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  1. Article ; Online: Briakinumab for the treatment of plaque psoriasis.

    Traczewski, Pawel / Rudnicka, Lidia

    BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy

    2012  Volume 26, Issue 1, Page(s) 9–20

    Abstract: Psoriasis is a chronic inflammatory skin disorder affecting approximately 2% of individuals worldwide. An improved understanding of the pathogenesis of psoriasis has led to the development of targeted biologic therapies. Briakinumab (ABT-874) is a ... ...

    Abstract Psoriasis is a chronic inflammatory skin disorder affecting approximately 2% of individuals worldwide. An improved understanding of the pathogenesis of psoriasis has led to the development of targeted biologic therapies. Briakinumab (ABT-874) is a recombinant human antibody that blocks the biological activity of the cytokines interleukin (IL)-12 and IL-23 through their shared subunit p40. IL-12 and IL-23 are key mediators in T-cell differentiation and have been shown to play a significant role in maintaining inflammation and abnormal keratinocyte function in psoriasis patients through development and stimulation of Th1 and Th17 subsets, respectively. In one phase II and four phase III studies (including two 52-week trials), the Psoriasis Area and Severity Index (PASI)-75 score at weeks 12 and 52 was achieved by at least 80.6% and 66.2% (p < 0.001) of patients receiving more than one dose of briakinumab every 4 weeks, respectively, with high proportions of patients achieving PASI-90 and PASI-100 scores (at least 55.4% and 28.8%, respectively; p < 0.001). These studies indicate safety and tolerance of briakinumab therapy for patients with moderate-to-severe chronic plaque psoriasis. In one clinical trial, therapy was associated with increased incidence of major cardiac events. Available results from two briakinumab trials show its positive impact on health-related quality of life. However, the manufacturer has now withdrawn the application in the EU and US.
    MeSH term(s) Animals ; Antibodies, Monoclonal/adverse effects ; Antibodies, Monoclonal/pharmacology ; Antibodies, Monoclonal/therapeutic use ; Clinical Trials as Topic/adverse effects ; Clinical Trials as Topic/statistics & numerical data ; Dermatologic Agents/adverse effects ; Dermatologic Agents/pharmacology ; Dermatologic Agents/therapeutic use ; Drug Approval ; Humans ; Interleukin-12/antagonists & inhibitors ; Interleukin-12/immunology ; Interleukin-23/antagonists & inhibitors ; Interleukin-23/immunology ; Psoriasis/drug therapy ; Psoriasis/immunology
    Chemical Substances Antibodies, Monoclonal ; Dermatologic Agents ; Interleukin-23 ; Interleukin-12 (187348-17-0) ; briakinumab (978I8M0P8X)
    Language English
    Publishing date 2012-02-01
    Publishing country New Zealand
    Document type Journal Article ; Review
    ZDB-ID 1364202-9
    ISSN 1179-190X ; 1173-8804
    ISSN (online) 1179-190X
    ISSN 1173-8804
    DOI 10.2165/11595940-000000000-00000
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Treatment of systemic lupus erythematosus with epratuzumab.

    Traczewski, Pawel / Rudnicka, Lidia

    British journal of clinical pharmacology

    2011  Volume 71, Issue 2, Page(s) 175–182

    Abstract: Systemic lupus erythematosus is a prototypic autoimmune disease characterized by abnormalities in the activity of B-cells and T-cells. A novel specific treatment for autoimmune diseases is B-cell depletion with monoclonal antibodies. Epratuzumab is a ... ...

    Abstract Systemic lupus erythematosus is a prototypic autoimmune disease characterized by abnormalities in the activity of B-cells and T-cells. A novel specific treatment for autoimmune diseases is B-cell depletion with monoclonal antibodies. Epratuzumab is a monoclonal antibody that targets CD22 antigen on B-cells. Initial phase II and two terminated early phase III studies suggest that treatment of systemic lupus erythematosus with this immunomodulatory agent is effective, well tolerated and significantly improves the patient's quality of life. In vitro studies and clinical trials with non-Hodgkin lymphoma patients indicate epratuzumab can potentially serve as a complementary drug in combination therapy with another inhibitor of B-cell activity, rituximab, which is a monoclonal anti-CD20 antibody.
    MeSH term(s) Animals ; Antibodies, Monoclonal/adverse effects ; Antibodies, Monoclonal/immunology ; Antibodies, Monoclonal/therapeutic use ; Antibodies, Monoclonal, Humanized ; Antibodies, Monoclonal, Murine-Derived/therapeutic use ; B-Lymphocytes/immunology ; Drug Therapy, Combination ; Humans ; Immunosuppressive Agents/adverse effects ; Immunosuppressive Agents/immunology ; Immunosuppressive Agents/therapeutic use ; Lupus Erythematosus, Systemic/drug therapy ; Lupus Erythematosus, Systemic/immunology ; Rituximab ; Sialic Acid Binding Ig-like Lectin 2/immunology ; Structure-Activity Relationship ; Treatment Outcome
    Chemical Substances Antibodies, Monoclonal ; Antibodies, Monoclonal, Humanized ; Antibodies, Monoclonal, Murine-Derived ; CD22 protein, human ; Immunosuppressive Agents ; Sialic Acid Binding Ig-like Lectin 2 ; epratuzumab (3062P60MH9) ; Rituximab (4F4X42SYQ6)
    Language English
    Publishing date 2011-01-28
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 188974-6
    ISSN 1365-2125 ; 0306-5251 ; 0264-3774
    ISSN (online) 1365-2125
    ISSN 0306-5251 ; 0264-3774
    DOI 10.1111/j.1365-2125.2010.03767.x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Adalimumab in dermatology.

    Traczewski, Pawel / Rudnicka, Lidia

    British journal of clinical pharmacology

    2008  Volume 66, Issue 5, Page(s) 618–625

    Abstract: Adalimumab is a biological agent, one of the tumour necrosis factor-alpha inhibitors. Pivotal studies evaluating its efficacy in plaque psoriasis (CHAMPION, REVEAL) and psoriatic arthritis (PsA) (ADEPT) were carried out in recent years. Adalimumab proved ...

    Abstract Adalimumab is a biological agent, one of the tumour necrosis factor-alpha inhibitors. Pivotal studies evaluating its efficacy in plaque psoriasis (CHAMPION, REVEAL) and psoriatic arthritis (PsA) (ADEPT) were carried out in recent years. Adalimumab proved highly effective in psoriasis patients and in PsA patients previously unresponsive to nonsteroidal anti-inflammatory drugs. Results of smaller studies suggest therapy with the drug may be successful in psoriasis resistant to other biologics and PsA unresponsive to disease-modifying antirheumatic drugs. Adalimumab has also been shown to improve patients' quality of life significantly. Although they should be further extended as far as dermatological conditions are concerned, available data indicate adalimumab is safe and well tolerated. Numerous case reports featuring its off-label use suggest the drug could be helpful in treating hidradenitis suppurativa, pyoderma gangrenosum, Sweet's syndrome, cutaneous sarcoidosis, pemphigus, systemic vasculitides, multicentric reticulohistiocytosis and stomatitis.
    MeSH term(s) Adalimumab ; Anti-Inflammatory Agents/adverse effects ; Anti-Inflammatory Agents/therapeutic use ; Antibodies, Monoclonal/adverse effects ; Antibodies, Monoclonal/therapeutic use ; Antibodies, Monoclonal, Humanized ; Arthritis, Psoriatic/drug therapy ; Humans ; Psoriasis/drug therapy ; Skin Diseases/drug therapy
    Chemical Substances Anti-Inflammatory Agents ; Antibodies, Monoclonal ; Antibodies, Monoclonal, Humanized ; Adalimumab (FYS6T7F842)
    Language English
    Publishing date 2008-07-11
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 188974-6
    ISSN 1365-2125 ; 0306-5251 ; 0264-3774
    ISSN (online) 1365-2125
    ISSN 0306-5251 ; 0264-3774
    DOI 10.1111/j.1365-2125.2008.03263.x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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