XAFTY®
A broad-spectrum antiviral for XAFTY®
XAFTY®
A broad-spectrum antiviral for XAFTY®
Antiviral drug
About XAFTY®
XAFTY® is a broad-spectrum antiviral that activates intracellular autophagy, enabling the body to eliminate viruses after they have entered host cells. Through this mechanism, it demonstrates strong therapeutic efficacy across a wide range of viral diseases, including COVID-19.
Its active ingredient, niclosamide, has shown efficacy against 31 viral infections—including COVID-19, SARS, MERS, Ebola, HIV, and influenza—highlighting its potential as a versatile treatment option for various viral diseases.
Maximized Bioavailability
Maximizing Bioavailability
Niclosamide sustains therapeutically effective plasma concentrations for over 24 hours. Leveraging our DDS platform technology, we have increased the bioavailability of this poorly water-soluble compound by up to 40-fold.
Niclosamide Innovation
Efficacy of XAFTY®
Antiviral Efficacy of Niclosamide, the Active Ingredient in XAFTY®
In the scientific community, extensive efforts have been made to rapidly identify antiviral agents by screening FDA-approved drugs for antiviral activity. As a result, in the early 2000s, niclosamide was found to exhibit antiviral properties against the SARS virus.
Subsequent studies have shown that niclosamide is effective not only against SARS but also against a wide range of viruses, including Zika virus, hepatitis viruses, and Ebola virus. Notably, its antiviral activity has been demonstrated regardless of viral family, highlighting its potential as a broad-spectrum antiviral agent.
※ Niclosamide : The active ingredient in Yomesan, an antiparasitic drug first introduced in Germany in 1962 by Bayer. Its safety has been well established over decades of use and it is listed on the WHO Model List of Essential Medicines.
MULTI TARGET DRUG NICOLOSAMIDE
Niclosamide, a leading candidate for host-targeted antiviral therapy, has demonstrated antiviral efficacy across a broad spectrum of viruses, regardless of virus type, in studies exploring broad-spectrum antiviral agents.
Spotlight on Niclosamide
Niclosamide : A Focus of Medical Interest

Nature
Identified as one of the most effective inhibitors of COVID-19 viral replication and lung injury

Institut Pasteur Korea
Among 3,000 FDA-approved drugs, identified as one of the most promising candidates for COVID-19 treatment

Korea Disease Control and Prevention Agency (KDCA)
Niclosamide shows up to 7× greater efficacy against the Omicron variant compared to remdesivir
Major Viral
Diseases & Treatments
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Antiviral drug
About XAFTY®
XAFTY® is a broad-spectrum antiviral that activates intracellular autophagy, enabling the body to eliminate viruses after they have entered host cells. Through this mechanism, it demonstrates strong therapeutic efficacy across a wide range of viral diseases, including COVID-19.
Its active ingredient, niclosamide, has shown efficacy against 31 viral infections—including COVID-19, SARS, MERS, Ebola, HIV, and influenza—highlighting its potential as a versatile treatment option for various viral diseases.
Maximized Bioavailability
Maximizing Bioavailability
Niclosamide sustains therapeutically effective plasma concentrations for over 24 hours.
Leveraging our DDS platform technology, we have increased the bioavailability
of this poorly water-soluble compound by up to 40-fold.
Niclosamide Innovation
Efficacy of XAFTY®
Antiviral Efficacy of Niclosamide, the Active Ingredient in XAFTY®
In the scientific community, extensive efforts have been made to rapidly identify antiviral agents by screening FDA-approved drugs for antiviral activity. As a result, in the early 2000s, niclosamide was found to exhibit antiviral properties against the SARS virus.
Subsequent studies have shown that niclosamide is effective not only against SARS but also against a wide range of viruses, including Zika virus, hepatitis viruses, and Ebola virus. Notably, its antiviral activity has been demonstrated regardless of viral family, highlighting its potential as a broad-spectrum antiviral agent.
※ Niclosamide : The active ingredient in Yomesan, an antiparasitic drug first introduced in Germany in 1962 by Bayer. Its safety has been well established over decades of use and it is listed on the WHO Model List of Essential Medicines.
MULTI TARGET DRUG NICOLOSAMIDE
Niclosamide, a leading candidate for host-targeted antiviral therapy, has demonstrated antiviral efficacy across a broad spectrum of viruses, regardless of virus type, in studies exploring broad-spectrum antiviral agents.
Spotlight on Niclosamide
Niclosamide : A Focus of Medical Interest

Nature
Identified as one of the most effective
inhibitors of COVID-19 viral replication
and lung injury

Institut Pasteur Korea
Among 3,000 FDA-approved drugs,
identified as one of the most promising
candidates for COVID-19 treatment

