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

NCT01351935 · ClinicalTrials.gov registry record · Phase 1

Escalating Dose Study in Subjects With Relapsed or Refractory B Cell Non-Hodgkin Lymphoma, Chronic Lymphocytic Leukemia, and Waldenstrom's Macroglobulinemia

A Phase 1 study, sponsored by Celgene.

Completed
Registry status
Phase 1
Development phase
113
Enrollment target

NCT01351935 is a Phase 1 study that has completed, run by Celgene. The registered enrollment target is 113 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01351935, a Phase 1 study, has completed, sponsored by Celgene.

COMPLETED
Registry status
Phase 1
Development phase
113 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the safety and tolerability of AVL-292 as monotherapy in subjects with relapsed or refractory B cell non-Hodgkin lymphoma (B-NHL), chronic lymphocytic leukemia (CLL) or Waldenstrom's macroglobulinemia (WM).

Interventions

  • DRUG AVL-292

Trial Details

FieldValue
Enrollment Target 113 participants
Start Date 2011-07-18
Est. Completion 2015-06-26
Phase Phase 1

Sponsor

Celgene

308 total trials

What the Registry Record Tells You About NCT01351935

The ClinicalTrials.gov registry entry for NCT01351935 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 113 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Celgene, which has 308 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which AVL-292 is the first listed.

NCT01351935 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01351935 about?

NCT01351935 is a clinical study titled "Escalating Dose Study in Subjects With Relapsed or Refractory B Cell Non-Hodgkin Lymphoma, Chronic Lymphocytic Leukemia, and Waldenstrom's Macroglobulinemia". The purpose of this study is to evaluate the safety and tolerability of AVL-292 as monotherapy in subjects with relapsed or refractory B cell non-Hodgkin lymphoma (B-NHL), chronic lymphocytic leukemia (CLL) or Waldenstrom's macroglobulinemia (WM).

What is the current status of trial NCT01351935?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 113 participants. The study started on 2011-07-18. Estimated completion is 2015-06-26.

What interventions are being tested in trial NCT01351935?

The interventions under investigation include: AVL-292 (DRUG).

Who is sponsoring clinical trial NCT01351935?

This trial is sponsored by Celgene, which has 308 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.