← Eichor
Study identifier: NCT06769425 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

HS-10502 Combination Treatment in Patients With Advanced Solid Tumors

Condition: Recurrent Ovarian Cancer · HER2-negative · Advanced Breast Cancer  ·  Sponsor: Jiangsu Hansoh Pharmaceutical Co., Ltd.

PhasePhase 1
Planned participants157
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

HS-10502 is a PARP1-specific selective inhibitor. The purpose if this study is to assess the safety, tolerability, pharmacokinetics (PK), and efficacy of HS-10502 Combination Treatment in subjects with advanced solid tumors.

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

Talk to the study team

Xi Yan  ·  18721195312  ·  yanx1@hspharm.com

Always discuss trial participation with your own doctor first.

Locations (1)

Fudan University Shanghai Cancer CenterShanghai, Shanghai Municipality, ChinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06769425