Abstract: Background. Progression from mild to severe SARS-CoV-2 infection correlates
with humoral and cellular immune signatures that adjust to a multiplying viral load.
Enhancing immunity with host-directed therapy, such as sargramostim (yeastderived, recombinant human granulocyte-macrophage colony-stimulating factor
[GM-CSF]), may prevent disease progression and reduce severity.
Methods. This prospective, randomized, double-blind, placebo-controlled study
enrolled symptomatic vaccinated and unvaccinated non-hospitalized patients with
mild/moderate COVID-19 at high risk for progression. Patients received daily sargramostim 250 mcg or placebo, inhaled via nebulizer, for 5 days. Figure 1 lists study
endpoints.
Abstract citation ID: ofad500.351
279. Inhaled Sargramostim (rhu GM-CSF) Leads to Enhanced SARS-CoV-2
Virus-Specific Immune Response and Viral Clearance: Results of the Biomarker
Cohort of a Randomized, Double-Blind, Placebo-Controlled Phase 2b Trial in
Non-Hospitalized Patients with COVID-19
Ila Joshi, PhD1; Fiona Garner, PhD1; Debasish F. Roychowdhury, MD1;
Lorinda Simms, MSc1; Sanjeev Ahuja, MD1; John L. McManus, n/a1; Edwin P. Rock,
MD, PhD1; Rodolfo Perez, MD2; Sandro Bacchelli, MD2; Robert PaineIII, MD3;
1
Partner Therapeutics, Inc., Lexington, Massachusetts; 2Encore Medical Research,
Hollywood, Florida; 3University of Utah, Salt Lake City, Utah
Session: 41. Basic Science and Translational Studies
Thursday, October 12, 2023: 12:15 PM
S184 • OFID 2023:10 (Suppl 2) • Poster Abstracts
Results. From April 28, 2021 to January 31, 2022, 101 patients consented and
provided samples for the biomarker cohort (Fig 2).
No difference was seen in the overall study primary endpoint (n=21/301
sargramostim, n=16/299 placebo, p=0.4). Treatment-emergent adverse events were
similar in both arms. In the biomarker cohort, SARS-CoV-2 viral clearance by day
14 was enhanced on the sargramostim arm (p=0.0064, Fig 3). Virus was
undetectable in a larger proportion on the sargramostim arm. Sargramostim
reduced viral load more in vaccinated than unvaccinated patients. Inflammatory
cytokine levels did not increase with treatment.
Kinetics and magnitude of antibody response against SARS-CoV-2 antigens
differed by group. After an initial IgM-titer peak at day 14, IgM titers at day 28
were lower in the vaccinated-sargramostim arm than the vaccinated-placebo arm
(Fig 4A). The unvaccinated-sargramostim arm maintained higher IgM titers than
the unvaccinated-placebo arm. Overall IgG titers were higher for vaccinated
patients across both treatment arms. However, the vaccinated-sargramostim arm
had higher IgG4 titers associated with IgG4-isotype-class switching than the
vaccinated-placebo arm (Fig 4B).
Conclusion. The primary clinical endpoint was not met. Biomarker analyses suggest inhaled sargramostim reduces SARS-CoV-2 viral load and alters humoral kinetics
and expression, more so in those vaccinated. Results suggest the potential of sargramostim as a virus agnostic, host-directed immunomodulator.
Disclosures. Ila Joshi, PhD, Partner Therapeutics, Inc.: Patents|Partner
Therapeutics, Inc.: Salary|Partner Therapeutics, Inc.: Stocks/Bonds Fiona Garner,
PhD, Partner Therapeutics, Inc.: Employment|Partner Therapeutics, Inc.: Stocks/
Bonds..
