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NCT03681561 · ClinicalTrials.gov registry record · Phase 1

Nivolumab With Ruxolitinib in Relapsed or Refractory Classical Hodgkin Lymphoma

A Phase 1 study of Hodgkin Lymphoma, sponsored by Veronika Bachanova.

Recruiting
Registry status
Phase 1
Development phase
54
Enrollment target
6
Study locations

NCT03681561 is a Phase 1 study of Hodgkin Lymphoma that is actively recruiting participants, run by Veronika Bachanova. The registered enrollment target is 54 participants, below the 165-participant average among 71 other Hodgkin Lymphoma trials with a reported enrollment target (67% lower). The trial reports 6 study locations across 6 states.

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The verdict

NCT03681561, a Phase 1 study of Hodgkin Lymphoma, is actively recruiting participants, sponsored by Veronika Bachanova.

RECRUITING
Registry status
Phase 1
Development phase
54 participants
Enrollment target
6
Study locations

Study Summary

This is a Phase I/II, multicenter, open-label, dose escalation/dose-expansion study to evaluate the tolerability, safety, and the maximum tolerated dose (MTD) of ruxolitinib when given with fixed dose nivolumab in patients with relapsed or refractory classical Hodgkin lymphoma (cHL).

Conditions Studied

Interventions

  • DRUG Nivolumab
  • DRUG Ruxolitinib

Study Locations (6)

Illinois

  • University of Illinois Cancer Center - Chicago

Indiana

  • Indiana Melvin and Bren Simon Comprehensive Cancer Center - Indianapolis

Iowa

  • University of Iowa Hospitals and Clinics - Iowa City

Minnesota

  • University of Minnesota - Minneapolis

Ohio

  • Ohio State University Comprehensive Cancer Center - Columbus

Wisconsin

  • University of Wisconsin - Madison

Trial Details

FieldValue
Enrollment Target 54 participants
Start Date 2018-09-13
Est. Completion 2027-07
Phase Phase 1

Sponsor

Veronika Bachanova

1 total trials

What the Registry Record Tells You About NCT03681561

The ClinicalTrials.gov registry entry for NCT03681561 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 54 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 165-participant average among 71 other Hodgkin Lymphoma trials with a reported enrollment target (67% lower). The listed sponsor is Veronika Bachanova, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Hodgkin Lymphoma appearing as the primary indexed condition, and to 2 interventions - of which Nivolumab is the first listed.

NCT03681561 reports 6 study locations spanning 6 distinct geographic areas - top geographies include Illinois, Indiana, Iowa.

Frequently Asked Questions

What is clinical trial NCT03681561 about?

NCT03681561 is a clinical study titled "Nivolumab With Ruxolitinib in Relapsed or Refractory Classical Hodgkin Lymphoma". This is a Phase I/II, multicenter, open-label, dose escalation/dose-expansion study to evaluate the tolerability, safety, and the maximum tolerated dose (MTD) of ruxolitinib when given with fixed dose nivolumab in patients with relapsed or refractory classical Hodgkin lymphoma (cHL).

What is the current status of trial NCT03681561?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 54 participants. The study started on 2018-09-13. Estimated completion is 2027-07.

What conditions does trial NCT03681561 study?

This clinical trial studies the following conditions: Hodgkin Lymphoma.

What interventions are being tested in trial NCT03681561?

The interventions under investigation include: Nivolumab (DRUG), Ruxolitinib (DRUG).

Who is sponsoring clinical trial NCT03681561?

This trial is sponsored by Veronika Bachanova, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03681561 being conducted?

This trial has 6 study locations across Illinois, Indiana, Iowa, Minnesota, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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