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  1. Article ; Online: Evolution of Antidrug Antibody Assays During the Development of Anti-Tissue Factor Pathway Inhibitor Monoclonal Antibody Marstacimab.

    Donley, Jean / Jani, Darshana / Zhu, Tong / Xiang, Yuhong / Gorovits, Boris / Arkin, Steven

    The AAPS journal

    2023  Volume 25, Issue 5, Page(s) 84

    Abstract: Tissue factor pathway inhibitor (TFPI) is an endogenous inhibitor of the extrinsic coagulation pathway. In patients with hemophilia A or B, inhibition of TFPI is an alternative therapeutic approach that augments the extrinsic coagulation pathway. ... ...

    Abstract Tissue factor pathway inhibitor (TFPI) is an endogenous inhibitor of the extrinsic coagulation pathway. In patients with hemophilia A or B, inhibition of TFPI is an alternative therapeutic approach that augments the extrinsic coagulation pathway. Marstacimab is an investigational fully human monoclonal antibody that binds and neutralizes TFPI and is being evaluated as a prophylactic treatment to prevent or reduce the frequency of bleeding episodes in patients with severe hemophilia A or B, with or without inhibitors (antibodies against coagulation factors). However, the efficacy, safety, and pharmacokinetics of marstacimab may be affected by the induction of antidrug antibody (ADA) responses. Here, we describe the evolution and validation of three quasi-quantitative electrochemiluminescence-based methods to detect marstacimab ADAs, starting from their use in a first-in-human phase 1 study to their use in phase 2 and 3 clinical studies of patients with severe hemophilia. For all three methods, validation criteria evaluated the performance of the assays in screening and confirmatory cut points, precision, selectivity, drug tolerance, target interference, and stability. Additional criteria for validation were dilution linearity (Methods 1 and 2) and low positive control concentration, prozone effect, plate homogeneity, and robustness (Method 3). The three methods met validation criteria and are a potentially valuable tool in detecting the induction of marstacimab ADAs during treatment in patients with hemophilia.
    MeSH term(s) Humans ; Hemophilia A/drug therapy ; Antibodies, Monoclonal, Humanized ; Antibodies, Monoclonal
    Chemical Substances marstacimab (0UB3OA67O7) ; lipoprotein-associated coagulation inhibitor ; Antibodies, Monoclonal, Humanized ; Antibodies, Monoclonal
    Language English
    Publishing date 2023-08-23
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1550-7416
    ISSN (online) 1550-7416
    DOI 10.1208/s12248-023-00847-w
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: A phase 2 pharmacodynamic dose-finding, safety, and efficacy study of dalteparin for pediatric venous thromboembolism treatment in children with and without cancer.

    Hartman, Lisa R / Nurmeev, Ildar / Svirin, Pavel / Wolter, Kevin D / Yan, Jean Li / Jani, Darshana / Goldenberg, Neil A / Sherman, Nancy

    Pediatric blood & cancer

    2022  Volume 69, Issue 8, Page(s) e29764

    Abstract: Data from registrational trials of pediatric venous thromboembolism (VTE) treatment are sparse, especially among cancer patients. We conducted a prospective, multicenter, open-label trial (NCT00952380) on dose-finding, safety, and efficacy (measured by ... ...

    Abstract Data from registrational trials of pediatric venous thromboembolism (VTE) treatment are sparse, especially among cancer patients. We conducted a prospective, multicenter, open-label trial (NCT00952380) on dose-finding, safety, and efficacy (measured by 90-day risks of clinically relevant bleeding [CRB] and symptomatic recurrent VTE [srVTE]) of twice-daily subcutaneous dalteparin for acute VTE treatment in patients ≤18 years old. Among 38 patients (cancer, n = 26; noncancer, n = 12), median dalteparin dose requirements per kilogram varied with age but not cancer status. Risks of CRB and srVTE were <4% in cancer and noncancer subgroups. Dalteparin is an important FDA-approved treatment for pediatric VTE, particularly with cancer.
    MeSH term(s) Adolescent ; Anticoagulants/adverse effects ; Child ; Dalteparin/adverse effects ; Hemorrhage/chemically induced ; Hemorrhage/drug therapy ; Humans ; Neoplasms/complications ; Neoplasms/drug therapy ; Prospective Studies ; Venous Thromboembolism/drug therapy
    Chemical Substances Anticoagulants ; Dalteparin (S79O08V79F)
    Language English
    Publishing date 2022-06-09
    Publishing country United States
    Document type Clinical Trial, Phase II ; Journal Article ; Multicenter Study ; Research Support, Non-U.S. Gov't
    ZDB-ID 2131448-2
    ISSN 1545-5017 ; 1545-5009
    ISSN (online) 1545-5017
    ISSN 1545-5009
    DOI 10.1002/pbc.29764
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Population Pharmacokinetic Analysis of Dalteparin in Pediatric Patients With Venous Thromboembolism.

