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A Study With ABBV-155 Alone and in Combination With Taxane Therapy in Adults With Relapsed and/or Refractory Solid Tumors

Completed · Phase 1 · NCT03595059

Conditions: Advanced Solid Tumors

At a glance

Research payments reported, 2025
$124,060
U.S. investigators named
7
Sites paid
7
Planned or actual enrollment
168

About the trial

Sponsor
AbbVie
Tested
ABBV-155 (drug), Paclitaxel (drug), Docetaxel (drug)
Dates
Started 2018-07-13; completion 2025-09-12
Results posted
Not yet

An open-label, dose-escalation (Part 1), dose-expansion (Part 2) study to assess the safety, pharmacokinetics (PK), and preliminary efficacy of ABBV-155 alone and in combination with paclitaxel or docetaxel. In Part 1 (dose escalation), participants will receive escalating doses of ABBV-155 monotherapy (Part 1a) or ABBV-155 in combination with paclitaxel or docetaxel (Part 1b). In Part 2 (dose expansion), participants will receive ABBV-155 monotherapy or in combination therapy. The ABBV-155 monotherapy cohort will enroll participants with relapsed or refractory (R/R) small cell lung cancer (SCLC) (Part 2a); the ABBV-155 plus a taxane (paclitaxel or docetaxel) combination cohort will enrol…

From ClinicalTrials.gov, last updated 2025-12-10. Full record, eligibility and contacts (opens in a new tab)

Industry funding

AbbVie Inc. reported $124,060 in research payments for this study in 2025 (28 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.