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Sun Protection Factor (SPF) Efficacy Assay | Clinical Trials | Clareo Health

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COMPLETEDNANCT02885805

Sun Protection Factor (SPF) Efficacy Assay

Evaluation of the effectiveness of a sunscreen product by determining its Sun Protection Factor (SPF) on the skin of human subjects.

Lead sponsor: Bayer•1 U.S. locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Bayer

Age

18 - 70 years

Sex

ALL

Healthy Volunteers

Yes

Inclusion Criteria

•Fitzpatrick Skin Type I, II and/or 111 for UVB testing; Fitzpatrick Skin Type II, 111 and/or IV for UVA testing.
•Sex: Male or female.
•Age: 18-70 years.
•Good health as determined from the HRL SHF.
•Signed and dated lnformed Consent Form.
•Signed and dated HIPAA Form.
•An unambiguous MED or MPPD

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Evaluation of the Stinging Potential of Products in Human Eyes

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: December 12, 2018Terms

Trial snapshot

StatusCOMPLETED

PhaseNA

Enrollment11

Start dateJun 2015

Last updatedDec 12, 2018

Condition

Sunscreen Agents

Locations shown

Union, New Jersey

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: December 12, 2018Data synced to Clareo: June 28, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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