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Phase 2 N=63 Treatment

Ibrutinib (PCI-32765) in Waldenstrom's Macroglobulinemia

Waldenstrom's Macroglobulinemia

Enrolled (actual)
63
Serious AEs
47.6%
Results posted
Jan 2020
Primary outcome: Primary: Overall Response Rate — 57 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
PCI-32765 (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Dana-Farber Cancer Institute
Primary completion
Sep 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Overall Response Rate
57
SECONDARY
Safety and Tolerability of PCI-32765
62
SECONDARY
Determine Progression Free Survival
39
SECONDARY
To Determine Time to Next Therapy (TTNT) of PCI-32765 in Symptomatic WM Patients With Relapsed/Refractory Disease
49
SECONDARY
Major Response Rates
49
SECONDARY
Very Good Partial Response Rate
17

Summary

This research study is a Phase II clinical trial. Phase II clinical trials test the effectiveness of an investigational drug, PCI-32765, to learn whether PCI-32765 works in treating a specific cancer. "Investigational" means that PCI-32765 is still being studied and that research doctors are trying to find out more about it-such as the safest dose to use, the side effects it may cause, and if PCI-32765 is effective for treating different types of cancer. It also means that the FDA has not yet approved PCI-32765 for use in patients, including people with Waldenstrom's Macroglobulinemia. PCI-32765 is a newly discovered drug that is being developed as an anti-cancer agent. PCI-32765 is a Bruton's tyrosine kinase (Btk) inhibitor drug which interrupts B cell receptor (BCR) signaling in lymphomas by selectively and irreversibly binding to the Btk protein, which then results in malignant cell death. This drug has been used in laboratory experiments and other research studies in B-cell malignancies and information from those other research studies suggests that PCI-32765 may be a treatment strategy for B-cell malignancies, including Waldenstrom's Macroglobulinemia. In this research study, the investigators are testing the safety and efficacy of PCI-32765 as a treatment option for relapsed or refractory Waldenstrom's Macroglobulinemia.

Eligibility Criteria

Inclusion Criteria

  • Clinicopathological diagnosis of Waldenstrom's Macroglobulinemia
  • Measurable disease
  • Have received at least one prior therapy for WM therapies
  • Disease free of prior malignancies
  • Able to adhere to study visit schedule and other protocol requirement

Exclusion Criteria

  • Pregnant or breastfeeding
  • Any other serious medical condition
  • Concurrent use of other anti-cancer agents or treatments
  • Prior exposure to PCI-32765
  • Known CNS lymphoma
  • Significant cardiovascular disease
  • Any disease affecting gastrointestinal function
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01614821). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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