Sun Protection Factor Assay (SPF Assay 104/2016)

Completed · Not applicable

Conditions studied: Sunscreening Agents

In brief

To evaluate the Sun Protection Factor efficacy on human skin.

Key facts

Study ID

NCT02891057

Run by

Bayer

People needed

10

Starts

2016-08-15

Expected to finish

2016-08-24

Last updated by the study team

2018-12-13

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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 (Subject History Form).
• Signed and dated Informed Consent Form.
• Signed and dated HIPAA (Health Insurance Portability and Accountability Act) form.
• An unambiguous MED (Minimal Erythema Dose) or MPPD (Minimal Persistent Pigment Darkening Dose)

You may not qualify if…

• 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.

Where it is running

• Study site — Union, New Jersey, United States

Full record on ClinicalTrials.gov

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