Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01700049 · ClinicalTrials.gov registry record · Phase 2

Study Evaluating the Efficacy of Oral Vismodegib in Various Histologic Subtypes

A Phase 2 study, sponsored by Mayo Clinic.

Completed
Registry status
Phase 2
Development phase
28
Enrollment target

NCT01700049: Completed Phase 2 study, sponsored by Mayo Clinic.

NCT01700049 is a Phase 2 study that has completed, run by Mayo Clinic. The registered enrollment target is 28 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (79% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT01700049, a Phase 2 study, has completed, sponsored by Mayo Clinic.

COMPLETED
Registry status
Phase 2
Development phase
28 participants
Enrollment target

Study Summary

The purpose of this study is to investigate the safety and effectiveness of oral vismodegib therapy in the treatment of different 'histologic subtypes' of basal cell skin cancer (BCC). The term 'histologic subtype' refers to how the cells and tumor tissue looks under the microscope. Three different 'histologic subtypes' of basal cell skin cancer (infiltrative/morpheaform, nodular and superficial) will be examined in this study.

Primary Outcome

The efficacy of vismodegib was defined as the number of tumor biopsies with positive pathology after 24 weeks. Subjects had one target lesion and up to 3 additional non-target lesions. A cumulative total of 65 tumors was measured after 24 weeks of treatment. Histopathological subtypes were categorized primarily as infiltrative, nodular and superficial.

Interventions

  • DRUG vismodegib (150 mg PO daily)

Trial Details

FieldValue
Enrollment Target 28 participants
Start Date 2013-01-14
Est. Completion 2018-07-03
Phase Phase 2
Mayo Clinic

2,844 total trials

What the finished NCT01700049 record still lists

NCT01700049 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 28 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (79% lower).

The record links to 0 conditions, and to 1 intervention - of which vismodegib (150 mg PO daily) is the first listed.

NCT01700049 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01700049 about?

NCT01700049 is a clinical study titled "Study Evaluating the Efficacy of Oral Vismodegib in Various Histologic Subtypes". The purpose of this study is to investigate the safety and effectiveness of oral vismodegib therapy in the treatment of different 'histologic subtypes' of basal cell skin cancer (BCC). The term 'histologic subtype' refers to how the cells and tumor tissue looks under the microscope. Three different ...

What is the current status of trial NCT01700049?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 28 participants. The study started on 2013-01-14. Estimated completion is 2018-07-03.

What interventions are being tested in trial NCT01700049?

The interventions under investigation include: vismodegib (150 mg PO daily) (DRUG).

Who is sponsoring clinical trial NCT01700049?

This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01700049's enrollment target sits among peer trials

28 1677th of 2000 higher than 304 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03471117 · 28 participants · Phase 4

    Pioglitazone to Reduce Sympathetic Overactivity in CKD Patients

  • NCT03523975 · 28 participants · Phase 1

    Venetoclax, Lenalidomide and Rituximab in Patients With Previously Untreated Mantle Cell Lymphoma

  • NCT03608631 · 28 participants · Phase 1

    iExosomes in Treating Participants With Metastatic Pancreas Cancer With KrasG12D Mutation

  • NCT03810651 · 28 participants · Early Phase 1

    Pencil Beam Scanning in Patients With Renal Tumors

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT01700049, the US trial registry maintained by the National Library of Medicine. NCT01700049 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.