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Study to Evaluate Adverse Events, Change in Disease Activity, and How ABBV-706 Moves Through the Body When Intravenously (IV) Infused Alone or in Combination With IV Infused Budigalimab, Cisplatin, or Carboplatin in Adult Participants With Advanced Solid Tumors

Active, not recruiting · Phase 1 · NCT05599984

Conditions: Advanced Solid Tumors

At a glance

Research payments reported, 2025
$4.7M
U.S. investigators named
27
Sites paid
27
Planned or actual enrollment
288

About the trial

Sponsor
AbbVie
Tested
ABBV-706 (drug), Cisplatin (drug), Budigalimab (drug), Carboplatin (drug)
Dates
Started 2022-12-05; completion 2027-11
Results posted
Not yet

Cancer is a condition where cells in a specific part of body grow and reproduce uncontrollably. The purpose of this study is to assess safety, tolerability, pharmacokinetics and preliminary efficacy of ABBV-706 as a monotherapy and in combination with budigalimab, carboplatin, or cisplatin. ABBV-706 is an investigational drug being developed for the treatment of small cell lung cancer (SCLC), high-grade central nervous system (CNS) tumors and high-grade neuroendocrine carcinomas (NECs). There are multiple treatment arms in this study. Participants will either receive ABBV-706 as a single agent or in combination with budigalimab (another investigational drug), carboplatin or cisplatin at d…

From ClinicalTrials.gov, last updated 2026-05-07. Full record, eligibility and contacts (opens in a new tab)

Industry funding

AbbVie Inc. reported $4.7M in research payments for this study in 2025 (2,170 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.