Korea Disease Control and Prevention Agency (KDCA)
Niclosamide shows up to 7× greater
efficacy against the Omicron variant
compared to remdesivir
Major Viral
Diseases & Treatments
Family | Virus Name | Associated Diseases | Approved Treatment | Reference |
Coronaviridae | MERS-CoV | MERS | ✕ | Gasen et al., Nature Communications (2019) 10:5770 |
SARS-CoV-1 | SARS | ✕ | Wu et al., Antimicrobial Agents and Chemotherapy (2004) 48, 2693–2696 | |
SARS-CoV-2 | COVID-19 | Remdesivir, Paxlovid, Lagevrio | Jeon et al., Antimicrobial Agents and Chemotherapy (2020) 64(7): e00819-20 | |
Retrovirus | Human Immunodeficiency Virus (HIV) | AIDS | Zidovudine, Zalcitabine, Stavudine, Abacavir, Didanosine, etc. | Jeon et al., Antimicrobial Agents and Chemotherapy (2020) 64(7): e00819-20 |
Adenoviridae | Human Adenovirus | Acute Infection, Respiratory Disease | ✕ | Jeon et al., Antimicrobial Agents and Chemotherapy (2020) 64(7): e00819-20 |
Flaviviridae | Zika virus | Microcephaly in Infants | ✕ | Simeonov et al., Nature Medicine (2016) 22, 1101–1107 |
Dengue virus 2 (DENV-2) | Dengue Fever | ✕ | Li et al., Cell Research (2017) 26, 1046–1064 | |
West Nile virus (WNV) | West Nile Fever | ✕ | Li et al., Cell Research (2017) 26, 1046–1064 | |
Yellow fever virus (YFV) | Yellow Fever | ✕ | Li et al., Cell Research (2017) 26, 1046–1064 | |
Japanese encephalitis virus (JEV) | Japanese Encephalitis | ✕ | Li et al., Cell Research (2017) 26, 1046–1064 | |
Hepatitis C virus (HCV) | Hepatitis C | Mavyret, Harvoni, Sovaldi, etc | Edwards et al., Journal of Medicinal Chemistry (2011) 54, 8670–8680 | |
Hepeviridae | Hepatitis E virus (HEV) | Hepatitis E | ✕ | Edwards et al., Journal of Medicinal Chemistry (2011) 54, 8670–8680 |
Filoviridae | Ebola virus | Ebola | ✕ | Madrid et al., ACS Infectious Diseases (2015) 1, 317–326 |
Orthomyxoviridae | Influenza virus | Flu | Rapivab, Relenza, Tamiflu, etc. | Jurgel et al., PLoS Pathogens (2012) 8(10): e1002976 |
Picornaviridae | Human Rhinovirus (HRV) | Common Cold | ✕ | Jurgel et al., PLoS Pathogens (2012) 8(10): e1002976 |
Coxsackievirus (CV) | Hand, Foot, and Mouth Disease (HFMD) | ✕ | Jurgel et al., PLoS Pathogens (2012) 8(10): e1002976 | |
Herpesviridae | Herpes virus 1 (HSV-1) | Herpes | ✕ | Jurgel et al., PLoS Pathogens (2012) 8(10): e1002976 |
Epstein–Barr virus (EBV) | Infectious Mononucleosis | ✕ | Huang et al., Antiviral Research (2017) 38, 68–78 | |
Kaposi’s sarcoma–associated herpesvirus (KSHV) | Kaposi’s Sarcoma | ✕ | Huang et al., Antiviral Research (2017) 38, 68–78 | |
Togaviridae | Chikungunya virus (CHIKV) | Chikungunya Fever | ✕ | Wang et al., Antiviral Research (2016) 135, 81–90 |
Sindbis virus (SINV) | Sindbis Fever | ✕ | Wang et al., Antiviral Research (2016) 135, 81–90 | |
Semliki Forest virus (SFV) | Semliki Forest Fever | ✕ | Wang et al., Antiviral Research (2016) 135, 81–90 | |
Arenaviridae | Lassa virus (LASV) | Lassa Fever | ✕ | Herring et al., Antimicrobial Agents and Chemotherapy (2021) 65(4) |
Pneumovirida | Respiratory Syncytial Virus (RSV) | Acute Respiratory Infection | ✕ | Nyomdecha et al., Virus Research (2021) 295:198277 |

CEO geunwoo jin
Email contact@hyundaibio.com
Tel 1544-3194 | Fax 053-756-4055
Address Hyundai Bioscience Co., Ltd., 8th Floor, Botanic Gate, 166, Magokdong-ro, Gangseo-gu, Seoul, 07790, Korea
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CEO geunwoo jin | Email contact@hyundaibio.com | Tel 1544-3194 | Fax 053-756-4055
Address Hyundai Bioscience Co., Ltd., 8th Floor, Botanic Gate, 166, Magokdong-ro, Gangseo-gu, Seoul, 07790, Korea
Copyright ⓒ 2026 HYUNDAI BIOSCIENCE All rights reserved.