A Study to Compare the Oral Bioavailability of Single Doses of Three Vapendavir Drug Formulations in Healthy Volunteers

Owner of Study Record: Vaxart Inc.

Inclusion Criteria:

1. Must be a healthy male or female between 19 and 60 years of age (inclusive) at the
time of signing the informed consent and weigh ≥50 kg with a BMI between 18 and 32.0
kg/m2 (inclusive);

2. Capable of giving written informed consent;

3. Subject is able to understand and comply with the protocol requirements, instructions
and restrictions;

4. Healthy on the basis of physical examination, medical history, VS, ECGs, and clinical
laboratory tests;

5. Female subjects who are not postmenopausal for at least 2 years or surgically sterile
with complete hysterectomy or bilateral oophorectomy and male subjects, who are not
surgically sterile via vasectomy, must agree to use a double barrier method of birth
control, such as, a condom plus spermicidal agent (foam/gel/film/cream/suppository)
from Study Day 0 until 30 days after completion of the study. This includes female
subjects who are using hormonal contraception;

6. Female subjects must not be breastfeeding or pregnant.

Exclusion Criteria:

1. Positive results at screening for hepatitis B, hepatitis C, or HIV;

2. No use of tobacco products, as well as electronic cigarettes, within 14 days of Study
Day 1 or unwilling to abstain during study participation;

3. A medical history or clinical evidence of any clinical condition that may, in the
opinion of the Investigator or Medical Monitor, impact on the subject's ability to
participate in the study, or on the study results;

4. Current or recent respiratory or other infection within 14 days of screening;

5. Presence or history of significant allergy requiring treatment;

6. Clinically significant abnormalities on ECG;

7. Vital signs representing abnormal systolic blood pressure and/or abnormal diastolic
blood pressure;

8. Safety laboratory abnormalities at screening or Study Day 0 which are clinically
significant;

9. Subject has a history of drug abuse or alcohol abuse in the past 2 years or current
evidence of such abuse or addiction;

10. A positive urine drug screen test at screening or admission to the study facility;

11. A positive breathalyzer for alcohol at screening or admission to the study facility;

12. A positive pregnancy test at screening or admission to the study facility;

13. Abstinence from alcohol must be employed from 72 hours before Study Day 1 and
throughout the duration of study participation;

14. Use of chronic prescription medications within 90 days, with the exception of hormonal
contraceptives (or contraceptive device containing hormonal contraceptive) being taken
by female subjects within 14 days, or over-the-counter (OTC) medications, including
vitamin, herbal, and mineral supplements, within the 7 days prior to Study Day 1 and
throughout study participation;

15. Received an investigational drug or investigational vaccine within 30 days, or use of
an investigational medical device within 30 days prior to Study Day 1;

16. Any prior use of vapendavir or inclusion in a previous vapendavir investigational
study or ongoing participation in a vapendavir investigational study;

17. Donation or loss of whole blood within 60 days or plasma within 14 days of Study Day 1
or anytime from screening to 30 days after completion of the study.