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Use Of Oral Itraconazole In Patients With Locally Limited Basocellular Carcinoma Of Skin.

Evaluation Of The Treatment With Oral Itraconazole In Patients With Basocellular Carcinoma Of Skin, Locally Limited Disease.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03972748
Enrollment
28
Registered
2019-06-04
Start date
2018-01-05
Completion date
2021-06-01
Last updated
2019-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Basal Cell Carcinoma, Hedgehog Pathway

Keywords

Itraconazole

Brief summary

Patients with localized basocellular carcinoma of the skin, will receive oral Itraconazole, 200 mg twice daily, for 60 days, prior to curative intent surgery.

Detailed description

Patients with localized basocellular carcinoma of the skin, will receive oral Itraconazole, 200 mg once daily, for 60 days, before surgery with curative intent. Tumor area regression will be measured through dermatologic evaluation and photographic documentation on baseline and at the end of the 60 day treatment period. The activity of the Hedgehog pathway will be measured on tissue samples obtained at the time of diagnosis and at the time of curative intent surgery, through the measuring of the Ki67 index.

Interventions

Oral Itraconazole capsules, 200 mg, twice daily, for 60 days prior to surgery with curative intent.

Sponsors

Hospital de Clinicas de Porto Alegre
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with diagnosis of Basocellular Carcinoma (BCC) of the Skin, histologically confirmed. * At least one BCC lesion with 10 mm in the longest diameter * Disease amenable to surgical intervention with curable intent. * Signed Informed Consent * PS ECOG 0 to 3

Exclusion criteria

* Chronic renal disease, with a glomerular filtration rate of less than 30 ml/min * Acute or chronic liver disease, as measured by: total bilirubin \> than 1.5 x ULN and AST and ALT \> than 5 x ULN. * Symptomatic cardiac insufficiency or an ejection fraction lower than 50% measured through echocardiography, * Other active malignancies in the last year. * Uncontrolled systemic hypertension, * Any chronic infections such as tuberculosis, viral hepatitis and HIV. * Pregnancy, suspected or confirmed. * Known intolerance to the use of Itraconazole.

Design outcomes

Primary

MeasureTime frameDescription
clinical response60 daystumor area response registered through dermatologic evaluation
hedgehog pathway activity60 daysMeasured through the Ki67 index on pathological specimens at the beginning and at the end of treatment.

Countries

Brazil

Contacts

Primary ContactRenato M Bakos, Ph. D.
rbakos@hcpa.edu.br+555133598000
Backup ContactRodrigo P Pereira, M.D.
rppereira@hcpa.edu.br+555133598000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026