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Chlorpheniramine Intranasal Spray to Accelerate COVID-19 Clinical Recovery in an Outpatient Setting: The ACCROS Trials

Valerio-Pascua et al., Research Square, doi:10.21203/rs.3.rs-2167465/v1, ACCROS-I, NCT05449405
Oct 2022  
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Recovery, all symptoms.. 61% Improvement Relative Risk Recovery, anosmia 67% Recovery, ageusia 89% Recovery, cough 53% Recovery, fatigue 67% Recovery, nasal congestion 59% PASC score 74% Chlorpheniramine  ACCROS-I  EARLY TREATMENT  DB RCT Is early treatment with chlorpheniramine beneficial for COVID-19? Double-blind RCT 101 patients in Honduras (June 2021 - July 2022) Improved recovery (p=0.00018) and lower PASC (p=0.001) c19early.org Valerio-Pascua et al., Research Square, Oct 2022 Favorschlorpheniramine Favorscontrol 0 0.5 1 1.5 2+
40th treatment shown to reduce risk in December 2022, now with p < 0.00000000001 from 3 studies.
Lower risk for recovery.
No treatment is 100% effective. Protocols combine treatments.
5,100+ studies for 112 treatments. c19early.org
RCT and retrospective study of chlorpheniramine nasal spray for COVID-19. The RCT included 101 outpatients showing significantly faster recovery with treatment. The retrospective study results are listed separately1. Long COVID results are from Valerio-Pascua (B) et al..
4 studies use direct respiratory tract administration3-6
Targeted administration to the respiratory tract provides treatment directly to the typical source of initial SARS-CoV-2 infection and replication, and allows for rapid onset of action, higher local drug concentration, and reduced systemic side effects.
Study covers antihistamine H1RAs and chlorpheniramine.
risk of no recovery, 61.4% lower, RR 0.39, p < 0.001, treatment 61, control 40, all symptoms combined.
risk of no recovery, 67.2% lower, RR 0.33, p = 0.15, treatment 3 of 61 (4.9%), control 6 of 40 (15.0%), NNT 9.9, day 7, anosmia.
risk of no recovery, 89.1% lower, RR 0.11, p = 0.01, treatment 1 of 61 (1.6%), control 6 of 40 (15.0%), NNT 7.5, day 7, ageusia.
risk of no recovery, 53.2% lower, RR 0.47, p = 0.05, treatment 10 of 61 (16.4%), control 14 of 40 (35.0%), NNT 5.4, day 7, cough.
risk of no recovery, 67.2% lower, RR 0.33, p = 0.21, treatment 2 of 61 (3.3%), control 4 of 40 (10.0%), NNT 15, day 7, fatigue.
risk of no recovery, 59.0% lower, RR 0.41, p = 0.13, treatment 5 of 61 (8.2%), control 8 of 40 (20.0%), NNT 8.5, day 7, nasal congestion.
relative PASC score, 73.5% better, RR 0.26, p < 0.001, treatment 55, control 46, relative average composite PASC score.
Effect extraction follows pre-specified rules prioritizing more serious outcomes. Submit updates
Valerio-Pascua et al., 18 Oct 2022, Double Blind Randomized Controlled Trial, placebo-controlled, Honduras, preprint, 16 authors, study period June 2021 - July 2022, trial NCT05449405 (history) (ACCROS-I). Contact: rahaghf@ccf.org.
