Analgesics
Antiandrogens
Antihistamines
Azvudine
Bromhexine
Budesonide
Colchicine
Conv. Plasma
Curcumin
Famotidine
Favipiravir
Fluvoxamine
Hydroxychlor..
Ivermectin
Lifestyle
Melatonin
Metformin
Minerals
Molnupiravir
Monoclonals
Naso/orophar..
Nigella Sativa
Nitazoxanide
PPIs
Paxlovid
Quercetin
Remdesivir
Thermotherapy
Vitamins
More

Other
Feedback
Home
Top
Results
Abstract
All chlorpheniramine studies
Meta analysis
 
Feedback
Home
next
study
previous
study
c19early.org COVID-19 treatment researchChlorpheniramineChlorphenira.. (more..)
Melatonin Meta
Metformin Meta
Antihistamines Meta
Azvudine Meta Molnupiravir Meta
Bromhexine Meta
Budesonide Meta
Colchicine Meta Nigella Sativa Meta
Conv. Plasma Meta Nitazoxanide Meta
Curcumin Meta PPIs Meta
Famotidine Meta Paxlovid Meta
Favipiravir Meta Quercetin Meta
Fluvoxamine Meta Remdesivir Meta
Hydroxychlor.. Meta Thermotherapy Meta
Ivermectin Meta

All Studies   Meta Analysis       

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  
  Post
  Facebook
Share
  Source   PDF   All Studies   Meta AnalysisMeta
Recovery, all symptoms.. 61% Improvement Relative Risk Recovery, anosmia 67% Recovery, ageusia 89% Recovery, cough 53% Recovery, fatigue 67% Recovery, nasal congestion 59% 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 with chlorpheniramine (p=0.00018) 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 109 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.
3 studies use direct respiratory tract administration2-4
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.
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
References
Alexander, Early multidrug treatment of SARS-CoV-2 infection (COVID-19) and reduced mortality among nursing home (or outpatient/ambulatory) residents, Med Hypotheses
Basu, A model-based approach to improve intranasal sprays for respiratory viral infections, medRxiv
Basu, Computational characterization of inhaled droplet transport to the nasopharynx, Sci Rep
Black, Molecular Modeling and Preliminary Clinical Data Suggesting Antiviral Activity for Chlorpheniramine (Chlorphenamine) Against COVID-19, Cureus
Blanco, Antihistamines and azithromycin as a treatment for COVID-19 on primary health care -A retrospective observational study in elderly patients, Pulm Pharmacol Ther
Bousquet, Visual analog scales can assess the severity of rhinitis graded according to ARIA guidelines, Allergy
Carey, Taste Receptors: Regulators of Sinonasal Innate Immunity, Laryngoscope Investig Otolaryngol
Chang, Chlorpheniramine attenuates histamine-mediated aquaporin 5 downregulation in human nasal epithelial cells via suppression of NF-κB activation, Int J Med Sci
Fang, Druce, Baraniuk, Anticholinergic properties of brompheniramine, chlorpheniramine, and atropine in human nasal mucosa in vitro, Am J Rhinol
Gies, Beyond Anti-viral Effects of Chloroquine/Hydroxychloroquine, Front Immunol
Grassin-Delyle, Bitter Taste Receptors (TAS2Rs) in Human Lung Macrophages: Receptor Expression and Inhibitory Effects of TAS2R Agonists, Frontiers in Physiology
Groenewold, Increases in Health-Related Workplace Absenteeism Among Workers in Essential Critical Infrastructure Occupations During the COVID-19 Pandemic -United States, March-April 2020, MMWR Morb Mortal Wkly Rep
