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NCT05228015 · ClinicalTrials.gov registry record · Phase 1

Oral TEAD Inhibitor Targeting the Hippo Pathway in Subjects with Advanced Solid Tumors

A Phase 1 study, sponsored by Ikena Oncology.

Terminated
Registry status
Phase 1
Development phase
67
Enrollment target

NCT05228015 is a Phase 1 study that was terminated before completion, run by Ikena Oncology. The registered enrollment target is 67 participants.

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The verdict

NCT05228015, a Phase 1 study, was terminated before completion, sponsored by Ikena Oncology.

TERMINATED
Registry status
Phase 1
Development phase
67 participants
Enrollment target

Study Summary

This is a Phase 1, first-in-human (FIH) clinical study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary antitumor activity of IK-930, an oral TEAD inhibitor, administered orally (PO) as monotherapy in subjects with advanced solid tumors with or without gene alterations in the Hippo pathway for whom there are no further treatment options known to confer clinical benefit. The study consists of two phases, an initial Dose Escalation phase followed by a Dose Expansion phase.

Interventions

  • DRUG Osimertinib
  • DRUG IK-930

Trial Details

FieldValue
Enrollment Target 67 participants
Start Date 2022-01-07
Est. Completion 2024-09-09
Phase Phase 1

Sponsor

Ikena Oncology

5 total trials

What the Registry Record Tells You About NCT05228015

The ClinicalTrials.gov registry entry for NCT05228015 describes a study currently listed as terminated, categorized as Phase 1. The registered enrollment target is 67 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ikena Oncology, which has 5 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Osimertinib is the first listed.

NCT05228015 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05228015 about?

NCT05228015 is a clinical study titled "Oral TEAD Inhibitor Targeting the Hippo Pathway in Subjects with Advanced Solid Tumors". This is a Phase 1, first-in-human (FIH) clinical study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary antitumor activity of IK-930, an oral TEAD inhibitor, administered orally (PO) as monotherapy in subjects with advanced solid tumors with or with...

What is the current status of trial NCT05228015?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 67 participants. The study started on 2022-01-07. Estimated completion is 2024-09-09.

What interventions are being tested in trial NCT05228015?

The interventions under investigation include: Osimertinib (DRUG), IK-930 (DRUG).

Who is sponsoring clinical trial NCT05228015?

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

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.