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NCT04432207 · ClinicalTrials.gov registry record · Phase 1

A Study of IMU-201 (PD1-Vaxx), a B-Cell Immunotherapy, in Adults With Non-Small Cell Lung Cancer

A Phase 1 study, sponsored by Imugene Limited.

Terminated
Registry status
Phase 1
Development phase
24
Enrollment target

NCT04432207: Clinical Trial Phase 1 study, sponsored by Imugene Limited.

NCT04432207 is a Phase 1 study that was terminated before completion, run by Imugene Limited. The registered enrollment target is 24 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (60% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04432207, a Phase 1 study, was terminated before completion, sponsored by Imugene Limited.

TERMINATED
Registry status
Phase 1
Development phase
24 participants
Enrollment target

Study Summary

An Open Label, Multi-Center, Dose Escalation/Expansion, Phase 1/1b Study of IMU 201 (PD1-Vaxx), a B-Cell Immunotherapy as monotherapy or in combination with atezolizumab with or without chemotherapy, in Adults with Non-Small Cell Lung Cancer (IMPrinter).

Primary Outcome

Safety and Tolerability Measures include: Frequency of adverse events (AEs) graded per terminology criteria for adverse events (CTCAE) version 5.00.

Interventions

  • DRUG Atezolizumab
  • BIOLOGICAL IMU-201 (administered as PD1-Vaxx) - Regimen 1
  • BIOLOGICAL IMU-201 (administered as PD1-Vaxx) - Regimen 2
  • BIOLOGICAL IMU-201 (administered as PD1-Vaxx) - Regimen 3
  • DRUG Standard of care chemotherapy

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2020-11-30
Est. Completion 2024-11-07
Phase Phase 1
Imugene Limited

5 total trials

Why NCT04432207 stopped before completion

NCT04432207 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (60% lower).

The record links to 0 conditions, and to 5 interventions - of which Atezolizumab is the first listed.

NCT04432207 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04432207 about?

NCT04432207 is a clinical study titled "A Study of IMU-201 (PD1-Vaxx), a B-Cell Immunotherapy, in Adults With Non-Small Cell Lung Cancer". An Open Label, Multi-Center, Dose Escalation/Expansion, Phase 1/1b Study of IMU 201 (PD1-Vaxx), a B-Cell Immunotherapy as monotherapy or in combination with atezolizumab with or without chemotherapy, in Adults with Non-Small Cell Lung Cancer (IMPrinter).

What is the current status of trial NCT04432207?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 24 participants. The study started on 2020-11-30. Estimated completion is 2024-11-07.

What interventions are being tested in trial NCT04432207?

The interventions under investigation include: Atezolizumab (DRUG), IMU-201 (administered as PD1-Vaxx) - Regimen 1 (BIOLOGICAL), IMU-201 (administered as PD1-Vaxx) - Regimen 2 (BIOLOGICAL), IMU-201 (administered as PD1-Vaxx) - Regimen 3 (BIOLOGICAL), Standard of care chemotherapy (DRUG).

Who is sponsoring clinical trial NCT04432207?

This trial is sponsored by Imugene Limited, which has 5 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04432207's enrollment target sits among peer trials

24 1520th of 2000 higher than 405 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04432207, the US trial registry maintained by the National Library of Medicine. NCT04432207 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.