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OTEZLA® Significantly Improved Measures Of Disease Severity In Adults With Mild-To-Moderate Plaque Psoriasis

Amgen today announced Otezla ® improved measures of disease severity in adults with mild-to-moderate plaque psoriasis regardless of their Body Surface Area affected by the disease, according to findings from the placebo-controlled, Phase 3 ADVANCE trial. Results were presented at the American Academy of Dermatology Virtual Meeting Experience 2021. “Many people with mild-to-moderate plaque psoriasis still report … Amgen (NASDAQ:AMGN) today announced Otezla ® (apremilast) improved measures of disease severity in adults with mild-to-moderate plaque psoriasis regardless of their Body Surface Area (BSA) affected by the disease, according to findings from the placebo-controlled, Phase 3 ADVANCE trial. Results were presented at the American Academy of Dermatology Virtual Meeting Experience 2021.

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Burt s Bees Research at AAD VMX 2021 Shows Nature-Based Ingredients Protect Against Evolving Skincare Challenges

Share this article Share this article DURHAM, N.C., April 23, 2021 /PRNewswire/  Burt s Bees, a pioneer in natural skin care, today announced its latest research findings on the benefits of nature-based ingredients to address today s evolving skincare needs. The data will be presented at the American Academy of Dermatology Virtual Meeting Experience (AAD VMX 2021) from April 23-25, 2021. The latest research findings from Burt s Bees highlight: For Burt’s Bees, the power of nature meets the proof of science at the American Academy of Dermatology Virtual Meeting Experience (AAD VMX 2021). Burt’s Bees, a pioneer in natural skin care, today announced its latest research findings on the benefits of nature-based ingredients to address today’s evolving skincare needs.

Redirecting to LEO Pharma Presents Long-Term Safety and Efficacy Data for Tralokinumab in Adults With Moderate-to-Severe Atopic Dermatitis at AAD VMX 2021

2.0 (2.4) Participants included 1,174 patients from ECZTEND at data cut-off.1 Observed outcomes for all patients enrolled 60 weeks prior to data cut-off (n=513) were analyzed at Week 56.1 At parent-trial baseline, ECZTEND baseline, and Week 56, median EASI score was 26.6, 4.7, and 1.8, respectively.1 At Week 56, IGA and EASI response rates were 49.7% (IGA 0/1), 95.1% (EASI-50), 82.8% (EASI-75), 61.0% (EASI-90), and 79.7% (EASI ≤7). An EASI score of ≤7 corresponds to mild atopic dermatitis.1 At the same 56-week data cut-off, measurements of itch and sleep disruptions due to itch were also reported.1 At Week 56, the mean worst weekly pruritus (i.e. itch) numeric rating scale (NRS) score was 3.3 (parent-trial baseline was 7.7) while the mean eczema-related weekly sleep NRS score was 2.0 (parent-trial baseline was 6.9).1

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