Thymalfasin (Thymosin Alpha 1; Ta1) as an Enhancer of Vaccine Response Among Older Adults Receiving Booster Doses of COVID-19 Vaccine

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age65-100
SponsorThe Methodist Hospital Research Institute

About this trial

The goal of this research is to learn more about ZADAXIN® (trade name; thymalfasin generic; Ta1 for short) and determine if Ta1 has any benefit in increasing the immune response to the COVID-19 vaccine. Ta1 has been shown to stimulate the immune system to fight infections.

This research study will test the safety and possible harms of Ta1 when it is given to people at different dose levels before COVID-19 vaccination.

Eligibility criteria

Qualifiers

Age 65 or greater.

Able and willing to provide informed consent or have consent provided by a legally authorized representative (LAR).

Scheduled for SARS-CoV-2 mRNA vaccination booster dose.

If a male subject, the subject must agree to use barrier contraception (ie, condoms) from Day 1 through 30 days following the last dose of study drug.

Disqualifiers

Hypoxemia for any reason, defined as either oxygen saturation (SpO2) ≤ 93% on room air or a requirement for supplemental oxygen support.

Acute liver failure defined as INR ≥ 1.5 and altered mental status in a patient without cirrhosis or pre-existing liver disease.

Acute kidney failure defined as an increase in serum creatinine of ≥0.3 mg/dL within 48 hours or ≥50% within 7 days OR urine output of <0.5 mL/kg/hour for >6 hours

Heart failure with NYHA functional classification III or IV.

Trial design

Treatments tested in this trial

  • Thymalfasin (Thymosin alpha 1, Ta1)

Treatment groups

75 Participants
are divided into 3 treatment groups