Oral Paclitaxel + Encequidar vs IV Paclitaxel in Treatment of HER2 Negative Metastatic Breast Cancer

Launched by HEALTH HOPE PHARMA · Feb 14, 2025

Keywords

ClinConnect Summary

This clinical trial is studying a new way to treat metastatic breast cancer, specifically for patients whose cancer is HER2 negative. The researchers want to see if an oral medication called Paclitaxel, combined with another drug called Encequidar, can be as effective as the standard intravenous (IV) Paclitaxel that many patients currently receive. The trial will first determine the best dose of the oral medication and then compare it to the IV treatment to see which works better.

To join the trial, participants need to be at least 18 years old and have a confirmed diagnosis of HER2 negative metastatic breast cancer. They should also not have received certain other cancer treatments recently and must meet specific health guidelines, such as having good blood counts and liver function. If eligible, participants will receive either the oral treatment or the IV treatment and will be monitored closely by the research team. It's important for potential participants to discuss this trial with their healthcare provider to understand if it's the right option for them.

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Eligibility criteria

• Inclusion Criteria:
• • 1. Signed written informed consent
• • 2. ≥18 years of age
• • 3. Histologically or cytologically confirmed HER2 negative breast cancer for whom IV paclitaxel monotherapy has been recommended.
• • 4. HER2 negative per American Society of Clinical Oncology (ASCO) College of American Pathologists (CAP) guideline. Subjects can be estrogen receptor/progesterone receptor (ER/PR) positive or negative per ASCO CAP guideline, but ER/PR and HER2 receptor status must be known.
• • 5. Metastatic breast cancer with target lesions measurable by CT scan per RECIST v1.1 criteria confirmed by BICR
• 6. Adequate hematologic status as demonstrated by not requiring granulocyte colony stimulating factor (G CSF) or transfusion support within 30 days prior to randomization to achieve the following at screening:
• • Absolute neutrophil count (ANC) ≥1500/mm3
• • Platelet count ≥100,000/mm3
• • Hemoglobin ≥9 g/dL
• 7. Adequate liver function as demonstrated by:
• • Total bilirubin ≤upper limit of normal (ULN) unless the subject has Gilbert's disease, for which bilirubin must be ≤2.0 × ULN
• • Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤1.5 × ULN
• • 8. Adequate renal function as demonstrated by estimated glomerular filtration rate (eGFR) ≥60 mL/min
• • 9. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
• • 10. Life expectancy at least 6 months, in the judgment of the Investigator
• • 11. Female subjects must be postmenopausal (≥12 months without menses) or surgically sterile (ie, by hysterectomy, bilateral oophorectomy, or bilateral tubal ligation) or must be using effective contraception (ie, non-hormonal intrauterine device, double barrier method of condom and spermicide) and agree to continue use of contraception for 30 days after their last dose of assigned study treatment.
• • 12. Women of childbearing potential must have a negative screening serum pregnancy test and urine test within 4 days prior to start of dosing in the study and not be breast feeding.
• • 13. Sexually active male subjects must use a barrier method of contraception during the study and agree to continue the use of male contraception for at least 30 days after the last dose of investigational product (IP).
• Exclusion Criteria:
• • 1. Not recovered to ≤grade 1 toxicity from previous anticancer treatments or previous investigational product (IP) except alopecia
• • 2. QTcF interval ≥470 msec at baseline
• • 3. Relapsed less than 6 months following treatment with a taxane (paclitaxel or docetaxel) as part of anthracycline-based adjuvant chemotherapy or for metastatic disease
• • 4. Known active central nervous system metastasis, including leptomeningeal involvement
• • 5. Currently receiving other medications intended for the treatment of their malignancy
• • 6. Received other IPs within 14 days or 5 half-lives of the first study dosing day, whichever is longer
• • 7. Received biologics or monoclonal antibodies intended for the treatment of their malignancy within 30 days of the first study dosing day
• • 8. Received radiation therapy within 2 weeks prior to signing informed consent or radiation therapy is planned within 6 months from the time of signing informed consent
• • 9. Taking a medication known to be a moderate or strong cytochrome P450 (CYP) 3A4 inhibitor or inducer or neurokinin-1 receptor antagonist (NK-1) inhibitor within 14 days prior to start of dosing in the study
• • 10. Taking a medication known to be a moderate or strong CYP2C8 inhibitor or inducer within 14 days prior to start of dosing in the study
• • 11. Taking an oral medication with a narrow therapeutic index known to be a P-glycoprotein (P-gp) substrate within 24 hours prior to start of dosing in the study
• • 12. Taking a medication known to be a P-gp inhibitor or inducer within 14 days prior to start of dosing in the study
• • 13. Taking a medication known to be an organic anion transporting polypeptide 1B1/3 (OATP1B1/3) inhibitor
• • 14. Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, myocardial infarction within the last 6 months, unstable angina pectoris, cardiac arrhythmia, chronic pulmonary disease requiring oxygen, known bleeding disorders, or any concomitant illness or social situation that would limit compliance with study requirements
• • 15. Major surgery to the upper GI tract, inability to take oral medication, or have a history of GI disease or other medical condition that, in the opinion of the Investigator may interfere with oral drug absorption
• • 16. History of significant hypersensitivity-type reaction to paclitaxel or Cremophor EL that would contraindicate the use of IV paclitaxel
• • 17. Known allergic reaction or intolerance to contrast media
• • 18. Documented history of true systemic allergic reaction to 3 or more medications
• • 19. Active hepatitis B (as evidenced by being HBsAg positive) or active hepatitis C (HCV-RNA positive) or cirrhosis of the liver
• • 20. Known HIV infection
• • 21. The Investigator believes that participation in this study would not be acceptable