Skip to main content

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

Completed · Phase 1 · NCT03739931

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

At a glance

Research payments reported, 2025
$358,801
U.S. investigators named
7
Sites paid
6
Planned or actual enrollment
134

About the trial

Sponsor
ModernaTX, Inc. (with AstraZeneca)
Tested
mRNA-2752 (biological), Durvalumab (biological)
Dates
Started 2018-11-27; completion 2025-08-01
Results posted
Not yet

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.

From ClinicalTrials.gov, last updated 2025-08-15. Full record, eligibility and contacts (opens in a new tab)

Industry funding

ModernaTX, Inc. reported $358,801 in research payments for this study in 2025 (27 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.