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A Dose Escalation Study of AV-380 in Cancer Patients With Cachexia

Completed · Phase 1 · NCT05865535

Conditions: Cachexia

At a glance

Research payments reported, 2025
$737,176
U.S. investigators named
12
Sites paid
14
Planned or actual enrollment
24

About the trial

Sponsor
AVEO Pharmaceuticals, Inc.
Tested
AV-380 (biological)
Dates
Started 2023-06-13; completion 2026-09-25
Results posted
Not yet

This open label ascending dose study is designed to evaluate the safety, pharmacokinetics (PK), pharmacodynamics (PD), and immunogenicity of AV-380 in cancer patients with Cachexia. AV-380 is an immunoglobulin (Ig) G1 monoclonal antibody (mAb) intended to bind circulating human growth differentiation factor 15 (GDF-15), a cytokine involved in cancer-induced cachexia.

From ClinicalTrials.gov, last updated 2026-11-09. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Aveo Pharmaceuticals, Inc. reported $737,176 in research payments for this study in 2025 (335 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.