Higdon, A Systematic Review of Coronavirus Disease 2019 Vaccine E cacy and Effectiveness Against Severe Acute Respiratory Syndrome Coronavirus 2 Infection and Disease, Open Forum Infect Dis
Klussmann, COVID-19: Azelastine nasal spray Reduces Virus-load In Nasal swabs (CARVIN). Early with azelastine nasal sprays reduces viral load in SARS-CoV-2 infected patients. First report on a double-blind placebo-controlled phase II clinical trial
Kumar, Cheng, A hypothesis: Bitter taste receptors as a therapeutic target for the clinical symptoms of SARS-CoV-2, Pharmazie
Lee, ACE2 localizes to the respiratory cilia and is not increased by ACE inhibitors or ARBs, Nature Communications
Lee, Bitter and sweet taste receptors regulate human upper respiratory innate immunity, J Clin Invest
Li, Existing bitter medicines for ghting 2019-nCoV-associated infectious diseases, Faseb j
Malone, COVID-19: Famotidine, Histamine, Mast Cells, and Mechanisms, Front Pharmacol
Mostafa, FDA-Approved Drugs with Potent In Vitro Antiviral Activity against Severe Acute Respiratory Syndrome Coronavirus 2, Pharmaceuticals
Nathwani, Impact of COVID-2019 on school attendance problems, J Glob Health
Ontai, Early multidrug treatment of SARS-CoV-2 (COVID-19) and decreased case fatality rates in Honduras, medRxiv
Orzechowski, Currie, Valancius, Comparative anticholinergic activities of 10 histamine H1 receptor antagonists in two functional models, Eur J Pharmacol
Osmanov, Risk factors for post-COVID-19 condition in previously hospitalised children using the ISARIC Global follow-up protocol: a prospective cohort study, European Respiratory Journal
Pocock, Simon, Sequential treatment assignment with balancing for prognostic factors in the controlled clinical trial, Biometrics
Popa, Bronchodilating activity of an H1 blocker, chlorpheniramine, J Allergy Clin Immunol
Rizvi, Chlorpheniramine, an Old Drug with New Potential Clinical Applications: A Comprehensive Review of the Literature, Current Reviews in Clinical and Experimental Pharmacology
Sanchez-Gonzalez, A Pathophysiological Perspective on COVID-19's Lethal Complication: From Viremia to Hypersensitivity Pneumonitis-like Immune Dysregulation, Infect Chemother
Sanchez-Gonzalez, A Randomized Controlled Pilot Trial to Test the E cacy of Intranasal Chlorpheniramine Maleate With Xylitol for the Treatment of Allergic Rhinitis, Cureus
Sanchez-Gonzalez, Intranasal Chlorpheniramine Maleate for the treatment of COVID-19: Translational and Clinical Evidence, Medical Research Archives
Sarkar, The Association between Early-Life Gut Microbiota and Long-Term Health and Diseases, J Clin Med
Taha, Treatment Protocol for COVID-19 Based on T2R Phenotype, Viruses
Torres, Chlorpheniramine Maleate Nasal Spray In COVID-19 Patients: Case Series, J Clin Exp Pharmacol
Valerio Pascua, Repurposing Drugs for Covid-19 by a Developing Country, Epidemol Int J
Vitiello, Sars-Cov-2 and risk of antiviral drug resistance, Ir J Med Sci
Westover, In Vitro Virucidal Effect of Intranasally Delivered Chlorpheniramine Maleate Compound Against Severe Acute Respiratory Syndrome Coronavirus 2, Cureus
Wu, SARS-CoV-2-triggered mast cell rapid degranulation induces alveolar epithelial in ammation and lung injury, Signal Transduction and Targeted Therapy
