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Eribulin in Combination With Capecitabine for Adjuvant Treatment in Estrogen Receptor-Positive Early Stage Breast Cancer

This study is ongoing, but not recruiting participants.
Sponsor:
Information provided by (Responsible Party):
Eisai Inc.
ClinicalTrials.gov Identifier:
NCT01439282
First received: September 19, 2011
Last updated: February 7, 2014
Last verified: February 2014

September 19, 2011
February 7, 2014
August 2011
May 2014   (final data collection date for primary outcome measure)
To evaluate the feasibility of adjuvant treatment eribulin plus capecitabine for each individual subject the regimen is considered feasible if that subject is able to achieve relative dose intensity (RDI) of at least 85% of the 4 cycles of treatment. [ Time Frame: 12 wks ] [ Designated as safety issue: No ]

Relative dose intensity for each subject will be calculated as follows:

(1) based on each subject's body surface area (BSA), a total planned dose for both eribulin (Dep) and capecitabine (Dcp) calculated for a full 4-cycle regimen; (2) actual total dose of eribulin (Dea) and capecitabine (Dca) for the full 4-cycle regimen as collected on the case report form; (3) overall RDI = (Dea/Dep + Dca/Dcp)/2.

Same as current
Complete list of historical versions of study NCT01439282 on ClinicalTrials.gov Archive Site
Number of patients with adverse events of 4 cycles of eribulin plus capecitabine in the adjuvant setting [ Time Frame: 12 weeks ] [ Designated as safety issue: Yes ]
Safety will be assessed by the monitoring and recording of all AEs and serious adverse events (SAEs), regular monitoring of hematology and clinical chemistry, vital signs, ECGs, ECOG performance status, regular physician assessments, concomitant medications, medical histories, and physical examinations.
Same as current
Not Provided
Not Provided
 
Eribulin in Combination With Capecitabine for Adjuvant Treatment in Estrogen Receptor-Positive Early Stage Breast Cancer
A Phase II, Multicenter, Single-Arm, Feasibility Study of Eribulin in Combination With Capecitabine for Adjuvant Treatment in Estrogen Receptor-Positive Early Stage Breast Cancer

This is a Phase 2, multicenter, single-arm, feasibility study evaluating eribulin in combination with capecitabine as an adjuvant chemotherapy regimen in approximately 65 subjects with early-stage (I-II), human epidermal growth factor receptor 2 (HER2)- normal, estrogen receptor (ER)-positive breast cancer.

Not Provided
Interventional
Phase 2
Allocation: Non-Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Estrogen Receptor Positive Tumor
  • Breast Cancer
Drug: E7389 (eribulin mesylate) and capecitabine
eribulin mesylate (E7389) and capecitabine Eribulin 1.4 mg/m2 intravenously over 2 - 5 minutes Day 1 and Day 8 plus capecitabine 900 mg/m2 orally BID Days 1 - 14 of a 21-day cycle for 4 cycles
Other Name: BOLD
Experimental: Eribulin + Capecitabine
Intervention: Drug: E7389 (eribulin mesylate) and capecitabine
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
67
Not Provided
May 2014   (final data collection date for primary outcome measure)

Inclusion Criteria:

  1. Male subjects aged ≥ 18 years and female subjects who must be postmenopausal (at least 12 months consecutive amenorrheic or have had a bilateral oophorectomy or, if they have had a hysterectomy but with ovaries intact, then females must be age 55 or older and with postmenopausal follicle-stimulating hormone [FSH] levels).
  2. Subject is a candidate for chemotherapy in the adjuvant setting.

    • Adjuvant therapy must begin within 84 days of the final surgical procedure for breast cancer.

  3. Histologically confirmed Stage I to II invasive breast cancer. Subjects may have more than one synchronous primary breast tumor.
  4. Receptor Status:

    • HER2-normal as determined by a negative fluorescence in situ hybridization (FISH) result or 0 to 1+ by immunohistochemistry (IHC) staining result
    • ER-positive, node-negative or ER-positive Grade 1 or 2 node-positive breast cancer
  5. ECOG performance status of 0 or 1
  6. Adequate renal function as evidenced by serum creatinine ≤ 1.5 mg/dL or calculated creatinine clearance ≥ 50 mL/min per the Cockcroft and Gault formula
  7. Adequate bone marrow function as evidenced by ANC ≥ 1.5 x 109/L, hemoglobin ≥ 10.0 g/dL, and platelet count ≥ 100 x 109/L
  8. Adequate liver function as evidenced by bilirubin ≤ 1.5 times the upper limits of normal (ULN) and alkaline phosphatase, alanine aminotransferase (ALT), and aspartate aminotransferase (AST) ≤ 3 x ULN
  9. Male subjects must have had a successful vasectomy (confirmed azoospermia), or their female partners must not be of childbearing potential, or male subjects must agree to use and have their female partners use a highly effective method of contraception (e.g., total abstinence, an intrauterine device, a double-barrier method [such as condom plus diaphragm with spermicide] throughout the entire study period and for 30 days after study drug discontinuation..
  10. Voluntary agreement to provide written informed consent and willingness and ability to comply with all aspects of the protocol

Exclusion Criteria:

  1. Stage III and IV invasive breast cancer
  2. Prior chemotherapy, radiation therapy, immunotherapy or biotherapy for current breast cancer
  3. Nonmalignant systemic disease (cardiovascular, renal, hepatic, etc) that would preclude any of the study therapy drugs
  4. Subjects with a concurrently active second malignancy other than adequately treated nonmelanoma skin cancers or in situ cervical cancer
  5. Subjects with pre-existing neuropathy > Grade 2
  6. Subjects with known positive human immunodeficiency virus (HIV) status
  7. Females of childbearing potential. Females will be considered to be of childbearing potential unless they are postmenopausal (at least 12 months consecutive amenorrheic or have had a bilateral oophorectomy or, if they have had a hysterectomy but with ovaries intact, then females must be age 55 or older and with postmenopausal FSH levels).
  8. Subjects with current gastrointestinal disease or other condition resulting in an inability to take or absorb oral medications
  9. Subjects with known allergy or hypersensitivity to eribulin mesylate or its excipients, or to fluoropyrimidine therapy (with or without documented dihydropyrimidine dehydrogenase [DPD] deficiency)
  10. A clinically significant electrocardiogram (ECG) abnormality, including a marked baseline prolongation of QT/QTc interval (time between the start of the Q wave and the end of the T wave / QT interval corrected for heart rate) (e.g., repeated demonstration of a QTc interval > 500 ms)
  11. Any medical or other condition which, in the opinion of the investigator, would preclude participation in a clinical trial
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01439282
E7389-A001-212
Not Provided
Eisai Inc.
Eisai Inc.
Not Provided
Study Director: David Cox Eisai Inc.
Eisai Inc.
February 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP