Iparomlimab and Tuvonralimab (QL1706) in Patients With HR-positive, HER2-negative Advanced Breast Cancer

This is a prospective, randomised, controlled, multicentre study to evaluate the efficacy and safety of Iparomlimab and Tuvonralimab (QL1706) in patients with hormone receptor-positive/human epidermal growth factor receptor 2-negative advanced breast cancer.

Trial Details

NCT ID
NCT07180160
Phase
PHASE2
Sponsor
Wenjin Yin
Status
RECRUITING
Cancer Type
HER2 Positive Breast Cancer
Interventions
  • QL1706
  • CDK4/6 inhibitor
  • Fulvestrant
Locations (sample)
  • Shanghai, China|31.22222,121.45806

Key Eligibility Criteria

  • Female, age≥18 years old
  • Expected survival ≥12 weeks
  • Pathologically confirmed recurrent or metastatic breast cancer not amenable to curative surgery
  • ER and/or PR positive, HER2 negative

For full eligibility, visit ClinicalTrials.gov.

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