Use of an alternative method to evaluate erythema severity in a clinical trial: difference in vehicle response with evaluation of baseline and postdose photographs for effect of oxymetazoline cream 1·0% for persistent erythema of rosacea in a phase IV study.


Journal

The British journal of dermatology
ISSN: 1365-2133
Titre abrégé: Br J Dermatol
Pays: England
ID NLM: 0004041

Informations de publication

Date de publication:
05 2019
Historique:
accepted: 23 11 2018
pubmed: 1 12 2018
medline: 4 7 2020
entrez: 1 12 2018
Statut: ppublish

Résumé

Once-daily topical oxymetazoline cream 1·0% significantly reduced persistent facial erythema of rosacea in trials requiring live, static patient assessments. To evaluate critically the methodology of clinical trials that require live, static patient assessments by determining whether assessment of erythema is different when reference to the baseline photograph is allowed. In two identically designed, randomized, phase III trials, adults with persistent facial erythema of rosacea applied oxymetazoline or vehicle once daily. This phase IV study evaluated standardized digital facial photographs from the phase III trials to record ≥ 1-grade Clinician Erythema Assessment (CEA) improvement at 1, 3, 6, 9 and 12 h postdose. Among 835 patients (oxymetazoline n = 415, vehicle n = 420), significantly greater proportions of patients treated with oxymetazoline vs. vehicle achieved ≥ 1-grade CEA improvement. For the comparison between phase IV study results and the original phase III analysis, when reference to baseline photographs was allowed while evaluating post-treatment photographs, the results for oxymetazoline were similar to results of the phase III trials (up to 85.7%), but a significantly lower proportion of vehicle recipients achieved ≥ 1-grade CEA improvement (up to 29.7% [phase 4] vs. 52.3% [phase 3]; P<0.001). In the phase IV study, up to 80·2% of patients treated with oxymetazoline achieved at least moderate erythema improvement vs. up to 22·9% of patients treated with vehicle. The association between patients' satisfaction with facial skin redness and percentage of erythema improvement was statistically significant. Assessment of study photographs, with comparison to baseline, confirmed significant erythema reduction with oxymetazoline on the first day of application. Compared with the phase III trial results, significantly fewer vehicle recipients attained ≥ 1-grade CEA improvement, suggesting a mitigated vehicle effect. This methodology may improve the accuracy of clinical trials evaluating erythema severity.

Sections du résumé

BACKGROUND
Once-daily topical oxymetazoline cream 1·0% significantly reduced persistent facial erythema of rosacea in trials requiring live, static patient assessments.
OBJECTIVES
To evaluate critically the methodology of clinical trials that require live, static patient assessments by determining whether assessment of erythema is different when reference to the baseline photograph is allowed.
METHODS
In two identically designed, randomized, phase III trials, adults with persistent facial erythema of rosacea applied oxymetazoline or vehicle once daily. This phase IV study evaluated standardized digital facial photographs from the phase III trials to record ≥ 1-grade Clinician Erythema Assessment (CEA) improvement at 1, 3, 6, 9 and 12 h postdose.
RESULTS
Among 835 patients (oxymetazoline n = 415, vehicle n = 420), significantly greater proportions of patients treated with oxymetazoline vs. vehicle achieved ≥ 1-grade CEA improvement. For the comparison between phase IV study results and the original phase III analysis, when reference to baseline photographs was allowed while evaluating post-treatment photographs, the results for oxymetazoline were similar to results of the phase III trials (up to 85.7%), but a significantly lower proportion of vehicle recipients achieved ≥ 1-grade CEA improvement (up to 29.7% [phase 4] vs. 52.3% [phase 3]; P<0.001). In the phase IV study, up to 80·2% of patients treated with oxymetazoline achieved at least moderate erythema improvement vs. up to 22·9% of patients treated with vehicle. The association between patients' satisfaction with facial skin redness and percentage of erythema improvement was statistically significant.
CONCLUSIONS
Assessment of study photographs, with comparison to baseline, confirmed significant erythema reduction with oxymetazoline on the first day of application. Compared with the phase III trial results, significantly fewer vehicle recipients attained ≥ 1-grade CEA improvement, suggesting a mitigated vehicle effect. This methodology may improve the accuracy of clinical trials evaluating erythema severity.

Identifiants

pubmed: 30500065
doi: 10.1111/bjd.17462
pmc: PMC6850476
doi:

Substances chimiques

Oxymetazoline 8VLN5B44ZY

Types de publication

Clinical Trial, Phase IV Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1050-1057

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2018 The Authors. British Journal of Dermatology published by John Wiley & Sons Ltd on behalf of British Association of Dermatologists.

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Auteurs

L F Eichenfield (LF)

University of California, San Diego, CA, U.S.A.
Rady Children's Hospital, San Diego, CA, U.S.A.

J Q Del Rosso (JQ)

JDR Dermatology Research/Thomas Dermatology, Las Vegas, NV, U.S.A.

J K L Tan (JKL)

Windsor Clinical Research Inc., Windsor, ON, Canada.

A A Hebert (AA)

UTHealth McGovern Medical School, Department of Dermatology, Houston, TX, U.S.A.

G F Webster (GF)

Webster Dermatology, P.A., Hockessin, DE, U.S.A.

J Harper (J)

Dermatology and Skin Care Center of Birmingham, Birmingham, AL, U.S.A.

H E Baldwin (HE)

The Acne Treatment and Research Center, Morristown, NJ, U.S.A.

L H Kircik (LH)

DermResearch, PLLC, Louisville, KY, U.S.A.
Icahn School of Medicine at Mount Sinai, New York, NY, U.S.A.

L Stein-Gold (L)

Henry Ford Health System, West Bloomfield, MI, U.S.A.

A Kaoukhov (A)

Allergan plc, Irvine, CA, U.S.A.

N Alvandi (N)

Allergan plc, Irvine, CA, U.S.A.

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