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Status unknownNCT05255523Updated Feb 24, 2022

Pyrotinib Plus Trastuzumab After First-line TH (P) Treatment With HER-2 Positive Breast Cancer

A Phase 2 interventional study of pyrotinib in Advanced Breast Cancer, sponsored by Fujian Medical University Union Hospital. Status unknown. Open to female participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2022-02-24.

Sponsored by Fujian Medical University Union Hospital · Phase 2, Interventional, and Prevention

The sponsor has not verified this record recently (last verified Feb 2022), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Enrollment
60
Allocation
Not applicable
Ages
18 Years to 75 Years
Sex
Female
01

Study summary

The purpose of this study is to assess the effect of pyrotinib

Read the detailed description

The purpose of this study is to assess the effect of pyrotinib combined with trastuzumab in the maintenance phase delay/reduction of brain metastases after first-line TH(P) therapy for HER-2-positive advanced breast cancer

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Conditions studied

  • Advanced Breast Cancer

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Keywords

  • pyrotinib;CNS;breast cancer; HER-2 positivity
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In context

Breast Neoplasms

12,544 studies on the registry are indexed under Breast Neoplasms; 2,892 are open to participants now.

This study's planned enrollment of 60 is below the median of 72 across 9,303 interventional studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

Fujian Medical University Union Hospital is the lead sponsor of 100 studies on the registry; 72 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  1. age:18-75 years old, female;
  2. HER2 positive advanced breast cancer diagnosed by pathology, cytology or radiology, including inoperable breast cancer with stage IV, or recurrent/metastatic breast cancer.HER-2 positivity was confirmed by histopathological test: immunohistochemistry(IHC) results of 3 + or in situ hybridization (ISH) results of amplification of HER2;
  3. Disease progression occurs after treatment with trastuzumab (stopping the drug for more than 12 months) or newly diagnosed IV stage breast cancer patients;
  4. Eastern Cooperative Oncology Group (ECOG) performance status of 0-1;
  5. Life expectancy greater than or equal to 6 months;
  6. The main organs function well, and the inspection indicators meet the following requirements:
  1. For results of blood routine test HB≥90g/L; ANC≥1.5×109/L; PLT≥90×109/L; 2) For results of blood biochemical test ALT and AST≤2×ULN, but≤5×ULN if the transferanse elevation is due to liver metastases; TBIL≤1.5×ULN; Serum creatinine ≤1.5×ULN; 7. The researchers believed that the subjects were preference to benefit; 8. Participants were willing to join in this study, and written informed consent.

Exclusion criteria

Exclusion Criteria:

  1. Patients with brain metastases by CT or MRI;
  2. More factors affecting of oral drugs (gastrointestinal surgery history, inability to swallow, chronic diarrhea, intestinal obstruction);
  3. Study drug and excipient allergy;
  4. History of psychiatric drugs abuse and can't quit or patients with mental disorders;
  5. Pregnant or lactating female patients;
  6. Less than 4 weeks from the last clinical trial;
  7. The researchers think inappropriate.
05

Study design

Phase
Phase 2
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    Arm 1

    Pyrotinib:400mg qd po continuous medication Capecitabine: 1000 mg/m2 bid po for 14 consecutive days with 7 days off, every 21 days as a cycle.

    Drug: pyrotinib

Interventions

  • Drugpyrotinib

    After 4-6 cycles of taxane chemotherapeutics combined with trastuzumab±pertuzumab, the assessment result reaches CR or PR, and the subsequent sequential pyrrotinib plus capecitabine±trastuzumab to CNS Progress

    Also known as: capecitabine

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What researchers measure

Primary outcomes

  1. Incidence of first progression with brain metastases

    Incidence of first progression with brain metastases

    Time frame: 24 month

Secondary outcomes

  1. ORR without CNS

    Baseline to measured stable disease without central nervous system

    Time frame: 24 month

  2. TTBM

    Time to brain metastases

    Time frame: 24 month

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 24, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05255523
Lead sponsor
Fujian Medical University Union Hospital
Responsible party
Sponsor
First posted
Feb 24, 2022
Start date
Feb 20, 2022 (estimated)
Primary completion
Nov 5, 2023 (estimated)
Completion
Dec 20, 2024 (estimated)
Last update
Feb 24, 2022

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Feb 2022. You cannot join it, but the record below documents what was studied.

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