COVID-19 studies:     IvermectinIVM Vitamin DV.D PXPX FLVFLV PVP-IPI HC QHCQ BHBH CICI BLBL NZNZ COCO BUBU More..
COVID-19 early treatment: real-time analysis of 598 studies
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PX 92% 2
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
FV 89% 2
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
PI 85% 3
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
BU 82% 1
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
V.D 81% 2
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
IVM 81% 18
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
BH 79% 2
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
BL 75% 3
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
CI 66% 2
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
(H)CQ 65% 26
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
NZ 49% 5
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Zn 42% 2
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
FPV 38% 3
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
V.C 18% 1
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
RD - 0
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
CO - 0
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
IC - 0
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Global adoption of early treatments. Studies and improvement refer to early treatment. Countries ordered by population. Official:
 
  Unofficial:
 
00.250.50.7511.251.51.752+Proxalutamide0.09[0.05-0.13]331,041RCTsStudiesPatientsRRCIFluvoxamine0.11[0.01-0.85]12277Iota-carrageenan0.20[0.04-0.91]11394Ivermectin0.28[0.22-0.36]275217,557Casirivimab/imde..0.30[0.19-0.48]444,793Povidone-Iodine0.32[0.12-0.81]441,994Nitazoxanide0.42[0.14-1.30]461,464Bamlanivimab0.43[0.23-0.81]563,121Budesonide0.46[0.11-1.96]221,806Vitamin D0.49[0.39-0.63]52222,660Bromhexine0.56[0.40-0.78]55291Colchicine0.57[0.38-0.85]495,719Zinc0.61[0.52-0.71]3106,913Favipiravir0.71[0.54-0.93]781,178Hydroxychloroquine0.73[0.68-0.77]31237363,648Remdesivir0.76[0.62-0.92]51422,358Vitamin C0.82[0.67-0.99]581,168All studies combined (pooled effects, all stages)c19early.com 4/29/21Lower RiskIncreased Risk
All studies combined (pooled effects, all stages)
MedicationImprovementStudies AuthorsPatients
Proxalutamide 92% [87‑95%] 3 20 1,041
Fluvoxamine 89% [15‑99%] 2 13 277
Iota-carrageenan 80% [9‑96%] 1 18 394
Ivermectin 72% [64‑78%] 52 426 17,557
Casiri/imdevimab 70% [52‑81%] 4 4 4,793
Povidone-Iodine 68% [19‑88%] 4 44 1,994
Nitazoxanide 58% [-30‑86%] 6 87 1,464
Bamlanivimab 57% [19‑77%] 6 64 3,121
Budesonide 54% [-96‑89%] 2 48 1,806
Vitamin D 51% [37‑61%] 22 225 22,660
Bromhexine 44% [22‑60%] 5 56 291
Colchicine 43% [15‑62%] 9 182 5,719
Zinc 39% [29‑48%] 10 96 6,913
Favipiravir 29% [7‑46%] 8 169 1,178
Hydroxychloroquine 27% [23‑32%] 237 3,761 363,648
Remdesivir 24% [8‑38%] 14 232 22,358
Vitamin C 18% [1‑33%] 8 96 1,168
00.250.50.7511.251.51.752+Proxalutamide0.08[0.04-0.18]22451RCTsStudiesPatientsRRCIFluvoxamine0.11[0.01-0.85]12277Povidone-Iodine0.15[0.05-0.48]33640Budesonide0.18[0.04-0.79]11146Vitamin D0.19[0.06-0.61]02114Ivermectin0.19[0.09-0.39]11181,937Bromhexine0.21[0.06-0.72]2296Bamlanivimab0.25[0.12-0.54]331,374Casirivimab/imde..0.34[0.18-0.65]222,879Hydroxychloroquine0.35[0.25-0.50]62644,235Nitazoxanide0.51[0.12-2.27]351,414Zinc0.58[0.16-2.11]12626Favipiravir0.62[0.38-1.02]33410Vitamin C0.82[0.23-2.91]1198Early treatment studies (pooled effects)c19early.com 4/29/21Lower RiskIncreased Risk
Early treatment studies (pooled effects)
MedicationImprovementStudies AuthorsPatients
Proxalutamide 92% [82‑96%] 2 15 451
