Drugs / OM-89

Trials 3 · a red edge is where a trial was stopped

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 21 trial
Phase 2 NCT02591901 Apr 2018 → Aug 2019 urinary tract infection Buckinghamshire Healthcare NHS Trust Completed No outcome recorded
Phase 42 trials
Phase 4 NCT06345014 Dec 2023 → Dec 2025 chronic pain syndrome, chronic prostatitis AJU Pharm Co., Ltd. Unknown No outcome recorded
Phase 4 NCT04049994 Jun 2020 → Sep 2023 spinal cord injury, urinary tract infection Swiss Paraplegic Research, Nottwil Completed No outcome recorded
Also used as a comparator or background therapy in 2 trials
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 3 NCT06588010 Comparator Dec 2024 → Dec 2027 expected cauda equina syndrome with neurogenic bladder Centre Hospitalier Universitaire Dijon Recruiting No outcome recorded
Phase 3 NCT00521924 Comparator Jun 2007 → Apr 2008 rheumatoid arthritis Merck Sharp & Dohme LLC Terminated No outcome recorded

Evidence & citations 5 cited values

Every value below carries the sentence it was read from. 6 sources stand behind the page.

FieldValueCited text
Known as OM 89 ClinicalTrials.gov intervention name — accepted as the source's own label NCT00521924
2

NCT06588010

NCT06345014

Known as Uro-Vaxom “Immunomodulation therapy with UroVaxom is a very promising method for the prevention of UTI, however data in individuals with SCI are very limited.” NCT04049994
4

“lyophilized lysate of E. coli strains for oral application (Uro-Vaxom®, OM Pharma SA, Meyrin, Switzerland).” PMID 34607600 Oct 2021

“OM-89 [Uro-Vaxom® Capsule]” NCT06588010

NCT02591901

NCT04049994

Known as Uro-Vaxom Capsule “OM-89 [Uro-Vaxom® Capsule]” NCT06345014
Modality Vaccine “orally administered, bacterial vaccineNCT02591901
Route Oral orally administered” NCT02591901