Open-label Trial of SUBA™-Itraconazole (SUBA-Cap) in Subjects With Basal Cell Carcinoma Nevus Syndrome (BCCNS)

HedgePath Pharmaceuticals

Status and phase

Completed

Phase 2

Conditions

Basal Cell Carcinoma in Basal Cell Nevus Syndrome

Treatments

Drug: SUBA-Itraconazole

Study type

Interventional

Funder types

Industry

Identifiers

NCT02354261

HP2001

SCORING (Other Identifier)

Details and patient eligibility

About

The study will assess the safety and efficacy of SUBA-Cap in subjects with Basal Cell Carcinoma Nevus Syndrome.

Full description

Single arm, phase IIb, multi-center, open-label study evaluating the use of oral SUBA-Cap in subjects with Basal Cell Carcinoma Nevus Syndrome and non-metastatic Basal Cell Carcinoma.

Following informed consent, subjects will undergo a skin biopsy for Gli1 analysis and an assessment of extent of disease using both tumor measurements (using modified Response Evaluation Criteria in Solid Tumors criteria) and color photographs of the skin.

Subjects will receive daily oral SUBA-Cap, at a starting dose of 150 mg twice daily (BID). Reassessments of disease will be conducted at weeks 4, 8, 16, and then every 8 weeks thereafter. Subjects with evidence of response (partial or complete) will be re-evaluated at least 4 weeks later for confirmation. Subjects may continue to receive SUBA-Cap until disease progression (defined as the appearance of one or more new lesions or ulceration of a target lesion) that requires a change in therapy (surgical intervention or use of other systemic therapy) or the appearance of unacceptable side effects. Pharmacokinetic assessments (serial trough levels) will be performed at defined intervals and, when possible, prior to and following any dose adjustment. Skin biopsies will be taken for Gli1 expression at defined intervals.

Enrollment

38 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

ECOG performance status of 0 or 1
Diagnosis of Basal Cell Carcinoma Nevus Syndrome (BCCNS)
Histologic confirmation of BCC from at least one lesion
History of surgical removal of at least ten (10) prior BCCs
Measurable disease as defined, namely at least ten (10) measurable lesions such that the sum of the longest diameters of the measurable lesions is at least 40 mm.
Has failed, refused, or is not eligible for standard of care therapy for BCC
Willingness to abstain from the use of non-study treatments for BCC, including but not limited to topical medications, PDT, and/or irradiation therapy.
At least four weeks from prior major surgery
Women who are pre-menopausal or not surgically sterile must be willing to use an acceptable contraceptive method for the duration of the study and for 30 days following the last dose of study drug
Sexually active men must be willing to use an acceptable contraceptive method for the duration of time on study and for 30 days following the last dose of study drug
Clinical laboratory values within the following ranges:
1. Negative serum pregnancy test
2. Adequate hematologic function (ANC ≥1.5 x 10^9/L; platelet count ≥75x10^9/L; hemoglobin ≥9g/dL (in the absence of red blood cell transfusions in the prior 14 days)
3. Prothrombin time (PT-INR) or activated partial thromboplastin time (APTT) <1.5 times the upper limit of normal range, unless currently receiving anticoagulants
4. Serum creatinine ≤ 1.5 x ULN or calculated creatinine clearance ≥60 mL/min
5. Total bilirubin ≤ 1.5x the upper limit of normal unless considered due to Gilbert syndrome in which case, ≤ 3x the upper limit of normal
6. Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels ≤ the upper limit of normal
Willingness to undergo biopsies (BCC lesions and normal skin)
Willingness to provide prior and study-related BCC biopsies for central review
Willingness to participate in collection of pharmacokinetic samples
Willingness to not donate blood, semen, or eggs for the duration of the study and for 3 months following discontinuation of SUBA-Cap
Willingness to delay removal of otherwise surgically eligible BCC's

Exclusion criteria

Presence of metastatic BCC
Subjects who would be disserved significantly by a delay in conventional therapy, such as surgical intervention of their BCC
Prior use of a hedgehog inhibitor (e.g., sonidegib, vismodegib) or Itraconazole within the past 6 months
History of progressive disease on a hedgehog inhibitor (e.g., sonidegib, vismodegib) or other Hh pathway inhibitors for the treatment of BCC
Pregnant and/or nursing women
Use of any medications metabolized by the cytochrome P450 3A4 isoenzyme system (CYP3A4) known to lead to potentially serious and/or life threatening adverse events when used in conjunction with itraconazole
Any illness that is likely to reduce absorption of oral medications
Corrected QT (Fridericia) interval of >450 msec for females and >430 msec for males
Use of any medications known to result in a prolongation of the QT interval
History of congestive heart failure or other cardiac abnormality that would contraindicate the use of itraconazole
Any condition or situation which in the Investigator's opinion may put the subject at significant risk, could confound the study results, or could interfere significantly with the subject's participation in the study
Any indication of compromised liver function that would otherwise contraindicate use of itraconazole
Any concurrent malignancy, except for squamous cell carcinoma of the skin and cervical carcinoma in situ, that is likely to require treatment within the next two years or would interfere with study requirements
Psychiatric illness and/or social situations (e.g., excessive alcohol use or use of illicit drugs) that would interfere with study compliance
Known HIV infection, active hepatitis B or active hepatitis C infection (testing not required unless indicated by history)
Known allergy to itraconazole or any of its excipients