AZD0284
/ AstraZeneca
- LARVOL DELTA
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September 01, 2021
AZD0284, a Potent, Selective, and Orally Bioavailable Inverse Agonist of Retinoic Acid Receptor-Related Orphan Receptor C2.
(PubMed, J Med Chem)
- "Inverse agonists of the nuclear receptor RORC2 have been widely pursued as a potential treatment for a variety of autoimmune diseases. In two preclinical in vivo studies, compound 20 reduced thymocyte numbers in mice and showed dose-dependent reduction of IL-17A containing γδ-T cells and of IL-17A and IL-22 RNA in the imiquimod induced inflammation model. Based on these data and a favorable safety profile, 20 was progressed to phase 1 clinical studies."
Journal • Immunology • Inflammation • IL17A • IL22
October 16, 2017
Study to Determine if AZD0284 is Effective and Safe in Treating Plaque Psoriasis
(clinicaltrials.gov)
- P1b; N=25; Not yet recruiting; Sponsor: AstraZeneca
Clinical • New P1 trial • Dermatology • Immunology • Psoriasis • IL17A
April 11, 2018
Study to Determine if AZD0284 is Effective and Safe in Treating Plaque Psoriasis
(clinicaltrials.gov)
- P1b; N=25; Suspended; Sponsor: AstraZeneca; Recruiting ➔ Suspended
Clinical • Trial suspension • Dermatology • Immunology • Psoriasis • IL17A
April 25, 2019
Study to Determine if AZD0284 is Effective and Safe in Treating Plaque Psoriasis
(clinicaltrials.gov)
- P1b; N=9; Terminated; Sponsor: AstraZeneca; N=25 ➔ 9; Suspended ➔ Terminated; The study is temporarily suspended due to preclinical findings that are currently under evaluation
Clinical • Enrollment change • Trial termination • Dermatology • Immunology • Psoriasis • IL17A
December 21, 2017
Study to Determine if AZD0284 is Effective and Safe in Treating Plaque Psoriasis
(clinicaltrials.gov)
- P1b; N=25; Recruiting; Sponsor: AstraZeneca; Not yet recruiting ➔ Recruiting
Clinical • Enrollment open • Dermatology • Immunology • Psoriasis • IL17A
February 21, 2020
Pharmacokinetics, Pharmacodynamics, and Safety of the Inverse Retinoic Acid-Related Orphan Receptor γ Agonist AZD0284.
(PubMed, Br J Clin Pharmacol)
- "AZD0284 was well tolerated, rapidly and dose-dependently absorbed, and reduced stimulated IL-17A release after single and multiple dosing. The results of this study support further clinical development of AZD0284."
Clinical • Journal • PK/PD data • IL17A
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