Skip to main content

Extended Treatment Protocol for Subjects Continuing to Benefit From Ibrutinib.

Active, not recruiting · Phase 4 · NCT03229200

Conditions: Lymphoma, B-Cell, Lymphoma, Non-Hodgkin, Leukemia, B-cell, Graft Vs Host Disease, Solid Tumor

At a glance

Research payments reported, 2025
$143,968
U.S. investigators named
22
Sites paid
22
Planned or actual enrollment
297

About the trial

Sponsor
Pharmacyclics Switzerland GmbH (with Janssen Biotech, Inc., including Johnson & Johnson)
Tested
Ibrutinib (drug)
Dates
Started 2017-05-22; completion 2027-05-10
Results posted
Not yet

Multicenter, open-label, prospective treatment protocol that provides continued access to ibrutinib to subjects who have completed parent ibrutinib studies, are still benefitting from treatment with ibrutinib, and have no access to commercial ibrutinib for their underlying disease within their region.

From ClinicalTrials.gov, last updated 2025-10-30. Full record, eligibility and contacts (opens in a new tab)

Industry funding

AbbVie Inc. reported $143,968 in research payments for this study in 2025 (156 payments).

Products named: Imbruvica

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.