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A First-in-Human Study of HH160 in Participants With Advanced or Metastatic Solid Tumors
Sponsor: Huahui Health
Summary
This study is evaluating the safety, side effects, how the body processes HH160, and its early anticancer activity when given alone or with other cancer treatments in participants with advanced solid tumors. The study will also identify the recommended dose for future studies. The trial includes two phases and is expected to last about 4 years, with treatment and follow-up lasting approximately 6-12 months each.
Official title: An Open-Label, Multicenter, Phase 1 Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, Immunogenicity and Preliminary Antitumor Activity of HH160 Alone or in Combination With Other Antitumor Agents in Patients With Advanced or Metastatic Solid Tumors
Key Details
Gender
All
Age Range
18 Years - 75 Years
Study Type
INTERVENTIONAL
Enrollment
299
Start Date
2026-06-11
Completion Date
2028-08
Last Updated
2026-08-21
Healthy Volunteers
No
Conditions
Interventions
HH160
Administered by intravenous infusion on Day 1 of each 21-day (Q3W) cycle or 14-day (Q2W) cycle.
Locations (3)
Calvary Mater Newcastle
Waratah, New South Wales, Australia
Tasman Health Care
Southport, Queensland, Australia
Shandong Tumour Hospital Dongyuan Unit
Jinan, Shandong, China