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COMPLETED Phase 1

Dose Escalation Study of mRNA-2752 for Intratumoral Injection to Participants in Advanced Malignancies

NCT03739931 · View on ClinicalTrials.gov ↗

Study Summary

The clinical study will assess the safety and tolerability of escalating intratumoral doses of mRNA-2752 in participants with relapsed/refractory solid tumor malignancies or lymphoma.

Interventions

  • BIOLOGICAL Durvalumab
  • BIOLOGICAL mRNA-2752

Study Locations (20)

Massachusetts

  • Massachusetts General Hospital — Boston
  • Cancer Center at Beth Israel Deaconess Medical Center — Boston
  • Dana-Farber Cancer Institute — Boston

New York

  • NYU Langone Medical Center — New York
  • Icahn School of Medicine at Mount Sinai — New York
  • James P. Wilmot Cancer Center — Rochester

Other

  • Alfred Health — Melbourne
  • Westmead Hospital — Westmead
  • Melanoma Institute of Australia — Wollstonecraft

California

  • UCSF Helen Diller Family Comprehensive Cancer Center — San Francisco
  • Providence St. John's Health Center — Santa Monica

Colorado

  • University of Colorado Denver — Aurora

Connecticut

  • Yale Cancer Center — New Haven

Florida

  • Sarah Cannon Research Institute at Florida Cancer Specialists — Sarasota

Illinois

  • The University of Chicago Medicine — Chicago

Trial Details

FieldValue
Enrollment Target 134 participants
Start Date 2018-11-27
Est. Completion 2025-08-01
Phase Phase 1

Sponsor

ModernaTX

67 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03739931

The ClinicalTrials.gov registry entry for NCT03739931 describes a study currently listed as completed. 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 134 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is ModernaTX, which has 67 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Dose Escalation: Relapsed/Refractory Solid Tumor Malignancies or Lymphoma appearing as the primary indexed condition, and to 2 interventions — of which Durvalumab 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: NCT03739931 reports 20 study locations spanning 13 distinct geographic areas — top geographies include Massachusetts, New York, Other. 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 NCT03739931 about?

NCT03739931 is a clinical study titled "Dose Escalation Study of mRNA-2752 for Intratumoral Injection to Participants in Advanced Malignancies". The clinical study will assess the safety and tolerability of escalating intratumoral doses of mRNA-2752 in participants with relapsed/refractory solid tumor malignancies or lymphoma.

What is the current status of trial NCT03739931?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 134 participants. The study started on 2018-11-27. Estimated completion is 2025-08-01.

What conditions does trial NCT03739931 study?

This clinical trial studies the following conditions: Dose Escalation: Relapsed/Refractory Solid Tumor Malignancies or Lymphoma, Dose Expansion: Triple Negative Breast Cancer, HNSCC, Non-Hodgkins, Urothelial Cancer, Immune Checkpoint Refractory Melanoma, and NSCLC Lymphoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03739931?

The interventions under investigation include: Durvalumab (BIOLOGICAL), mRNA-2752 (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03739931?

This trial is sponsored by ModernaTX, which has 67 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03739931 being conducted?

This trial has 20 study locations across California, Colorado, Connecticut, Florida, Illinois. 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