COVID-19 Positive Individuals Needed for Nationwide Study: Recruitment in Seattle

COVID-19 Positive Individuals Needed for Nationwide Study: Recruitment in Seattle

UW Medicine researchers are recruiting people in the Seattle area who have recently tested positive for COVID-19 for four treatment therapies being evaluated in a nationwide study. The therapies include infusions, injections, and an inhalant. Part of the ACTIV-2 clinical trial, the National Institutes of Health (NIH) launched the “Rise Above COVID: Accelerating COVID-91 Therapeutic Interventions and Vaccines” last April.  TrialSite informed last year that the NIH via NIAID reorganized a number of National Institute of Allergy and Infectious Diseases (NIAID) trial site networks for a centralized, organized response to the pandemic, with an aim at accelerating trial recruitment, among other important objectives.

The AIDS Clinical Trials Unit, a research center based at Harborview Medical Center, is conducting the current trial, known as ACTIV-2. It is one of more than 200 sites involved and was a key research center for NIAID. These academic medical centers 

Study Eligibility and Goal

The study team at Harborview Medical Center must recruit participants that have tested positive for SARS-CoV-2, the virus that causes COVID-19, in an outpatient setting within 10 days and must have begun to experience symptoms within seven days of enrolling.

Dr. Rachel Bender Ignacio leads the effort for UW Medicine, directing the AIDS Clinical Trials Unit.  The investigator went on the record:

“The goal of ACTIV-2 is to identify treatments that can keep people who acquire COVID-19 from getting sicker and requiring hospitalization. These treatments also have the potential to help people with mild illness feel better more quickly, return to work faster, or prevent long COVID.”

People who acquired COVID-19 despite being vaccinated are eligible to participate in the trial, she said.

Study Treatments

In addition to studying the safety and efficacy of these investigational therapies, ACTIV-2 also aims to determine whether they are able to decrease viral shedding, thereby reducing transmission of SARS-CoV-2. Participants will be randomized to receive one of the following agents or a placebo:

  • BMS-986414 and BMS-986413 are monoclonal antibodies administered as two subcutaneous injections (shots) given at one visit. Because they target different parts of SARS-CoV-2, the hope is that the combination therapy will improve efficacy, cover multiple variants, and reduce the likelihood that the virus will develop resistance to the treatment. (Rockefeller University and Bristol Myers Squibb, Phase 2 study)
     
  • SAB-185 is the first polyclonal antibody (a treatment containing many different antibodies) to be evaluated in ACTIV-2. SAB-185 is derived from cows that have been genetically engineered to make human antibodies. Once the cows develop an immune response and generate antibodies against the spike protein on the surface of SARS-CoV-2, samples of their blood are collected and the antibodies are separated out and purified. SAB-185 is administered through an intravenous infusion. (SAB Biotherapeutics, Phase 2 study)
     
  • SNG001 is a nebulized formulation of beta interferon being studied as an inhalant. SNG001 is a self-administered dosage that participants inhale once daily for 14 days at home. ACTIV-2 is the first U.S. study to evaluate SNG001 among non-hospitalized people with COVID-19. (Synairgen, Phase 2 study)
     
  • BRII-196 plus BRII-198 are two monoclonal antibodies administered as separate infusions during a single visit. They were derived from antibodies made by people who had recovered from COVID-19. (Brii Biosciences, Phase 3 study)

For more information about ACTIV-2, visit the AIDS Clinical Trial Unit ACTIV-2 site or Rise Above COVID: ACTIV-2 Study.

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