RecruitingPhase 1Phase 2NCT06380660

Study of ACE-86225106 to Treat Patients With Advanced Solid Tumors

A Phase I/II, Open-label, Multicentre Study to Assess the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy of Ascending Doses of ACE-86225106 as Monotherapy in Patients With Advanced Solid Tumors


Sponsor

Acerand Therapeutics (Shanghai) Limited

Enrollment

298 participants

Start Date

Mar 22, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to determine if the experimental treatment with poly-ADP ribose polymerase (PARP) inhibitor, ACE-86225106 is safe, tolerable and has anti-cancer activity in adult patients with advanced solid tumors.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This early-phase study tests a new experimental drug called ACE-86225106 in patients with advanced solid tumors (cancers in organs or tissues) that have not responded to standard treatments. The study aims to find the right dose and assess safety. **You may be eligible if...** - You are 18 or older (in most cases) - You have an advanced solid tumor that is hard to treat or that you cannot tolerate standard treatments for - You are in good general health (ECOG 0-1) - Your cancer can be measured on scans - Your expected survival is at least 3 months - You are able to provide tumor tissue and blood samples for genetic testing **You may NOT be eligible if...** - You recently received anti-cancer drugs, major surgery, or radiation - Your organ function is inadequate - You have certain other cancers or serious medical conditions 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

DRUGACE-86225106 tablet

ACE-86225106 will be administered orally daily as a continuous regimen. Subjects will continue to receive study treatment until PD as judged by local investigator review, development of unacceptable toxicity, or withdrawal of consent.


Locations(14)

Chongqing Cancer Hospital

Chongqing, Chongqing Municipality, China

Fujian Cancer Hospital

Fuzhou, Fujian, China

Sun Yat-Sen University Cancer Center

Guangzhou, Guangdong, China

Anyang Cancer Hospital

Anyang, Henan, China

Henan Cancer Hospital

Zhengzhou, Henan, China

Hubei Cancer Hospital

Wuhan, Hubei, China

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

Wuhan, Hubei, China

Hunan Cancer Hospital

Changsha, Hunan, China

Jinan Central Hospital

Jinan, Shandong, China

Qilu Hospital Shangdong University

Jinan, Shandong, China

Fudan University Shanghai Cancer Center

Shanghai, Shanghai Municipality, China

Second Hospital Affiliated to Shanxi Medical University

Taiyuan, Shanxi, China

Zhejiang Cancer Hospital

Hangzhou, Zhejiang, China

First Hospital Affiliated to Wenzhou Medical University

Wenzhou, Zhejiang, China

View Full Details on ClinicalTrials.gov

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NCT06380660


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