Trial · NCT04664829
The Role of Bexarotene in Inducing Susceptibility to Chemotherapy in Metastatic TNBC
NCT04664829, Phase 1, Completed, National Cancer Centre, Singapore
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. The Role of Bexarotene in Inducing Susceptibility to Chemotherapy in Metastatic TNBC. Trials, record NCT04664829. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04664829
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- The Role of Bexarotene in Inducing Susceptibility to Chemotherapy in Metastatic TNBC
- NCT number
- NCT04664829
- Status
- Completed
- Phases
- Phase 1
- Enrollment
- 12 participants, actual
- Lead sponsor
- National Cancer Centre, Singapore
- Conditions
- Metastatic Triple-Negative Breast Carcinoma
- Interventions
- Bexarotene, Capecitabine
- First posted
- 2020-12-11
- Last updated
- 2025-09-23
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Tumour transcriptome by RNA sequencing | From time of first biopsy before the start of treatment, to disease progression, up to 2 years | To characterize the changes in tumour transcriptome upon treatment |
| Primary | Tumour protein profile by multiplex immunohistochemistry | From time of first biopsy before the start of study treatment, to disease progression, up to 2 years | To characterize the changes in tumour protein profile upon treatment |
| Secondary | Incidences of treatment related adverse events | From time of start of study treatment, to 28 days after last dose of study treatment, up to 2 years |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT04664829
GET https://conductscience.org/api/trials/v1/NCT04664829/registered