deltatrials
Unknown PHASE1/PHASE2 INTERVENTIONAL 1-arm NCT04609215

ImmunoBreast - A Phase Ib Study

ImmunoBreast - A Phase Ib Study to Investigate the Safety, Tolerability and Trends of Efficacy of ALECSAT Treatment as an add-on Therapy to Carboplatin and Gemcitabine in Patients With Locally Advanced or Metastatic Triple-negative Breast Cancer

Sponsor: CytoVac A/S

Interventions ALECSAT
Updated 6 times since 2020 Last updated: Apr 19, 2022 Started: Apr 21, 2020 Primary completion: May 21, 2023 Completion: May 21, 2023
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

This PHASE1/PHASE2 trial investigates Breast Cancer and Metastatic Breast Cancer and is currently ongoing. CytoVac A/S leads this study, which shows 6 recorded versions since 2020 — indicating limited longitudinal coverage. As an oncology study, it adds to the longitudinal record of treatment development for this indication.

Status Flow

~Nov 2020 – ~Jan 2021 · 2 months · monthly snapshot~Jan 2021 – ~May 2022 · 16 months · monthly snapshotRecruiting~May 2022 – ~May 2024 · 24 months · monthly snapshotRecruiting~May 2024 – ~Jul 2024 · 2 months · monthly snapshot~Jul 2024 – ~Sep 2024 · 2 months · monthly snapshot~Sep 2024 – present · 24 months · monthly snapshotUnknown

Change History

6 versions recorded
  1. Sep 2024 — Present [monthly]

    Unknown PHASE1/PHASE2

  2. Jul 2024 — Sep 2024 [monthly]

    Unknown PHASE1/PHASE2

    Status: Unknown StatusUnknown · Phase: PHASE1_PHASE2PHASE1/PHASE2

  3. May 2024 — Jul 2024 [monthly]

    Unknown Status PHASE1_PHASE2

    Status: RecruitingUnknown Status

  4. May 2022 — May 2024 [monthly]

    Recruiting PHASE1_PHASE2

  5. Jan 2021 — May 2022 [monthly]

    Recruiting PHASE1_PHASE2

Show 1 earlier version
  1. Nov 2020 — Jan 2021 [monthly]

    Recruiting PHASE1_PHASE2

    First recorded

Apr 2020

Trial started

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

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:
  • CytoVac A/S
  • Henrik Ditzel
  • National Board of Health, Denmark
Data source: Odense University Hospital

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

Study Locations