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Trial · NCT01815840

Outcomes12

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYMean Percent Change From Baseline in the Number of Clinically Evident Basal Cell Carcinomas at Week 73 (After 72 Weeks of Treatment)Baseline; Week 73
Participants in the Intent-to-Treat analysis population (defined as all randomized participants) with available data were included in the analysis. The last observation carried forward method was used.
percent changeMEAN
SECONDARYPercentage of Participants Who Discontinued Study Treatment Due to Tolerability IssuesBaseline to Week 73Intent-to-Treat Analysis Population, defined as all randomized participants.percentage of participantsNUMBER
SECONDARYMean Percent Change From Baseline in Total Size of Three Target Basal Cell Carcinoma Lesions in Individual Participants at Week 73Baseline; Week 73Participants in the Intent-to-Treat Analysis Population (defined as all randomized participants) with available data were included in the analysis.percent changeMEAN
SECONDARYPercentage of Participants With at Least 50% Reduction in the Number of Basal Cell Carcinomas at Week 73Baseline; Week 73Intent-to-Treat Analysis Population, defined as all randomized participants.percentage of participantsNUMBER
SECONDARYPercentage of Participants With New Basal Cell Carcinomas at Week 73Baseline; Week 73Participants in the Intent-to-Treat Analysis Population (defined as all randomized participants) with available data were included in the analysis.percentage of participantsNUMBER
SECONDARYPercent Change in Total Number of Basal Cell Carcinomas Relative to Baseline at Week 85 (12 Weeks Following End of Treatment) (Recurrence Rate)Baseline; Week 85Participants in the Intent-to-Treat Analysis Population (defined as all randomized participants) with available data were included in the analysis.percent changeMEAN
SECONDARYPercent Change in Total Number of Basal Cell Carcinomas Relative to Baseline at Week 97 (24 Weeks Following End of Treatment) (Recurrence Rate)Baseline; Week 97Participants in the Intent-to-Treat Analysis Population (defined as all randomized participants) with available data were included in the analysis.percent changeMEAN
SECONDARYPercent Change in Total Number of Basal Cell Carcinomas Relative to Baseline at Week 125 (52 Weeks Following End of Treatment) (Recurrence Rate)Baseline; Week 125Participants in the Intent-to-Treat Analysis Population (defined as all randomized participants) with available data were included in the analysis.percent changeMEAN
SECONDARYPercentage of Participants Experiencing Any Adverse EventUp to 125 weeksSafety Analysis Population: participants in the Intent-to-Treat Analysis Population (defined as all randomized participants) who received at least one dose of study treatment.percentage of participantsNUMBER
SECONDARYPercent Change From Baseline in the Skindex-16 Symptom Domain Score at Week 73Baseline; Week 73Participants in the Intent-to-Treat Analysis Population (defined as all randomized participants) with available data were included in the analysis.percent changeMEAN
SECONDARYPercent Change From Baseline in the Skindex-16 Emotion Domain Score at Week 73Baseline; Week 73Participants in the Intent-to-Treat Analysis Population (defined as all randomized participants) with available data were included in the analysis.percent changeMEAN
SECONDARYPercent Change From Baseline in the Skindex-16 Function Domain Score at Week 73Baseline; Week 73Participants in the Intent-to-Treat Analysis Population (defined as all randomized participants) with available data were included in the analysis.percent changeMEAN

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

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

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Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT01815840/outcomes