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A First-in-human, Dose Escalation and Dose Expansion Study of SAR445877 in Adult Participants With Advanced Solid Tumors

Recruiting · Phase 1, Phase 2 · NCT05584670

Conditions: Solid Tumor

At a glance

Research payments reported, 2025
$4.1M
U.S. investigators named
7
Sites paid
8
Planned or actual enrollment
542

About the trial

Sponsor
Sanofi
Tested
SAR445877 (drug), Cetuximab (drug), ADG126 (drug), Bevacizumab (drug), Nivolumab (drug), Ipilimumab (drug)
Dates
Started 2022-11-29; completion 2028-06-28
Results posted
Not yet

This is a Phase 1/2, open label, multiple cohort study to assess the safety and preliminary efficacy of SAR445877 as a monotherapy or in combination with other anticancer therapies for participants aged at least 18 years with advanced unresectable or metastatic solid tumors. The study will include 2 parts: A dose escalation Part 1: for finding the therapeutic dose(s) of SAR445877 in a monotherapy given every 2 weeks (Q2W) or weekly (QW) and in combination with other anticancer therapies when applicable. A multicohort dose expansion/dose optimization Part 2: for the assessment of safety and preliminary efficacy of SAR445877 in monotherapy and in combination with cetuximab or with next gene…

From ClinicalTrials.gov, last updated 2026-06-23. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Sanofi US Services Inc. reported $4.1M in research payments for this study in 2025 (122 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.