Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-26 @ 10:46 PM
Ignite Modification Date:
2025-12-26 @ 10:46 PM
NCT ID:
NCT02366312
Eligibility Criteria:
Inclusion Criteria:
* Males and females, 18 years of age and above at the time the informed consent form is signed;
* Able to understand and sign the Informed Consent Form and other necessary paperwork prior to initiation of study procedures;
* Able to communicate with the investigator/study site personnel, understand and comply with the study requirements, and willing to return for specified visits at the appointed time;
* Patients who have received prior treatment for their KCOT and with a diagnosis of recurrent (maxillary or mandibular) sporadic KCOT or NBCCS-associated KCOT (single or multiple);
* Diagnosis of KCOT will be done by past pathology report or by biopsy at the study site, if applicable;
* Willingness to consent to biopsy of the lesion, if needed;
* Willingness to delay excision of the target tumor site, unless evidence of disease progression or lack of drug tolerability;
* Willingness to donate blood for genetic testing;
* For female patients of childbearing potential, agreement to use two acceptable methods of birth control, including one barrier method during the study and 7 months after discontinuation of study drug;
* For males with female partners of childbearing potential, agreement to use a male condom (with spermicide) and to advise their female partners to use an acceptable method of birth control during the study and for 2 months after the discontinuation of the study drug;
* Agreement not to donate blood/blood products during the study and for 7 months after the discontinuation of the study drug;
* For males not to donate sperm products or semen during treatment and for 2 months after the discontinuation of the study drug;
* Able and willing to swallow pill;
* No malabsorption syndrome or other condition that would interfere with enteral absorption;
* At least 4 weeks since last chemotherapy, investigational therapy, radiotherapy or major surgical procedure and recovered from the first study drug administration;
* KCOT measures at least 1 cm in one dimension on pretreatment volumetric CT scan;
* No clinically significant abnormalities with clinical laboratory assessments;
Exclusion Criteria:
* Concurrent anti-tumor therapy;
* Completion of the most recent anti-tumor therapy (including Vismodegib) less than 4 weeks prior to the initiation of treatment (first study drug administration);
* Uncontrolled medical illness;
* Pregnancy or lactation; female patients who are planning to become pregnant for the duration of the study and 7 months post-treatment;
* Inability or unwillingness to swallow capsules;
* Any medical or psychological illness or condition preventing adequate consent;
* History of significant atherosclerotic disease, including the following:
* Coronary artery disease (i.e., myocardial infarction within the past year or unstable angina);
* Documented carotid atheroma;
* Known HIV infection;
* Current alcohol abuse;
* History of resistance to vismodegib (patients who previous received vismodegib for BCC and had no clinical response will be excluded).
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02366312
Study Brief:
Protocol Section:
NCT02366312