{ '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. Open Forum Infect Dis, ' '2022. 9(6): p.\xa0ofac138.', 'journal-title': 'Open Forum Infect Dis'}, { 'key': 'ref2', 'volume-title': "A Pathophysiological Perspective on COVID-19's Lethal Complication: From " 'Viremia to Hypersensitivity Pneumonitis-like Immune Dysregulation', 'author': 'Sanchez-Gonzalez MA', 'year': '2020', 'unstructured': 'Sanchez-Gonzalez, M.A., et al., A Pathophysiological Perspective on ' "COVID-19's Lethal Complication: From Viremia to Hypersensitivity " 'Pneumonitis-like Immune Dysregulation. Infect Chemother, 2020.'}, { 'issue': '1', 'key': 'ref3', 'doi-asserted-by': 'crossref', 'first-page': '428', 'DOI': '10.1038/s41392-021-00849-0', 'article-title': 'SARS-CoV-2-triggered mast cell rapid degranulation induces alveolar ' 'epithelial inflammation and lung injury', 'volume': '6', 'author': 'Wu M-L', 'year': '2021', 'unstructured': 'Wu, M.-L., et al., SARS-CoV-2-triggered mast cell rapid degranulation ' 'induces alveolar epithelial inflammation and lung injury. Signal ' 'Transduction and Targeted Therapy, 2021. 6(1): p.\xa0428.', 'journal-title': 'Signal Transduction and Targeted Therapy'}, { 'key': 'ref4', 'doi-asserted-by': 'crossref', 'first-page': '633680', 'DOI': '10.3389/fphar.2021.633680', 'article-title': 'COVID-19: Famotidine, Histamine, Mast Cells, and Mechanisms', 'volume': '12', 'author': 'Malone RW', 'year': '2021', 'unstructured': 'Malone, R.W., et al., COVID-19: Famotidine, Histamine, Mast Cells, and ' 'Mechanisms. Front Pharmacol, 2021. 12: p.\xa0633680.', 'journal-title': 'Front Pharmacol'}, { 'issue': '3', 'key': 'ref5', 'doi-asserted-by': 'crossref', 'DOI': '10.3390/jcm10030459', 'article-title': 'The Association between Early-Life Gut Microbiota and Long-Term Health ' 'and Diseases', 'volume': '10', 'author': 'Sarkar A', 'year': '2021', 'unstructured': 'Sarkar, A., et al., The Association between Early-Life Gut Microbiota ' 'and Long-Term Health and Diseases. J Clin Med, 2021. 10(3).', 'journal-title': 'J Clin Med'}, { 'key': 'ref6', 'doi-asserted-by': 'crossref', 'first-page': '110622', 'DOI': '10.1016/j.mehy.2021.110622', 'article-title': 'Early multidrug treatment of SARS-CoV-2 infection (COVID-19) and ' 'reduced mortality among nursing home (or outpatient/ambulatory) ' 'residents', 'volume': '153', 'author': 'Alexander PE', 'year': '2021', 'unstructured': 'Alexander, P.E., et al., Early multidrug treatment of SARS-CoV-2 ' 'infection (COVID-19) and reduced mortality among nursing home (or ' 'outpatient/ambulatory) residents. Med Hypotheses, 2021. 153: p.\xa0' '110622.', 'journal-title': 'Med Hypotheses'}, { 'key': 'ref7', 'author': 'Ontai S', 'year': '2021', 'unstructured': 'Ontai, S., et al., Early multidrug treatment of SARS-CoV-2 (COVID-19) ' 'and decreased case fatality rates in Honduras. medRxiv, 2021: p.\xa0' '2021.07.21.21260223.'}, { 'issue': '2', 'key': 'ref8', 'article-title': 'Repurposing Drugs for Covid-19 by a Developing Country', 'volume': '6', 'author': 'Valerio Pascua F', 'year': '2022', 'unstructured': 'Valerio Pascua, F., et al., Repurposing Drugs for Covid-19 by a ' 'Developing Country. Epidemol Int J, 2022. 