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NCT06500819 · ClinicalTrials.gov registry record · Phase 1

Autologous B7-H3 Chimeric Antigen Receptor T Cells in Relapsed/Refractory Solid Tumors

A Phase 1 study of Sarcoma and Neuroblastoma, sponsored by Crystal Mackall, MD.

Recruiting
Registry status
Phase 1
Development phase
41
Enrollment target
1
Study location

NCT06500819 is a Phase 1 study of Sarcoma and Neuroblastoma that is actively recruiting participants, run by Crystal Mackall, MD. The registered enrollment target is 41 participants, below the 921-participant average among 122 other Sarcoma trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06500819, a Phase 1 study of Sarcoma and Neuroblastoma, is actively recruiting participants, sponsored by Crystal Mackall, MD.

RECRUITING
Registry status
Phase 1
Development phase
41 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to test the manufacturing feasibility and safety of intravenous (IV) administration of B7-H3CART in children and young adult subjects with relapsed and/or refractory solid tumors expressing B7-H3 target using a standard 3+3 dose escalation design.

Interventions

  • DRUG B7-H3CART Dose (Intravenous)

Study Locations (1)

California

  • Stanford University - Palo Alto

Trial Details

FieldValue
Enrollment Target 41 participants
Start Date 2024-07-11
Est. Completion 2029-07
Phase Phase 1

Sponsor

Crystal Mackall, MD

1 total trials

What the Registry Record Tells You About NCT06500819

The ClinicalTrials.gov registry entry for NCT06500819 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 41 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 921-participant average among 122 other Sarcoma trials with a reported enrollment target (96% lower). The listed sponsor is Crystal Mackall, MD, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Sarcoma appearing as the primary indexed condition, and to 1 intervention - of which B7-H3CART Dose (Intravenous) is the first listed.

NCT06500819 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT06500819 about?

NCT06500819 is a clinical study titled "Autologous B7-H3 Chimeric Antigen Receptor T Cells in Relapsed/Refractory Solid Tumors". The purpose of this study is to test the manufacturing feasibility and safety of intravenous (IV) administration of B7-H3CART in children and young adult subjects with relapsed and/or refractory solid tumors expressing B7-H3 target using a standard 3+3 dose escalation design.

What is the current status of trial NCT06500819?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 41 participants. The study started on 2024-07-11. Estimated completion is 2029-07.

What conditions does trial NCT06500819 study?

This clinical trial studies the following conditions: Sarcoma, Neuroblastoma, Osteosarcoma.

What interventions are being tested in trial NCT06500819?

The interventions under investigation include: B7-H3CART Dose (Intravenous) (DRUG).

Who is sponsoring clinical trial NCT06500819?

This trial is sponsored by Crystal Mackall, MD, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06500819 being conducted?

This trial has 1 study location across California. 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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