Phase I/IIa Study of Pharmacokinetics and Safety of Epidiferphane™ and Taxanes in Breast Cancer Patients

Phase 1

Withdrawn

• Conditions: Breast Cancer
• Interventions: Drug: Epidiferphane; Drug: Taxane Chemotherapy

• Registration Number: NCT03611985
• Lead Sponsor: University of Florida

Brief Summary

Patients with breast cancer are commonly treated with taxane chemotherapy. Some very common side effects of taxanes, such as anemia and peripheral neuropathy, are often as not well addressed during treatment, resulting in dose reductions, dose delays and early discontinuation (collectively called relative dose intensity) of these chemotherapy agents in 15-80 % of patients on these drugs. This reduction in relative dose intensity (RDI) results in worse clinical outcomes such as progression free and overall survival. Pre-clinical studies in mouse models subjected to standardized chemotherapy regimens containing paclitaxel or oxaliplatin have shown that the nutritional supplement Epidiferphane™ reduces both neuropathy and anemia. This study will investigate whether the use of Epidiferphane™ in patients with breast cancer receiving taxane chemotherapy results in an attenuation of the side effects experienced, as well as an improvement in tumor response rate. The safety and maximum tolerated dose of Epidiferphane™ in this patient population will also be determined in this study.

Detailed Description

Not available

Basic Information
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Recruitment & Eligibility
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Study & Design

Study Timeline

• Study First Submitted: 2018-07-06
• Study First Submitted QC: 2018-07-26
• Study First Posted: 2018-08-02
• Status Verified: 2020-01
• Last Update Submitted: 2020-01-09
• Last Update Posted: 2020-01-13
• Study Start: 2020-03
• Primary Completion: 2023-03
• Study Completion: 2023-03

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• Must be at least 18 years of age
• Subjects on the phase I portion must have a clinical diagnosis of metastatic breast cancer. Subjects on the phase IIa portion must have a clinical diagnosis of breast cancer of any stage and histology.
• Must be about to start a new chemotherapy treatment regimen containing either paclitaxel given weekly or docetaxel given every 3 weeks at UF Health
• Must continue cancer therapy at UF Health for at least the next three months
• A functioning digestive tract with no obstruction
• Subjects must be willing to avoid regular consumption of green tea for the duration of trial participation.
• Written informed consent obtained from the subject or the subject's legal representative and the ability for the subject to comply with all the study-related procedures.
• Women of childbearing potential (WOCBP) must be using an adequate method of contraception to avoid pregnancy throughout the study.
• Males with female partners of child-bearing potential must agree to use physician-approved contraceptive methods (e.g., abstinence, condoms, vasectomy) throughout the study.

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Exclusion Criteria

• Must not be receiving any other investigational agents
• Females or males of childbearing potential who are unwilling or unable to use an acceptable method to avoid pregnancy for the entire study period and following completion of taxane therapy for an additional 6 months for women of child bearing potential and 3 months for men with partners of child bearing potential.
• Females who are pregnant or breastfeeding
• Active systemic infection considered to be opportunistic, life threatening or clinically significant at the time of treatment.
• Psychiatric illness or social situation that would limit compliance with trial requirements.
• Known allergy to turmeric, broccoli, or green tea.
• Subjects must not be on treatment with verapamil or tacrolimus during the trial.
• History of any other disease, metabolic dysfunction, physical examination finding, or clinical laboratory finding (e.g. hemoglobin < 10 mg/dL, CTCAE v 5.0 grade 3 or higher neutropenia or thrombocytopenia) giving reasonable suspicion of a disease or condition that contraindicates the use of protocol therapy or that might affect the interpretation of the results of the study or that puts the subject at high risk for treatment complications, in the opinion of the treating physician.
• Prisoners or subjects who are involuntarily incarcerated.
• Subjects who are compulsorily detained for treatment of either a psychiatric or physical illness.
• Subjects demonstrating an inability to comply with the study and/or follow-up procedures.
• CTCAE v 5.0 grade 2 or higher peripheral sensory or motor neuropathy
• CTCAE v 5.0 grade 1 or higher paresthesia
• Alanine aminotransferase (ALT) or Aspartate aminotransferase (AST) >2.5 × the upper limit of normal (ULN)
• Total bilirubin (TBL) >1.5 × ULN or >3 × ULN in the presence of documented Gilbert's Syndrome (unconjugated hyperbilirubinemia)
• Glomerular filtration rate (GFR) <50 mL/min

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SEQUENTIAL

Arm && Interventions

Group	Intervention	Description
Epidiferphane + taxane chemotherapy	Epidiferphane	-
Epidiferphane + taxane chemotherapy	Taxane Chemotherapy	-

Primary Outcome Measures

Name	Time	Method
Cmax of Epidiferphane's components	24 hours	The Cmax of each of Epidiferphane's components will be based on blood concentration measured prior to taxane chemotherapy administration, as well as at 1, 2 and 24 hours after taxane chemotherapy administration.
Rate of occurrence of DLTs by dose level in patients with breast cancer who are being treated with taxanes	4 months	This will be assessed by the rate of occurrence of DLTs by Epidiferphane dose level
Maximum tolerated dose of Epidiferphane in patients with breast cancer who are being treated with taxanes	3 months
Cmax of taxanes	3 weeks	The Cmax of the taxane chemotherapy agents given will be based on blood concentrations measured prior to taxane chemotherapy administration, as well as at 1, 2 and 24 hours after taxane chemotherapy administration.
Number of adverse events (graded according to CTCAE v5.0 criteria) by epidiferphane dose level	4 months
Concentration at 24 hours (C24 hours) of Epidiferphane's components	24 hours	The C24 hours of each of Epidiferphane's components will be based on blood concentration measured 24 hours after taxane chemotherapy administration.
Concentration at 24 hours (C24 hours) of taxanes	24 hours	The C24 hours of the taxanes given will be based on blood concentration measured 24 hours after taxane chemotherapy administration.

Secondary Outcome Measures

Name	Time	Method
Change in CTCAE grade 2 or higher neuropathy and anemia, as compared to historically reported rates for the occurrence of each of these events	4 months
Effect of Epidiferphane on tumor response rate, as measured by RECIST 1.1 criteria and pathologic tumor response at surgery	3 months
Effect of Epidiferphane on the neuropathy marker NF-kB, as measured by multiplex cytokine bead analysis	3 weeks
Effect of Epidiferphane on the neuropathy marker VEGFA, as measured by multiplex cytokine bead analysis	3 weeks
Effect of Epidiferphane on the neuropathy marker Nrf2, as measured by multiplex cytokine bead analysis	3 weeks
Effect of Epidiferphane on the neuropathy marker IL18, as measured by multiplex cytokine bead analysis	3 weeks
Effect of Epidiferphane on quality of life, as measured by the EORTC QLQ-C30 scale	3 months	The EORTC QLQ-C30 measures ability to perform everyday activities and whether the subject has experienced select physical symptoms on a scale of 1-4 (with 1 meaning "Not at all" and 4 meaning "Very much"), as well as overall quality of life and overall healt over the past week on a scale from 1-7 (with 1 meaning "Very Poor" and 7 meaning "Excellent").
Effect of Epidiferphane on quality of life, as measured by the FACT-Taxane scale	3 months	The FACT-Taxane measures various aspects of physical, social, emotional, and functional well-being, as well as whether the subject has experienced select physical symptoms over the past 7 days, on a scale of 0-4 (with 0 meaning "Not at all" and 4 meaning "Very much").