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Sun Protection Factor (SPF) Efficacy Assay

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Bayer

Status

Completed

Conditions

Sunscreen Agents

Treatments

Drug: SPF 15 Control
Drug: BAY987516

Study type

Interventional

Funder types

Industry

Identifiers

Details and patient eligibility

About

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

Enrollment

11 patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

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

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

11 participants in 1 patient group

SPF evaluation + Control
Experimental group
Description:
Fair-skinned subjects in good health with Skin Types I, II or III.
Treatment:
Drug: SPF 15 Control
Drug: BAY987516

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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