    Damle, Bharat / Jen, Frank / Sherman, Nancy / Jani, Darshana / Sweeney, Kevin

    Journal of clinical pharmacology

    2020  Volume 61, Issue 2, Page(s) 172–180

    Abstract: This article describes the population pharmacokinetics (PK) of dalteparin in pediatric patients with venous thromboembolism (VTE). A prospective multicenter open-label study was conducted in children who required anticoagulation for the treatment of VTE. ...

    Abstract This article describes the population pharmacokinetics (PK) of dalteparin in pediatric patients with venous thromboembolism (VTE). A prospective multicenter open-label study was conducted in children who required anticoagulation for the treatment of VTE. The study population included children with and without cancer. The goal was to describe the pharmacokinetics of dalteparin using anti-Xa as a surrogate marker and to determine the dose required to achieve therapeutic anti-Xa levels (0.5-1.0 IU/mL). The anti-Xa data were supplemented with 2 published studies and analyzed using population pharmacokinetic approaches. The pharmacokinetics of dalteparin following subcutaneous injection in pediatric patients was described by a 1-compartment model with linear absorption and elimination. Body weight was added as a covariate on both CL/F and Vd/F as a power function with fixed exponents of 0.75 and 1.0, respectively. The estimates of CL/F and Vd/F in the full model were 929 mL/h and 7180 mL, respectively, for a reference female patient aged 12 years with body weight of 43 kg. Body weight-normalized CL/F decreased with age. Cancer status and sex did not have significant effects on CL/F and Vd/F. Simulations were conducted to select starting doses of dalteparin that would rapidly achieve therapeutic anti-Xa levels. These simulations suggested that the recommended starting doses of dalteparin administered subcutaneously in pediatric patients of different age cohort groups for treatment of VTE were 150 IU/kg every 12 hours (1 month to <2 years), 125 IU/kg every 12 hours (≥2 to <8 years), and 100 IU/kg every 12 hours (≥8 to <19 years).
    MeSH term(s) Adolescent ; Age Factors ; Anticoagulants/administration & dosage ; Anticoagulants/adverse effects ; Anticoagulants/pharmacokinetics ; Anticoagulants/therapeutic use ; Biomarkers ; Body Weight ; Child ; Child, Preschool ; Dalteparin/administration & dosage ; Dalteparin/adverse effects ; Dalteparin/pharmacokinetics ; Dalteparin/therapeutic use ; Factor Xa Inhibitors/pharmacokinetics ; Factor Xa Inhibitors/therapeutic use ; Female ; Humans ; Infant ; Infant, Newborn ; Injections, Subcutaneous ; Male ; Metabolic Clearance Rate ; Prospective Studies ; Sex Factors ; Venous Thromboembolism/drug therapy
    Chemical Substances Anticoagulants ; Biomarkers ; Factor Xa Inhibitors ; Dalteparin (S79O08V79F)
    Language English
    Publishing date 2020-08-21
    Publishing country England
    Document type Journal Article ; Multicenter Study
    ZDB-ID 188980-1
    ISSN 1552-4604 ; 0091-2700 ; 0021-9754
    ISSN (online) 1552-4604
    ISSN 0091-2700 ; 0021-9754
    DOI 10.1002/jcph.1716
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Feasibility of immuno-PCR technology platforms as an ultrasensitive tool for the detection of anti-drug antibodies.

