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JAK Inhibitor Tops Mab for Eczema

JAK Inhibitor Tops Mab for Eczema
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United statesUpadacitinib rinvoqJohn geverAndrew blauveltOregon medical research centerEczema areaSeverity indexMedpage todayManaging editorஒன்றுபட்டது மாநிலங்களில்ஆண்ட்ரூ ப்ளானுவெல்ட்ஓரிகந் மருத்துவ ஆராய்ச்சி மையம்அரிக்கும் தோலழற்சி பரப்பளவுதீவிரம் குறியீட்டுநிர்வகித்தல் ஆசிரியர்

JAMA Dermatology Publishes Data Showing RINVOQ® Achieved Superiority Versus DUPIXENT® for Primary and All Ranked Secondary Endpoints in Phase 3b Head-to-Head Study in Adults with Atopic Dermatitis

JAMA Dermatology Publishes Data Showing RINVOQ® Achieved Superiority Versus DUPIXENT® for Primary and All Ranked Secondary Endpoints in Phase 3b Head-to-Head Study in Adults with Atopic Dermatitis
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United statesAndrew blauveltOregon medical research centerDrug administrationExchange commissionEuropean medicines agencyAbbvie incCommittee for medicinal products human useEczema severity indexWorst pruritus numerical rating scaleWorst pruritusMedicinal productsHuman useImportant safety informationMississippi riverFull prescribing information

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

LEO Pharma LEO Pharma Presents Long-Term Safety and Efficacy Data for Tralokinumab in Adults With Moderate-to-Severe Atopic Dermatitis at AAD VMX 2021 Monday, April 26, 2021 1:00PM IST (7:30AM GMT) Ballerup, Denmark & Madison, N.J., United States: Interim analysis at 56 weeks from ECZTEND, an open-label extension trial, demonstrates sustainable and durable efficacy of tralokinumab in adult patients 1 Patients enrolled in ECZTRA 1 and 2 parent trials who continued into ECZTEND have now been treated with tralokinumab for two years 1 1 LEO Pharma A/S, a global leader in medical dermatology, today announced results on the long-term safety and efficacy profile of tralokinumab in adult patients with moderate-to-severe atopic dermatitis. Results were shared as an oral presentation during the American Academy of Dermatology Virtual Meeting Experience (AAD VMX) 2021.

United statesLinda mayerAndrew blauveltOregon medical research centerGlobal researchEuropean medicines agency onAmerican academy of dermatology virtual meeting experienceNational library of medicineCommittee for medicinal products human useGlobal product communicationsAmerican academyDermatology virtual meeting experienceInvestigator global assessmentEczema areaSeverity indexExecutive vice president

Taltz® Delivers More Cumulative Days with Completely Clear Skin for Adults with Psoriasis Compared to Seven Other Biologics in Novel Network Meta-Analysis

Share this article Share this article INDIANAPOLIS, April 23, 2021 /PRNewswire/ Through clinical trial meta-analysis and real-world evidence, Eli Lilly and Company s (NYSE: LLY) Taltz ® (ixekizumab) demonstrated greater success in key measured treatment outcomes compared to other biologics in adults with moderate to severe plaque psoriasis. In the first one-year network meta-analysis based on area under the curve, Taltz showed numerically greater cumulative benefits on completely clear skin over one year compared to seven other biologics, as measured by Psoriasis Area Severity Index (PASI) 100. In three real-world analyses of U.S. claims data ranging from one to three years, patients treated with Taltz stayed on treatment longer, were more adherent to the prescription and had more days on monotherapy compared to the other biologics studied. These results are being presented virtually at the American Academy of Dermatology s Virtual Meeting Experience (AAD VMX), April 23-25, 20

United statesKevin hernMarkg lebwohlMarlo scottAndrew blauveltEli lillyExchange commissionAmerican academy of dermatology virtual meeting experienceOregon medical research centerIcahn school of medicine at mount sinaiPsoriasis area severity indexAmerican academyVirtual meeting experienceLotus mallbrisProvided patientsLongest lasting complete skin clearance

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

United statesAndrew blauveltOregon medical research centerAmerican academy of dermatology virtual meeting experienceGlobal researchNational library of medicineEuropean medicines agency onCommittee for medicinal products human useAmerican academyDermatology virtual meeting experienceInvestigator global assessmentEczema areaSeverity indexExecutive vice presidentMedicinal productsHuman use