6(2).', 'journal-title': 'Epidemol Int J'}, { 'key': 'ref9', 'article-title': 'COVID-19: Azelastine nasal spray Reduces Virus-load In Nasal swabs ' '(CARVIN). Early intervention with azelastine nasal sprays reduces viral ' 'load in SARS-CoV-2 infected patients. First report on a double-blind ' 'placebo-controlled phase II clinical trial', 'volume': 'COVID-19', 'author': 'Klussmann JP', 'year': '2021', 'unstructured': 'Klussmann, J.P., et al., COVID-19: Azelastine nasal spray Reduces ' 'Virus-load In Nasal swabs (CARVIN). Early intervention with azelastine ' 'nasal sprays reduces viral load in SARS-CoV-2 infected patients. First ' 'report on a double-blind placebo-controlled phase II clinical trial. ' 'COVID-19, 2021.'}, { 'key': 'ref10', 'doi-asserted-by': 'crossref', 'first-page': '101989', 'DOI': '10.1016/j.pupt.2021.101989', 'article-title': 'Antihistamines and azithromycin as a treatment for COVID-19 on primary ' 'health care - A retrospective observational study in elderly patients', 'volume': '67', 'author': 'Morán Blanco JI', 'year': '2021', 'unstructured': 'Morán Blanco, J.I., et al., Antihistamines and azithromycin as a ' 'treatment for COVID-19 on primary health care - A retrospective ' 'observational study in elderly patients. Pulm Pharmacol Ther, 2021. 67: ' 'p.\xa0101989.', 'journal-title': 'Pulm Pharmacol Ther'}, { 'issue': '3', 'key': 'ref11', 'doi-asserted-by': 'crossref', 'DOI': '10.18103/mra.v10i3.2752', 'article-title': 'Intranasal Chlorpheniramine Maleate for the treatment of COVID-19: ' 'Translational and Clinical Evidence', 'volume': '10', 'author': 'Sanchez-Gonzalez MA', 'year': '2022', 'unstructured': 'Sanchez-Gonzalez, M.A., et al., Intranasal Chlorpheniramine Maleate for ' 'the treatment of COVID-19: Translational and Clinical Evidence. Medical ' 'Research Archives, 2022. 10(3).', 'journal-title': 'Medical Research Archives'}, { 'issue': '3', 'key': 'ref12', 'article-title': 'Treatment Protocol for COVID-19 Based on T2R Phenotype', 'volume': '13', 'author': 'Taha MA', 'year': '2021', 'unstructured': 'Taha, M.A., et al., Treatment Protocol for COVID-19 Based on T2R ' 'Phenotype. Viruses, 2021. 13(3).', 'journal-title': 'Viruses'}, { 'key': 'ref13', 'doi-asserted-by': 'crossref', 'first-page': '03084', 'DOI': '10.7189/jogh.11.03084', 'article-title': 'Impact of COVID-2019 on school attendance problems', 'volume': '11', 'author': 'Nathwani G', 'year': '2021', 'unstructured': 'Nathwani, G., et al., Impact of COVID-2019 on school attendance ' 'problems. J Glob Health, 2021. 11: p.\xa003084.', 'journal-title': 'J Glob Health'}, { 'issue': '2', 'key': 'ref14', 'doi-asserted-by': 'crossref', 'first-page': '2101341', 'DOI': '10.1183/13993003.01341-2021', 'article-title': 'Risk factors for post-COVID-19 condition in previously hospitalised ' 'children using the ISARIC Global follow-up protocol: a prospective ' 'cohort study', 'volume': '59', 'author': 'Osmanov IM', 'year': '2022', 'unstructured': 'Osmanov, I.M., et al., Risk factors for post-COVID-19 condition in ' 'previously hospitalised children using the ISARIC Global follow-up ' 'protocol: a prospective cohort study. European Respiratory Journal, ' '2022. 59(2): p.