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NCT05849207 · ClinicalTrials.gov registry record · Phase 1

Post-Transplant Cyclophosphamide in Patients Aged >/= 65 Years Undergoing Haploidentical Transplant

A Phase 1 study of Hematologic Malignancies, sponsored by Ronald Paquette.

Recruiting
Registry status
Phase 1
Development phase
26
Enrollment target
1
Study location

NCT05849207 is a Phase 1 study of Hematologic Malignancies that is actively recruiting participants, run by Ronald Paquette. The registered enrollment target is 26 participants, below the 2,711-participant average among 45 other Hematologic Malignancies trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05849207, a Phase 1 study of Hematologic Malignancies, is actively recruiting participants, sponsored by Ronald Paquette.

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

Study Summary

The purpose of this phase 1 study is to determine the optimal dose of the immune suppressive drug, cyclophosphamide, following standard allogeneic stem cell transplant in patients aged \>/= 65 years with hematologic malignancies.

Conditions Studied

Interventions

  • DRUG Cyclophosphamide

Study Locations (1)

California

  • Cedars-Sinai Medical Center - Los Angeles

Trial Details

FieldValue
Enrollment Target 26 participants
Start Date 2023-10-24
Est. Completion 2028-07-01
Phase Phase 1

Sponsor

Ronald Paquette

2 total trials

What the Registry Record Tells You About NCT05849207

The ClinicalTrials.gov registry entry for NCT05849207 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 26 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,711-participant average among 45 other Hematologic Malignancies trials with a reported enrollment target (99% lower). The listed sponsor is Ronald Paquette, which has 2 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Hematologic Malignancies appearing as the primary indexed condition, and to 1 intervention - of which Cyclophosphamide is the first listed.

NCT05849207 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT05849207 about?

NCT05849207 is a clinical study titled "Post-Transplant Cyclophosphamide in Patients Aged >/= 65 Years Undergoing Haploidentical Transplant". The purpose of this phase 1 study is to determine the optimal dose of the immune suppressive drug, cyclophosphamide, following standard allogeneic stem cell transplant in patients aged \>/= 65 years with hematologic malignancies.

What is the current status of trial NCT05849207?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 26 participants. The study started on 2023-10-24. Estimated completion is 2028-07-01.

What conditions does trial NCT05849207 study?

This clinical trial studies the following conditions: Hematologic Malignancies.

What interventions are being tested in trial NCT05849207?

The interventions under investigation include: Cyclophosphamide (DRUG).

Who is sponsoring clinical trial NCT05849207?

This trial is sponsored by Ronald Paquette, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05849207 being conducted?

This trial has 1 study location across California. 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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