Effect of the P-Selectin Inhibitor Crizanlizumab on Survival Free of Organ Support in Patients Hospitalized for COVID-19: A Randomized Controlled Trial

Author:

Solomon Scott D.1ORCID,Lowenstein Charles J.2ORCID,Bhatt Ankeet S.13,Peikert Alexander1ORCID,Vardeny Orly4,Kosiborod Mikhail N.5ORCID,Berger Jeffrey S.6ORCID,Reynolds Harmony R.6ORCID,Mavromichalis Stephanie6,Barytol Anya1,Althouse Andrew D.7ORCID,Luther James F.7,Leifer Eric S.8,Kindzelski Andrei L.8,Cushman Mary9ORCID,Gong Michelle N.10ORCID,Kornblith Lucy Z.11,Khatri Pooja12ORCID,Kim Keri S.13ORCID,Baumann Kreuziger Lisa14ORCID,Wahid Lana15ORCID,Kirwan Bridget-Anne16,Geraci Mark W.7ORCID,Neal Matthew D.7ORCID,Hochman Judith S.6ORCID,

Affiliation:

1. Cardiovascular Medicine Division, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA (S.D.S., A.S.B., A.P., A.B.).

2. Johns Hopkins School of Medicine, Baltimore, MD (C.J.L.).

3. Kaiser Permanente San Francisco Medical Center, CA (A.S.B.).

4. University of Minnesota and the Minneapolis VA Medical Center (O.V.).

5. Saint Luke’s Mid America Heart Institute, University of Missouri–Kansas City (M.N.K.).

6. Cardiovascular Clinical Research Center, NYU Grossman School of Medicine, New York (J.S.B., H.R.R., S.M., J.S.H.).

7. University of Pittsburgh, PA (A.D.A., J.F.L., M.W.G., M.D.N.).

8. National Heart, Lung, and Blood Institute, Bethesda, MD (E.S.L., A.L.K.).

9. Larner College of Medicine, University of Vermont, Burlington (M.C.).

10. Albert Einstein College of Medicine, Bronx, NY (M.N.G.).

11. University of California, San Francisco (L.Z.K.).

12. University of Cincinnati Medical Center, OH (P.K.).

13. University of Illinois, Chicago (K.S.K.).

14. Versity Blood Research Institute, Milwaukee, WI (L.B.K.).

15. Duke University, Durham, NC (L.W.).

16. Socar Research SA, Nyon, Switzerland (B.-A.K.).

Abstract

BACKGROUND: COVID-19 has been associated with endothelial injury, resultant microvascular inflammation and thrombosis. Activated endothelial cells release and express P-selectin and von Willebrand factor, both of which are elevated in severe COVID-19 and may be implicated in the disease pathophysiology. We hypothesized that crizanlizumab, a humanized monoclonal antibody to P-selectin, would reduce morbidity and death in patients hospitalized for COVID-19. METHODS: An international, adaptive, randomized controlled platform trial, funded by the National Heart, Lung, and Blood Institute, randomly assigned 422 patients hospitalized with COVID-19 with moderate or severe illness to receive either a single infusion of the P-selectin inhibitor crizanlizumab (at a dose of 5 mg/kg) plus standard of care or standard of care alone in an open-label 1:1 ratio. The primary outcome was organ support–free days, evaluated on an ordinal scale consisting of the number of days alive free of organ support through the first 21 days after trial entry. RESULTS: The study was stopped for futility by the data safety monitoring committee. Among 421 randomized patients with known 21-day outcomes, 163 patients (77%) randomized to the crizanlizumab plus standard-of-care arm did not require any respiratory or cardiovascular organ support compared with 169 (80%) in the standard-of-care–alone arm. The adjusted odds ratio for the effect of crizanlizumab on organ support–free days was 0.70 (95% CI, 0.43–1.16), where an odds ratio >1 indicates treatment benefit, yielding a posterior probability of futility (odds ratio <1.2) of 98% and a posterior probability of inferiority (odds ratio <1.0) of 91%. Overall, there were 37 deaths (17.5%) in the crizanlizumab arm and 27 deaths (12.8%) in the standard-of-care arm (hazard ratio, 1.33 [95% CrI, 0.85-2.21]; [probability of hazard ratio>1] = 0.879). CONCLUSIONS: Crizanlizumab, a P-selectin inhibitor, did not result in improvement in organ support–free days in patients hospitalized with COVID-19. REGISTRATION: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT04505774.

Funder

National Heart Lung and Blood Institute

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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