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Search / Trial NCT04664829

The Role of Bexarotene in Inducing Susceptibility to Chemotherapy in Metastatic TNBC

Launched by NATIONAL CANCER CENTRE, SINGAPORE · Dec 7, 2020

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Bexarotene

ClinConnect Summary

This clinical trial is studying a drug called Bexarotene to see if it can help make chemotherapy more effective for women with metastatic triple-negative breast cancer (TNBC). TNBC is a type of breast cancer that is known to be aggressive and can be tough to treat, especially when patients have already received certain chemotherapy drugs and their cancer has continued to grow. The researchers believe that by changing the state of the cancer cells, they may be able to make them more responsive to future treatments.

To participate in this trial, women must be at least 21 years old and have been diagnosed with metastatic TNBC that has not improved after receiving prior treatment with a certain type of chemotherapy called taxanes. Participants will undergo tests to ensure they are healthy enough for the study and will have the chance to have their cancer biopsied (a small sample taken) before, during, and after the treatment. The trial is currently recruiting participants and aims to provide insight into new ways to tackle this challenging form of cancer.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Patients with histologically or cytologically proven metastatic TNBC
  • Patients whose TNBC has progressed after prior taxane therapy in the (neo)adjuvant or metastatic setting, and have not received Capecitabine or 5-fluorouracil
  • Females aged 21 years and older
  • ECOG performance status 0 or 1
  • Life expectancy greater than three months
  • Patients have normal organ and marrow function
  • Site(s) of disease amenable to serial bedside biopsies before, during and after study treatment
  • Exclusion Criteria:
  • Previous palliative radiotherapy to potentially biopsy-able lesion
  • Active symptomatic central nervous system (CNS) metastases
  • Spinal cord compression not definitively treated with surgery and/or radiation
  • Uncontrolled pleural effusion, pericardial effusion, ascites requiring recurrent drainage procedures

About National Cancer Centre, Singapore

The National Cancer Centre Singapore (NCCS) is a leading institution dedicated to cancer treatment, research, and education in Asia. As a premier clinical trial sponsor, NCCS focuses on advancing oncology through innovative therapies and comprehensive clinical studies. With a multidisciplinary team of experts and state-of-the-art facilities, the center is committed to improving patient outcomes and contributing to global cancer research initiatives. NCCS actively collaborates with various stakeholders, including academic institutions and pharmaceutical companies, to foster groundbreaking discoveries and enhance the understanding of cancer management and treatment.

Locations

Singapore, , Singapore

Patients applied

0 patients applied

Trial Officials

Elaine Lim, MD

Principal Investigator

National Cancer Centre, Singapore

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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