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NCT03850366 · ClinicalTrials.gov registry record · Phase 2

HLA-Haploidentical Peripheral Blood Stem Cell Transplantation With Post-transplant Cyclophosphamide and Bortezomib

A Phase 2 study of Hematological Malignancy, sponsored by Henry Ford Health System.

Recruiting
Registry status
Phase 2
Development phase
15
Enrollment target
1
Study location

NCT03850366 is a Phase 2 study of Hematological Malignancy that is actively recruiting participants, run by Henry Ford Health System. The registered enrollment target is 15 participants, below the 120-participant average among 9 other Hematological Malignancy trials with a reported enrollment target (87% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03850366, a Phase 2 study of Hematological Malignancy, is actively recruiting participants, sponsored by Henry Ford Health System.

RECRUITING
Registry status
Phase 2
Development phase
15 participants
Enrollment target
1
Study location

Study Summary

Now haplo stem cell transplant using bone marrow or peripheral blood is becoming more feasible with better regimens to prevent graft versus host disease (GVHD) like post transplant cyclophosphamide , tacrolimus, mycophenolate . Recently Bortezomib has also been shown to inhibit dendritic cells maturation and function and possesses a number of other favorable immunomodulatory effect that can prevent GVHD and help enhance immune reconstitution. this study is to assess the engraftment rate in patients with hematologic malignancies who need allogeneic stem cell transplant but do not have a suitable matched related or unrelated stem cell donor and will get T-cell replete HLA-Haploidentical allogeneic peripheral stem cell transplantation using post transplant Cyclophosphamide and bortezomib

Conditions Studied

Interventions

  • DRUG Bortezomib

Study Locations (1)

Michigan

  • Henry Ford hospital - Detroit

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2016-03-08
Est. Completion 2028-01-01
Phase Phase 2

Sponsor

Henry Ford Health System

234 total trials

What the Registry Record Tells You About NCT03850366

The ClinicalTrials.gov registry entry for NCT03850366 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 120-participant average among 9 other Hematological Malignancy trials with a reported enrollment target (87% lower). The listed sponsor is Henry Ford Health System, which has 234 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Hematological Malignancy appearing as the primary indexed condition, and to 1 intervention - of which Bortezomib is the first listed.

NCT03850366 reports 1 study location spanning 1 distinct geographic area - top geographies include Michigan.

Frequently Asked Questions

What is clinical trial NCT03850366 about?

NCT03850366 is a clinical study titled "HLA-Haploidentical Peripheral Blood Stem Cell Transplantation With Post-transplant Cyclophosphamide and Bortezomib". Now haplo stem cell transplant using bone marrow or peripheral blood is becoming more feasible with better regimens to prevent graft versus host disease (GVHD) like post transplant cyclophosphamide , tacrolimus, mycophenolate . Recently Bortezomib has also been shown to inhibit dendritic cells matur...

What is the current status of trial NCT03850366?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 15 participants. The study started on 2016-03-08. Estimated completion is 2028-01-01.

What conditions does trial NCT03850366 study?

This clinical trial studies the following conditions: Hematological Malignancy.

What interventions are being tested in trial NCT03850366?

The interventions under investigation include: Bortezomib (DRUG).

Who is sponsoring clinical trial NCT03850366?

This trial is sponsored by Henry Ford Health System, which has 234 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03850366 being conducted?

This trial has 1 study location across Michigan. 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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