This PaperChlorphenira..All
Chlorpheniramine Intranasal Spray to Accelerate COVID-19 Clinical Recovery in an Outpatient Setting: The ACCROS Trials
Fernando Valerio-Pascua, Estela Jackeline Pineda Mejia, Mari L Tesch, Jancy Godoy, Carlos López Fuentes, Gloria B Erazo, Marco Bermúdez, Miguel Fernando Vargas Pineda, Syed A A Rivzi, Armando Cabrera, Zeeshan Chauhan, Scarlet Grullón-Franco, Jorge L Paulino-Then, Natalia Garcia, Jeffrey D Williams, Franck F Rahaghi
doi:10.21203/rs.3.rs-2167465/v1
Purpose: Our group demonstrated the safety, e cacy, and antiviral effect of intranasally administered Chlorpheniramine Maleate (CPM) for treating coronavirus disease 2019 . Since the nasal cavity is the portal of entry for COVID pathogens, sensory and upper respiratory symptoms (URS) (e.g., cough, ageusia, anosmia, nasal congestion, etc.) are signi cant symptoms in the course of the disease. Intranasal therapies could alleviate the disease-induced URS faster. This study evaluated the effectiveness and safety of intranasal CPM for treating mild to moderate COVID-19-induced URS in the outpatient setting. Methods: The two-part Accelerating COVID-19 Clinical Recovery in an Outpatient Setting (ACCROS) research study was conducted to collect evidence from a randomized, double-blinded placebo-controlled trial (ACCROS-I). Both parts enrolled patients with mild to moderate COVID-19 con rmed by reverse transcription-polymerase chain reaction. The primary endpoint in ACCROS-I was time to clinical recovery, de ned as the change from baseline to day 7 in COVID-19 symptoms reported as the percent change (Δ%) in the daily symptoms score (DSS) and the severity of the disease symptoms using a visual analog scale (VAS), on a scale of 1-10 (10=worst symptoms). COVID-19 patients (n = 101) were recruited and assigned to either a 10-day CPM treatment (n=61) or placebo (PLB) (n=40) in addition to standard of care (SoC). Secondary endpoints included the incidence of hospitalization and the proportion of patients with URS on day 7. ACCROS-II data were collected from medical records of COVID-positive subjects using a standardized form. Cohorts of patients treated with CPM and SoC (CPM+Soc) were compared for the duration of general symptoms and URS. Patient information was collected as part of routine visits and telehealth consultations. Results ACCROS-I: There was a statistically signi cant difference in the rate of clinical recovery (P<0.05) in Δ%DSS (M -18.8±SEM 7.9%) and Δ%VAS (-8.6±5.1%), such that the CPM group reported fewer symptoms than PLB. The proportion of patients who reported sensory de cits and URS at day 7 was signi cantly lower (P<0.05) in CPM vs. PLB for ageusia (1.7% vs. 15.0%), cough (16.4% vs. 35.0%) and nasal congestion (8.1%vs.20%). None of the patients required hospitalization. ACCROS-II: There was a statistically signi cant reduction (P<0.05) in total days reporting URS for general symptoms of COVID-19 in CPM+SoC (5.1 ± 0.1) compared to SoC (11.0 ± 0.2). CPM+SoC users also showed fewer days with cough, anosmia, and ageusia. Persistent anosmia (over 29 days) was found in 3% of the patients on SoC, whereas no persistent anosmia was reported in the CPM+SoC cohort (X 2 = 10.18; P<0.001). Conclusion: The result of this two-part study supports the conclusion that intranasal CPM is an antiviral agent that can be administered intranasally to treat COVID-19-induced symptoms effectively. Intranasal CPM accelerates clinical recovery and reduces..
