A Phase II Study of HLX22 in Combination With Trastuzumab Deruxtecan in HER2-low, Hormone Receptor Positive Locally Advanced or Metastatic Breast Cancer Patients
This is a Phase II Study of HLX22 in Combination with Trastuzumab Deruxtecan (T-DXd) in HER2-low, Hormone Receptor Positive Locally Advanced or Metastatic Breast Cancer Patients with Disease Progression or Intolerable Adverse Reaction on Standard of Care. Eligible subjects will be treated with the study drug until the loss of clinical benefit, death, intolerable toxicity, withdrawal of informed consent, or other reasons specified by the protocol (whichever occurs first).
Conditions studied
HER2-low Hormone Receptor Positive Breast Cancer
About this study
This is a Phase II Study of HLX22 in Combination with Trastuzumab Deruxtecan (T-DXd) in HER2-low, Hormone Receptor Positive Locally Advanced or Metastatic Breast Cancer Patients with Disease Progression or Intolerable Adverse Reaction on Standard of Care. Eligible subjects will be treated with the study drug until the loss of clinical benefit, death, intolerable toxicity, withdrawal of informed consent, or other reasons specified by the protocol (whichever occurs first).
Interventions
- Drug: HLX22 — HLX22 15mg/kg Q3W
- Drug: Trastuzumab Deruxtecan — Trastuzumab Deruxtecan 5.4mg/kg Q3W
Primary outcomes
- Progression-Free Survival (PFS) (Up to 5 years)
- Objective response rate (ORR) (Up to 2 years)
Eligibility information
Study locations
- Fudan University Shanghai Cancer Center, Shanghai, Shanghai Municipality 200000 China
Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-10-15.