DOI record:
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"abstract": "<jats:title>Abstract</jats:title>\n <jats:sec>\n <jats:title>Background</jats:title>\n <jats:p>Progression from mild to severe SARS-CoV-2 infection correlates with humoral and cellular immune signatures that adjust to a multiplying viral load. Enhancing immunity with host-directed therapy, such as sargramostim (yeast-derived, recombinant human granulocyte-macrophage colony-stimulating factor [GM-CSF]), may prevent disease progression and reduce severity.</jats:p>\n </jats:sec>\n <jats:sec>\n <jats:title>Methods</jats:title>\n <jats:p>This prospective, randomized, double-blind, placebo-controlled study enrolled symptomatic vaccinated and unvaccinated non-hospitalized patients with mild/moderate COVID-19 at high risk for progression. Patients received daily sargramostim 250 mcg or placebo, inhaled via nebulizer, for 5 days. Figure 1 lists study endpoints.</jats:p>\n </jats:sec>\n <jats:sec>\n <jats:title>Results</jats:title>\n <jats:p>From April 28, 2021 to January 31, 2022, 101 patients consented and provided samples for the biomarker cohort (Fig 2).</jats:p>\n <jats:p>No difference was seen in the overall study primary endpoint (n=21/301 sargramostim, n=16/299 placebo, p=0.4). Treatment-emergent adverse events were similar in both arms. In the biomarker cohort, SARS-CoV-2 viral clearance by day 14 was enhanced on the sargramostim arm (p=0.0064, Fig 3). Virus was undetectable in a larger proportion on the sargramostim arm. Sargramostim reduced viral load more in vaccinated than unvaccinated patients. Inflammatory cytokine levels did not increase with treatment.</jats:p>\n <jats:p>Kinetics and magnitude of antibody response against SARS-CoV-2 antigens differed by group. After an initial IgM-titer peak at day 14, IgM titers at day 28 were lower in the vaccinated-sargramostim arm than the vaccinated-placebo arm (Fig 4A). The unvaccinated-sargramostim arm maintained higher IgM titers than the unvaccinated-placebo arm. Overall IgG titers were higher for vaccinated patients across both treatment arms. However, the vaccinated-sargramostim arm had higher IgG4 titers associated with IgG4-isotype-class switching than the vaccinated-placebo arm (Fig 4B).</jats:p>\n </jats:sec>\n <jats:sec>\n <jats:title>Conclusion</jats:title>\n <jats:p>The primary clinical endpoint was not met. Biomarker analyses suggest inhaled sargramostim reduces SARS-CoV-2 viral load and alters humoral kinetics and expression, more so in those vaccinated. Results suggest the potential of sargramostim as a virus agnostic, host-directed immunomodulator.</jats:p>\n </jats:sec>\n <jats:sec>\n <jats:title>Disclosures</jats:title>\n <jats:p>Ila Joshi, PhD, Partner Therapeutics, Inc.: Patents|Partner Therapeutics, Inc.: Salary|Partner Therapeutics, Inc.: Stocks/Bonds Fiona Garner, PhD, Partner Therapeutics, Inc.: Employment|Partner Therapeutics, Inc.: Stocks/Bonds Debasish F. Roychowdhury, MD, Partner Therapeutics, Inc.: Employment|Partner Therapeutics, Inc.: Ownership Interest|Partner Therapeutics, Inc.: Stocks/Bonds Lorinda Simms, MSc, Partner Therapeutics, Inc.: Advisor/Consultant|Partner Therapeutics, Inc.: Stocks/Bonds Sanjeev Ahuja, MD, Partner Therapeutics, Inc.: Employment|Partner Therapeutics, Inc.: Stocks/Bonds|Scioto Biosciences: Past Employee John L. McManus, n/a, JPEO-CBRND's Joint Project Manager for Chemical, Biological, Radiological, and Nuclear Medical: Project agreement MCDC2006-012. Included references to commercial products do not constitute an endorsement by the US DoD or the JPEO-CBRND.|Partner Therapeutics, Inc.: Employment|Partner Therapeutics, Inc.: Stocks/Bonds Edwin P. Rock, MD, PhD, Partner Therapeutics: Employment Robert Paine III, MD, Partner Therapeutics, Inc.: Advisor/Consultant</jats:p>\n </jats:sec>",
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