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RECRUITING Phase 1

A Study of ADRX-0405 in Subjects With Select Advanced Solid Tumors

NCT06710379 · View on ClinicalTrials.gov ↗

Study Summary

The primary purpose of this study is to assess the safety, tolerability, and pharmacokinetics, and to identify the optimal dose of ADRX-0405 in patients with select advanced solid tumors.

Conditions Studied

Interventions

  • DRUG ADRX-0405

Study Locations (8)

California

  • City of Hope — Duarte
  • UCLA — Santa Monica

Texas

  • NEXT Austin — Austin
  • The University of Texas MD Anderson Cancer Center — Houston

Michigan

  • START Midwest — Grand Rapids

Minnesota

  • University of Minnesota Masonic Cancer Center — Minneapolis

Utah

  • START Mountain Region — West Valley City

Virginia

  • NEXT Virginia — Fairfax

Trial Details

FieldValue
Enrollment Target 68 participants
Start Date 2024-12-30
Est. Completion 2026-12
Phase Phase 1

Sponsor

Adcentrx Therapeutics

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06710379

The ClinicalTrials.gov registry entry for NCT06710379 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 68 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Adcentrx Therapeutics, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Solid Tumors appearing as the primary indexed condition, and to 1 intervention — of which ADRX-0405 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06710379 reports 8 study locations spanning 6 distinct geographic areas — top geographies include California, Texas, Michigan. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06710379 about?

NCT06710379 is a clinical study titled "A Study of ADRX-0405 in Subjects With Select Advanced Solid Tumors". The primary purpose of this study is to assess the safety, tolerability, and pharmacokinetics, and to identify the optimal dose of ADRX-0405 in patients with select advanced solid tumors.

What is the current status of trial NCT06710379?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 68 participants. The study started on 2024-12-30. Estimated completion is 2026-12.

What conditions does trial NCT06710379 study?

This clinical trial studies the following conditions: Solid Tumors. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06710379?

The interventions under investigation include: ADRX-0405 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06710379?

This trial is sponsored by Adcentrx Therapeutics, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06710379 being conducted?

This trial has 8 study locations across California, Michigan, Minnesota, Texas, Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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