    Jani, Darshana / Savino, Edward / Goyal, Jaya

    Bioanalysis

    2015  Volume 7, Issue 3, Page(s) 285–294

    Abstract: Aim: During the early clinical development of a receptor-IgG1 fusion protein (Drug X), a risk based strategy was utilized to evaluate immunogenicity from Phase I through Proof of Concept clinical studies.: Materials & methods: Three different ... ...

    Abstract Aim: During the early clinical development of a receptor-IgG1 fusion protein (Drug X), a risk based strategy was utilized to evaluate immunogenicity from Phase I through Proof of Concept clinical studies.
    Materials & methods: Three different technology platforms, enzyme-linked immunosorbant assay, electrochemiluminescent assay and newly emerging immuno-PCR were utilized for evaluation of immunogenic response.
    Results: An ELISA with adequate sensitivity but significant drug interference was replaced by electrochemiluminescent method with improved drug tolerance; however, an inverse correlation was observed between the administered dose and the incidence of anti-drug antibodies. Further evaluation of an immuno-PCR showed reduced drug interference enabling the detection of anti-drug antibodies in the presence of excess amount of Drug X.
    Conclusion: Immuno PCR assay proved to be a feasible platform for anti-drug antibody characterization.
    MeSH term(s) Antibodies/analysis ; Antibodies/blood ; Antibodies/immunology ; Biological Therapy ; Enzyme-Linked Immunosorbent Assay/methods ; Feasibility Studies ; Humans ; Limit of Detection ; Luminescent Measurements ; Pharmaceutical Preparations ; Polymerase Chain Reaction/methods ; Recombinant Fusion Proteins/immunology ; Recombinant Fusion Proteins/therapeutic use
    Chemical Substances Antibodies ; Pharmaceutical Preparations ; Recombinant Fusion Proteins
    Language English
    Publishing date 2015
    Publishing country England
    Document type Journal Article
    ISSN 1757-6199
    ISSN (online) 1757-6199
    DOI 10.4155/bio.14.245
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Neutralizing Antibody Assay Development with High Drug and Target Tolerance to Support Clinical Development of an Anti-TFPI Therapeutic Monoclonal Antibody.

    Xiang, Yuhong / Parng, Chuenlei / Olson, Katrina / Seletskaia, Elena / Gorovits, Boris / Jani, Darshana / Caiazzo, Teresa / Joyce, Alison / Donley, Jean

    The AAPS journal

    2019  Volume 21, Issue 3, Page(s) 46

    Abstract: Immunogenicity is a major challenge for protein therapeutics which can potentially reduce drug efficacy and safety and is often being monitored by anti-drug antibody (ADA) and neutralizing antibody (NAb) assays. Circulating targets and residual drugs in ... ...

    Abstract Immunogenicity is a major challenge for protein therapeutics which can potentially reduce drug efficacy and safety and is often being monitored by anti-drug antibody (ADA) and neutralizing antibody (NAb) assays. Circulating targets and residual drugs in matrices can have significant impacts on accuracy of results from ADA and NAb assays, and sufficient drug and target tolerance for these assays are necessary. Here, we report the development of a competitive ligand binding (CLB) NAb assay for an anti-TFPI (tissue factor pathway inhibitor) monoclonal antibody (PF-06741086) with high drug and target tolerance to support ongoing clinical studies. A double acid affinity capture elution approach was used to mitigate drug interference, and a robust target removal strategy was employed to enhance target tolerance. The validated NAb assay has sensitivity of 313 ng/mL, drug tolerance of 50 μg/mL, and target tolerance of 1200 ng/mL. A step-by-step tutorial of assay development is described in this manuscript along with the rationale for using a high drug/target tolerant NAb assay. The NAb assay cut point factor obtained was 0.78. Other assay performance characteristics, e.g., precision and selectivity, are also discussed. This validated method demonstrated a superior drug and target tolerance to warrant specific and precise characterization of the NAb responses in support of ongoing clinical studies.
    MeSH term(s) Antibodies, Monoclonal, Humanized/immunology ; Antibodies, Monoclonal, Humanized/pharmacology ; Antibodies, Neutralizing/immunology ; Binding, Competitive ; Biological Assay/methods ; Drug Development/methods ; Drug Tolerance/immunology ; Humans ; Immune Tolerance ; Immunoassay/methods ; Ligands ; Lipoproteins/antagonists & inhibitors ; Protein Binding ; Recombinant Proteins/metabolism
    Chemical Substances Antibodies, Monoclonal, Humanized ; Antibodies, Neutralizing ; Ligands ; Lipoproteins ; Recombinant Proteins ; lipoprotein-associated coagulation inhibitor ; marstacimab (0UB3OA67O7)
    Language English
    Publishing date 2019-03-29
    Publishing country United States
    Document type Journal Article ; Validation Study
    ISSN 1550-7416
    ISSN (online) 1550-7416
    DOI 10.1208/s12248-019-0320-3
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Neutralizing Antibody Validation Testing and Reporting Harmonization.

