A Study of HS-20110 for Advanced Solid Tumors
This study is testing a drug called HS-20110 in people with advanced solid tumors. HS-20110 is an antibody-drug conjugate, which means it's designed to deliver a drug directly to cancer cells. The main goals are to find the safest dose of HS-20110 and see how well it shrinks tumors. You may be able to join if you are 18 or older and have advanced solid tumors that have been confirmed by a doctor. The study is open-label, meaning both you and your doctors will know you are receiving HS-20110. The study plans to enroll 475 participants.
- Study design
- This is an open-label study, meaning everyone knows what treatment is being given. It plans to enroll 475 participants with advanced solid tumors.
- What's involved
- HS-20110 will be given through an IV infusion in 21-day cycles. The study will explore different doses of the drug.
- Compensation
- Not stated in the trial record.
- Follow-up
- Your safety will be monitored from the first day of treatment until one month after your last dose. Tumor response will be measured from screening until two months after your last dose.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
A Study of HS-20110 in Participants With Advanced Solid Tumors
At a glance
Conditions
NCT06892379
Where you'd take part
This study runs at 8 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Carolina BioOncology Institute
Huntersville, North Carolinastudy coordinator listed
Recruiting
BRCR Medical Center INC
Tamarac, Floridano site contact published
Recruiting
Fort Wayne Medical Oncology and Hematology
Fort Wayne, Indianano site contact published
Recruiting
NEXT Dallas
Irving, Texasno site contact published
Recruiting
NEXT Oncology
San Antonio, Texasno site contact published
Recruiting
NEXT Virginia
Fairfax, Virginiano site contact published
Recruiting
SUN YAT-SEN University Cancer Center
Guangzhou, Guangdong, Chinano site contact published
Recruiting
The University of Texas MD Anderson Cancer Center
Houston, Texasno site contact published
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- Maximum tolerated dose (MTD) or maximum applicable dose (MAD)From day 1 to one months after the last dose in Phase 1a
- Objective response rate (ORR) as per RECIST v1.1From screening to 2 months after the last dose