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Updated: May 3, 2026

Cell Population Analyses During Skin Carcinogenesis
Published on: August 21, 2013
Smoothened inhibitors in the treatment of advanced basal cell carcinomas
1Division of General Dermatology, Department of Dermatology, Medical University of Vienna, Vienna, Austria.
Purpose Of Review:
The Hedgehog pathway has been identified as a key element in the development of many forms of cancer. Smoothened (Smo) inhibitors are known to beneficially interfere with the Hedgehog pathway and are currently under investigation as anticancer drugs for many tumor entities. Reviewed here are the most recent developments in clinical research on Smo inhibitors for the treatment of advanced basal cell carcinoma (BCC).
Recent Findings:
When reviewing the literature of the past 12 months, it is striking to see the rapid evolution of the field. Compounds that have been presented as powerful new drug candidates 12 months ago have now been discontinued, whereas new ones have emerged. Reports on 13 drug candidates have been identified: one marketed, vismodegib, eight currently under development (phase I-II) and four for which clinical investigation for BCC is currently not being pursued.
Summary:
Smo inhibitors are a promising drug class for the treatment of BCC. To date, most candidates are in early stage development and are expected to enter the market in approximately 5-8 years, if successful.
Insights
Smoothened (Smo) inhibitors show promise for treating advanced basal cell carcinoma (BCC) by targeting the Hedgehog pathway. While the field is rapidly evolving, new drug candidates are emerging for this cancer treatment.
Area of Science:
- Oncology
- Molecular Biology
- Dermatology
Background:
- The Hedgehog pathway is crucial in the development of various cancers.
- Smoothened (Smo) inhibitors disrupt the Hedgehog pathway and are investigated as anticancer agents.
- Advanced basal cell carcinoma (BCC) is a significant target for novel cancer therapies.
Purpose of the Study:
- To review recent clinical research developments in Smo inhibitors for advanced BCC treatment.
- To assess the current landscape of Smo inhibitor drug candidates in clinical development.
- To understand the therapeutic potential of Smo inhibitors in oncology.
Main Methods:
- Literature review of clinical research on Smo inhibitors over the past 12 months.
- Identification and categorization of drug candidates based on development stage.
- Analysis of clinical investigation status for BCC.
Main Results:
- The field of Smo inhibitors has evolved rapidly in the last year.
- Thirteen drug candidates were identified: one marketed (vismodegib), eight in early-stage development (Phase I-II), and four not currently pursued for BCC.
- Many previously promising compounds have been discontinued, with new candidates emerging.
Conclusions:
- Smo inhibitors represent a promising therapeutic class for BCC.
- Most Smo inhibitor candidates are in early development stages.
- Successful candidates may reach the market in 5-8 years, pending further clinical trials.
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