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NCT07140315 · ClinicalTrials.gov registry record · Phase 1

DK222 Study at Hopkins

A Phase 1 study, sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins.

Recruiting
Registry status
Phase 1
Development phase
6
Enrollment target

NCT07140315: Recruiting Phase 1 study, sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins.

NCT07140315 is a Phase 1 study that is actively recruiting participants, run by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins. The registered enrollment target is 6 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07140315, a Phase 1 study, is actively recruiting participants, sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins.

RECRUITING
Registry status
Phase 1
Development phase
6 participants
Enrollment target

Study Summary

This Phase 1 clinical trial will test a new drug called \[18F\]DK222 in people with cancer. The goal is to see if the drug is safe, how it spreads through the body, how long it stays in the body, and how much radiation it gives off. \[18F\]DK222 is designed to attach strongly and specifically to a protein called PD-L1, which helps cancer hide from the immune system. This is a first in human study to collect preliminary safety and toxicity data of \[18F\]DK222.

Primary Outcome

Any grade 3-5 toxicity attributed to \[¹⁸F\]DK222 administration will be considered as not meeting the safety endpoint. All adverse events (AEs) will be graded according to the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.

Interventions

  • DRUG [18F]DK222 radiotracer

Trial Details

FieldValue
Enrollment Target 6 participants
Start Date 2026-07-01
Est. Completion 2027-07-01
Phase Phase 1

What NCT07140315 shows while recruiting

NCT07140315 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 6 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (90% lower).

The record links to 0 conditions, and to 1 intervention - of which [18F]DK222 radiotracer is the first listed.

NCT07140315 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07140315 about?

NCT07140315 is a clinical study titled "DK222 Study at Hopkins". This Phase 1 clinical trial will test a new drug called \[18F\]DK222 in people with cancer. The goal is to see if the drug is safe, how it spreads through the body, how long it stays in the body, and how much radiation it gives off. \[18F\]DK222 is designed to attach strongly and specifically to a p...

What is the current status of trial NCT07140315?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 6 participants. The study started on 2026-07-01. Estimated completion is 2027-07-01.

What interventions are being tested in trial NCT07140315?

The interventions under investigation include: [18F]DK222 radiotracer (DRUG).

Who is sponsoring clinical trial NCT07140315?

This trial is sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, which has 523 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07140315's enrollment target sits among peer trials

6 1974th of 2000 higher than 12 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 NCT07140315, the US trial registry maintained by the National Library of Medicine. NCT07140315 (small enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.