Drugs / EOM613
Trials 1
| Phase | Registry id | Dates | Indication | Sponsor | Status | Outcome |
|---|---|---|---|---|---|---|
| Phase 1 | NCT05212532 | Aug 2021 → Feb 2022 | COVID-19, acute respiratory distress syndrome, pneumonia | EOM Pharmaceuticals | Unknown | No outcome recorded |
News releases announcing trial results or a regulatory action · 1
| Date | Issuer | Release |
|---|---|---|
| 2020-12-24 | EOM Pharmaceuticals | Regulatory EOM PHARMACEUTICALS ANNOUNCES ITS PRE-IND MEETING REQUEST WITH U.S. FDA TO EVALUATE PLANS FOR A PHASE 2 CLINICAL TRIAL OF ITS INVESTIGATIONAL DUAL-ACTING, BROAD-SPECTRUM IMMUNOMODULATOR IN COVID-19 PATIENTS eompharma.com ↗ |
All press releases naming this drug 2 releases
Evidence & citations 4 cited values
Every value below carries the sentence it was read from. 1 source stands behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | EOM613 | ClinicalTrials.gov intervention name — accepted as the source's own label NCT05212532 ↗ |
| Modality | Oligonucleotide (other) | “EOM613 is a peptide nucleic acid with novel immune-modulating properties” NCT05212532 ↗ |
| Route | Subcutaneous | “EOM613 is to be administered subcutaneously (SC) at a dose of 2 mL once daily (QD) for 10 days” NCT05212532 ↗ |
| Target | IL6 | “including modulation of IL-6 expression” NCT05212532 ↗ |