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NCT02876510 · ClinicalTrials.gov registry record · Phase 1

ACTolog in Patients With Solid Cancers

A Phase 1 study, sponsored by Immatics US.

Completed
Registry status
Phase 1
Development phase
38
Enrollment target

NCT02876510: Completed Phase 1 study, sponsored by Immatics US.

NCT02876510 is a Phase 1 study that has completed, run by Immatics US. The registered enrollment target is 38 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (37% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02876510, a Phase 1 study, has completed, sponsored by Immatics US.

COMPLETED
Registry status
Phase 1
Development phase
38 participants
Enrollment target

Study Summary

The study purpose is to learn about the safety and tolerability of IMA101 alone (Cohort 1) or in combination with atezolizumab (Cohort 2) in patients with advanced solid cancers that express pre-defined Immatics tumor targets.

Interventions

  • DRUG Cyclophosphamide
  • DRUG Fludarabine
  • BIOLOGICAL IMA101 product
  • BIOLOGICAL Recombinant human interleukin-2
  • DIAGNOSTIC_TEST IMADetect

Trial Details

FieldValue
Enrollment Target 38 participants
Start Date 2017-06-30
Est. Completion 2021-09-22
Phase Phase 1
Immatics US

7 total trials

What the finished NCT02876510 record still lists

NCT02876510 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 38 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (37% lower).

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

NCT02876510 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02876510 about?

NCT02876510 is a clinical study titled "ACTolog in Patients With Solid Cancers". The study purpose is to learn about the safety and tolerability of IMA101 alone (Cohort 1) or in combination with atezolizumab (Cohort 2) in patients with advanced solid cancers that express pre-defined Immatics tumor targets.

What is the current status of trial NCT02876510?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 38 participants. The study started on 2017-06-30. Estimated completion is 2021-09-22.

What interventions are being tested in trial NCT02876510?

The interventions under investigation include: Cyclophosphamide (DRUG), Fludarabine (DRUG), IMA101 product (BIOLOGICAL), Recombinant human interleukin-2 (BIOLOGICAL), IMADetect (DIAGNOSTIC_TEST).

Who is sponsoring clinical trial NCT02876510?

This trial is sponsored by Immatics US, which has 7 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02876510's enrollment target sits among peer trials

38 1197th of 2000 higher than 797 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 NCT02876510, the US trial registry maintained by the National Library of Medicine. NCT02876510 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.