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Trial · NCT01791894

Arsenic Trioxide in Treating Patients With Basal Cell Carcinoma

NCT01791894, Phase 1, Phase 2, Completed, Stanford University; results first posted 2016-10-28

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. Arsenic Trioxide in Treating Patients With Basal Cell Carcinoma. Trials, record NCT01791894. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01791894

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Arsenic Trioxide in Treating Patients With Basal Cell Carcinoma
NCT number
NCT01791894
Status
Completed
Phases
Phase 1, Phase 2
Enrollment
5 participants, actual
Lead sponsor
Stanford University
Conditions
Basal Cell Carcinoma of the Skin, Recurrent Skin Cancer
Interventions
arsenic trioxide
First posted
2013-02-15
Last updated
2018-06-08
Results first posted
2016-10-28

Source ClinicalTrials.gov

Registered outcomes4

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryPercent Change in Biomarker (GLI2 Protein) Levelsbaseline to day 33
SecondaryPatients With Stable Disease Post TreatmentAfter 3 cycles of treatment (approx. 61 days)Number of patients with stable disease post treatment by RECIST criteria
SecondaryPatients With Progressive Disease Post Treatment by RECIST CriteriaAfter 3 treatment cycles (approx. 61 days)Patients with a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions
SecondaryIncidence of Grade 3/4 Adverse Events as Assessed by Common Terminology Criteria for Adverse Events (CTCAE) Version 3.0Baseline to cycle 3

Outcomes4

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYPercent Change in Biomarker (GLI2 Protein) Levelsbaseline to day 33We recruited patients with biopsy-confirmed metastatic basal cell carcinoma who were had progressed on SMO inhibitors such as vismodegib (GDC 0449), IPI- 926, LEQ506 and LDE225.percentage decreaseMEAN
SECONDARYPatients With Stable Disease Post TreatmentAfter 3 cycles of treatment (approx. 61 days)4 patients completed 3 cycles of treatmentparticipantsNUMBER
SECONDARYPatients With Progressive Disease Post Treatment by RECIST CriteriaAfter 3 treatment cycles (approx. 61 days)participantsNUMBER
SECONDARYIncidence of Grade 3/4 Adverse Events as Assessed by Common Terminology Criteria for Adverse Events (CTCAE) Version 3.0Baseline to cycle 3number of occurrencesNUMBER

Results by group4

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Percent Change in Biomarker (GLI2 Protein) LevelsTreatment (Arsenic Trioxide)75Standard Deviation 11percentage decrease
Patients With Stable Disease Post TreatmentTreatment (Arsenic Trioxide)3participants
Patients With Progressive Disease Post Treatment by RECIST CriteriaIV ATO1participants
Incidence of Grade 3/4 Adverse Events as Assessed by Common Terminology Criteria for Adverse Events (CTCAE) Version 3.0IV ATO2number of occurrences

Participant flow3

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDIV ATO5
Overall StudyCOMPLETEDIV ATO4
Overall StudyNOT COMPLETEDIV ATO1

Adverse events4

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
othergrade 1 asymptomatic atrial flutterCardiac disordersTreatment (Arsenic Trioxide)151
othertransaminitisInvestigationsTreatment (Arsenic Trioxide)151
seriousgrade 3 infectionBlood and lymphatic system disordersTreatment (Arsenic Trioxide)151
seriousgrade 4 leukopeniaBlood and lymphatic system disordersTreatment (Arsenic Trioxide)151

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityTreatment (Arsenic Trioxide)
Total, other adverse eventsTreatment (Arsenic Trioxide)15
Total, serious adverse eventsTreatment (Arsenic Trioxide)15

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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT01791894

GET https://conductscience.org/api/trials/v1/NCT01791894/registered