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Sun Protection Factor (SPF) Assay: UVA Protection Factor Assay on Minimal Persistent Pigment-Darkening Dose(MPPD). (NCT02779842)

To evaluate the Sun Protection Factor efficacy on human skin.
  • Drug: Coppertone (BAY 987517)
    Each 50 cm*2 test site area of a subject requires 100 mg of a test material to obtain a standard 2 mg/cm*2 test application. formulation number SR15-39-Z12-002.
    Ages eligible for Study
    18 Years to 70 Years
    Genders eligible for Study
    All
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Inclusion Criteria:
    • Fitzpatrick Skin Type l, ll and/or lll for UVB testing. Fitzpatrick Skin Type ll, lll and/or lV for UVA testing.
    • Male and female
    • Aged between 18-70 years old.
    • Good health as determined from the HRL SHF
    • Signed and dated Informed Consent Form
    • Signed and dated HIPAA Form
    • An unambiguous MED or MPPD (Minimal Persistent Pigment Darkening Dose)
    Exclusion Criteria:
    • Subjects on test at any other research laboratory or clinic.
    • Known allergy or sensitivity to sunscreens, cosmetics and toiletries, topical drugs and/or ultraviolet light.
    • Pre-existing dermatologic conditions which have been diagnoses by a medical professional (e.g. psoriasis, eczema, etc.) which would interfere with this study.
    • Pre-existing other medical conditions (e.g. adult asthma. diabetes).
    • Treatment with antihistamines or corticosteroids within one week prior to initiation of the test.
    • Treatment with antibiotics within two weeks prior to initiation of the test.
    • Chronic medication which could affect the results of the study.
    • Known pregnant or nursing women.

    1 locations

    United States (1)
    • Not specified
      Union, New Jersey, United States, 07083
    Status:
    unknown
    Type:
    Interventional
    Phase:
    -
    Start:
    30 June, 2015
    Updated:
    18 May, 2016
    Participants:
    6
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