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Personalized Phage Treatment in Covid-19 Patients With Bacterial Co-Infections Microbials for Pneumonia or Bacteremia/Septicemia

Expanded Access Study of Phage Treatment in Covid-19 Patients on Anti-Microbials for Pneumonia or Bacteremia/Septicemia Due to A. Baumannii, P. Aeruginosa or S. Aureus

Status
NO_LONGER_AVAILABLE
Phases
Unknown
Study type
Expanded Access
Source
ClinicalTrials.gov
Registry ID
NCT04636554
Enrollment
Unknown
Registered
2020-11-19
Start date
Unknown
Completion date
Unknown
Last updated
2021-12-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acinetobacter Baumannii Infection, Bacteremia, Covid19, Pseudomonas Aeruginosa Infection, Septicemia, Staph Aureus Infection

Keywords

Covid19, Bacteriophage, Phage, Bacteremia, Septicemia, Acinetobacter, baumannii, Pseudomonas, Aeruginosa, Infection, Staph, Aureus

Brief summary

Phage Treatment in Covid-19 Patients with Bacterial Co-Infections

Detailed description

The treatment approach will be to make phage therapy available to institutions who care for Covid-19 patients with bacterial co-infections due to A. baumannii, P. aeruginosa or S. aureus. Patient bacterial isolates will be tested to determine phage susceptibility prior to and during phage therapy. The primary objectives are to determine the feasibility of developing, producing and providing a personalized intravenous phage for Covid-19 patients who have pneumonia, bacteremia or septicemia due to A. baumannii, P. aeruginosa or S. aureus and to evaluate the safety of intravenous phage in Covid-19 patients along with anti-microbial treatment for pneumonia, bacteremia or septicemia due to A. baumannii, P. aeruginosa or S. aureus.

Interventions

Personalized intravenous phage therapy in Covid-19 patients along with anti-microbial treatment for pneumonia, bacteremia or septicemia due to A. baumannii, P. aeruginosa or S. aureus.

Sponsors

Adaptive Phage Therapeutics, Inc.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Covid-19 patients with pneumonia or bacteremia/septicemia who have culture-confirmed bacterial co-infection with A. baumannii, P. aeruginosa or S. aureus. * Patient provided informed and signed consent.

Exclusion criteria

* Patient eligible for another APT sponsored trial. * Patient participating in another clinical trial at the same time or patients \< 4 weeks from participating in an alternative investigational protocol/study * Patient with known allergy to infusion of phage products * Patients with a history of Meningitis or encephalitis at time of study entry, Primary immune deficiency disease or tuberculosis or Stroke, transient ischemic attack (TIA), or untreated deep vein thrombosis.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026