Recruiting
Phase 2

2-HOBA

Sponsor:

Vanderbilt University Medical Center

Code:

NCT07189936

Conditions

Post-Acute COVID-19 Syndrome

Postural Tachycardia Syndrome (POTS)

SARS CoV 2 Infection

Long COVID19

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

To Measure levels of circulating monocyte/ T cell doublets at Baseline

To measure levels of circulating monocyte/ T cell doublets after 28 days of 2 HOBA treatment

To measure levels of circulating monocyte/ T cell doublets after 28 days of Placebo treatment

To Measure Splanchnic venous capacitance after 28 days of Treatment with 2HOBA

To Measure Splanchnic venous capacitance after 28 days of Treatment with Placebo

Study Details

Brief summary:

Long COVID is defined by a range of symptoms affecting multiple organs that persist for more than three months following an acute SARS-CoV-2 infection. Approximately 7% of individuals who recover from SARS-Cov-2 infection develop Long COVID.

Long COVID Postural Orthostatic Tachycardia Syndrome (LCPOTS) symptoms include fatigue, exercise intolerance, orthostatic intolerance, syncope, and heightened orthostatic tachycardia.

Research has found that decreased parasympathetic activity in LCPOTS increases the production of highly immunogenic neoantigens Isolevuglandins (IsoLG-adducts). IsoLG-adducts induce formation of circulating monocyte/T cell complexes(doublets) leading to the persistent and unresolved immune response that continues after the initial infection.

The purpose of the this research, is to study the effects of 2-hydroxybenzylamine (2-HOBA), an Iso-LG-adduct scavenger, its effects in immune markers and compare it with Placebo

Conditions

Post-Acute COVID-19 Syndrome

Postural Tachycardia Syndrome (POTS)

SARS CoV 2 Infection

Long COVID19

Study ID

NCT07189936

Start date

Dec 18, 2025

Status verified date

Jan, 2026

Completion date

Jun 30, 2029

Anticipated

Primary completion date

Jun 30, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

All participants should meet diagnostic criteria for Long COVID and POTS and as outlined below:

Long COVID (LC) is defined by a range of symptoms affecting multiple organs that persist for more than three months following an acute SARS-CoV-2 infection.

POTS: the presence of chronic symptoms lasting more than 3 months, along with orthostatic tachycardia (a HR increase over 30 bpm upon standing or exceeding 120 bpm without orthostatic hypotension) within 10 minutes upon standing or 75-degree head up tilt.

For patients aged 18 and 21, an increase of more than 40 bpm or a standing HR over 130 bpm will be required for inclusion in the study.

2 Patients need confirmation of POTS diagnosis based on orthostatic vital signs obtained prior to enrollment in the study.

SARS-CoV-2 infection 3 or more months prior identified by the follow signs:

A. Meets the clinical OR epidemiological criteria.

1. Clinical criteria: Acute onset of fever AND cough (influenza-like illness) OR Acute onset of ANY THREE OR MORE of the following signs or symptoms: fever, cough, general, weakness/fatigue, headache, myalgia, sore throat, coryza, dyspnea, nausea, diarrhea, anorexia.
2. Epidemiological criteria: Contact of a probable or confirmed case or linked to a COVID-19 cluster; or B. Presents with acute respiratory infection with history of fever or measured fever of ≥ 38°C; and cough; with onset within the last 10 days; and who requires hospitalization); or C. Presents with no clinical signs or symptoms, NOR meeting epidemiologic criteria with a positive professional use or self-test SARS-CoV-2 antigen-Rapid Diagnostic Test.

D. A person with a positive nucleic acid amplification test, regardless of clinical criteria OR epidemiological criteria; or E. Meeting clinical criteria AND/OR epidemiological criteria (See A). With a positive professional use or self-test, SARS-CoV-2 Antigen-Rapid Diagnostic Test.

F. Documented by health care provider in clinical note or encounter.

Exclusion Criteria:

1. Known active acute SARS-Cov-2 infection (4 weeks from onset)
2. Moderate or severe immunocompromised patients,
3. Known history of cardiovascular disease (atrioventricular block (AV block), myocardial infarction, angina, heart failure, pacemaker, stroke, transient ischemic attack within 6 months before enrollment),
4. Uncontrolled hypertension (BP>140/90 despite appropriate treatment);
5. Type 1 or type 2 diabetes mellitus;
6. Impaired hepatic function (AST or ALT greater than 1.5x the upper limit of normal or with total bilirubin ≥1.5mg/dl),
7. Impaired renal function test (eGFR<60 mL/min/1.73m2),
8. Anemia (hemoglobin <10 g/dl),
9. Pregnant or breastfeeding women,
10. Known history of autoimmune disease, steroid use or other immunotherapies,
11. Inability to provide informed consent.

