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

NCT04666649 · ClinicalTrials.gov registry record · Phase 1

Pegcrisantaspase in Combination With Venetoclax for Treatment of Relapsed or Refractory Acute Myeloid Leukemia (R/R AML)

A Phase 1 study, sponsored by University of Maryland, Baltimore.

Completed
Registry status
Phase 1
Development phase
27
Enrollment target

NCT04666649 is a Phase 1 study that has completed, run by University of Maryland, Baltimore. The registered enrollment target is 27 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04666649, a Phase 1 study, has completed, sponsored by University of Maryland, Baltimore.

COMPLETED
Registry status
Phase 1
Development phase
27 participants
Enrollment target

Study Summary

Evaluate the safety and tolerability of pegcrisantaspase in combination with venetoclax (Ven-PegC) and estimate the maximum tolerated doses and/or biologically active doses of Ven-PegC in patients with relapsed or refractory acute myeloid leukemia (R/R AML)

Interventions

  • DRUG Venetoclax and pegcrisantaspase

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2021-03-10
Est. Completion 2025-05-23
Phase Phase 1

Sponsor

University of Maryland, Baltimore

560 total trials

What the Registry Record Tells You About NCT04666649

The ClinicalTrials.gov registry entry for NCT04666649 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 27 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Maryland, Baltimore, which has 560 total studies on file at ClinicalTrials.gov.

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

NCT04666649 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04666649 about?

NCT04666649 is a clinical study titled "Pegcrisantaspase in Combination With Venetoclax for Treatment of Relapsed or Refractory Acute Myeloid Leukemia (R/R AML)". Evaluate the safety and tolerability of pegcrisantaspase in combination with venetoclax (Ven-PegC) and estimate the maximum tolerated doses and/or biologically active doses of Ven-PegC in patients with relapsed or refractory acute myeloid leukemia (R/R AML)

What is the current status of trial NCT04666649?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 27 participants. The study started on 2021-03-10. Estimated completion is 2025-05-23.

What interventions are being tested in trial NCT04666649?

The interventions under investigation include: Venetoclax and pegcrisantaspase (DRUG).

Who is sponsoring clinical trial NCT04666649?

This trial is sponsored by University of Maryland, Baltimore, which has 560 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.