Fluvoxamine 89% [15‑99%] 2 13 277
Povidone-Iodine 85% [52‑95%] 3 29 640
Budesonide 82% [21‑96%] 1 24 146
Vitamin D 81% [39‑94%] 2 13 114
Ivermectin 81% [61‑91%] 18 175 1,937
Bromhexine 79% [28‑94%] 2 21 96
Bamlanivimab 75% [46‑88%] 3 40 1,374
Casiri/imdevimab 66% [35‑82%] 2 2 2,879
Hydroxychloroquine 65% [50‑75%] 26 414 44,235
Nitazoxanide 49% [-127‑88%] 5 67 1,414
Zinc 42% [-111‑84%] 2 14 626
Favipiravir 38% [-2‑62%] 3 52 410
Vitamin C 18% [-191‑77%] 1 11 98
00.250.50.7511.251.51.752+Proxalutamide0.09[0.05-0.15]22804RCTsStudiesPatientsRRCIBromhexine0.09[0.01-1.57]22178Povidone-Iodine0.12[0.03-0.50]11606Ivermectin0.24[0.14-0.42]8187,267Vitamin D0.38[0.25-0.59]4138,432Nitazoxanide0.40[0.10-1.58]23923Bamlanivimab0.52[0.10-2.71]231,551Colchicine0.57[0.38-0.85]495,719Zinc0.63[0.54-0.74]164,591Remdesivir0.74[0.59-0.93]51322,216Vitamin C0.75[0.55-1.02]35626Hydroxychloroquine0.75[0.69-0.81]13146250,055Favipiravir1.15[0.68-1.94]22465All mortality results (all stages)c19early.com 4/29/21Lower RiskIncreased Risk
All mortality results (all stages)
MedicationImprovementStudies AuthorsPatients
Proxalutamide 91% [85‑95%] 2 12 804
Bromhexine 91% [-57‑99%] 2 18 178
Povidone-Iodine 88% [50‑97%] 1 6 606
Ivermectin 76% [58‑86%] 18 155 7,267
Vitamin D 62% [41‑75%] 13 116 8,432
Nitazoxanide 60% [-58‑90%] 3 32 923
Bamlanivimab 48% [-171‑90%] 3 24 1,551
Colchicine 43% [15‑62%] 9 182 5,719
Zinc 37% [26‑46%] 6 54 4,591
Remdesivir 26% [7‑41%] 13 225 22,216
Vitamin C 25% [-2‑45%] 5 64 626
Hydroxychloroquine 25% [19‑31%] 146 2,535 250,055
Favipiravir -15% [-94‑32%] 2 54 465
00.250.50.7511.251.51.752+Bamlanivimab0.08[0.00-1.43]11769RCTsStudiesPatientsRRCIBromhexine0.09[0.01-1.59]1178Povidone-Iodine0.12[0.03-0.50]11606Ivermectin0.16[0.04-0.63]24802Vitamin D0.19[0.06-0.61]02114Proxalutamide0.19[0.01-3.90]11214Zinc0.21[0.03-1.47]01518Hydroxychloroquine0.28[0.18-0.43]01140,652Favipiravir0.55[0.05-5.81]1192Nitazoxanide0.59[0.02-13.78]12873Early treatment mortality resultsc19early.com 4/29/21Lower RiskIncreased Risk
Early treatment mortality results
MedicationImprovementStudies AuthorsPatients
Bamlanivimab 92% [-43‑100%] 1 1 769
Bromhexine 91% [-59‑99%] 1 11 78
Povidone-Iodine 88% [50‑97%] 1 6 606
Ivermectin 84% [37‑96%] 4 37 802
Vitamin D 81% [39‑94%] 2 13 114
Proxalutamide 81% [-290‑99%] 1 7 214
Zinc 79% [-47‑97%] 1 3 518
Hydroxychloroquine 72% [57‑82%] 11 158 40,652
Favipiravir 45% [-481‑95%] 1 10 92
Nitazoxanide 41% [-1278‑98%] 2 12 873
Recent studies (see the individual treatment pages for all studies):

4/27
In Vitro Varese et al., bioRxiv, doi:10.1101/2021.04.27.441512 (Preprint) (In Vitro) in vitro Iota-carrageenan prevents the replication of SARS-CoV-2 on an in vitro respiratory epithelium model
In Vitro Calu-3 (human respiratory epithelial cell line) study showing that iota-carrageenan inhibits SARS-CoV-2.
4/26
Late Mohandas et al., (Peer Reviewed) death, ↑81.0%, p=0.007 Clinical review of COVID-19 patients presenting to a quaternary care private hospital in South India: A retrospective study
Retrospective 3,345 hospitalized patients in India, 11.5% treated with HCQ, showing unadjusted higher mortality with treatment. Confounding by indication and time based confounding (due to declining use over the period when overall treatm..
4/26
Levels Al-Daghri et al., Journal of Translational Medicine, doi:10.1186/s12967-021-02838-x (Peer Reviewed) Vitamin D status of Arab Gulf residents screened for SARS-CoV-2 and its association with COVID-19 infection: a multi-centre case–control study
Case control study with 220 adults showing significantly lower vitamin D levels in PCR+ patients.