We will also exclude individuals with known allergy sensitivity to components of the study medication, known contraindication to the study interventions, use of central acetylcholinesterase inhibitors (e.g., pyridostigmine, donezepil), aspirin allergy because salicylic acid is a metabolite of 2-HOBA; use of monoamine oxidase inhibitors (MAO-I) because of some inhibition of MAO-A is present in the anticipated therapeutic range of 2-HOBA.

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Study Design

Enrollment

50 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

placebo comparator: Levels of circulating monocyte/ T cell doublets, and inflammatory cytokines in 2 HoBA Vs Placebo

to test the effect of 28-day treatment with Iso-LG-adduct scavenger, 2-hydroxybenzylamine (2-HOBA) versus placebo on circulating monocyte/ T cell doublets (CD14+CD3+) , and inflammatory cytokines

placebo comparator: Effect of 2HOBA on Splanchnic venous capacitance and compare with placebo group on POTS patients

To test the hypothesis that IsoLG-adducts directly contribute to splanchnic vasodilation, by assessing changes in splanchnic venous capacitance with 2-HOBA treatment at head up Tilt

active comparator: Effect of 2HOBA on Orthostatic Tachycardia compare with placebo group during 30 minutes head up tilt

To test that IsoLG-adducts directly effect Orthostatic tachycardia in LCPOTS, during 30-minute head-up tilt.

Interventions

To Measure levels of circulating monocyte/ T cell doublets at Baseline

To determine the levels of circulating monocyte/ T cell doublets on all the LCPOTS subjects

To measure levels of circulating monocyte/ T cell doublets after 28 days of 2 HOBA treatment

Subjects will be randomized 1:1 to 2-HOBA or matching placebo. The levels of circulating monocyte/ T cell doublets (immune burden) after 28 days of 2 HOBA treatment

To measure levels of circulating monocyte/ T cell doublets after 28 days of Placebo treatment

The levels of circulating monocyte/ T cell doublets (immune burden) after 28 days of 2 HOBA treatment and compare it to the placebo arms

To Measure Splanchnic venous capacitance after 28 days of Treatment with 2HOBA

We will Measure changes in Splanchnic venous capacitance after 28 days of Treatment with 2HOBA and compare it with baseline during 30 Mins head up tilt . All the LCPOTS subjects will be randomized 1:1 to 2-HOBA or matching placebo

To Measure Splanchnic venous capacitance after 28 days of Treatment with Placebo

We will Measure changes in splanchnic venous capacitance during 30 mins head up tilt ,after 28 days of Treatment with Placebo, we will compare it to the subjects who received 2 HOBA for 28 days

To Measure Orthostatic Tachycardia after 28 days of Treatment with 2HOBA

To Measure changes in Orthostatic Tachycardia after 28 days of Treatment with 2HOBA at 30 minutes of head up Tilt

To Measure Orthostatic Tachycardia after 28 days of Treatment with Placebo

To Measure changes in Orthostatic Tachycardia after 28 days of Treatment with Placebo at 30 minutes of head up Tilt and compare it with the subjects who received 28 days of 2HOBA

Primary outcome measure

  • Effect IsoLG-adducts (2-HOBA) measured by levels of monocyte/T cell doublets in LCPOTS. [ Time Frame: Baseline (Day 0) to after 28 days of treatment ]
  • Changes in Splanchnic venous capacitance before and after 28 days of treatment [ Time Frame: Day 0- Day 28 days ]

Central Contacts and Locations

Central contacts

Locations

Cyndya Shibao

Recruiting

Nashville, Tennessee, United States, 37027

Contacts

Principal Investigator:

Cyndya A Shibao, MD

More Information

Sponsor

Vanderbilt University Medical Center

Last update posted

Jan 22, 2026

Last verified

Jan, 2026

Keywords

  • Long COVID

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Vanderbilt University Medical Center on 2026-01-22.