BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 38564770)

  • 1. Immunogenicity profile of rurioctocog alfa pegol in previously treated patients with severe congenital hemophilia A.
    Horling FM; Reipert BM; Allacher P; Engl W; Pan L; Tangada S
    Blood Adv; 2024 Jun; 8(11):2726-2739. PubMed ID: 38564770
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Efficacy, safety, and immunogenicity of rurioctocog alfa pegol for prophylactic treatment in previously treated patients with severe hemophilia A: a systematic review and meta-analysis of clinical trials.
    Witarto BS; Visuddho V; Witarto AP; Sutanto H; Wiratama BS; Wungu CDK
    F1000Res; 2021; 10():1049. PubMed ID: 35136579
    [No Abstract]   [Full Text] [Related]  

  • 3. Perioperative haemostasis with full-length, PEGylated, recombinant factor VIII with extended half-life (rurioctocog alfa pegol) in patients with haemophilia A: Final results of a multicentre, single-arm phase III trial.
    Gruppo R; López-Fernández MF; Wynn TT; Engl W; Sharkhawy M; Tangada S
    Haemophilia; 2019 Sep; 25(5):773-781. PubMed ID: 31353761
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Direct comparison of two extended half-life PEGylated recombinant FVIII products: a randomized, crossover pharmacokinetic study in patients with severe hemophilia A.
    Solms A; Shah A; Berntorp E; Tiede A; Iorio A; Linardi C; Ahsman M; Mancuso ME; Zhivkov T; Lissitchkov T
    Ann Hematol; 2020 Nov; 99(11):2689-2698. PubMed ID: 32974838
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Long-term safety and efficacy results from the phase 3b, open-label, multicentre Continuation study of rurioctocog alfa pegol for prophylaxis in previously treated patients with severe haemophilia A.
    Chowdary P; Mullins ES; Konkle BA; McGuinn C; Park YS; Stasyshyn O; Zulfikar B; Engl W; Tangada S
    Haemophilia; 2020 Jul; 26(4):e168-e178. PubMed ID: 32597029
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Real-world study of rurioctocog alfa pegol and emicizumab in US clinical practice among patients with hemophilia A.
    Sun SX; Frick A; Balasa V; Roberts JC
    Expert Rev Hematol; 2022 Oct; 15(10):943-950. PubMed ID: 36000620
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical efficacy of simoctocog alfa versus extended half-life recombinant FVIII concentrates in hemophilia A patients undergoing personalized prophylaxis using a matching-adjusted indirect comparison method.
    Kessler CM; Corrales-Medina FF; Mannucci PM; Jiménez-Yuste V; Tarantino MD
    Eur J Haematol; 2023 Nov; 111(5):757-767. PubMed ID: 37587687
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A Retrospective Observational Study of Rurioctocog Alfa Pegol in Clinical Practice in the United States.
    Aledort L; Milligan S; Watt M; Booth J
    J Manag Care Spec Pharm; 2020 Apr; 26(4):492-503. PubMed ID: 32223610
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Immunogenicity, safety, and efficacy of rurioctocog alfa pegol in previously untreated patients with severe hemophilia A: interim results from a phase 3, prospective, multicenter, open-label study.
    Sidonio RF; Thompson AA; Peyvandi F; Stasyshyn O; Yeoh SL; Sosothikul D; Antmen AB; Maggiore C; Engl W; Ewenstein B; Tangada S
    Expert Rev Hematol; 2023; 16(10):793-801. PubMed ID: 37646148
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Healthcare costs among hemophilia A patients in the United States treated with rurioctocog alfa pegol (FVIII-PEG) or antihemophilic factor (recombinant), FC fusion protein (rFVIIIFc) using real-world data.
    Farahbakhshian S; Fan Q; Schultz BG; Princic N; Park J; Bullano M
    J Med Econ; 2023; 26(1):1278-1286. PubMed ID: 37787429
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Safety and efficacy of damoctocog alfa pegol prophylaxis in patients with severe haemophilia A: Results of an interventional, post-marketing study.
    Holme PA; Poulsen LH; Tueckmantel C; Maas Enriquez M; Alvarez Román MT; De Cristofaro R
    Haemophilia; 2024 Mar; 30(2):388-394. PubMed ID: 38229269
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Rurioctocog alfa pegol PK-guided prophylaxis in hemophilia A: results from the phase 3 PROPEL study.
    Klamroth R; Windyga J; Radulescu V; Collins PW; Stasyshyn O; Ibrahim HM; Engl W; Tangada SD; Savage W; Ewenstein B
    Blood; 2021 Apr; 137(13):1818-1827. PubMed ID: 33150384
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Pharmacokinetics of recombinant factor VIII in adults with severe hemophilia A: fixed-sequence single-dose study of octocog alfa, rurioctocog alfa pegol, and efanesoctocog alfa.
    Lissitchkov T; Willemze A; Jan C; Zilberstein M; Katragadda S
    Res Pract Thromb Haemost; 2023 May; 7(4):100176. PubMed ID: 37538505
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Damoctocog Alfa Pegol: A Review in Haemophilia A.
    Paik J; Deeks ED
    Drugs; 2019 Jul; 79(10):1147-1156. PubMed ID: 31218660
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Microsimulation to compare activity-related bleed risks between pharmacokinetic-guided rurioctocog alfa pegol prophylaxis and emicizumab.
    Sun SX; Crawford S
    Expert Rev Hematol; 2023 Mar; 16(3):205-211. PubMed ID: 36655343
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Subgroup analysis of a phase 2/3 study of rurioctocog alfa pegol in patients with severe hemophilia A: efficacy and safety in previously treated Korean patients.
    You CW; Baek HJ; Park SK; Park YS; Shin HJ; Engl W; Tangada S
    Blood Res; 2019 Sep; 54(3):198-203. PubMed ID: 31730687
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Report on 4 cases with decreased recovery due to neutralizing antibodies specific for PEGylated recombinant factor VIII.
    Hillarp A; Holme PA; Wåland EP; Le MS; Henriksson CE; Tjønnfjord GE; Måseide RJ
    J Thromb Haemost; 2023 Oct; 21(10):2771-2775. PubMed ID: 37543216
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Factor VIII products and inhibitor development in previously treated patients with severe or moderately severe hemophilia A: a systematic review.
    Hassan S; Cannavò A; Gouw SC; Rosendaal FR; van der Bom JG
    J Thromb Haemost; 2018 Jun; 16(6):1055-1068. PubMed ID: 29665204
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Long-Term Outcomes of Previously Treated Adult and Adolescent Patients with Severe Hemophilia A Receiving Prophylaxis with Extended Half-Life FVIII Treatments: An Economic Analysis from a United Kingdom Perspective.
    Benson G; Morton T; Thomas H; Lee XY
    Clinicoecon Outcomes Res; 2021; 13():39-51. PubMed ID: 33500640
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Comparison of Real-World Dose and Consumption for Two Extended Half-Life Recombinant Factor VIII Products for the Treatment of Hemophilia A in the United States.
    Wu Y; Sun SX; Fan T
    J Blood Med; 2022; 13():517-524. PubMed ID: 36188439
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.