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NCT02540161 · ClinicalTrials.gov registry record · Phase 2

Phase 2 Study of Sym004 for Adult Patients With Recurrent Glioblastoma

A Phase 2 study, sponsored by Annick Desjardins.

Completed
Registry status
Phase 2
Development phase
43
Enrollment target

NCT02540161: Completed Phase 2 study, sponsored by Annick Desjardins.

NCT02540161 is a Phase 2 study that has completed, run by Annick Desjardins. The registered enrollment target is 43 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (68% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02540161, a Phase 2 study, has completed, sponsored by Annick Desjardins.

COMPLETED
Registry status
Phase 2
Development phase
43 participants
Enrollment target

Study Summary

The purpose of this study is to assess the activity of Sym004, a recombinant antibody mixture that specifically binds to EGFR, in patients diagnosed with recurrent glioblastoma whose tumor is EGFR amplified. This is a phase 2 study that will accrue patients with WHO grade IV recurrent malignant glioma (glioblastoma or gliosarcoma) in two cohorts to assess the efficacy of Sym004.

Primary Outcome

Within each cohort, the percentage of participants alive and progression-free at 6 months after the start of Sym004 treatment will be determined. PFS6 will be calculated from the date study treatment started until the date of progression or death, or the date of last follow-up if participants are alive without progression. Kaplan-Meier methods will be used to estimate survival.

Interventions

  • DRUG Sym004 - 18 mg/kg
  • DRUG Sym004 - 24 mg/kg

Trial Details

FieldValue
Enrollment Target 43 participants
Start Date 2016-02-01
Est. Completion 2020-04-27
Phase Phase 2
Annick Desjardins

9 total trials

What the finished NCT02540161 record still lists

NCT02540161 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 43 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (68% lower).

The record links to 0 conditions, and to 2 interventions - of which Sym004 - 18 mg/kg is the first listed.

NCT02540161 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02540161 about?

NCT02540161 is a clinical study titled "Phase 2 Study of Sym004 for Adult Patients With Recurrent Glioblastoma". The purpose of this study is to assess the activity of Sym004, a recombinant antibody mixture that specifically binds to EGFR, in patients diagnosed with recurrent glioblastoma whose tumor is EGFR amplified. This is a phase 2 study that will accrue patients with WHO grade IV recurrent malignant glio...

What is the current status of trial NCT02540161?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 43 participants. The study started on 2016-02-01. Estimated completion is 2020-04-27.

What interventions are being tested in trial NCT02540161?

The interventions under investigation include: Sym004 - 18 mg/kg (DRUG), Sym004 - 24 mg/kg (DRUG).

Who is sponsoring clinical trial NCT02540161?

This trial is sponsored by Annick Desjardins, which has 9 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02540161's enrollment target sits among peer trials

43 1332nd of 2000 higher than 662 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT02540161, the US trial registry maintained by the National Library of Medicine. NCT02540161 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.