    Myler, Heather / Pedras-Vasconcelos, João / Lester, Todd / Civoli, Francesca / Xu, Weifeng / Wu, Bonnie / Vainshtein, Inna / Luo, Linlin / Hassanein, Mohamed / Liu, Susana / Ramaswamy, Swarna Suba / Mora, Johanna / Pennucci, Jason / McCush, Fred / Lavelle, Amy / Jani, Darshana / Ambakhutwala, Angela / Baltrukonis, Daniel / Barker, Breann /
    Carmean, Rebecca / Chung, Shan / Dai, Sheng / DeWall, Stephen / Dholakiya, Sanjay L / Dodge, Robert / Finco, Deborah / Yan, Haoheng / Hays, Amanda / Hu, Zheng / Inzano, Cynthia / Kamen, Lynn / Lai, Ching-Ha / Meyer, Erik / Nelson, Robert / Paudel, Amrit / Phillips, Kelli / Poupart, Marie-Eve / Qu, Qiang / Abhari, Mohsen Rajabi / Ryding, Janka / Sheldon, Curtis / Spriggs, Franklin / Warrino, Dominic / Wu, Yuling / Yang, Lin / Pasas-Farmer, Stephanie

    The AAPS journal

    2023  Volume 25, Issue 4, Page(s) 69

    Abstract: Evolving immunogenicity assay performance expectations and a lack of harmonized neutralizing antibody validation testing and reporting tools have resulted in significant time spent by health authorities and sponsors on resolving filing queries. A team of ...

    Abstract Evolving immunogenicity assay performance expectations and a lack of harmonized neutralizing antibody validation testing and reporting tools have resulted in significant time spent by health authorities and sponsors on resolving filing queries. A team of experts within the American Association of Pharmaceutical Scientists' Therapeutic Product Immunogenicity Community across industry and the Food and Drug Administration addressed challenges unique to cell-based and non-cell-based neutralizing antibody assays. Harmonization of validation expectations and data reporting will facilitate filings to health authorities and are described in this manuscript. This team provides validation testing and reporting strategies and tools for the following assessments: (1) format selection; (2) cut point; (3) assay acceptance criteria; (4) control precision; (5) sensitivity including positive control selection and performance tracking; (6) negative control selection; (7) selectivity/specificity including matrix interference, hemolysis, lipemia, bilirubin, concomitant medications, and structurally similar analytes; (8) drug tolerance; (9) target tolerance; (10) sample stability; and (11) assay robustness.
    MeSH term(s) Antibodies, Neutralizing ; Pharmaceutical Preparations ; Drug Tolerance
    Chemical Substances Antibodies, Neutralizing ; Pharmaceutical Preparations
    Language English
    Publishing date 2023-07-08
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1550-7416
    ISSN (online) 1550-7416
    DOI 10.1208/s12248-023-00830-5
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Anti-drug Antibody Assay Validation: Improved Reporting of the Assay Selectivity via Simpler Positive Control Recovery Data Analysis.