\xa02101341.', 'journal-title': 'European Respiratory Journal'}, { 'issue': '27', 'key': 'ref15', 'doi-asserted-by': 'crossref', 'first-page': '853', 'DOI': '10.15585/mmwr.mm6927a1', 'article-title': 'Increases in Health-Related Workplace Absenteeism Among Workers in ' 'Essential Critical Infrastructure Occupations During the COVID-19 ' 'Pandemic - United States, March-April 2020', 'volume': '69', 'author': 'Groenewold MR', 'year': '2020', 'unstructured': 'Groenewold, M.R., et al., Increases in Health-Related Workplace ' 'Absenteeism Among Workers in Essential Critical Infrastructure ' 'Occupations During the COVID-19 Pandemic - United States, March-April ' '2020. MMWR Morb Mortal Wkly Rep, 2020. 69(27): p.\xa0853–858.', 'journal-title': 'MMWR Morb Mortal Wkly Rep'}, { 'key': 'ref16', 'first-page': '1', 'article-title': 'Chlorpheniramine, an Old Drug with New Potential Clinical Applications: ' 'A Comprehensive Review of the Literature', 'volume': '17', 'author': 'Rizvi AAS', 'year': '2022', 'unstructured': 'Rizvi, A.A.S., et al., Chlorpheniramine, an Old Drug with New Potential ' 'Clinical Applications: A Comprehensive Review of the Literature. Current ' 'Reviews in Clinical and Experimental Pharmacology, 2022. 17: p.\xa01–1.', 'journal-title': 'Current Reviews in Clinical and Experimental Pharmacology'}, { 'issue': '3', 'key': 'ref17', 'doi-asserted-by': 'crossref', 'first-page': '1393', 'DOI': '10.1172/JCI72094', 'article-title': 'Bitter and sweet taste receptors regulate human upper respiratory ' 'innate immunity', 'volume': '124', 'author': 'Lee RJ', 'year': '2014', 'unstructured': 'Lee, R.J., et al., Bitter and sweet taste receptors regulate human upper ' 'respiratory innate immunity. J Clin Invest, 2014. 124(3): p.\xa0' '1393–405.', 'journal-title': 'J Clin Invest'}, { 'issue': '1', 'key': 'ref18', 'first-page': 'e20980', 'article-title': 'Molecular Modeling and Preliminary Clinical Data Suggesting Antiviral ' 'Activity for Chlorpheniramine (Chlorphenamine) Against COVID-19', 'volume': '14', 'author': 'Black S', 'year': '2022', 'unstructured': 'Black, S., Molecular Modeling and Preliminary Clinical Data Suggesting ' 'Antiviral Activity for Chlorpheniramine (Chlorphenamine) Against ' 'COVID-19. Cureus, 2022. 14(1): p.\xa0e20980.', 'journal-title': 'Cureus'}, { 'key': 'ref19', 'author': 'Mostafa A', 'year': '2020', 'unstructured': 'Mostafa, A., et al., FDA-Approved Drugs with Potent In Vitro Antiviral ' 'Activity against Severe Acute Respiratory Syndrome Coronavirus 2. ' 'Pharmaceuticals (Basel), 2020. 13(12).'}, { 'issue': '9', 'key': 'ref20', 'first-page': 'e10501', 'article-title': 'In Vitro Virucidal Effect of Intranasally Delivered Chlorpheniramine ' 'Maleate Compound Against Severe Acute Respiratory Syndrome Coronavirus ' '2', 'volume': '12', 'author': 'Westover JB', 'year': '2020', 'unstructured': 'Westover, J.B., et al., In Vitro Virucidal Effect of Intranasally ' 'Delivered Chlorpheniramine Maleate Compound Against Severe Acute ' 'Respiratory Syndrome Coronavirus 2. Cureus, 2020. 12(9): p.\xa0e10501.', 'journal-title': 'Cureus'}, { 'issue': '3', 'key': 'ref21', 'first-page': 'e14206', 'article-title': 'A Randomized Controlled Pilot Trial to Test the Efficacy of Intranasal ' 'Chlorpheniramine Maleate With Xylitol for the Treatment of Allergic ' 'Rhinitis', 'volume': '13', 'author': 'Sanchez-Gonzalez M', 'year': '2021', 'unstructured': 'Sanchez-Gonzalez, M., et al., A Randomized Controlled Pilot Trial to ' 'Test the Efficacy of Intranasal Chlorpheniramine Maleate With Xylitol ' 'for the Treatment of Allergic Rhinitis. Cureus, 2021. 