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Pfizer Gets CDSCO Panel Nod to Study PF-06823859
New Delhi:The drug major Pfizer has got approval from the Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) to conduct the trial for the drug PF-06823859
This came after the firm presented phase 3 clinical study protocol no. C0251010 version original, dated 08 April 2024.
Dazukibart (PF-06823859) is under development for the treatment of moderate to severe dermatomyositis, cutaneous lupus erythematosus, subacute cutaneous lupus erythematosus (SCLE), chronic cutaneous lupus erythematosus (CCLE), systemic lupus erythematosus.
PF-06823859 is a potent, selective, humanised immunoglobulin 1-neutralising monoclonal antibody (mAb) directed against human IFNβ. Dazukibart is a monoclonal antibody, a type of biologic drug specifically designed to target and inhibit certain proteins associated with autoimmune diseases.
Dazukibart targets the IL-23 cytokine, a protein that is heavily involved in the body's immune response. IL-23 plays a pivotal role in the development and maintenance of chronic inflammation, a hallmark of many autoimmune conditions.
At the recent SEC meeting for Analgesic and Rheumatology held on October 3, 2024, the expert panel reviewed phase 3 clinical study protocol no. C0251010 version original dated 08 April 2024.
After detailed deliberation, the committee recommended granting permission to conduct the trial as presented by the firm.
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Dr Kamal Kant Kohli-MBBS, DTCD- a chest specialist with more than 30 years of practice and a flair for writing clinical articles, Dr Kamal Kant Kohli joined Medical Dialogues as a Chief Editor of Medical News. Besides writing articles, as an editor, he proofreads and verifies all the medical content published on Medical Dialogues including those coming from journals, studies,medical conferences,guidelines etc. Email: drkohli@medicaldialogues.in. Contact no. 011-43720751