To evaluate the Sun Protection Factor efficacy on human skin.
Drug: Coppertone (BAY 987517)
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Full eligibility criteria for NCT02779842
Ages eligible for Study
18 Years to 70 Years
Genders eligible for Study
Accepts Healthy Volunteers
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)
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.
All locations for NCT02779842
United States (1)
Union, New Jersey, United States, 07083
View full eligibility
Tris trial is registered with FDA with number: NCT02779842. The sponsor of the trial is Bayer and it is looking for 6 volunteers for the current phase.
Official trial title: Sun Protection Factor (SPF) Assay: UVA Protection Factor Assay on Minimal Persistent Pigment-Darkening Dose(MPPD).
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