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Myocet, Docetaxel & Trastuzumab as 1st Line Treatment of Patients With HER-2/Neu Positive Metastatic Breast Cancer

Phase I-II Study of Liposomal Doxorubicin (Myocet®), Docetaxel and Trastuzumab as First-Line Treatment of Patients With HER-2/Neu Positive Metastatic Breast Cancer

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00250874
Enrollment
45
Registered
2005-11-08
Start date
2003-12-31
Completion date
Unknown
Last updated
2005-11-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Metastatic Breast Cancer

Brief summary

To study the pharmacokinetic profile of the therapeutic schedule in order to demonstrate absence of negative interactions among the 3 drugs administered

Detailed description

1. To assess the maximum tolerated dose (MTD) of Myocet at different dosages in combination with Taxotere at the fixed dose of 35 mg/m2 on day 2 and 9 every 21 days and weekly Herceptin as first line therapy in patients affected by HER-2/neu positive metastatic breast cancer 2. To enhance the proportion of complete remission 3. To allow the feasibility of the combination of Herceptin with both Myocet and Taxotere without an enhanced risk of cardiotoxicity

Interventions

DRUGLiposomal Doxorubicin (Myocet), Docetaxel and Trastuzumab

Sponsors

Zeneus Pharma
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* HER-2/neu overexpression assessed by FISH test or with immunohistochemical methods: Dako(the result must be 3+ with dakotest); if the immunohistochemical test results 2+ it is needed a positive FISH test * Female \< 70yrs * Histologically or cytologically proven breast cancer. * Metastatic or locally advanced breast cancer (clinical stage: III-IV) * Adequate hematological, hepatic, renal and cardiac function, the latter confirmed by echocardiography with FEVS ≥50% * Prior adjuvant chemotherapy if doxorubicin total dose ≤300 mg/m2, epirubicin total dose ≤450 mg/m2

Exclusion criteria

* History of cardiopathy * Severe hepatic and renal diseases * Brain metastases as the only parameter of disease * Contraindication to the use of corticosteroids as premedication * Acute infectious diseases * Insulin-dependent diabetes * History of other cancers except for adequately treated basal cell skin cancer or in situ carcinoma of the cervix * Concurrent treatment with any other cancer therapy

Countries

Italy

Contacts

Primary ContactProfessor Amadori
segronco@ausl.fo.it+39 0543 731737
Backup ContactProfessor Gasparini

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026