phase 1 stage: inclusion criteria: male subjects aged 18-50 years; in good state of health, determined by medical history, physical exam, and normal laboratory tests at screening; are able to provide informed consent for participation; are able and willing to comply with the study schedule and procedures. exclusion criteria active sars-cov-2 infection demonstrated by positive polymerase chain reaction (pcr) at enrollment; requiring cpap for sleep apnea; pre-existing pulmonary disease; have any serious acute concomitant illness that, in the opinion of the investigator, would interfere with evaluation of safety of ap-003, or put the participant at risk of harm from study participation; are currently receiving an investigational agent, have participated in another study of an investigational agent within 30 days of enrollment, or were previously enrolled in the current study; are legally incompetent and unable to understand the study's purpose, significance, and consequences, and to make decisions accordingly; have known hypersensitivity to interferon alpha or any component of the study drug or placebo control. phase 2 stage: inclusion criteria: active sars-cov-2 infection demonstrated by positive polymerase chain reaction (pcr) ≤ 5 days at enrollment; symptomatic of mild or moderate covid-19 for ≤ 5 days at enrollment. symptoms can include fever, cough, sore throat, malaise, headache, muscle pain, gastrointestinal symptoms, chest pain, with or without shortness of breath on exertion/dyspnea; age ≥ 18 years; are able to provide informed consent for participation; are able and willing to comply with the study schedule and procedures. exclusion criteria patients requiring cpap for sleep apnea. patients with pre-existing pulmonary disease requiring chronic o2 supplementation. patients with known infection with influenza a or b; in the opinion of the investigator, should undergo ventilatory (cpap, mechanical ventilation, etc.) or circulatory support within 24 hours of study enrollment; have any serious acute concomitant illness that, in the opinion of the investigator, would interfere with evaluation of safety or efficacy, or put the participant at risk of harm from study participation; are currently receiving an investigational agent, have participated in another study of an investigational agent within 30 days of enrollment, or were previously enrolled in the current study; are legally incompetent and unable to understand the study's purpose, significance, and consequences, and to make decisions accordingly; women who are pregnant or breast-feeding, or planning to conceive in the next 30 days; have known hypersensitivity to interferon alpha or any component of the study drug or placebo control.

phase 1 stage: inclusion criteria: male subjects aged 18-50 years; in good state of health, determined by medical history, physical exam, and normal laboratory tests at screening; are able to provide informed consent for participation; are able and willing to comply with the study schedule and procedures. exclusion criteria active sars-cov-2 infection demonstrated by positive polymerase chain reaction (pcr) at enrollment; requiring cpap for sleep apnea; pre-existing pulmonary disease; have any serious acute concomitant illness that, in the opinion of the investigator, would interfere with evaluation of safety of ap-003, or put the participant at risk of harm from study participation; are currently receiving an investigational agent, have participated in another study of an investigational agent within 30 days of enrollment, or were previously enrolled in the current study; are legally incompetent and unable to understand the study's purpose, significance, and consequences, and to make decisions accordingly; have known hypersensitivity to interferon alpha or any component of the study drug or placebo control. phase 2 stage: inclusion criteria: active sars-cov-2 infection demonstrated by positive polymerase chain reaction (pcr) ≤ 5 days at enrollment; symptomatic of mild or moderate covid-19 for ≤ 5 days at enrollment. symptoms can include fever, cough, sore throat, malaise, headache, muscle pain, gastrointestinal symptoms, chest pain, with or without shortness of breath on exertion/dyspnea; age ≥ 18 years; are able to provide informed consent for participation; are able and willing to comply with the study schedule and procedures. exclusion criteria patients requiring cpap for sleep apnea. patients with pre-existing pulmonary disease requiring chronic o2 supplementation. patients with known infection with influenza a or b; in the opinion of the investigator, should undergo ventilatory (cpap, mechanical ventilation, etc.) or circulatory support within 24 hours of study enrollment; have any serious acute concomitant illness that, in the opinion of the investigator, would interfere with evaluation of safety or efficacy, or put the participant at risk of harm from study participation; are currently receiving an investigational agent, have participated in another study of an investigational agent within 30 days of enrollment, or were previously enrolled in the current study; are legally incompetent and unable to understand the study's purpose, significance, and consequences, and to make decisions accordingly; women who are pregnant or breast-feeding, or planning to conceive in the next 30 days; have known hypersensitivity to interferon alpha or any component of the study drug or placebo control.

phase 1 stage: inclusion criteria: 1. male subjects aged 18-50 years; 2. in good state of health, determined by medical history, physical exam, and normal laboratory tests at screening; 3. are able to provide informed consent for participation; 4. are able and willing to comply with the study schedule and procedures. exclusion criteria 1. active sars-cov-2 infection demonstrated by positive polymerase chain reaction (pcr) at enrollment; 2. requiring cpap for sleep apnea; 3. pre-existing pulmonary disease; 4. have any serious acute concomitant illness that, in the opinion of the investigator, would interfere with evaluation of safety of ap-003, or put the participant at risk of harm from study participation; 5. are currently receiving an investigational agent, have participated in another study of an investigational agent within 30 days of enrollment, or were previously enrolled in the current study; 6. are legally incompetent and unable to understand the study's purpose, significance, and consequences, and to make decisions accordingly; 7. have known hypersensitivity to interferon alpha or any component of the study drug or placebo control. phase 2 stage: inclusion criteria: 1. active sars-cov-2 infection demonstrated by positive polymerase chain reaction (pcr) ≤ 5 days at enrollment; 2. symptomatic of mild or moderate covid-19 for ≤ 5 days at enrollment. symptoms can include fever, cough, sore throat, malaise, headache, muscle pain, gastrointestinal symptoms, chest pain, with or without shortness of breath on exertion/dyspnea; 3. age ≥ 18 years; 4. are able to provide informed consent for participation; 5. are able and willing to comply with the study schedule and procedures. exclusion criteria 1. patients requiring cpap for sleep apnea. 2. patients with pre-existing pulmonary disease requiring chronic o2 supplementation. 3. patients with known infection with influenza a or b; 4. in the opinion of the investigator, should undergo ventilatory (cpap, mechanical ventilation, etc.) or circulatory support within 24 hours of study enrollment; 5. have any serious acute concomitant illness that, in the opinion of the investigator, would interfere with evaluation of safety or efficacy, or put the participant at risk of harm from study participation; 6. are currently receiving an investigational agent, have participated in another study of an investigational agent within 30 days of enrollment, or were previously enrolled in the current study; 7. are legally incompetent and unable to understand the study's purpose, significance, and consequences, and to make decisions accordingly; 8. women who are pregnant or breast-feeding, or planning to conceive in the next 30 days; 9. have known hypersensitivity to interferon alpha or any component of the study drug or placebo control.

phase 1 stage: inclusion criteria: 1. male subjects aged 18-50 years; 2. in good state of health, determined by medical history, physical exam, and normal laboratory tests at screening; 3. are able to provide informed consent for participation; 4. are able and willing to comply with the study schedule and procedures. exclusion criteria 1. active sars-cov-2 infection demonstrated by positive polymerase chain reaction (pcr) at enrollment; 2. requiring cpap for sleep apnea; 3. pre-existing pulmonary disease; 4. have any serious acute concomitant illness that, in the opinion of the investigator, would interfere with evaluation of safety of ap-003, or put the participant at risk of harm from study participation; 5. are currently receiving an investigational agent, have participated in another study of an investigational agent within 30 days of enrollment, or were previously enrolled in the current study; 6. are legally incompetent and unable to understand the study's purpose, significance, and consequences, and to make decisions accordingly; 7. have known hypersensitivity to interferon alpha or any component of the study drug or placebo control. phase 2 stage: inclusion criteria: 1. active sars-cov-2 infection demonstrated by positive polymerase chain reaction (pcr) ≤ 5 days at enrollment; 2. symptomatic of mild or moderate covid-19 for ≤ 5 days at enrollment. symptoms can include fever, cough, sore throat, malaise, headache, muscle pain, gastrointestinal symptoms, chest pain, with or without shortness of breath on exertion/dyspnea; 3. age ≥ 18 years; 4. are able to provide informed consent for participation; 5. are able and willing to comply with the study schedule and procedures. exclusion criteria 1. patients requiring cpap for sleep apnea. 2. patients with pre-existing pulmonary disease requiring chronic o2 supplementation. 3. patients with known infection with influenza a or b; 4. in the opinion of the investigator, should undergo ventilatory (cpap, mechanical ventilation, etc.) or circulatory support within 24 hours of study enrollment; 5. have any serious acute concomitant illness that, in the opinion of the investigator, would interfere with evaluation of safety or efficacy, or put the participant at risk of harm from study participation; 6. are currently receiving an investigational agent, have participated in another study of an investigational agent within 30 days of enrollment, or were previously enrolled in the current study; 7. are legally incompetent and unable to understand the study's purpose, significance, and consequences, and to make decisions accordingly; 8. women who are pregnant or breast-feeding, or planning to conceive in the next 30 days; 9. have known hypersensitivity to interferon alpha or any component of the study drug or placebo control.