Trial Search Results

Study of Patidegib Topical Gel, 2%, for the Reduction of Disease Burden of Persistently Developing Basal Cell Carcinomas (BCCs) in Subjects With Basal Cell Nevus Syndrome (Gorlin Syndrome)

This is a global, multicenter, randomized, double-blind, stratified, vehicle-controlled study of the efficacy and safety of Patidegib Topical Gel, 2%, applied topically twice daily to the face of adult participants with Gorlin syndrome. Participants will be required to apply the investigational product for 12 months. The primary endpoint is a comparison between the two treatment arms of the number of new surgically eligible BCCs (nSEBs) that develop over the 12 month period.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

PellePharm, Inc.

Stanford Investigator(s):

Intervention(s):

  • Drug: Patidegib Topical Gel, 2%
  • Drug: Patidegib Topical Gel, Vehicle

Phase:

Phase 3

Eligibility


Inclusion Criteria:

   1. The participant must be age at least 18 years of age at the Screening Visit.

   2. The participant must provide written informed consent prior to any study procedures.

   3. The participant must meet diagnostic criteria for the basal cell nevus (Gorlin)
   syndrome including major criterion #3a plus 1 additional major criterion or plus 2
   additional minor criteria listed below.

   Major criteria:

      1. >2 histologically confirmed BCCs or 1 for participant under age 20.

      2. Odontogenic keratocysts of the jaw confirmed histologically.

      3. ≥3 palmar and/or plantar pits seen at the Screening Visit.

      4. Bilamellar calcification of the falx cerebri present at less than 20 years of
      age.

      5. Fused, bifid, or markedly splayed ribs.

      6. First degree relative with Gorlin syndrome.

      7. Patched protein 1 (PTCH1) mutation predicted to be of functional significance in
      normal tissue.

   Minor criteria:

      1. Macrocephaly.

      2. Congenital malformations including frontal bossing, cleft lip or palate, "coarse
      face", moderate to severe hypertelorism.

      3. Skeletal abnormalities detectable clinically: Sprengel deformity, marked pectus
      deformity, or marked finger syndactyly.

      4. Skeletal abnormalities detectable radiographically: bridging of the sella
      turcica; vertebral abnormalities such as hemivertebrae, fusion or elongation of
      the vertebral bodies; modeling defects of the hands and feet; flame shaped
      lucencies of the hands or feet.

      5. Ovarian fibroma.

      6. Medulloblastoma (Modification of criteria of V Kimonis et al Am J Med Genet 69:
      299-308, 1997).

   4. The participant must have 10 (with at least 3 on the face) clinically typical BCCs
   present within 24 months prior to Randomization (Baseline/Day 1). Additionally, the
   subject must have at least 2 BCCs with longest diameter <5 mm present on the face
   prior to Randomization (Baseline/Day 1).

   5. The participant is willing to have blood collected to measure circulating drug levels.

   6. The participant is willing to abstain from application of a non-study topical
   medication (prescription or over the counter) to facial skin for the duration of the
   trial except as prescribed by the Investigator. Moisturizers and emollients are
   allowed. Participant will be encouraged to use their preferred sunscreen with a sun
   protector factor (SPF) of at least 30 daily on all exposed skin sites.

   7. If the participant is a woman of childbearing potential (WOCBP), she must be willing
   to use complete abstinence from sexual intercourse and/or she and her partner must be
   willing to use at least 2 highly-effective forms of birth control starting prior to
   Baseline, through the duration of the study, and for 12 months after last application
   of IP.

   8. If the participant is a male with a female sex partner who is a WOCBP, the participant
   must be willing to use condoms, even after a vasectomy, starting prior to Baseline,
   through the duration of the study, and for at least 8 months after the last
   application of IP.

   9. The participant is willing for all facial BCCs to be evaluated and treatment
   recommendations made only by the Investigator.

10. The participant is willing to forego treatment of facial BCCs with anything other than
   the study IP except when the Investigator believes that delay of treatment of a facial
   BCC potentially might compromise the health of the subject. During the trial the only
   allowed form of treatment is surgical. Non-facial BCCs may be removed at the
   discretion of the Investigator or Primary Skin Care Physician (PSCP).

Exclusion Criteria:

   1. The subject has previously participated in a clinical trial evaluating patidegib
   topical gel.

   2. The participant has used topical treatment to the face or systemic therapies that
   might interfere with the evaluation of the study IP. Among these are use of the
   following:

      1. 5-fluorouracil, imiquimod, diclofenac, or Ingenol mebutate (except as topical
      treatment to discrete non-facial BCCs) systemically or topically to the skin
      within the 2 months prior to the Screening Visit.

      2. Systemic chemotherapy within 1 year prior to the Screening Visit.

      3. Known inhibitors of the Hedgehog signaling pathway (such as vismodegib,
      sonidegib, itraconazole) topically or systemically within 3 months prior to the
      Screening Visit.

      4. Photodynamic therapy (PDT) except to localized non-facial, individual BCCs within
      2 months prior to the Screening Visit.

   3. The participant is known to have a hypersensitivity to any of the ingredients in the
   study medication formulation.

   4. The participant is unable or unwilling to make a good faith effort to return to the
   study site for all study visits and tests.

   5. The participant has uncontrolled systemic disease.

   6. The participant has been treated for invasive cancer within the past 5 years excluding
   non-melanoma skin cancer, Stage I cervical cancer, ductal carcinoma in situ of the
   breast, or chronic lymphocytic leukemia (CLL) Stage 0.

   7. The participant has current, recent (within five half-lives of the experimental drug
   or if half-life not known, within the past 6 months prior to the Screening Visit), or
   planned participation in an experimental drug study while enrolled in this study.

   8. The participant is a WOCBP who is unwilling or unable to comply with pregnancy
   prevention measures.

   9. The participant is pregnant or breastfeeding.

10. The participant has 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. This may
   include a history of other skin conditions (such as severe facial eczema) or diseases,
   metabolic dysfunction, physical examination findings, or clinical laboratory findings
   giving reasonable suspicion of a disease or condition that contraindicates use of an
   investigational drug or that might affect interpretation of the results of the study
   or render the participant at high risk from treatment complications.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Alexander Valencia
650-498-5185
Not Recruiting