A Study of Neoadjuvant Paclitaxel in Combination With Bavituximab in Early- Stage Triple- Negative Breast Cancer

Sponsor

Peregrine Pharmaceuticals (Industry)

Overall Status

Withdrawn

CT.gov ID

NCT02685306

Collaborator

(none)

Enrollment

Arms

Duration (Months)

Study Details

Study Description

Brief Summary

The primary purpose of this research study is to see whether adding bavituximab (an investigational drug) to the standard chemotherapy drug taxane, will improve the results of the treatment for early- stage Triple Negative Breast Cancer followed by Standard- of- Care surgery

Condition or Disease	Intervention/Treatment	Phase
Breast Cancer Triple Negative Breast Neoplasms Triple-Negative Breast Neoplasm Triple-Negative Breast Cancer Triple Negative Breast Cancer ER-Negative PR-Negative HER2-Negative Breast Neoplasms ER-Negative PR-Negative HER2-Negative Breast Cancer	Biological: Bavituximab Drug: Taxane	Phase 2

Detailed Description

This is an open-label randomized trial in patients with early- stage Triple Negative Breast Cancer. Patients will be treated with either paciltaxel alone or paclitaxel with bavituximab. Paclitaxel will be given weekly, and bavituximab will be given weekly. All therapy will continue for up to twelve doses of treatment followed by standard of care definitive surgical resection.

Study Design

Study Type:

Interventional

Actual Enrollment :

0 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

A Phase II Study to Determine the Pathological Complete Response Rate and Immunomodulatory Effects of Neoadjuvant Paclitaxel in Combination With Bavituximab in Early- Stage Triple- Negative Breast Cancer

Study Start Date :

Mar 1, 2016

Anticipated Primary Completion Date :

Apr 1, 2017

Anticipated Study Completion Date :

Sep 1, 2017

Arms and Interventions

Arm	Intervention/Treatment
Active Comparator: Taxane Taxane (Paclitaxel) weekly on Days 1, 8,15,22,29, 36, 43, 50, 57, 64, 71, 78	Drug: Taxane 12 weekly doses of taxane on Days 1, 8,15,22,29, 36, 43, 50, 57, 64, 71, 78 Other Names: Paclitaxel
Experimental: Bavituximab plus Taxane Bavituximab 3 mg/kg weekly PLUS Taxane (Paclitaxel) on Days 1, 8,15,22,29, 36, 43, 50, 57, 64, 71, 78	Biological: Bavituximab 12 weekly doses of bavituximab given on Days 1, 8,15,22,29, 36, 43, 50, 57, 64, 71, 78 Drug: Taxane 12 weekly doses of taxane on Days 1, 8,15,22,29, 36, 43, 50, 57, 64, 71, 78 Other Names: Paclitaxel

Arm

Intervention/Treatment

Active Comparator: Taxane

Taxane (Paclitaxel) weekly on Days 1, 8,15,22,29, 36, 43, 50, 57, 64, 71, 78

Drug: Taxane

12 weekly doses of taxane on Days 1, 8,15,22,29, 36, 43, 50, 57, 64, 71, 78

Other Names:

Paclitaxel

Experimental: Bavituximab plus Taxane

Bavituximab 3 mg/kg weekly PLUS Taxane (Paclitaxel) on Days 1, 8,15,22,29, 36, 43, 50, 57, 64, 71, 78

Biological: Bavituximab

12 weekly doses of bavituximab given on Days 1, 8,15,22,29, 36, 43, 50, 57, 64, 71, 78

Drug: Taxane

12 weekly doses of taxane on Days 1, 8,15,22,29, 36, 43, 50, 57, 64, 71, 78

Other Names:

Paclitaxel

Outcome Measures

Primary Outcome Measures

Pathological Complete Response (pCR) rate of neoadjuvant paclitaxel in combination with bavituximab in patients with early- stage triple- negative breast cancer (TNBC) [Approximately 24 months]

Secondary Outcome Measures

Safety Measures - Adverse Events and Laboratory Evaluations [approximately 24 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Written informed consent has been obtained prior to screening.
Target Population
Female or male at least 18 years of age.
Invasive breast cancer confirmed by pathology evaluation of core biopsy.
Early-stage TNBC according to the American Joint Committee on Cancer (AJCC) Staging Manual Clinical Stage I (T1c, > 1.5 cm), Stage II or Stage III invasive breast cancer.
Tumors must be ER/PgR status negative (IHC < 1%) and lack of HER2/neu overexpression or amplification as measured by local hospital pathology laboratory (IHC +/- fluorescence in situ hybridization (FISH) and IHC < 3+, and FISH < 2.2) as described in the NCCN Guidelines.
Patient must consent to a minimum of 1 tumor-containing formalin fixed paraffin embedded core (or archival tissue) or baseline research biopsy.
Eastern Cooperative Oncology Group Performance Status 0 or 1.
Adequate hematologic function (absolute neutrophil count ≥ 1,500 cells/µL; hemoglobin

9 g/dL, platelets > 100,000/µL.).

Adequate renal function (serum creatinine ≤ 1.5 mg/dL or calculated creatinine clearance ≥ 60 mL/min using Cockcroft-Gault equation).
Adequate hepatic function: total bilirubin ≤ upper limit of normal (ULN), serum albumin ≥≥ 3.0 g/dL, alanine aminotransferase and aspartate aminotransferase ≤ 1.5 x ULN.
Prothrombin time and/or international normalized ratio (INR) ≤ 1.5 x ULN and activated partial thromboplastin time ≤ 1.5 x ULN, if patient is not on anticoagulant therapy.
Female patients must have a negative serum human chorionic gonadotropin test within 1 week of Day 1 (pregnancy test not required for patients with bilateral oophorectomy and/or hysterectomy or for those patients who are > 1 year postmenopausal
Women of childbearing potential must avoid becoming pregnant and men must avoid fathering a child during and for 3 months after the end of study treatment.

Exclusion Criteria:

Surgically unresectable, inflammatory, or metastatic breast cancer.
Any prior treatment for current breast cancer including chemotherapy, hormonal therapy, radiation, or other experimental therapy.
Known history of bleeding diathesis or coagulopathy (e.g., von Willebrand disease or hemophilia).
Clinically significant bleeding, such as gross hematuria, gastrointestinal bleeding before screening (if clinically significant bleeding has occurred within 6 months of screening, but the cause has been identified and adequately treated [e.g., cystitis, ulcer], then this exclusion criterion does not apply. Minor biopsy-related bleeding lasting < 24 hours and resolved at least 1 week before Day 1 is allowed.
Thromboembolic events (e.g., deep vein thrombosis, pulmonary embolism, or arterial thrombosis) occurring within 6 months before screening.
Uncontrolled intercurrent disease (e.g., diabetes, hypertension, thyroid disease, active infections).
Autoimmune disease requiring treatment with chronic systemic immunosuppressive therapy. Prior allotransplantation.
History of hypersensitivity to any of the excipients of paclitaxel (e.g., Cremaphor).
Has an active infection requiring systemic therapy.
Major surgery within 4 weeks prior to Day 1
Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the subject's participation for the full duration of the trial, or is not in the best interest of the subject to participate, in the opinion of the treating investigator.
Investigational therapy within 28 days prior to Day 1.
Is pregnant or breastfeeding, or expecting to conceive within the projected duration of the trial.
Has a known history of human immunodeficiency virus (HIV) (HIV1/2 antibodies) or active hepatitis B (e.g., HBsAg reactive) or hepatitis C (e.g., hepatitis C virus RNA [qualitative] is detected.