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Find Drugs in Development News & Deals for Lebrikizumab

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Details:

Ebglyss (lebrikizumab) is an approved high-affinity and potent IL-13 inhibitor being studied in adult and adolescent patients 12 years of age and older with moderate-to-severe AD.


Lead Product(s): Lebrikizumab

Therapeutic Area: Dermatology Product Name: Ebglyss

Highest Development Status: ApprovedProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 10, 2024

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Ebglyss (lebrikizumab) is a monoclonal antibody that binds IL-13 with high affinity to specifically prevent the formation of the IL-13Rα1/IL-4Rα heterodimer complex. It is approved for the treatment of moderate-to-severe atopic dermatitis.


Lead Product(s): Lebrikizumab

Therapeutic Area: Dermatology Product Name: Ebglyss

Highest Development Status: ApprovedProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable November 17, 2023

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Ebglyss (lebrikizumab) is an investigational, monoclonal antibody that binds IL-13, and FDA has issued a complete response letter for the lebrikizumab biologic license application (BLA) for the treatment of moderate-to-severe atopic dermatitis (eczema).


Lead Product(s): Lebrikizumab

Therapeutic Area: Dermatology Product Name: Ebglyss

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 02, 2023

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Ebglyss (lebrikizumab) is an investigational, monoclonal antibody that binds IL-13, which is received positive CHMP opinion for moderate-to-severe atopic dermatitis.


Lead Product(s): Lebrikizumab

Therapeutic Area: Dermatology Product Name: Ebglyss

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 15, 2023

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LY3650150 (lebrikizumab) is an investigational high-affinity and potent IL-13 inhibitor being studied in adult and adolescent patients 12 years of age and older with moderate-to-severe AD.


Lead Product(s): Lebrikizumab

Therapeutic Area: Dermatology Product Name: LY3650150

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable May 01, 2023

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New, late-breaking data show lebrikizumab responders reported long-lasting results at one year of treatment across measures of improvement in skin clearance, itch and disease extent and severity.


Lead Product(s): Lebrikizumab

Therapeutic Area: Dermatology Product Name: LY3650150

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 08, 2022

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Lebrikizumab (LY3650150), is a novel, investigational, monoclonal antibody designed to bind IL-13 with high affinity to specifically prevent the formation of the IL-13Rα1/IL-4Rα heterodimer complex and subsequent signaling.


Lead Product(s): Lebrikizumab

Therapeutic Area: Dermatology Product Name: LY3650150

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable June 06, 2022

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Lebrikizumab is a novel, monoclonal antibody (mAb) that binds to the IL-13 protein with high affinity to specifically prevent the formation of IL-13Rα1/IL-4Rα (Type 2 receptor) which blocks downstream signaling through the IL-13 pathway.


Lead Product(s): Lebrikizumab,Corticosteroids

Therapeutic Area: Dermatology Product Name: LY3650150

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 11, 2022

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More than 50 percent of patients with moderate-to-severe atopic dermatitis (AD) experienced at least 75 percent reduction in disease severity (EASI-75) at 16 weeks when receiving lebrikizumab, an investigational IL-13 inhibitor monotherapy.


Lead Product(s): Lebrikizumab

Therapeutic Area: Dermatology Product Name: LY3650150

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 26, 2022

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Safety profile consistent with prior LY3650150 (lebrikizumab) studies met all primary and key secondary endpoints at week16, also significantly improved disease severity when combined with topical corticosteroids in people with moderate-to-severe atopic dermatitis.


Lead Product(s): Lebrikizumab

Therapeutic Area: Dermatology Product Name: LY3650150

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 21, 2021

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In the initial 16-week placebo-controlled period of ADvocate 1 and ADvocate 2, the incidence of treatment-emergent adverse events (AEs) and serious AEs among patients treated with lebrikizumab was consistent with that of the previous Phase 2 lebrikizumab study in AD.


Lead Product(s): Lebrikizumab

Therapeutic Area: Dermatology Product Name: LY3650150

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Eli Lilly

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable August 16, 2021

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In the initial 16-week placebo-controlled period of ADvocate 1 and ADvocate 2, the incidence of treatment-emergent adverse events (AEs) and serious AEs among patients treated with lebrikizumab was consistent with that of the previous Phase 2 lebrikizumab study in AD.


Lead Product(s): Lebrikizumab

Therapeutic Area: Dermatology Product Name: LY3650150

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Eli Lilly

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable August 16, 2021

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Data from this study suggests that treatment with lebrikizumab provided rapid and clinically meaningful improvements in itch, sleep and overall measures of quality of life.


Lead Product(s): Lebrikizumab

Therapeutic Area: Dermatology Product Name: LY3650150

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Eli Lilly

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable June 12, 2020

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The acquisition of Dermira also expands Lilly's portfolio of marketed dermatology medicines with the addition of QBREXZA® (glycopyrronium).


Lead Product(s): Lebrikizumab

Therapeutic Area: Dermatology Product Name: LY3650150

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Eli Lilly

Deal Size: $1,100.0 million Upfront Cash: $1,100.0 million

Deal Type: Acquisition February 20, 2020

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Lilly gets Dermira’s experimental treatment for atopic dermatitis, as well as an approved medicated cloth for excessive armpit sweating.


Lead Product(s): Lebrikizumab

Therapeutic Area: Dermatology Product Name: LY3650150

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Eli Lilly

Deal Size: $1,100.0 million Upfront Cash: $1,100.0 million

Deal Type: Acquisition January 10, 2020

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