CI

At a glance

ClinicalIndex Comparison Record
N/ARecruiting· 80 target
Drug / intervention
Vismodegib +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05463757
NCT05463757N/ARecruitingMonitorUpdated 14mo ago · Completion was 1mo ago
Slow Enrollment
Long Recruiting
Monitor

Registration of Oral Hedgehog Inhibitors Vismodegib and Sonidegib in the Treatment of Advanced and Multiple Basal Cell Carcinoma in the Netherlands: a Prospective Registration Study.

Maastricht University Medical Center·observational·Posted Jul 19, 2022·Updated Apr 4, 2025

In Brief

An observational study evaluating Vismodegib and Sonidegib for Basal Cell Carcinoma and 10 related conditions. Currently recruiting, targeting 80 participants across 8 sites.

Signals

Enrolling slower than its timeline implies

Detailed Summary

Background: Oral hedgehog inhibitors vismodegib and sonidegib have been used for the treatment of locally advanced (laBCC), metastatic basal cell carcinoma (mBCC) and in basal cell nevus syndrome (BCNS) patients. In the Netherlands, targeted therapy with vismodegib and sonidegib has been available since 2013 and 2021, respectively. No direct comparative studies have been performed between the two oral hedgehog inhibitors (HHI) vismodegib and sonidegib yet . In addition, data for sonidegib are not yet available. Objective: The aim of this study is 1) to evaluate the effectiveness of oral HHIs in the treatment of laBCC, mBCC and BCNS patients and 2) to compare the oral HHIs vismodegib and sonidegib. Study design: prospective registration study that includes all patients, regardless of age and gender, with histologically proven basal cell carcinoma receiving treatment with either vismodegib or sonidegib in the Netherlands. Patient, tumor and treatment information was gathered from patient records. Main study parameters/endpoints: The primary outcome for measuring efficacy/tumor response was median progression free survival (PFS) where the decrease, stagnation or increase in tumor size is measured by maximum diameter. Secondary outcomes are frequency, severity and reversibility of treatment-emergent adverse events and disease-specific quality of life expressed as mean scores on the EORTC-QLQ-C30 and aBCCdex questionnaires.

Study Details

Timeline

N/ARecruiting
202220232024202520262027
First PostedJul 19, 2022
Enrollment StartNov 1, 2021
Primary CompletionJun 1, 2026
Study CompletionDec 1, 2026
TodayJul 1, 2026
Enrollment to primary: 4.6 yearsPosted 3.9 years ago

Interventions

Vismodegibdrug

Oral vismodegib (Erivedge), taken daily or every other day (depending on doctor's description)

Sonidegibdrug

Sonidegib (Odomzo), taken daily or every other day (depending on doctor's description)