Literature DB >> 10605746

Prophylactic infusion regimens in the management of hemophilia.

R C Ljung1.   

Abstract

To summarize, prophylactic treatment of hemophilia begun at an early age has been gaining acceptance as the optimal therapeutic option in an increasing number of hemophilia centers in the developed world in recent years. In all too many parts of the world, however, this option must be viewed as a long-range goal in hemophilia care, since national economic resources are insufficient for regular prophylactic treatment to be feasible at the moment. The future development of prophylaxis seems to be focused on three different areas. First, research has focused on improving the cost-effectiveness of the current model by testing daily, frequent injections using novel devices for venous access or continuous infusion with portable or implantable mini-pumps and administration of bio-engineered concentrates with a prolonged half-life at a reduced price. Secondly, a break-through in gene therapy, which will enable us to introduce a gene producing an amount of clotting factor sufficient to provide a continuous prophylactic concentration in the blood. Finally, the most mind-challenging option makes most of the discussion in this chapter obsolete and focuses on the development of an oral compound, peptide, or peptidomimetic agent with the capacity to activate the coagulation cascade in a controllable way.

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Year:  1999        PMID: 10605746

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   5.249


  7 in total

Review 1.  Gene therapy for hemophilia.

Authors:  Amit C Nathwani
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2019-12-06

2.  Therapeutic levels of FVIII following a single peripheral vein administration of rAAV vector encoding a novel human factor VIII variant.

Authors:  Jenny McIntosh; Peter J Lenting; Cecilia Rosales; Doyoung Lee; Samira Rabbanian; Deepak Raj; Nishil Patel; Edward G D Tuddenham; Olivier D Christophe; John H McVey; Simon Waddington; Arthur W Nienhuis; John T Gray; Paolo Fagone; Federico Mingozzi; Shang-Zhen Zhou; Katherine A High; Maria Cancio; Catherine Y C Ng; Junfang Zhou; Christopher L Morton; Andrew M Davidoff; Amit C Nathwani
Journal:  Blood       Date:  2013-02-20       Impact factor: 22.113

3.  Ultrasound-mediated gene delivery of factor VIII plasmids for hemophilia A gene therapy in mice.

Authors:  Shuxian Song; Meghan J Lyle; Misty L Noble-Vranish; Dominic M Min-Tran; James Harrang; Weidong Xiao; Evan C Unger; Carol H Miao
Journal:  Mol Ther Nucleic Acids       Date:  2022-01-10       Impact factor: 8.886

4.  Efficacy, Safety and Pharmacokinetic Results of a Phase III, Open-Label, Multicenter Study with a Plasma-Derived Von Willebrand Factor (VWF)/Factor VIII (FVIII) Concentrate in Pediatric Patients <12 Years of Age with Hemophilia A (SWIFTLY-HA Study).

Authors:  Claudia Djambas Khayat; Genadi Iosava; Irina Romashevskaya; Oleksandra Stasyshyn; Marta Julia Lopez; Maria Teresa Pompa; Tobias Rogosch; Wilfried Seifert
Journal:  J Blood Med       Date:  2021-06-21

5.  Recombinant Factor IX Fc Fusion Protein Maintains Full Procoagulant Properties and Exhibits Prolonged Efficacy in Hemophilia B Mice.

Authors:  Garabet G Toby; Tongyao Liu; Yang Buyue; Xin Zhang; Alan J Bitonti; Glenn F Pierce; Jurg M Sommer; Haiyan Jiang; Robert T Peters
Journal:  PLoS One       Date:  2016-02-03       Impact factor: 3.240

6.  Preclinical evaluation of a next-generation, subcutaneously administered, coagulation factor IX variant, dalcinonacog alfa.

Authors:  Timothy C Nichols; Howard Levy; Elizabeth P Merricks; Robin A Raymer; Martin L Lee
Journal:  PLoS One       Date:  2020-10-28       Impact factor: 3.240

7.  Efficacy and safety of subcutaneous prophylaxis with dalcinonacog alfa in adults with haemophilia B.

Authors:  Johnny Mahlangu; Howard Levy; Martin Lee; Frank Del Greco
Journal:  Haemophilia       Date:  2021-05-06       Impact factor: 4.287

  7 in total

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