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RECRUITING
NCT07623369
PHASE1

A First-in-Human Study of HH160 in Participants With Advanced or Metastatic Solid Tumors

Sponsor: Huahui Health

View on ClinicalTrials.gov

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

Interventions

DRUG

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