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Study identifier: NCT06380660 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

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

Condition: Solid Tumor, Adult · BRCA1 Mutation · BRCA2 Mutation  ·  Sponsor: Acerand Therapeutics (Shanghai) Limited

PhasePhase 1/Phase 2
Planned participants298
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Teresa Shi  ·  8613916513539  ·  teresa.shi@acerand.com

Sherwin Cai, MD  ·  sherwin.cai@acerand.com

Always discuss trial participation with your own doctor first.

Locations (14)

Chongqing Cancer HospitalChongqing, Chongqing Municipality, ChinaRecruiting
Fujian Cancer HospitalFuzhou, Fujian, ChinaRecruiting
Sun Yat-Sen University Cancer CenterGuangzhou, Guangdong, ChinaRecruiting
Anyang Cancer HospitalAnyang, Henan, ChinaRecruiting
Henan Cancer HospitalZhengzhou, Henan, ChinaRecruiting
Hubei Cancer HospitalWuhan, Hubei, ChinaRecruiting
Union Hospital, Tongji Medical College, Huazhong University of Science and TechnologyWuhan, Hubei, ChinaRecruiting
Hunan Cancer HospitalChangsha, Hunan, ChinaRecruiting
Jinan Central HospitalJinan, Shandong, ChinaRecruiting
Qilu Hospital Shangdong UniversityJinan, Shandong, ChinaRecruiting
Fudan University Shanghai Cancer CenterShanghai, Shanghai Municipality, ChinaRecruiting
Second Hospital Affiliated to Shanxi Medical UniversityTaiyuan, Shanxi, ChinaRecruiting

+ 2 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06380660