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NCT06150664 · ClinicalTrials.gov registry record · Phase 1

A Phase 1 of CTX-8371 in Patients With Advanced Malignancies

A Phase 1 study of Non-Small Cell Lung Cancer and Head and Neck Squamous Cell Carcinoma, sponsored by Compass Therapeutics.

Recruiting
Registry status
Phase 1
Development phase
73
Enrollment target
7
Study locations

NCT06150664 is a Phase 1 study of Non-Small Cell Lung Cancer and Head and Neck Squamous Cell Carcinoma that is actively recruiting participants, run by Compass Therapeutics. The registered enrollment target is 73 participants, below the 659-participant average among 449 other Non-Small Cell Lung Cancer trials with a reported enrollment target (89% lower). The trial reports 7 study locations across 4 states.

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The verdict

NCT06150664, a Phase 1 study of Non-Small Cell Lung Cancer and Head and Neck Squamous Cell Carcinoma, is actively recruiting participants, sponsored by Compass Therapeutics.

RECRUITING
Registry status
Phase 1
Development phase
73 participants
Enrollment target
7
Study locations

Study Summary

This is a Phase 1, open-label, first-in-human study of CTX-8371 administered as a monotherapy in patients with metastatic or locally advanced malignancies. The study will be conducted in 2 cohorts: Dose Escalation and Dose Expansion.

Interventions

  • DRUG CTX-8371

Study Locations (7)

Florida

  • D&H Cancer Research Center - Margate
  • Florida Cancer Specialists - Lake Nona - Orlando
  • Florida Cancer Specialists - Sarasota - Sarasota

Massachusetts

  • Beth Israel Deaconess Medical Center - Boston
  • Dana-Farber Cancer Institute - Boston

New York

  • Roswell Park Cancer Institute - Buffalo

Tennessee

  • Tennessee Oncology - Nashville

Trial Details

FieldValue
Enrollment Target 73 participants
Start Date 2024-03-19
Est. Completion 2027-05
Phase Phase 1

Sponsor

Compass Therapeutics

5 total trials

What the Registry Record Tells You About NCT06150664

The ClinicalTrials.gov registry entry for NCT06150664 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 73 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 659-participant average among 449 other Non-Small Cell Lung Cancer trials with a reported enrollment target (89% lower). The listed sponsor is Compass Therapeutics, which has 5 total studies on file at ClinicalTrials.gov.

The record links to 5 conditions, with Non-Small Cell Lung Cancer appearing as the primary indexed condition, and to 1 intervention - of which CTX-8371 is the first listed.

NCT06150664 reports 7 study locations spanning 4 distinct geographic areas - top geographies include Florida, Massachusetts, New York.

Frequently Asked Questions

What is clinical trial NCT06150664 about?

NCT06150664 is a clinical study titled "A Phase 1 of CTX-8371 in Patients With Advanced Malignancies". This is a Phase 1, open-label, first-in-human study of CTX-8371 administered as a monotherapy in patients with metastatic or locally advanced malignancies. The study will be conducted in 2 cohorts: Dose Escalation and Dose Expansion.

What is the current status of trial NCT06150664?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 73 participants. The study started on 2024-03-19. Estimated completion is 2027-05.

What conditions does trial NCT06150664 study?

This clinical trial studies the following conditions: Non-Small Cell Lung Cancer, Head and Neck Squamous Cell Carcinoma, Triple Negative Breast Cancer, Hodgkin Lymphoma, Malignant Melanoma.

What interventions are being tested in trial NCT06150664?

The interventions under investigation include: CTX-8371 (DRUG).

Who is sponsoring clinical trial NCT06150664?

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

Where is trial NCT06150664 being conducted?

This trial has 7 study locations across Florida, Massachusetts, New York, Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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