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Sun Protection Factor (SPF) / UVA Protection Factor (UVAPF) Assay

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Bayer

Status

Completed

Conditions

Sunscreen Agents

Treatments

Drug: SPF 15 Control
Drug: BAY 987519

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

6 patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Male or female of an age of 18 to 70 years inclusive;
  • Fitzpatrick Skin Type I, II and/or III for SPF testing;
  • Good health as determined from the CRO Subject History Form (SHF);
  • Signed and dated Informed Consent Form;
  • Signed and dated Health Insurance Portability and Accountability Act (HIPAA) Form;
  • An unambiguous minimal erythema dose (MED).

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

6 participants in 1 patient group

SPF evaluation
Experimental group
Description:
Subjects with good health as determined from the CRO Subject History Form (SHF) and Fitzpatrick Skin Type I, II and/or III were included for SPF testing.
Treatment:
Drug: BAY 987519
Drug: SPF 15 Control

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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