Efficacy and Safety Study of Efgartigimod in Adults With Post-COVID-19 POTS
The study aims to investigate the safety, tolerability, efficacy, pharmacodynamics (PD), pharmacokinetics (PK), and immunogenicity of efgartigimod compared to placebo in participants with post-COVID-19 postural orthostatic tachycardia syndrome (POTS) (post-COVID-19 POTS).
A Phase 2 Randomized, Double-blinded, Placebo-controlled Study to Evaluate the Efficacy and Safety of Efgartigimod IV in Adult Patients With Post-COVID-19 Postural Orthostatic Tachycardia Syndrome (POTS)
The study aims to investigate the safety, tolerability, efficacy, pharmacodynamics (PD), pharmacokinetics (PK), and immunogenicity of efgartigimod compared to placebo in participants with post-COVID-19 postural orthostatic tachycardia syndrome (POTS) (post-COVID-19 POTS). Efgartigimod may be a viable treatment option for individuals diagnosed with post-COVID-19 POTS because it has been shown to reduce IgG levels, including IgG autoantibodies, which may underlie some of the autonomic disease manifestations in these patients.
Postural Orthostatic Tachycardia Syndrome, POTS, Long COVID, efgartigimod, Tachycardia, Syndrome
You can join if…
Open to people ages 18 years and up
- Reached the age of consent when signing the informed consent form
- Capable of providing signed informed consent and complying with protocol requirements
- Diagnosed with new-onset POTS post-COVID-19 established by the following:
- Prior COVID-19 confirmed by documentation of historical PCR test
- Tilt table or orthostatic vital sign measurements during screening consistent with consensus criteria: sustained HR increase of ≥30 bpm within 10 min of standing or head up tilt (≥40 bpm for individuals aged 18 to 19 years) and/or HR reaching >120 bpm within 10 min; absence of sustained 20 mmHg decrease in systolic blood pressure (SBP)
- Ongoing symptoms of POTS confirmed by the investigator with at least 3 symptoms in each of the following areas lasting longer than 12 weeks after either diagnosis of COVID-19 or after hospital discharge for COVID-19:
- Vasomotor symptoms: fatigue, orthostatic intolerance, brain fog, exertional dyspnea, difficulty with concentration, venous pooling, and exercise intolerance ii.
Sympathetic over-compensation symptoms: palpitation, heat intolerance, nausea with or without vomiting, insomnia, anxiety, lack of appetite, chest pain, and diaphoresis
- COMPASS 31 ≥35 at screening
Agree to use contraceptives consistent with local regulations regarding the methods of contraception for those participating in clinical studies and the following:
Male participants Female participants of childbearing potential must have a negative serum pregnancy test at screening and a negative urine pregnancy test at baseline before receiving IMP. Contraceptive requirements.
- Body mass index (BMI) <35 kg/m2
You CAN'T join if...
- Diagnosis of or receiving treatment for the following conditions before COVID-19: peripheral neuropathy, POTS, myalgic encephalomyelitis encephalitis/chronic fatigue syndrome, Ehlers Danlos syndrome confirmed by genetic testing, autonomic neuropathy, multiple sclerosis, stroke, spinal cord injury, or any known lesions in the central nervous system by imaging or neurological exam
- History of or currently being treated for clinically significant ongoing cardiac arrythmia, heart failure, myocarditis, pulmonary embolism requiring anticoagulation, pulmonary fibrosis, or critical illness-related polyneuropathy or myopathy
- Known autoimmune disease that, in the investigator's judgment, would interfere with an accurate assessment of clinical symptoms of post-COVID-19 POTS or puts the participant at undue risk
- Known HIV disease or common variable immunodeficiency
- History of malignancy unless considered cured by adequate treatment with no evidence of recurrence for ≥3 years before the first administration of IMP. Adequately-treated participants with the following cancers may be included at any time:
- Basal cell or squamous cell skin cancer
- Carcinoma in situ of the cervix
- Carcinoma in situ of the breast
- Incidental histological finding of prostate cancer (TNM stage T1a or T1b)
- Clinically significant uncontrolled active or chronic bacterial, viral, or fungal infection or positive SARS-CoV-2 PCR test at screening
- Positive serum test at screening for an active infection with any of the following:
- Hepatitis B virus (HBV) that is indicative of an acute or chronic infection, unless associated with a negative HB surface antigen (HBsAg) or negative HBV DNA test
- Hepatitis C virus (HCV) based on HCV antibody assay unless a negative RNA test is available
- A medical condition that could confound the results of the study or put the participant at undue risk in the investigator's judgment
Clinically significant disease, recent major surgery (within 3 months of screening), or intends to have surgery during the study; or any other condition that in the opinion of the investigator could confound the results of the study or put the participant at undue risk
10. Total IgG <4 g/L at screening 11. Received within 12 weeks or 5 half-lives (whichever is longer) before screening an
12. Received within 12 weeks before screening either intravenous immunoglobulin (Ig) IV or
SC or plasmapheresis/plasma exchange (PLEX)
13. Received a live or live-attenuated vaccine less than 4 weeks before screening 14. Known hypersensitivity to IMP or 1 of its excipients 15. Previously participated in an efgartigimod clinical study and received at least 1 dose
16. Currently participating in another interventional clinical study 17. History (within 12 months of screening) of or current alcohol, drug, or medication
18. Pregnant or lactating or intends to become pregnant during the study 19. Unwilling to remain on a stable regimen of medications during the study 20. Unwilling to avoid initiation of new physical rehabilitation or other
physician-prescribed exercise programs during the 24-week treatment period
- University of California, San Diego Sulpizio Cardiovascular Center
accepting new patients
La Jolla California 92037 United States
- Stanford Movement Disorder Center
accepting new patients
Palo Alto California 94304 United States
- accepting new patients
- Start Date
- Completion Date
- Phase 2 research study
- Study Type
- Expecting 42 study participants
- Last Updated
Please contact me about this study
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The study team should get back to you in a few business days.