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Recruiting Phase 1/2

A Study to Evaluate Safety and Efficacy of BEY1107 in Combination with Capecitabine in Patients with Metastatic Colorectal Cancer

NCT05093907 · tracked via the Priya Life Science South Korea tracker
Phase
Phase 1/2
Started
2021-08-31
Last updated
2025-03-10

Condition(s) studied

Metastatic Colorectal Cancer

Investigational drug(s) / intervention(s)

BEY1107 →Capecitabine

BEY1107: Administer once daily, PO, 3-week continuous dose.

Capecitabine: Administer twice daily, PO, 2-week continuous dose, followed by 1-week rest period.

Study summary

This is a Phase 1/2 study to evaluate the maximum tolerated dose, safety and efficacy of BEY1107 in combination with capecitabine in patients with metastatic colorectal cancer refractory or intolerant to standard of care (SoC).

Eligibility

Sex
ALL
Min age
19 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Adult males and females aged over 19 years or older at the time of Informed Consent. 2. Histopathologically or cytologically diagnosed with colorectal cancer. 3. Patients with unresectable metastatic lesion(s). 4. Patients who experienced treatment failure of colorectal cancer with the second-line or beyond standard chemotherapy (including fluoropyrimidine, oxaliplatin and irinotecan). 5. Subjects who have at least one measurable or evaluable lesion as per RECIST v1.1. 6. Subjects with ECOG performance status 0 or 1. 7. Women of childbearing potential who are not surgically sterile must consent to practice acceptable contraception until 6 months after the end of IP administration and also have the evidence of not being fertile. 8. Non-vasectomized men who consent to use an acceptable contraception by one-self and the partner until 3 months after the end of IP administration. 9. Patients who are fully informed of this trial, voluntarily decide to participate in the trial and provide written consent to comply with requirements for the trial. Exclusion Criteria: 1. Patients who received radiation therapy, chemotherapy or biological agent including hormone therapy recently. 2. Subjects who had a surgery with general anesthesia within 4 weeks of screening. 3. Subjects with symptomatic brain metastasis. 4. Subjects with peripheral neuropathy. 5. Subjects who had findings of affecting absorptin of the IP with gastrointestinal surgery or impossible oral drug administration. 6. Subjects with systemic disease not suitable for anticancer agent administration at the discretion of the investigator. 7. Subjects who had a cardiovascular disease as of screening. 8. Subjects with history of malignancy other than basal cell carcinoma of the skin or cervical carcinoma in situ or papillary thyroid cancer appropriately treated within 5 years. 9. Gastrointestinal bleeding or ulcer. 10. Dihydro-Pyridine Dehydrogenase (DPD) deficiency. 11. Galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption. 12. Hypersensitivity to the ingredient(s) of the investigational product (BEY 1107) or capecitabine, 5-FU (fluorouracil). 13. HIV Positive. 14. Ineligible result of HBV, HCV by the investigator. 15. Acute or severe infection. 16. Subjects who take a Sorivudine or brivudine in combination. 17. Subjects who take a combination of tegafur, gimeracil and oteracil potassium or discontinue within 7 days at the screening. 18. Subjects who take a Rifampin and azole class antifungal drugs in combination. 19. Subjects who has labortory findings of inadequate bone marrow, kidney and liver function. 20. Pregnant women, breastfeeding women, or positive findings on the pregnancy test at screening. 21. Subjects with life expectancy of less than 12 weeks by the investigator. 22. Subjects who had been administered other IP within 4 weeks prior to screening. 23. Subjects determined by the investigator to be ineligible for participation in this trial.

Primary outcome measure(s)

  • Maximum Tolerated Dose(MTD) assessed by investigator following administration of BEY1107 in combination with Capecitabine — From baseline up to disease progression, approximately 54 weeks
    MTD will be assessed based on adverse events(including DLT assessment), vital signs, 12-lead ECG, laboratory tests, etc.
  • Objective Response Rate(ORR)(Phase 2) assessed by investigator following administration of BEY1107 in combination with Capecitabine — From baseline up to disease progression, approximately 54 weeks
    ORR defined as proportion of subjects with a overall response of CR or PR

Trial sites (1)

FacilityCityRegionStatus
Seoul National University Hospial Seoul Jongro-go Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05093907 on ClinicalTrials.gov ↗ ← All trials in South Korea