiated Phase I Study of a Tankyrase Inhibitor RK-582 for Patients With Unresectable Metastatic Colorectal Cancer


Sponsor

Eiji Shinozaki

Enrollment

48 participants

Start Date

Mar 13, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Tankyrase, the fifth and sixth members of the poly(ADP-ribose) polymerase (PARP) family (PARP-5a/b), is responsible for poly(ADP-ribosyl)ation (PARylation), and was originally identified as a factor that promotes the function of telomerase, an enzyme that elongates telomeres. Subsequently, it was reported that tankyrase enhances Wnt/beta-catenin signaling by PARylation and subsequent degradation of AXIN, a negative regulator of Wnt/beta-catenin signaling, suggesting that tankyrase inhibitors may be a new treatment for colorectal cancer. RK-582 was discovered through lead optimization from a tankyrase inhibitor that suppresses the growth of human colorectal cancer cells. It was confirmed that RK-582 selectively inhibited tankyrase among the PARP family enzymes, suppressed the growth of Wnt/beta-catenin signal-dependent human colorectal cancer cells at both the levels of cultured cells and xenograft tumors in immunodeficient mice, and accumulated AXIN to decrease beta-catenin and downregulate the target gene expression as pharmacodynamic biomarkers. Based on these findings, RK-582 is thought to have potential as a new treatment for colorectal cancer patients. At present, however, the efficacy and safety of RK-582 in humans have not been confirmed. Thus, this clinical trial is conducted with the aim of investigating the tolerability and safety of RK-582 for patients with unresectable advanced or recurrent colorectal cancer as a first-in-human trial, in which RK-582 is administered to humans for the first time.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests a new oral medication called RK-582, which belongs to a class of drugs called tankyrase inhibitors, for people with advanced colorectal cancer that has spread and is no longer responding to standard treatments. **You may be eligible if:** - You have been diagnosed with colorectal cancer confirmed by biopsy - Your cancer is advanced (unresectable or metastatic) and has stopped responding to or you cannot tolerate standard treatments - You have measurable cancer on imaging - You are able to swallow capsules **You may NOT be eligible if:** - You have serious medical conditions affecting the gut, liver, lungs, heart, or blood - You have had interstitial lung disease - You have chronic nausea, vomiting, or diarrhea that would affect taking medication by mouth - You have a blood clot in your lungs or large veins - You are taking strong medications that interact with the study drug (CYP3A4 inhibitors or inducers) - You have osteoporosis or significant bone loss - You have obvious bone metastases in the legs or spine bearing your weight Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGRK-582

Dosing Frequency: Do single dose of RK-582 at the dose level specified for the cohort. Seven days after the first dose, Start repeated daily dose and continue until discontinuation criteria were met. Dose level per dose: Dose Level 1: 5 mg BID Dose level 2: 10 mg QD Dose level 3: 20 mg QD Dose level 4: 40 mg QD Dose Level 5: 60 mg QD Dose Level 6: 80 mg QD Dose Level 7: 100 mg QD Dose Level 8: 200 mg QD


Locations(1)

Cancer Institute Hospital of JFCR

Koto-ku, Tokyo, Japan

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NCT06853496