ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

Ibrutinib (PCI-32765) in Waldenstrom's Macroglobulinemia

ClinicalTrials.gov ID: NCT01614821

Public ClinicalTrials.gov record NCT01614821. 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 May 16, 2026, 4:47 PM EDT

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

Official title

Phase 2 Study of Bruton's Tyrosine Kinase (Btk) Inhibitor, Ibrutinib (PCI-32765), in Waldenstrom's Macroglobulinemia

Study identification

NCT ID
NCT01614821
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Dana-Farber Cancer Institute
Other
Enrollment
63 participants

Conditions and interventions

Interventions

  • PCI-32765 Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Apr 30, 2012
Primary completion
Sep 8, 2016
Completion
Sep 14, 2018
Last update posted
Jan 20, 2020

2012 – 2018

United States locations

U.S. sites
4
U.S. states
3
U.S. cities
3
Facility City State ZIP Site status
Stanford University Palo Alto California 94305
Brigham and Women's Hospital Boston Massachusetts 02215
Dana-Farber Cancer Institute Boston Massachusetts 02215
Memorial Sloan-Kettering Cancer Center New York New York 10065

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01614821, 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 Jan 20, 2020 · Synced May 16, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01614821 live on ClinicalTrials.gov.

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