13(3): p.\xa0' 'e14206.', 'journal-title': 'Cureus'}, { 'issue': '1', 'key': 'ref22', 'doi-asserted-by': 'crossref', 'first-page': '5453', 'DOI': '10.1038/s41467-020-19145-6', 'article-title': 'ACE2 localizes to the respiratory cilia and is not increased by ACE ' 'inhibitors or ARBs', 'volume': '11', 'author': 'Lee IT', 'year': '2020', 'unstructured': 'Lee, I.T., et al., ACE2 localizes to the respiratory cilia and is not ' 'increased by ACE inhibitors or ARBs. Nature Communications, 2020. 11(1): ' 'p.\xa05453.', 'journal-title': 'Nature Communications'}, { 'issue': '1', 'key': 'ref23', 'doi-asserted-by': 'crossref', 'first-page': '103', 'DOI': '10.2307/2529712', 'article-title': 'Sequential treatment assignment with balancing for prognostic factors ' 'in the controlled clinical trial', 'volume': '31', 'author': 'Pocock SJ', 'year': '1975', 'unstructured': 'Pocock, S.J. and R. Simon, Sequential treatment assignment with ' 'balancing for prognostic factors in the controlled clinical trial. ' 'Biometrics, 1975. 31(1): p.\xa0103–15.', 'journal-title': 'Biometrics'}, { 'key': 'ref24', 'author': 'FDA US', 'year': '2020', 'unstructured': 'FDA, U.S. Department of Health and Human Services Food and Drug ' 'Administration Center for Drug Evaluation and Research (CDER) Center for ' 'Biologics Evaluation and Research (CBER). Assessing COVID-19-Related ' 'Symptoms in Outpatient Adult and Adolescent Subjects in Clinical Trials ' 'of Drugs and Biological Products for COVID-19 Prevention or Treatment ' 'Guidance for Industry. 2020. https://www.fda.gov/media/142143/download. ' 'Accessed 12 May 2021. 2020.'}, { 'key': 'ref25', 'author': 'Basu S', 'year': '2022', 'unstructured': 'Basu, S., et al., A model-based approach to improve intranasal sprays ' 'for respiratory viral infections. medRxiv, 2022: p.\xa0' '2022.01.26.22269854.'}, { 'issue': '1', 'key': 'ref26', 'doi-asserted-by': 'crossref', 'first-page': '6652', 'DOI': '10.1038/s41598-021-85765-7', 'article-title': 'Computational characterization of inhaled droplet transport to the ' 'nasopharynx', 'volume': '11', 'author': 'Basu S', 'year': '2021', 'unstructured': 'Basu, S., Computational characterization of inhaled droplet transport to ' 'the nasopharynx. Sci Rep, 2021. 11(1): p.\xa06652.', 'journal-title': 'Sci Rep'}, { 'key': 'ref27', 'volume-title': 'Guidance for industry. Allergic rhinitis: clinical development programs ' 'for drug products.', 'year': '2018', 'unstructured': 'U.S. Department of Health & Human Services, U.S.F.a.D.A., Guidance for ' 'industry. Allergic rhinitis: clinical development programs for drug ' 'products., U.S.F.a.D.A. U.S. Department of Health & Human Services, ' 'Editor. 2018.'}, { 'issue': '4', 'key': 'ref28', 'doi-asserted-by': 'crossref', 'first-page': '367', 'DOI': '10.1111/j.1398-9995.2006.01276.x', 'article-title': 'Visual analog scales can assess the severity of rhinitis graded ' 'according to ARIA guidelines', 'volume': '62', 'author': 'Bousquet PJ', 'year': '2007', 'unstructured': 'Bousquet, P.J., et al., Visual analog scales can assess the severity of ' 'rhinitis graded according to ARIA guidelines. Allergy, 2007. 62(4): ' 'p.