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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: Completed Phase 1 study, sponsored by University of Maryland, Baltimore.

NCT04666649 is a Phase 1 study that has completed, run by University of Maryland, Baltimore. The registered enrollment target is 27 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (55% lower). According to ClinicalTrials.gov, the official US trial registry.

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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)

Primary Outcome

The period for determination of RLT will be from the first day of treatment until 30 days after receiving the first dose of Ven-PegC.

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
University of Maryland, Baltimore

560 total trials

What the finished NCT04666649 record still lists

NCT04666649 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 27 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (55% lower).

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

NCT04666649 does not publish any study locations in the registry export this page uses.

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.

How this trial's enrollment target compares

Where NCT04666649's enrollment target sits among peer trials

27 1463rd of 2000 higher than 519 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04666649, the US trial registry maintained by the National Library of Medicine. NCT04666649 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.