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NCT05743036 · ClinicalTrials.gov registry record · Phase 1

ZN-c3 in Adult Participants With Metastatic Colorectal Cancer

A Phase 1 study, sponsored by K-Group, Beta, Inc., a wholly owned subsidiary of Zentalis Pharmaceuticals.

Terminated
Registry status
Phase 1
Development phase
44
Enrollment target

NCT05743036: Clinical Trial Phase 1 study, sponsored by K-Group, Beta, Inc., a wholly owned subsidiary of Zentalis Pharmaceuticals.

NCT05743036 is a Phase 1 study that was terminated before completion, run by K-Group, Beta, Inc., a wholly owned subsidiary of Zentalis Pharmaceuticals. The registered enrollment target is 44 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (27% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05743036, a Phase 1 study, was terminated before completion, sponsored by K-Group, Beta, Inc., a wholly owned subsidiary of Zentalis Pharmaceuticals.

TERMINATED
Registry status
Phase 1
Development phase
44 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the safety, tolerability, and potential clinical benefits of ZN-c3 administered in combination with encorafenib and cetuximab in adult participants with metastatic BRAF V600E mutant colorectal cancer previously treated with one or two treatment regimens.

Primary Outcome

DLTs defined as treatment-related AEs occurring within the first 29 days after the start of any study treatment that in the opinion of the investigator cannot be reasonably attributed to the participant's underlying disease, concomitant medications, or pre-existing conditions.

Interventions

  • DRUG Cetuximab
  • DRUG Encorafenib
  • DRUG ZN-c3

Trial Details

FieldValue
Enrollment Target 44 participants
Start Date 2023-02-27
Est. Completion 2025-07-09
Phase Phase 1

Why NCT05743036 stopped before completion

NCT05743036 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 44 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (27% lower).

The record links to 0 conditions, and to 3 interventions - of which Cetuximab is the first listed.

NCT05743036 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05743036 about?

NCT05743036 is a clinical study titled "ZN-c3 in Adult Participants With Metastatic Colorectal Cancer". The purpose of this study is to evaluate the safety, tolerability, and potential clinical benefits of ZN-c3 administered in combination with encorafenib and cetuximab in adult participants with metastatic BRAF V600E mutant colorectal cancer previously treated with one or two treatment regimens.

What is the current status of trial NCT05743036?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 44 participants. The study started on 2023-02-27. Estimated completion is 2025-07-09.

What interventions are being tested in trial NCT05743036?

The interventions under investigation include: Cetuximab (DRUG), Encorafenib (DRUG), ZN-c3 (DRUG).

Who is sponsoring clinical trial NCT05743036?

This trial is sponsored by K-Group, Beta, Inc., a wholly owned subsidiary of Zentalis Pharmaceuticals, which has 8 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05743036's enrollment target sits among peer trials

44 1086th of 2000 higher than 901 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 NCT05743036, the US trial registry maintained by the National Library of Medicine. NCT05743036 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.