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Terminated Phase 3 Interventional Results available

A Safety and Efficacy Study of Ibrutinib in Pediatric and Young Adult Participants With Relapsed or Refractory Mature B-cell Non-Hodgkin Lymphoma

ClinicalTrials.gov ID: NCT02703272

Public ClinicalTrials.gov record NCT02703272. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 10:07 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Open-label, Safety and Efficacy Study of Ibrutinib in Pediatric and Young Adult Patients With Relapsed or Refractory Mature B-cell Non-Hodgkin Lymphoma

Study identification

NCT ID
NCT02703272
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Janssen Research & Development, LLC
Industry
Enrollment
72 participants

Conditions and interventions

Interventions

  • Ibrutinib Drug
  • Rituximab Drug
  • Ifosfamide Drug
  • Carboplatin Drug
  • Etoposide Drug
  • Vincristine Drug
  • Idarubicin Drug
  • Dexamethasone Drug

Drug

Eligibility (public fields only)

Age range
1 Year to 30 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 30, 2016
Primary completion
Jun 10, 2021
Completion
Jun 10, 2021
Last update posted
Dec 1, 2022

2016 – 2021

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
Not listed Los Angeles California
Not listed Orange California
Not listed Palo Alto California
Not listed Aurora Colorado
Not listed Washington D.C. District of Columbia
Not listed Atlanta Georgia
Not listed Baltimore Maryland
Not listed Boston Massachusetts
Not listed New York New York
Not listed Valhalla New York
Not listed Charlotte North Carolina
Not listed Cincinnati Ohio
Not listed Columbus Ohio
Not listed Philadelphia Pennsylvania
Not listed Dallas Texas
Not listed Salt Lake City Utah
Not listed Milwaukee Wisconsin

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 59 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02703272, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 1, 2022 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02703272 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →