Clinical Trial Will Assess IVIG for Treating COVID-19

Octapharma USA is supporting a new investigator-initiated clinical trial led by George Sakoulas, MD, of Sharp Memorial Hospital in San Diego, Calif., focused on treating the most critical coronavirus patients who are experiencing respiratory failure who become ventilator-dependent. The Randomized Open Label Study of Standard of Care Plus Intravenous Immunoglobulin (IVIG) Compared to Standard of Care Alone in the Treatment of COVID-19 Infection hopes to identify whether IVIG can halt coronavirus progression to respiratory failure requiring transfer into the intensive care unit (ICU) and mechanical ventilation in admitted COVID-19 patients, and whether adding IVIG to the standard of care will reduce days requiring oxygen therapy and total hospital days.

“It is currently believed that 80 percent of COVID-19 subjects will require no medical treatment, 15 percent will require non-ICU medical care and 5 percent may require ICU admission,” said Dr. Sakoulas. “The goals of this study are to evaluate three parameters: the rate of subjects requiring mechanical ventilation; number of days patients require oxygen therapy; and length of hospital stay.”

Secondary objectives of the study are to identify whether adding IVIG to the standard of care will reduce days requiring oxygen therapy, and to identify whether adding IVIG to the standard of care will reduce total hospital days.

“Although we are currently collecting convalescent plasma for future preparations, we need a treatment option for COVID-19 now for critical and soon-to-be critical patients,” said Octapharma USA President Flemming Nielsen. “There is no known effective treatment for patients who are infected with COVID-19. IVIG is wellunderstood to treat immune-mediated diseases and for prophylaxis and treatment of severe infections, especially in immunocompromised patients.”

In an earlier clinical trial in Wuhan, China, where the coronavirus outbreak began, it was noted that death from the disease is frequently the result of an abnormal pulmonary immune system response with multiple respiratory viral infections in which there is an elevation of cytokine and chemokine production referred to as a “cytokine storm” and associated with poor clinical outcomes.

“There have been few human cases analyzing the effects of utilizing IVIG for COVID-19 infection,” said Dr. Sakoulas. “One small case series of three patients from China demonstrated clinical improvement allowing hospital discharge in clinically deteriorating COVID-19 patients. Motivated by this small study, our team employed a similar algorithm in a 62- year-old female with diabetes, hypertension and a history of prior chemotherapy due to breast cancer who was clinically deteriorating from COVID-19 infection, with oxygen requirement increasing from 2L to 6L in the first 48 hours of hospitalization. After receiving IVIG, the patient demonstrated a remarkable clinical improvement, becoming afebrile and breathing normally without external oxygen treatment in less than 72 hours, accompanied by improvement in inflammatory markers. She was discharged home uneventfully. We believe that at least some COVID-19 patients may benefit from IVIG treatment, especially when given at the right time before full-blown acute respiratory distress syndrome sets in.”

Dr. Sakoulas hopes to enroll 20 adults hospitalized with COVID-19 requiring significant oxygen, but not on mechanical ventilation. Patients will be randomized to receive standard of care alone, or standard of care with IVIG treatment. For complete study information, contact Huub Kreuwel, vice president of scientific and medical affairs at Octapharma, at [email protected].