Supplementary Files This is a list of supplementary les associated with this preprint. Click to download. Tables.docx
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{ 'institution': [{'name': 'Research Square'}], 'indexed': { 'date-parts': [[2022, 10, 25]], 'date-time': '2022-10-25T05:06:49Z', 'timestamp': 1666674409162}, 'posted': {'date-parts': [[2022, 10, 18]]}, 'group-title': 'In Review', 'reference-count': 39, 'publisher': 'Research Square Platform LLC', 'license': [ { 'start': { 'date-parts': [[2022, 10, 18]], 'date-time': '2022-10-18T00:00:00Z', 'timestamp': 1666051200000}, 'content-version': 'unspecified', 'delay-in-days': 0, 'URL': 'https://creativecommons.org/licenses/by/4.0/'}], 'content-domain': {'domain': [], 'crossmark-restriction': False}, 'accepted': {'date-parts': [[2022, 10, 14]]}, 'abstract': '<jats:title>Abstract</jats:title>\n' ' <jats:p><jats:bold>Purpose: </jats:bold>Our group demonstrated the safety, efficacy, ' 'and antiviral effect of intranasally administered Chlorpheniramine Maleate (CPM) for treating ' 'coronavirus disease 2019 (COVID-19). Since the nasal cavity is the portal of entry for COVID ' 'pathogens, sensory and upper respiratory symptoms (URS) (e.g., cough, ageusia, anosmia, nasal ' 'congestion, etc.) are significant symptoms in the course of the disease. Intranasal therapies ' 'could alleviate the disease-induced URS faster. This study evaluated the effectiveness and ' 'safety of intranasal CPM for treating mild to moderate COVID-19-induced URS in the outpatient ' 'setting.\n' '<jats:bold>Methods: </jats:bold>The two-part <jats:bold>A</jats:bold>ccelerating ' '<jats:bold>C</jats:bold>OVID-19 <jats:bold>C</jats:bold>linical ' '<jats:bold>R</jats:bold>ecovery in an <jats:bold>O</jats:bold>utpatient ' '<jats:bold>S</jats:bold>etting (ACCROS) research study was conducted to collect evidence from ' 'a randomized, double-blinded placebo-controlled trial (ACCROS-I). Both parts enrolled ' 'patients with mild to moderate COVID-19 confirmed by reverse transcription-polymerase chain ' 'reaction. The primary endpoint in ACCROS-I was time to clinical recovery, defined as the ' 'change from baseline to day 7 in COVID-19 symptoms reported as the percent change (Δ%) in the ' 'daily symptoms score (DSS) and the severity of the disease symptoms using a visual analog ' 'scale (VAS), on a scale of 1-10 (10=worst symptoms). COVID-19 patients (n = 101) were ' 'recruited and assigned to either a 10-day CPM treatment (n=61) or placebo (PLB) (n=40) in ' 'addition to standard of care (SoC). Secondary endpoints included the incidence of ' 'hospitalization and the proportion of patients with URS on day 7. ACCROS-II data were ' 'collected from medical records of COVID-positive subjects using a standardized form. Cohorts ' 'of patients treated with CPM and SoC (CPM+Soc) were compared for the duration of general ' 'symptoms and URS. Patient information was collected as part of routine visits and telehealth ' 'consultations.\n' '<jats:bold>Results </jats:bold><jats:italic>ACCROS-I:</jats:italic> There was a statistically ' 'significant difference in the rate of clinical recovery (P&lt;0.05) in Δ%DSS (M -18.8±SEM ' '7.9%) and Δ%VAS (-8.6±5.1%), such that the CPM group reported fewer symptoms than PLB. The ' 'proportion of patients who reported sensory deficits and URS at day 7 was significantly lower ' '(P&lt;0.05) in CPM vs. PLB for ageusia (1.7% vs. 15.0%), cough (16.4% vs. 35.0%) and nasal ' 'congestion (8.1%vs.20%). None of the patients required hospitalization.\n' '<jats:italic>ACCROS-II</jats:italic>: There was a statistically significant reduction ' '(P&lt;0.05) in total days reporting URS for general symptoms of COVID-19 in CPM+SoC (5.1 ± ' '0.1) compared to SoC (11.0 ± 0.2). CPM+SoC users also showed fewer days with cough, anosmia, ' 'and ageusia. Persistent anosmia (over 29 days) was found in 3% of the patients on SoC, ' 'whereas no persistent anosmia was reported in the CPM+SoC cohort (X<jats:sup>2</jats:sup> = ' '10.18; P&lt;0.001).