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A Study on the Efficacy and Safety of IPyC for HER2+ MBC

F

Fujian Medical University

Status

Completed

Conditions

Breast Cancer

Treatments

Drug: Inetetamab and Pyrotinib Combined with Chemotherapy

Study type

Observational

Funder types

Other

Identifiers

NCT06990347
K2024-534-01

Details and patient eligibility

About

Between July 2020 and August 2024, 301 HER2-positive MBC patients from five tertiary centers received the regimen until disease progression or unacceptable toxicity. Efficacy endpoints included progression-free survival (PFS), objective response rate (ORR), and clinical benefit rate (CBR).

Enrollment

301 patients

Sex

Female

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients who underwent a biopsy of the metastatic site and were confirmed as having MBC
  • patients who received inetetamab + pyrotinib + chemotherapy as metastasis therapy.

Exclusion criteria

  • male patients or individuals with prior malignancy
  • patients with prior or current enrollment in interventional clinical trials for MBC
  • patients who received less than 2 cycles of treatment (6 weeks of inetetamab or 8 weeks of pyrotinib)
  • patients who were lost to follow-up during the therapeutic process

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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