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NCT03692429 · ClinicalTrials.gov registry record · Phase 1

alloSHRINK - Standard cHemotherapy Regimen and Immunotherapy With Allogeneic NKG2D-based CYAD-101 Chimeric Antigen Receptor T-cells

A Phase 1 study of Unresectable Metastatic Colorectal Cancer, sponsored by Celyad Oncology.

Recruiting
Registry status
Phase 1
Development phase
49
Enrollment target
4
Study locations

NCT03692429: Recruiting Phase 1 study of Unresectable Metastatic Colorectal Cancer, sponsored by Celyad Oncology.

NCT03692429 is a Phase 1 study of Unresectable Metastatic Colorectal Cancer that is actively recruiting participants, run by Celyad Oncology. The registered enrollment target is 49 participants, below the 135-participant average among 3 other Unresectable Metastatic Colorectal Cancer trials with a reported enrollment target (64% lower). The trial reports 4 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03692429, a Phase 1 study of Unresectable Metastatic Colorectal Cancer, is actively recruiting participants, sponsored by Celyad Oncology.

RECRUITING
Registry status
Phase 1
Development phase
49 participants
Enrollment target
4
Study locations

Study Summary

The purpose of the alloSHRINK study is to assess the safety, cell kinetics and clinical activity of CYAD-101 in patients with unresectable metastatic colorectal cancer administered after standard chemotherapy

Interventions

  • DRUG FOLFIRI
  • DRUG CYAD-101
  • DRUG FOLFOX

Study Locations (4)

Other

  • Institut Jules Bordet - Brussels
  • UZ Antwerpen - Edegem
  • UZ Leuven - Leuven

Florida

  • Moffit Cancer Center - Tampa

Trial Details

FieldValue
Enrollment Target 49 participants
Start Date 2018-11-28
Est. Completion 2036-02-17
Phase Phase 1
Celyad Oncology

6 total trials

What NCT03692429 shows while recruiting

NCT03692429 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 49 participants, a relatively small participant target, below the 135-participant average among 3 other Unresectable Metastatic Colorectal Cancer trials with a reported enrollment target (64% lower).

The record links to 1 condition, with Unresectable Metastatic Colorectal Cancer appearing as the primary indexed condition, and to 3 interventions - of which FOLFIRI is the first listed.

NCT03692429 reports a single indexed study location in Other, Florida.

Frequently Asked Questions

What is clinical trial NCT03692429 about?

NCT03692429 is a clinical study titled "alloSHRINK - Standard cHemotherapy Regimen and Immunotherapy With Allogeneic NKG2D-based CYAD-101 Chimeric Antigen Receptor T-cells". The purpose of the alloSHRINK study is to assess the safety, cell kinetics and clinical activity of CYAD-101 in patients with unresectable metastatic colorectal cancer administered after standard chemotherapy

What is the current status of trial NCT03692429?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 49 participants. The study started on 2018-11-28. Estimated completion is 2036-02-17.

What conditions does trial NCT03692429 study?

This clinical trial studies the following conditions: Unresectable Metastatic Colorectal Cancer.

What interventions are being tested in trial NCT03692429?

The interventions under investigation include: FOLFIRI (DRUG), CYAD-101 (DRUG), FOLFOX (DRUG).

Who is sponsoring clinical trial NCT03692429?

This trial is sponsored by Celyad Oncology, which has 6 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03692429 being conducted?

This trial has 4 study locations across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

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Source: ClinicalTrials.gov NCT03692429, the US trial registry maintained by the National Library of Medicine. NCT03692429 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.