4/23
Late Toya et al., SSRN (Preprint) A Cross-Country Analysis of the Determinants of COVID-19 Fatalities
Country based analysis finding lower mortality with the use of HCQ.
4/22
Late Reis et al., JAMA Network Open, doi:10.1001/jamanetworkopen.2021.6468 (Peer Reviewed) death, ↓66.0%, p=1.00 Effect of Early Treatment With Hydroxychloroquine or Lopinavir and Ritonavir on Risk of Hospitalization Among Patients With COVID-19 The TOGETHER Randomized Clinical Trial
Early terminated RCT in Brazil showing lower mortality and hospitalization with HCQ, but not reaching statistical significance. Although the title includes "early treatment", treatment was relatively late, with most patients bei..
4/21
Late Zhao et al., International Immunopharmacology, doi:10.1016/j.intimp.2021.107702 (Peer Reviewed) viral+, ↓59.0%, p=0.06 Favipiravir in the treatment of patients with SARS-CoV-2 RNA recurrent positive after discharge: a multicenter, open-label, randomized trial
RCT with 55 patients (36 favipiravir, 19 control) who were PCR+ after recovery, showing improved viral clearance with treatment.
4/20
Review Sukhatme et al., Front. Pharmacol., doi:10.3389/fphar.2021.652688 (Review) (Peer Reviewed) review Fluvoxamine: A Review of Its Mechanism of Action and Its Role in COVID-19
Review of mechanisms of action of fluvoxamine and other SSRIs that could be beneficial for COVID-19 treatment, including lower platelet aggregation, decreased mast cell degranulation, interference with endolysosomal viral trafficking, reg..
4/20
Early Rossignol et al., medRxiv, doi:10.1101/2021.04.19.21255441 (Preprint) death, ↑206.0%, p=0.49 Early treatment with nitazoxanide prevents worsening of mild and moderate COVID-19 and subsequent hospitalization
RCT with 184 outpatients treated with an extended release formulation of nitazoxanide, and 195 controls, showing lower hospitalization and progression to severe disease with treatment. There was one COVID-19 related death in the treatment..
4/19
Review DiNicolantonio et al., Open Heart, doi:10.1136/openhrt-2021-001655 (Review) (Peer Reviewed) review Anti-inflammatory activity of ivermectin in late-stage COVID-19 may reflect activation of systemic glycine receptors
Review suggesting that the effectiveness of ivermectin in the cytokine storm phase of COVID-19 may be, at least in part, an anti-inflammatory effect mediated by increased activation of glycine receptors on leukocytes and possibly vascular..
4/19
Late Favipiravir Observational Study Group, Fujita Health University (Preprint) Favipiravir Observational Study Interim Report 3
Retrospective analysis of favipiravir use in 10,986 hospitalized patients, including analysis of changes in clinical status and side effects. Common adverse events were uric acid level increase and liver function enzyme increase. Authors ..
4/17
Review Shah Alam et al., International Immunopharmacology, doi:10.1016/j.intimp.2021.107686 (Review) (Peer Reviewed) review The role of vitamin D in reducing SARS-CoV-2 infection: An update
Review of vitamin D for COVID-19 noting that infections are likely to be more prevalent in the winter season; clinical trials show vitamin D as a potential therapeutic agent; vitamin D is beneficial against COVID-19 by reducing inflammato..
4/17
Early Fujii et al., Journal of Infection and Chemotherapy, doi:10.1016/j.jiac.2021.04.013 (Peer Reviewed) Early favipiravir treatment was associated with early defervescence in non-severe COVID-19 patients
Retrospective 41 favipiravir patients finding that early treatment was more successful.
4/16
PrEP Morgenstern et al., medRxiv, doi:10.1101/2021.04.10.21255248 (Preprint) hosp., ↓80.0%, p=0.50 Retrospective cohort study of Ivermectin as a SARS-CoV-2 pre-exposure prophylactic method in Healthcare Workers
Propensity matched retrospective prophylaxis study of healthcare workers in the Dominican Republic showing significantly lower cases with treatment, and no hospitalization with treatment (versus 2 in the PSM matched control group). The ca..
4/15
PrEP Alzahrani et al., Rheumatology International , doi:10.1007/s00296-021-04857-9 (Peer Reviewed) death, ↓58.8%, p=1.00 Clinical characteristics and outcome of COVID-19 in patients with rheumatic diseases
Retrospective 47 rheumatic disease patients not finding significant differences with HCQ.