    Gorovits, Boris / Roldan, Marcela Araya / Baltrukonis, Daniel / Cai, Chun-Hua / Donley, Jean / Jani, Darshana / Kamerud, John / McCush, Frederick / Thomas, Jeffrey S / Wang, Ying

    The AAPS journal

    2019  Volume 21, Issue 5, Page(s) 76

    Abstract: Anti-drug antibody (ADA) assay selectivity is evaluated during assay validation to assess the potential for individual matrices to interfere with detection of ADA. While current EMA and FDA guideline documents suggest comparative analysis with and ... ...

    Abstract Anti-drug antibody (ADA) assay selectivity is evaluated during assay validation to assess the potential for individual matrices to interfere with detection of ADA. While current EMA and FDA guideline documents suggest comparative analysis with and without matrix, they do not provide specific recommendations on the acceptance criteria such as an acceptable percent positive control (PC) recovery range or positive rate. Industry has adopted an approach where recovery of PC spiked sample is expected to fall within ± 20% (80 to 120%) vs. that for the PC material spiked in negative control matrix or assay buffer. Here, it is proposed that ADA assay selectivity evaluated using a qualitative assessment of PC recovery vs. a PK-like quantitative method may be more appropriate. The PC recovery test should focus on the reliability of the method to detect the low PC level in individual samples and avoid false-negative ADA reporting. Therefore, it is proposed that assessment of high PC level as well as the assessment of quantitative percent recovery (within ± 20%) should not be included in the test. The recovery test may be viewed as acceptable should a pre-selected number of individual samples (for example at least 8 or 9 out of 10) prepared at the low PC concentration of the assay score as ADA positive.
    MeSH term(s) Antibodies/immunology ; Antibodies, Monoclonal/immunology ; Humans ; Immunoassay/methods ; Reproducibility of Results
    Chemical Substances Antibodies ; Antibodies, Monoclonal
    Language English
    Publishing date 2019-06-18
    Publishing country United States
    Document type Journal Article ; Validation Study
    ISSN 1550-7416
    ISSN (online) 1550-7416
    DOI 10.1208/s12248-019-0347-5
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Recommendations for the development and validation of confirmatory anti-drug antibody assays.

    Jani, Darshana / Marsden, Robin / Mikulskis, Alvydas / Gleason, Carol / Klem, Thomas / Krinos Fiorotti, Corinna / Myler, Heather / Yang, Lin / Fiscella, Michele

    Bioanalysis

    2015  Volume 7, Issue 13, Page(s) 1619–1631

    Abstract: Identification and characterization of anti-drug antibodies is a critical component of biopharmaceutical drug development. The tiered approach for immunogenicity testing consists of screening, confirmatory, and characterization assays. Herein, we provide ...

    Abstract Identification and characterization of anti-drug antibodies is a critical component of biopharmaceutical drug development. The tiered approach for immunogenicity testing consists of screening, confirmatory, and characterization assays. Herein, we provide recommendations for confirmatory assays by expanding upon published guidance and present common practices across the industry. The authors recommend scientific approaches for development and validation of confirmatory assays using competition methods in ligand-binding assays, along with statistical formulae for routine use and validation. The paper will assist in understanding the confirmatory assay, and carefully implementing validation criteria a priori, as well as during sample analysis. These approaches represent the authors' current knowledge and practices, with the aim that more uniform practices will be applied across the industry.
    MeSH term(s) Antibodies, Monoclonal/immunology ; Antibody Formation ; Biological Assay/methods ; Drug Design ; Humans
    Chemical Substances Antibodies, Monoclonal
    Language English
    Publishing date 2015
    Publishing country England
    Document type Journal Article
    ISSN 1757-6199
    ISSN (online) 1757-6199
    DOI 10.4155/bio.15.96
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Recommendations for Selection and Characterization of Protein Biomarker Assay Calibrator Material.

    Cowan, Kyra J / Amaravadi, Lakshmi / Cameron, Mark J / Fink, Damien / Jani, Darshana / Kamat, Medha / King, Lindsay / Neely, Robert J / Ni, Yan / Rhyne, Paul / Riffon, Renee / Zhu, Yuda

    The AAPS journal

    2017  Volume 19, Issue 6, Page(s) 1550–1563

    Abstract: As biomarkers continue to become an integral part of drug development and decision-making, there are increased expectations for reliable and quantitative assays. Protein biomarker assay results are directly influenced by the calibrator material. The ... ...

