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Novel Tissue Factor Inhibition for Thromboprophylaxis in COVID-19: Primary Results of the ASPEN-COVID-19 Trial.
Hess, Connie N; Hsia, Judith; Carroll, Ian A; Nehler, Mark R; Ruf, Wolfram; Morrow, David A; Nicolau, Jose C; Berwanger, Otavio; Szarek, Michael; Capell, Warren H; Johri, Shilpa; Pursley, Michael S; Gupta, Ryan; Meehan, Patrick S; Franchi, Francesco; Effron, Mark B; Marshall, Debra; Graybill, Christopher A; Huebler, Sophia P; Keuer, Thomas; Bristow, Michael R; Bonaca, Marc P.
Afiliação
  • Hess CN; Department of Medicine (C.N.H., J.H., M.S., W.H.C., M.R.B., M.P.B.), University of Colorado, Aurora.
  • Hsia J; CPC Clinical Research, Aurora, CO (C.N.H., J.H., M.R.N., M.S., W.H.C., R.G., M.P.B.).
  • Carroll IA; Department of Medicine (C.N.H., J.H., M.S., W.H.C., M.R.B., M.P.B.), University of Colorado, Aurora.
  • Nehler MR; CPC Clinical Research, Aurora, CO (C.N.H., J.H., M.R.N., M.S., W.H.C., R.G., M.P.B.).
  • Ruf W; ARCA biopharma, Westminster, CO (I.A.C., D.M., C.A.G., S.P.H., T.K., M.R.B.).
  • Morrow DA; Department of Surgery (M.R.N., R.G.), University of Colorado, Aurora.
  • Nicolau JC; CPC Clinical Research, Aurora, CO (C.N.H., J.H., M.R.N., M.S., W.H.C., R.G., M.P.B.).
  • Berwanger O; Johannes Gutenberg University Medical Center, Mainz, Germany (W.R.).
  • Szarek M; Scripps Research, La Jolla, CA (W.R.).
  • Capell WH; Brigham and Women's Hospital, Harvard Medical School, Boston, MA (D.A.M.).
  • Johri S; Instituto do Coracao (InCor), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, SP, Brazil (J.C.N.).
  • Pursley MS; Hospital Israelita Albert Einstein, Sao Paulo, Brazil (O.B.).
  • Gupta R; Department of Medicine (C.N.H., J.H., M.S., W.H.C., M.R.B., M.P.B.), University of Colorado, Aurora.
  • Meehan PS; CPC Clinical Research, Aurora, CO (C.N.H., J.H., M.R.N., M.S., W.H.C., R.G., M.P.B.).
  • Franchi F; The State University of New York Downstate Health Sciences University, Brooklyn (M.S.).
  • Effron MB; Department of Medicine (C.N.H., J.H., M.S., W.H.C., M.R.B., M.P.B.), University of Colorado, Aurora.
  • Marshall D; CPC Clinical Research, Aurora, CO (C.N.H., J.H., M.R.N., M.S., W.H.C., R.G., M.P.B.).
  • Graybill CA; Pulmonary Associates of Richmond, VA (S.J.).
  • Huebler SP; Eastern Shore Research Institute, Fairhope, AL (M.S.P.).
  • Keuer T; Department of Surgery (M.R.N., R.G.), University of Colorado, Aurora.
  • Bristow MR; CPC Clinical Research, Aurora, CO (C.N.H., J.H., M.R.N., M.S., W.H.C., R.G., M.P.B.).
  • Bonaca MP; MultiCare Pulmonary Specialists, Tacoma, WA (P.S.M.).
Arterioscler Thromb Vasc Biol ; 43(8): 1572-1582, 2023 08.
Article em En | MEDLINE | ID: mdl-37381988
ABSTRACT

BACKGROUND:

Thrombo-inflammation is central to COVID-19-associated coagulopathy. TF (tissue factor), a driver of disordered coagulation and inflammation in viral infections, may be a therapeutic target in COVID-19. The safety and efficacy of the novel TF inhibitor rNAPc2 (recombinant nematode anticoagulation protein c2) in COVID-19 are unknown.

METHODS:

ASPEN-COVID-19 was an international, randomized, open-label, active comparator clinical trial with blinded end point adjudication. Hospitalized patients with COVID-19 and elevated D-dimer levels were randomized 112 to lower or higher dose rNAPc2 on days 1, 3, and 5 followed by heparin on day 8 or to heparin per local standard of care. In comparisons of the pooled rNAPc2 versus heparin groups, the primary safety end point was major or nonmajor clinically relevant International Society of Thrombosis and Haemostasis bleeding through day 8. The primary efficacy end point was proportional change in D-dimer concentration from baseline to day 8, or discharge if before day 8. Patients were followed for 30 days.

RESULTS:

Among 160 randomized patients, median age was 54 years, 43.1% were female, and 38.8% had severe baseline COVID-19. There were no significant differences between rNAPc2 and heparin in bleeding or other safety events. Overall, median change in D-dimer was -16.8% (interquartile range, -45.7 to 36.8; P=0.41) with rNAPc2 treatment and -11.2% (-36.0 to 34.4; P=0.91) with heparin (Pintergroup=0.47). In prespecified analyses, in severely ill patients, D-dimer levels tended to increase more within the heparin (median, 29.0% [-14.9 to 145.2]; P=0.02) than the rNAPc2 group (median, 25.9% [-49.1 to 136.4]; P=0.14; Pintergroup=0.96); in mildly ill patients, D-dimer levels were reduced within each group with a numerically greater reduction with rNAPc2 versus heparin (rNAPc2 median, -32.7% [-44.7 to 4.3]; P=0.007 and heparin median, -16.8% [-36.0 to 0.5]; P=0.008, Pintergroup=0.34).

CONCLUSIONS:

rNAPc2 treatment in hospitalized patients with COVID-19 was well tolerated without excess bleeding or serious adverse events but did not significantly reduce D-dimer more than heparin at day 8. REGISTRATION URL https//www. CLINICALTRIALS gov; Unique identifier NCT04655586.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos da Coagulação Sanguínea / Produtos de Degradação da Fibrina e do Fibrinogênio / Tromboembolia Venosa / COVID-19 / Antifibrinolíticos Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Arterioscler Thromb Vasc Biol Assunto da revista: ANGIOLOGIA Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos da Coagulação Sanguínea / Produtos de Degradação da Fibrina e do Fibrinogênio / Tromboembolia Venosa / COVID-19 / Antifibrinolíticos Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Arterioscler Thromb Vasc Biol Assunto da revista: ANGIOLOGIA Ano de publicação: 2023 Tipo de documento: Article