deltatrials
Terminated PHASE1 INTERVENTIONAL 4-arm NCT05429021

IMM-BCP-01 in Mild to Moderate COVID-19

A Randomized, Double-Blind, Placebo-Controlled, First-in-Human, Phase 1 Study to Evaluate the Safety, Pharmacokinetics, and Viral Clearance of Single Ascending Doses of IMM-BCP-01 Administered Intravenously in Adults With Mild to Moderate COVID-19

Sponsor: Immunome, Inc.

Updated 5 times since 2022 Last updated: Sep 24, 2024 Started: Jun 3, 2022 Primary completion: Jan 6, 2023 Completion: Jan 6, 2023
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

Terminated

Business decision to discontinue the study based on strategic prioritization.

Listed as NCT05429021, this PHASE1 trial focuses on COVID-19 and SARS-CoV2 Infection and remains terminated or withdrawn. Sponsored by Immunome, Inc., it has been updated 5 times since 2022, reflecting limited change activity. This study is part of the global effort to build evidence for infectious disease interventions.

Status Flow

~Jul 2022 – ~Sep 2022 · 2 months · monthly snapshotRecruiting~Sep 2022 – ~Jul 2024 · 22 months · monthly snapshotRecruiting~Jul 2024 – ~Sep 2024 · 2 months · monthly snapshotRecruiting~Sep 2024 – ~Oct 2024 · 30 days · monthly snapshotUnknown~Oct 2024 – present · 21 months · monthly snapshotTerminated

Change History

5 versions recorded
  1. Oct 2024 — Present [monthly]

    Terminated PHASE1

    Status: UnknownTerminated

  2. Sep 2024 — Oct 2024 [monthly]

    Unknown PHASE1

    Status: RecruitingUnknown

  3. Jul 2024 — Sep 2024 [monthly]

    Recruiting PHASE1

  4. Sep 2022 — Jul 2024 [monthly]

    Recruiting PHASE1

  5. Jul 2022 — Sep 2022 [monthly]

    Recruiting PHASE1

    First recorded

Jun 2022

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:
  • Immunome, Inc.
  • United States Department of Defense
Data source: Immunome, Inc.

For direct contact, visit the study record on ClinicalTrials.gov .