    Abstract As biomarkers continue to become an integral part of drug development and decision-making, there are increased expectations for reliable and quantitative assays. Protein biomarker assay results are directly influenced by the calibrator material. The selection of calibrator material presents many challenges that impact the relative accuracy and performance of the assay. There is an industry-wide challenge finding reliable and well-characterized calibrator material with good documentation. Several case studies are presented that demonstrate some of the challenges involved in selecting appropriate calibrators along with the resolutions that were ultimately applied. From these experiences, we present here a set of recommendations for selecting and characterizing calibrator material based on the intended purpose of the assay. Finally, we introduce a commutability approach, based on common clinical chemistry practices, which can be used to demonstrate inter-changeability with calibrator materials across multiple lots and technology platforms for all types of protein biomarker assays.
    MeSH term(s) Biomarkers/analysis ; Calibration ; Proteins/analysis
    Chemical Substances Biomarkers ; Proteins
    Language English
    Publishing date 2017-10-02
    Publishing country United States
    Document type Journal Article
    ISSN 1550-7416
    ISSN (online) 1550-7416
    DOI 10.1208/s12248-017-0146-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Anti-drug Antibody Sample Testing and Reporting Harmonization.

    Jani, Darshana / Marsden, Robin / Gunsior, Michele / Hay, Laura Schild / Ward, Bethany / Cowan, Kyra J / Azadeh, Mitra / Barker, Breann / Cao, Liching / Closson, Kristin R / Coble, Kelly / Dholakiya, Sanjay L / Dusseault, Julie / Hays, Amanda / Herl, Carina / Hodsdon, Michael E / Irvin, Susan C / Kirshner, Susan / Kolaitis, Gerry /
    Kulagina, Nadia / Kumar, Seema / Lai, Ching Ha / Lipari, Francesco / Liu, Susana / Merdek, Keith D / Moldovan, Ioana R / Mozaffari, Reza / Pan, Luying / Place, Corina / Snoeck, Veerle / Manning, Marta Starcevic / Stocker, Dennis / Tary-Lehmann, Magdalena / Turner, Amy / Vainshtein, Inna / Verthelyi, Daniela / Williams, William T / Yan, Haoheng / Yan, Weili / Yang, Lili / Yang, Lin / Zemo, Jennifer / Zhong, Zhandong Don

    The AAPS journal

    2022  Volume 24, Issue 6, Page(s) 113

    Abstract: A clear scientific and operational need exists for harmonized bioanalytical immunogenicity study reporting to facilitate communication of immunogenicity findings and expedient review by industry and health authorities. To address these key bioanalytical ... ...

    Abstract A clear scientific and operational need exists for harmonized bioanalytical immunogenicity study reporting to facilitate communication of immunogenicity findings and expedient review by industry and health authorities. To address these key bioanalytical reporting gaps and provide a report structure for documenting immunogenicity results, this cross-industry group was formed to establish harmonized recommendations and a develop a submission template to facilitate agency filings. Provided here are recommendations for reporting clinical anti-drug antibody (ADA) assay results using ligand-binding assay technologies. This publication describes the essential bioanalytical report (BAR) elements such as the method, critical reagents and equipment, study samples, results, and data analysis, and provides a template for a suggested structure for the ADA BAR. This publication focuses on the content and presentation of the bioanalytical ADA sample analysis report. The interpretation of immunogenicity data, including the evaluation of the impact of ADA on safety, exposure, and efficacy, is out of scope of this publication.
    MeSH term(s) Antibodies ; Antibodies, Neutralizing
    Chemical Substances Antibodies ; Antibodies, Neutralizing
    Language English
    Publishing date 2022-10-28
    Publishing country United States
    Document type Journal Article
    ISSN 1550-7416
    ISSN (online) 1550-7416
    DOI 10.1208/s12248-022-00762-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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