\xa0367–72.', 'journal-title': 'Allergy'}, { 'issue': '2', 'key': 'ref29', 'first-page': '3', 'article-title': 'Chlorpheniramine Maleate Nasal Spray In COVID-19 Patients: Case Series', 'volume': '10', 'author': 'Torres J', 'year': '2021', 'unstructured': 'Torres, J., et al., Chlorpheniramine Maleate Nasal Spray In COVID-19 ' 'Patients: Case Series. J Clin Exp Pharmacol, 2021. 10(2): p.\xa03.', 'journal-title': 'J Clin Exp Pharmacol'}, { 'key': 'ref30', 'doi-asserted-by': 'crossref', 'first-page': '1409', 'DOI': '10.3389/fimmu.2020.01409', 'article-title': 'Beyond Anti-viral Effects of Chloroquine/Hydroxychloroquine', 'volume': '11', 'author': 'Gies V', 'year': '2020', 'unstructured': 'Gies, V., et al., Beyond Anti-viral Effects of ' 'Chloroquine/Hydroxychloroquine. Front Immunol, 2020. 11: p.\xa01409.', 'journal-title': 'Front Immunol'}, { 'key': 'ref31', 'first-page': '1', 'article-title': 'Sars-Cov-2 and risk of antiviral drug resistance', 'author': 'Vitiello A', 'year': '2021', 'unstructured': 'Vitiello, A., Sars-Cov-2 and risk of antiviral drug resistance. Ir J Med ' 'Sci, 2021: p.\xa01–2.', 'journal-title': 'Ir J Med Sci'}, { 'issue': '5', 'key': 'ref32', 'doi-asserted-by': 'crossref', 'first-page': '6008', 'DOI': '10.1096/fj.202000502', 'article-title': 'Existing bitter medicines for fighting 2019-nCoV-associated infectious ' 'diseases', 'volume': '34', 'author': 'Li X', 'year': '2020', 'unstructured': 'Li, X., et al., Existing bitter medicines for fighting ' '2019-nCoV-associated infectious diseases. Faseb j, 2020. 34(5): p.\xa0' '6008–6016.', 'journal-title': 'Faseb j'}, { 'issue': '4', 'key': 'ref33', 'doi-asserted-by': 'crossref', 'first-page': '88', 'DOI': '10.1002/lio2.26', 'article-title': 'Taste Receptors: Regulators of Sinonasal Innate Immunity', 'volume': '1', 'author': 'Carey RM', 'year': '2016', 'unstructured': 'Carey, R.M., et al., Taste Receptors: Regulators of Sinonasal Innate ' 'Immunity. Laryngoscope Investig Otolaryngol, 2016. 1(4): p.\xa088–95.', 'journal-title': 'Laryngoscope Investig Otolaryngol'}, { 'issue': '1267', 'key': 'ref34', 'article-title': 'Bitter Taste Receptors (TAS2Rs) in Human Lung Macrophages: Receptor ' 'Expression and Inhibitory Effects of TAS2R Agonists', 'volume': '10', 'author': 'Grassin-Delyle S', 'year': '2019', 'unstructured': 'Grassin-Delyle, S., et al., Bitter Taste Receptors (TAS2Rs) in Human ' 'Lung Macrophages: Receptor Expression and Inhibitory Effects of TAS2R ' 'Agonists. Frontiers in Physiology, 2019. 10(1267).', 'journal-title': 'Frontiers in Physiology'}, { 'issue': '2', 'key': 'ref35', 'first-page': '43', 'article-title': 'A hypothesis: Bitter taste receptors as a therapeutic target for the ' 'clinical symptoms of SARS-CoV-2', 'volume': '76', 'author': 'Kumar SA', 'year': '2021', 'unstructured': 'Kumar, S.A. and W. Cheng, A hypothesis: Bitter taste receptors as a ' 'therapeutic target for the clinical symptoms of SARS-CoV-2. Pharmazie, ' '2021. 76(2): p.\xa043–54.', 'journal-title': 'Pharmazie'}, { 'issue': '3', 'key': 'ref36', 'doi-asserted-by': 'crossref', 'first-page': '257', 'DOI': '10.1016/j.ejphar.2004.11.006', 'article-title': 'Comparative anticholinergic activities of 10 histamine H1 receptor ' 'antagonists in two functional models', 'volume': '506', 'author': 'Orzechowski RF', 'year': '2005', 'unstructured': 'Orzechowski, R.F., D.S. Currie, and C.A. Valancius, Comparative ' 'anticholinergic activities of 10 histamine H1 receptor antagonists in ' 'two functional models. Eur J Pharmacol, 2005. 