Trial Condition(s):

Sunscreening Agent

18670 - Sun Protection Factor Assay (SPF Assay)

Bayer Identifier:

18670

ClinicalTrials.gov Identifier:

NCT02801929

EudraCT Number:

Not Available

Study Completed

Trial Purpose

To evaluate the Sun Protection Factor efficacy on human skin.

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(Self 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)
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.

Trial Summary

Enrollment Goal
10
Trial Dates
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Phase
N/A
Could I receive a placebo?
No
Products
BAY987518
Accepts Healthy Volunteers
Yes

Where to Participate

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Locations
Status
LocationsStatus
Locations

Investigative Site

Union, United States, 07083

Status
Completed
 

Trial Design