Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02548962 · ClinicalTrials.gov registry record · Phase 1

Study of Ibrutinib in Combination With Pomalidomide and Dexamethasone in Subjects With Relapsed/Refractory Multiple Myeloma

A Phase 1 study, sponsored by Pharmacyclics.

Terminated
Registry status
Phase 1
Development phase
11
Enrollment target

NCT02548962: Clinical Trial Phase 1 study, sponsored by Pharmacyclics.

NCT02548962 is a Phase 1 study that was terminated before completion, run by Pharmacyclics. The registered enrollment target is 11 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (82% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02548962, a Phase 1 study, was terminated before completion, sponsored by Pharmacyclics.

TERMINATED
Registry status
Phase 1
Development phase
11 participants
Enrollment target

Study Summary

Phase 1 is an open-label, dose finding, multicenter study of ibrutinib in combination with pomalidomide and dexamethasone in subjects with relapsed/refractory multiple myeloma. Phase 2b is a randomized, double-blind, multicenter study of ibrutinib or placebo, in combination with pomalidomide and dexamethasone in subjects with relapsed/refractory multiple myeloma.

Primary Outcome

The overall response rate, defined as the proportion of subjects achieving a best overall response of PR or better per investigator assessment per IMWG at or prior to initiation of subsequent anticancer therapy

Interventions

  • DRUG Placebo
  • DRUG Dexamethasone
  • DRUG Pomalidomide
  • DRUG Ibrutinib

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2016-03
Est. Completion 2018-06-13
Phase Phase 1
Pharmacyclics

54 total trials

Why NCT02548962 stopped before completion

NCT02548962 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 11 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (82% lower).

The record links to 0 conditions, and to 4 interventions - of which Placebo is the first listed.

NCT02548962 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02548962 about?

NCT02548962 is a clinical study titled "Study of Ibrutinib in Combination With Pomalidomide and Dexamethasone in Subjects With Relapsed/Refractory Multiple Myeloma". Phase 1 is an open-label, dose finding, multicenter study of ibrutinib in combination with pomalidomide and dexamethasone in subjects with relapsed/refractory multiple myeloma. Phase 2b is a randomized, double-blind, multicenter study of ibrutinib or placebo, in combination with pomalidomide and de...

What is the current status of trial NCT02548962?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 11 participants. The study started on 2016-03. Estimated completion is 2018-06-13.

What interventions are being tested in trial NCT02548962?

The interventions under investigation include: Placebo (DRUG), Dexamethasone (DRUG), Pomalidomide (DRUG), Ibrutinib (DRUG).

Who is sponsoring clinical trial NCT02548962?

This trial is sponsored by Pharmacyclics, which has 54 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02548962's enrollment target sits among peer trials

11 1911th of 2000 higher than 88 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03114462 · 11 participants · Phase 1

    Trial of Stereotactic HYpofractionateD RadioAblative (HYDRA) Treatment of Laryngeal Cancer

  • NCT06039709 · 11 participants · Phase 1

    Sonodynamic Therapy in Patients With Recurrent GBM

  • NCT06425380 · 11 participants · NA

    Pilot Open-Label Trial of Resistant Potato Starch in Patients With Cirrhosis and Overt Hepatic Encephalopathy

  • NCT06472661 · 11 participants · Early Phase 1

    FUSA With Intratumoral PolyICLC in Regionally Advanced Resectable Melanoma

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02548962, the US trial registry maintained by the National Library of Medicine. NCT02548962 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.