4/15
PrEP Figueroa et al., medRxiv, doi:10.1101/2021.04.13.21255409 (Preprint) symp. case, ↓79.8%, p=0.04 Efficacy of a nasal spray containing Iota-Carrageenan in the prophylaxis of COVID-19 in hospital personnel dedicated to patients care with COVID-19 disease A pragmatic multicenter, randomized, double-blind, placebo-controlled trial (CARR-COV-02)
Prophylaxis RCT with 394 healthcare workers, 196 treated with iota-carrageenan, showing significantly lower symptomatic cases with treatment. There were no deaths or hospitalizations. There was a significant number of PCR- symptomatic cas..
4/15
Levels Skalny et al., Metabolites, doi:10.3390/metabo11040244 (Peer Reviewed) Serum Zinc, Copper, and Other Biometals Are Associated with COVID-19 Severity Markers
Analysis of serum metal levels in 150 COVID-19 patients and 44 controls, finding that COVID-19 severity was associated with lower serum Ca, Fe, Se, Zn levels when compared to controls.
4/15
PrEP Alegiani et al., Rheumatology, doi:10.1093/rheumatology/keab348 (Peer Reviewed) death, ↑8.0%, p=0.64 Risk of COVID-19 hospitalization and mortality in rheumatic patients treated with hydroxychloroquine or other conventional DMARDs in Italy
Retrospective database analysis case control study of rheumatic patients. When compared with other cDMARDs, HCQ users had significantly lower hospitalization, however there was no significant difference in mortality. Results differ signif..
4/14
Late Hakamifard et al., Immunopathologia Persa, doi:10.34172/ipp.2021.xx (Peer Reviewed) ICU, ↓46.3%, p=0.46 The effect of vitamin E and vitamin C in patients with COVID-19 pneumonia; a randomized controlled clinical trial
RCT with 38 patients treated with vitamin C and vitamin E, and 34 control patients, showing lower ICU admission with treatment, but not statistically significant.
4/14
PEP Seet et al., International Journal of Infectious Diseases, doi:10.1016/j.ijid.2021.04.035 (Peer Reviewed) severe case, ↓49.8%, p=0.01 Positive impact of oral hydroxychloroquine and povidone-iodine throat spray for COVID-19 prophylaxis: an open-label randomized trial
Prophylaxis RCT in Singapore with 3,037 low risk patients, showing lower serious cases, lower symptomatic cases, and lower confirmed cases of COVID-19 with all treatments (ivermectin, HCQ, PVP-I, and Zinc + vitamin C) compared to vitamin ..
4/12
PEP Regeneron Press Release (Preprint) hosp./ER, ↓88.9%, p=0.06 Phase 3 prevention trial showed 81% reduced risk of symptomatic SARS-CoV-2 infections with subcutaneous administration of REGEN-COV™ (casirivimab and imdevimab)
Press release for a phase 3 prophylaxis trial reporting lower hospitalization/ER and symptomatic cases, and faster recovery with 1,200mg subcutaneous casirivimab with imdevimab.
4/12
Late Yu et al., medRxiv, doi:10.1101/2021.04.10.21254672 (Preprint) hosp./death, ↓17.5%, p=0.24 Inhaled budesonide for COVID-19 in people at higher risk of adverse outcomes in the community: interim analyses from the PRINCIPLE trial
Interim results from the PRINCIPLE trial, 751 treated with budesonide starting a median of 6 days after symptom onset, showing lower hospitalization/death, and faster recovery with treatment.
4/10
In Silico Bello et al., Journal of Biomolecular Structure and Dynamics, doi:10.1080/07391102.2021.1911857 (Peer Reviewed) Elucidation of the inhibitory activity of ivermectin with host nuclear importin α and several SARS-CoV-2 targets
In Silico analysis finding that the in vitro activity of ivermectin may explained by acting as an inhibitor of importin-α, dimeric 3CLpro, and Nsp9.
We aim to cover the most promising early treatments for COVID-19. We use pre-specified effect extraction criteria that prioritizes more serious outcomes, for details see methods. For specific outcomes and different treatment stages see the individual pages. Treatments with only 3 or fewer studies are shown in grey. Not all treatments are covered here, effectiveness has been reported for many other treatments in studies. Of the 598 studies, 445 present results comparing with a control group, 393 are treatment studies, and 52 analyze outcomes based on serum levels.
Please send us corrections, updates, or comments. Vaccines and treatments are both extremely valuable and complementary; multiple approaches are required to cover all people and all existing 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. Treatment protocols for physicians are available from the FLCCC.
Thanks for your feedback! Please search before submitting papers and note that studies are listed under the date they were first available, which may be the date of an earlier preprint.
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