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Bristol Myers Squibb Presents Positive Data from Two Pivotal Phase 3 Psoriasis Studies Demonstrating Superiority of Deucravacitinib Compared to Placebo and Otezla®


Bristol Myers Squibb Presents Positive Data from Two Pivotal Phase 3 Psoriasis Studies Demonstrating Superiority of Deucravacitinib Compared to Placebo and Otezla®
Significantly more patients treated with deucravacitinib achieved PASI 75 and sPGA 01 compared to patients treated with placebo and Otezla at Week 16, with an increased benefit versus Otezla at Week 24 and maintained through Week 52 Deucravacitinib was well tolerated with a low rate of discontinuation due to adverse events Deucravacitinib is a first-in-class, oral, selective tyrosine kinase 2 inhibitor with a unique …
Significantly more patients treated with deucravacitinib achieved PASI 75 and sPGA 0/1 compared to patients treated with placebo and Otezla at Week 16, with an increased benefit versus Otezla at Week 24 and maintained through Week 52 ....

United States , April Armstrong , Kirby Hosea , Nina Goworek , Mary Beth Harler , Bristol Myers Squibb , Thomas Alva Edison , American Academy Of Dermatology Virtual Meeting , Research Abstracts , University Of Southern California , Bristol Myers Squibb Company , Exchange Commission , American Academy Of Dermatology , Amgen Inc , Fibrosis Development , Dermatology Virtual Meeting Experience , Myers Squibb , Psoriasis Area , Severity Index , Global Assessment , Business Wire , Associate Dean , Deucravacitinib Versus Placebo , Psoriasis Symptoms , Signs Diary , Life Quality Index ,

Dermavant Sciences: Dermavant to Showcase PASI90, Itch and Quality of Life Data from Phase 3 Pivotal Trials for Tapinarof at AAD VMX 2021


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- Approximately One in Five Tapinarof Patients Achieved At Least 90% Disease Clearance -
- A Significantly Higher Portion of Psoriasis Patients Experienced Clinically Meaningful Improvements in Itch with Tapinarof Compared to Vehicle -
- Improvements in DLQI Exceeded MCID at Week 12 with Statistical Significance Compared to Vehicle -
- Data Will Be Included in NDA Submission for Tapinarof, Expected Mid-2021 -
Dermavant Sciences, a clinical-stage biopharmaceutical company dedicated to developing and commercializing innovative therapeutics in immuno-dermatology, will present data from its two pivotal Phase 3 trials for tapinarof for the treatment of psoriasis in adults, PSOARING 1 (tapinarof 1%, n=340; vehicle, n=170) and PSOARING 2 (tapinarof 1%, n=343; vehicle, n=172), at the American Academy of Dermatology Virtual Meeting Experience 2021 (AAD VMX 2021) on April 23-25, 2021. ....

United States , Laurence Watts , Kostenloser Wertpapierhandel , Angela Salerno Robin , American Academy Of Dermatology Virtual Meeting , Roivant Sciences , Program For Tapinarof , Dermavant Sciences , Linkedin Dermavant Sciences , Five Tapinarof Patients Achieved At Least , Disease Clearance , Significantly Higher Portion , Tapinarof Compared , Statistical Significance Compared , Will Be Included , American Academy , Dermatology Virtual Meeting Experience , Psoriasis Area , Severity Index , Peak Pruritis Numerical Rating Scale , Dermatology Life Quality Index , Secondary Efficacy Endpoints , Patient Reported Outcomes , North America , Vice President , Media Relations ,