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NCT06859762 · ClinicalTrials.gov registry record · Phase 1

A First-in-Human Study of YL217 in Patients With Advanced Solid Tumors

A Phase 1 study of Advanced Solid Tumor, sponsored by MediLink Therapeutics (Suzhou) Co..

Recruiting
Registry status
Phase 1
Development phase
220
Enrollment target
19
Study locations

NCT06859762 is a Phase 1 study of Advanced Solid Tumor that is actively recruiting participants, run by MediLink Therapeutics (Suzhou) Co.. The registered enrollment target is 220 participants, above the 192-participant average among 189 other Advanced Solid Tumor trials with a reported enrollment target (15% higher). The trial reports 19 study locations across 17 states.

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The verdict

NCT06859762, a Phase 1 study of Advanced Solid Tumor, is actively recruiting participants, sponsored by MediLink Therapeutics (Suzhou) Co..

RECRUITING
Registry status
Phase 1
Development phase
220 participants
Enrollment target
19
Study locations

Study Summary

A Phase 1 First-in-Human study of YL217 in Patients with Advanced Solid Tumors

Conditions Studied

Interventions

  • DRUG YL217

Study Locations (19)

Ohio

  • University of Cincinnati Medical Center - Cincinnati
  • Cleveland Clinic Taussig Cancer Institute - Cleveland

Texas

  • The University of Texas MD Anderson Cancer Center - Houston
  • UT Health San Antonio - Mays Cancer Center - San Antonio

Arizona

  • Mayo Clinic Arizona - Phoenix

California

  • UCLA Hematology/Oncology - Santa Monica - Santa Monica

Connecticut

  • Yale Cancer Center - New Haven

Kansas

  • The University of Kansas Cancer Center (KUCC) - Kansas City

Maryland

  • University of Maryland Medical Center-Greenebaum Cancer Ctr - Medical Oncology - Baltimore

Michigan

  • Karmanos Cancer Institute - Detroit

Trial Details

FieldValue
Enrollment Target 220 participants
Start Date 2025-07-02
Est. Completion 2027-07
Phase Phase 1

What the Registry Record Tells You About NCT06859762

The ClinicalTrials.gov registry entry for NCT06859762 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 220 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 192-participant average among 189 other Advanced Solid Tumor trials with a reported enrollment target (15% higher). The listed sponsor is MediLink Therapeutics (Suzhou) Co., which has 7 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Advanced Solid Tumor appearing as the primary indexed condition, and to 1 intervention - of which YL217 is the first listed.

NCT06859762 reports 19 study locations spanning 17 distinct geographic areas - top geographies include Ohio, Texas, Arizona.

Frequently Asked Questions

What is clinical trial NCT06859762 about?

NCT06859762 is a clinical study titled "A First-in-Human Study of YL217 in Patients With Advanced Solid Tumors". A Phase 1 First-in-Human study of YL217 in Patients with Advanced Solid Tumors

What is the current status of trial NCT06859762?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 220 participants. The study started on 2025-07-02. Estimated completion is 2027-07.

What conditions does trial NCT06859762 study?

This clinical trial studies the following conditions: Advanced Solid Tumor.

What interventions are being tested in trial NCT06859762?

The interventions under investigation include: YL217 (DRUG).

Who is sponsoring clinical trial NCT06859762?

This trial is sponsored by MediLink Therapeutics (Suzhou) Co., which has 7 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06859762 being conducted?

This trial has 19 study locations across Arizona, California, Connecticut, Kansas, Maryland. 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

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.