506(3): p.\xa0257–64.', 'journal-title': 'Eur J Pharmacol'}, { 'issue': '1', 'key': 'ref37', 'doi-asserted-by': 'crossref', 'first-page': '54', 'DOI': '10.1016/0091-6749(77)90177-4', 'article-title': 'Bronchodilating activity of an H1 blocker, chlorpheniramine', 'volume': '59', 'author': 'Popa VT', 'year': '1977', 'unstructured': 'Popa, V.T., Bronchodilating activity of an H1 blocker, chlorpheniramine. ' 'J Allergy Clin Immunol, 1977. 59(1): p.\xa054–63.', 'journal-title': 'J Allergy Clin Immunol'}, { 'issue': '2', 'key': 'ref38', 'doi-asserted-by': 'crossref', 'first-page': '131', 'DOI': '10.2500/105065898781390271', 'article-title': 'Anticholinergic properties of brompheniramine, chlorpheniramine, and ' 'atropine in human nasal mucosa in vitro', 'volume': '12', 'author': 'Fang SY', 'year': '1998', 'unstructured': 'Fang, S.Y., H.M. Druce, and J.N. Baraniuk, Anticholinergic properties of ' 'brompheniramine, chlorpheniramine, and atropine in human nasal mucosa in ' 'vitro. Am J Rhinol, 1998. 12(2): p.\xa0131–3.', 'journal-title': 'Am J Rhinol'}, { 'issue': '12', 'key': 'ref39', 'doi-asserted-by': 'crossref', 'first-page': '1268', 'DOI': '10.7150/ijms.21573', 'article-title': 'Chlorpheniramine attenuates histamine-mediated aquaporin 5 ' 'downregulation in human nasal epithelial cells via suppression of NF-κB ' 'activation', 'volume': '14', 'author': 'Chang YL', 'year': '2017', 'unstructured': 'Chang, Y.L., et al., Chlorpheniramine attenuates histamine-mediated ' 'aquaporin 5 downregulation in human nasal epithelial cells via ' 'suppression of NF-κB activation. Int J Med Sci, 2017. 14(12): p.\xa0' '1268–1275.', 'journal-title': 'Int J Med Sci'}], 'container-title': [], 'original-title': [], 'link': [ { 'URL': 'https://www.researchsquare.com/article/rs-2167465/v1', 'content-type': 'text/html', 'content-version': 'vor', 'intended-application': 'text-mining'}, { 'URL': 'https://www.researchsquare.com/article/rs-2167465/v1.html', 'content-type': 'unspecified', 'content-version': 'vor', 'intended-application': 'similarity-checking'}], 'deposited': { 'date-parts': [[2022, 10, 24]], 'date-time': '2022-10-24T04:15:00Z', 'timestamp': 1666584900000}, 'score': 1, 'resource': {'primary': {'URL': 'https://www.researchsquare.com/article/rs-2167465/v1'}}, 'subtitle': [], 'short-title': [], 'issued': {'date-parts': [[2022, 10, 18]]}, 'references-count': 39, 'URL': 'http://dx.doi.org/10.21203/rs.3.rs-2167465/v1', 'relation': {}, 'published': {'date-parts': [[2022, 10, 18]]}, 'subtype': 'preprint'}
Loading..
Please send us corrections, updates, or comments. c19early involves the extraction of 100,000+ datapoints from thousands of papers. Community updates help ensure high accuracy. Treatments and other interventions are complementary. All practical, effective, and safe means should be used based on risk/benefit analysis. No treatment or intervention is 100% available and effective for all current and future variants. We do not provide medical advice. Before taking any medication, consult a qualified physician who can provide personalized advice and details of risks and benefits based on your medical history and situation. FLCCC and WCH provide treatment protocols.
  or use drag and drop   
Submit