Live Breaking News & Updates on ஓரிகந் மருத்துவ ஆராய்ச்சி மையம்

Stay updated with breaking news from ஓரிகந் மருத்துவ ஆராய்ச்சி மையம். Get real-time updates on events, politics, business, and more. Visit us for reliable news and exclusive interviews.

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 States , Linda Mayer , Andrew Blauvelt , Oregon Medical Research Center , Global Research , European Medicines Agency On , American Academy Of Dermatology Virtual Meeting Experience , National Library Of Medicine , Committee For Medicinal Products Human Use , Global Product Communications , American Academy , Dermatology Virtual Meeting Experience , Investigator Global Assessment , Eczema Area , Severity Index , Executive Vice President , Medicinal Products , Human Use , European Medicines Agency , Term Extension , Improvements Observed , Tralokinumab Treatment , Moderate To Severe Atopic Dermatitis , Interim Readout , Long Term Extension , Long Term Extension Trial ,

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), Apr ....

United States , Kevin Hern , Markg Lebwohl , Marlo Scott , Andrew Blauvelt , Eli Lilly , Exchange Commission , American Academy Of Dermatology Virtual Meeting Experience , Oregon Medical Research Center , Icahn School Of Medicine At Mount Sinai , Psoriasis Area Severity Index , American Academy , Virtual Meeting Experience , Lotus Mallbris , Provided Patients , Longest Lasting Complete Skin Clearance , Clinical Therapeutics , Icahn School , Mount Sinai , Helped Patients Stay , Prescribed Treatment , Taltz Took Treatment , More Frequent , Prior Biologic Use Were More Likely , Continue Treatment , Prescribed Compared ,

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 States , Andrew Blauvelt , Oregon Medical Research Center , American Academy Of Dermatology Virtual Meeting Experience , Global Research , National Library Of Medicine , European Medicines Agency On , Committee For Medicinal Products Human Use , American Academy , Dermatology Virtual Meeting Experience , Investigator Global Assessment , Eczema Area , Severity Index , Executive Vice President , Medicinal Products , Human Use , European Medicines Agency , Term Extension , Improvements Observed , Tralokinumab Treatment , Moderate To Severe Atopic Dermatitis , Interim Readout , Long Term Extension , Long Term Extension Trial , Subjects With Atopic Dermatitis Who Participated , Previous Tralokinumab Trials ,