Dose Escalation and Dose Expansion Study of MDX2004 in Participants With Advanced Tumors

NCT07110584 · Status: RECRUITING · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 235

Last updated 2026-03-05

No results posted yet for this study

Summary

This study is designed to characterize the safety, tolerability, and anti-tumor activity of MDX2004 in patients with advanced tumors.

Conditions

  • Advanced Tumors

Interventions

DRUG

MDX2004

MDX2004 intravenous infusion

Sponsors & Collaborators

  • ModeX Therapeutics, An OPKO Health Company

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SEQUENTIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-10-01
Primary Completion
2031-06-30
Completion
2031-06-30

Countries

  • Australia
  • Israel

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07110584 on ClinicalTrials.gov