\n' '<jats:bold>Conclusion:</jats:bold> The result of this two-part study supports the conclusion ' 'that intranasal CPM is an antiviral agent that can be administered intranasally to treat ' 'COVID-19-induced symptoms effectively. Intranasal CPM accelerates clinical recovery and ' "reduces URS in patients with mild to moderate COVID-19. This study's important implications " 'include individuals returning to daily life faster, reducing community and individual ' 'economic burden, and decreasing healthcare utilization.\n' '<jats:bold>Trial registration:</jats:bold> ClinicalTrials.gov.; ID: NCT05449405 ACCROS-I ' 'retrospectively registered on 7/13/2022, NCT05520944 ACCROS-R retrospectively registered on ' '08/27/2022.</jats:p>', 'DOI': '10.21203/rs.3.rs-2167465/v1', 'type': 'posted-content', 'created': { 'date-parts': [[2022, 10, 18]], 'date-time': '2022-10-18T18:11:18Z', 'timestamp': 1666116678000}, 'source': 'Crossref', 'is-referenced-by-count': 0, 'title': 'Chlorpheniramine Intranasal Spray to Accelerate COVID-19 Clinical Recovery in an Outpatient ' 'Setting: The ACCROS Trials', 'prefix': '10.21203', 'author': [ { 'given': 'Fernando', 'family': 'Valerio-Pascua', 'sequence': 'first', 'affiliation': [{'name': 'Hospital CEMESA Cortés'}]}, { 'given': 'Estela Jackeline Pineda', 'family': 'Mejia', 'sequence': 'additional', 'affiliation': [{'name': 'Hospital CEMESA Cortés'}]}, { 'given': 'Mari L.', 'family': 'Tesch', 'sequence': 'additional', 'affiliation': [{'name': 'Aventura Hospital Pulmonary and Critical Care Fellowship'}]}, { 'given': 'Jancy', 'family': 'Godoy', 'sequence': 'additional', 'affiliation': [{'name': 'Hospital Leonardo Martínez Valenzuela'}]}, { 'given': 'Carlos López', 'family': 'Fuentes', 'sequence': 'additional', 'affiliation': [{'name': 'Universidad Católica de Honduras'}]}, { 'given': 'Gloria B.', 'family': 'Erazo', 'sequence': 'additional', 'affiliation': [{'name': 'Universidad Católica de Honduras'}]}, { 'given': 'Marco', 'family': 'Bermúdez', 'sequence': 'additional', 'affiliation': [{'name': 'Universidad Católica de Honduras'}]}, { 'given': 'Miguel Fernando Vargas', 'family': 'Pineda', 'sequence': 'additional', 'affiliation': [{'name': 'Saint Barnabas Hospital'}]}, { 'given': 'Syed A.A.', 'family': 'Rivzi', 'sequence': 'additional', 'affiliation': [{'name': 'Hampton University School of Pharmacy'}]}, { 'given': 'Armando', 'family': 'Cabrera', 'sequence': 'additional', 'affiliation': [{'name': 'Aventura Hospital Pulmonary and Critical Care Fellowship'}]}, { 'given': 'Zeeshan', 'family': 'Chauhan', 'sequence': 'additional', 'affiliation': [{'name': 'Aventura Hospital Pulmonary and Critical Care Fellowship'}]}, { 'given': 'Scarlet', 'family': 'Grullón-Franco', 'sequence': 'additional', 'affiliation': [{'name': 'Clinica Universitaria Union Medica'}]}, { 'given': 'Jorge L.', 'family': 'Paulino-Then', 'sequence': 'additional', 'affiliation': [{'name': 'Clinica Universitaria Union Medica'}]}, { 'given': 'Natalia', 'family': 'Garcia', 'sequence': 'additional', 'affiliation': [{'name': 'Clinica Universitaria Union Medica'}]}, { 'given': 'Jeffrey D.', 'family': 'Williams', 'sequence': 'additional', 'affiliation': [{'name': 'The George Washington University'}]}, { 'given': 'Franck F.', 'family': 'Rahaghi', 'sequence': 'additional', 'affiliation': [{'name': 'Cleveland Clinic'}]}], 'member': '8761', 'reference': [ { 'issue': '6', 'key': 'ref1', 'doi-asserted-by': 'crossref', 'first-page': 'ofac138', 'DOI': '10.1093/ofid/ofac138', 'article-title': 'A Systematic Review of Coronavirus Disease 2019 Vaccine Efficacy and ' 'Effectiveness Against Severe Acute Respiratory Syndrome Coronavirus 2 ' 'Infection and Disease', 'volume': '9', 'author': 'Higdon MM', 'year': '2022', 'unstructured': 'Higdon, M.M., et al., A Systematic Review of Coronavirus Disease 2019 ' 'Vaccine Efficacy and Effectiveness Against Severe Acute Respiratory ' 'Syndrome Coronavirus 2 Infection and Disease. 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