Trial Condition(s):

Sunscreening Agents

18751-Sun Protection Factor Assay. (SPF Assay)

Bayer Identifier:

18751

ClinicalTrials.gov Identifier:

NCT02739802

EudraCT Number:

Not Available

Study Completed

Trial Purpose

To evaluate the Sun Protection Factor (SPF) 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 or female - Aged between 18-70 years old. - Good health - Signed and dated Informed Consent Form - Signed and dated Health Insurance Portability and Accountability Authorization (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.

Trial Summary

Enrollment Goal
10
Trial Dates
black-arrow
Phase
N/A
Could I receive a placebo?
No
Products
BAY987517
Accepts Healthy Volunteers
Yes

Where to Participate

Loading...
Locations
Status
LocationsStatus
Locations

Investigative Site

Union, United States, 07083

Status
Completed
 

Trial Design