Eli Lilly`s Biologic Taltz (Ixekizumab) Receives Suppl Approvals in US
Eli Lilly's Biologic Taltz (Ixekizumab) Receives Approval in the U.S.
Eli Lilly forays into dermatological space with launch of psoriasis drug
Eli Lilly and Company (NYSE: LLY) announced today the availability of a new, citrate-free formulation of Taltz® (ixekizumab) injection 80 mg/mL. The...
Eli Lilly Taltz (Ixekizumab) Receives Supplemental Approval in the U.S.
Drug has been cleared for use in patients whose condition is not controlled well enough with conventional therapy
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, 2021.
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TORONTO, April 2, 2021 /CNW/ - On March 29, 2021, Health Canada issued a Notice of Compliance for Taltz® (ixekizumab) injection, 80 mg/mL, for the treatment of pediatric patients from six to less than 18 years of age with moderate-to-severe plaque psoriasis who are candidates for systemic therapy or phototherapy. About one million Canadians, including children, live with psoriasis.1