Clinical trial · Interventional
Pharmacokinetic Study of Pyrotinib and Docetaxel in Combination With Trastuzumab in Patients With HER2 Metastatic Breast Cancer
An Open, Single-arm and Multi-center Pharmacokinetic Study of Pyrotinib and Docetaxel Plus Trastuzumab in Patients With HER2 Positive Recurrent or Metastasis Breast Cancer.
NCT04367090CI-TRIAL-00069677completedPhase 1ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The primary objective of the study is to study the pharmacokinetics of pyrotinib and docetaxel plus Trastuzumab in HER2 Positive MBC. The secondary objective of the study is to evaluate the safety and efficacy (ORR) of pyrotinib and docetaxel plus Trastuzumab in HER2 Positive MBC.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Metastatic Breast Cancer | Malignant Breast Neoplasm | CURATED_BROADER | 0.78 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Docetaxel, trastuzumab | Drug | — | UNRESOLVED |
| Pyrotinib | Drug | Pyrotinib | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Pyrotinib and docetaxel plus trastuzumab
- interventionNames
- Drug: Docetaxel, trastuzumab
- Drug: Pyrotinib
Primary outcomes (2)
- measure
- Pharmacokinetic parameter: Cmax of pyrotinib and docetaxel
- timeFrame
- Approximately 2 months
- description
- Peak Plasma Concentration (Cmax) of pyrotinib
- measure
- Pharmacokinetic parameter: AUC of pyrotinib and docetaxel
- timeFrame
- Approximately 2 months
- description
- Area under the plasma concentration versus time curve (AUC) of pyrotinib and docetaxel
Secondary outcomes (4)
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: 1. HER2 positive recurrent or metastasis breast cancer. 2. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1. 3. Adequate organ function. 4. Signed, written inform consent obtained prior to any study procedure. Exclusion Criteria: 1. Patients received more than 1 line of chemotherapy or immunotherapy in the phase of recurrence / metastasis. 2. History of HER tyrosine kinase inhibitors or monoclonal antibody for breast cancer in any treatment setting,except trastuzumab ,or Pertuzumab used in the neo-adjuvant or adjuvant setting. 3. Assessed by the investigator to be unable receive systemic chemotherapy. 4. History of other malignancy within the last 5 years,except for carcinoma in situ of cervix,basal cell carcinoma or squamous cell carcinoma of the skin that has been previously treated with curative intent. 5. Pregnant or lactating women,or for women of childbearing potential unwilling to use a highly-effective contraception during of the study treatment and for at least 7 months after the last dose of study treatment.
References
Publications (1)
- DERIVEDDai L, Gao T, Guo R, Chen Y, Wang J, Zhou S, Tang Y, Chen D, Huang S. Efficacy and safety of pyrotinib-based regimens in HER2 positive metastatic breast cancer: A retrospective real-world data study. Neoplasia. 2024 Oct;56:101029. doi: 10.1016/j.neo.2024.101029. Epub 2024 Jul 17. PMID 39024777