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NCT04512105 · ClinicalTrials.gov registry record · Phase 1

Pitavastatin in Combination With Venetoclax for Chronic Lymphocytic Leukemia or Acute Myeloid Leukemia

A Phase 1 study, sponsored by University of California, Irvine.

Completed
Registry status
Phase 1
Development phase
6
Enrollment target

NCT04512105: Completed Phase 1 study, sponsored by University of California, Irvine.

NCT04512105 is a Phase 1 study that has completed, run by University of California, Irvine. The registered enrollment target is 6 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04512105, a Phase 1 study, has completed, sponsored by University of California, Irvine.

COMPLETED
Registry status
Phase 1
Development phase
6 participants
Enrollment target

Study Summary

This is a phase I, dose-escalation, open-label clinical trial determining the safety and tolerability of adding Pitavastatin to Venetoclax in subjects with chronic lymphocytic leukemia (CLL) or acute myeloid leukemia (AML). These are subjects who are newly diagnosed subjects with AML who are ineligible for intensive induction chemotherapy, relapsed/refractory CLL or newly diagnosed CLL.

Primary Outcome

Determination of the maximum tolerated dose (MTD) will be utilized to evaluate the safety and tolerability of adding to PIT to treatment with stable doses of VEN ± anti-CD20 antibodies (patients with CLL) or VEN with hypomethylating agents (patients with AML).

Interventions

  • DRUG Venetoclax
  • DRUG Pitavastatin

Trial Details

FieldValue
Enrollment Target 6 participants
Start Date 2020-12-02
Est. Completion 2025-02-05
Phase Phase 1
University of California, Irvine

368 total trials

What the finished NCT04512105 record still lists

NCT04512105 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 6 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (90% lower).

The record links to 0 conditions, and to 2 interventions - of which Venetoclax is the first listed.

NCT04512105 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04512105 about?

NCT04512105 is a clinical study titled "Pitavastatin in Combination With Venetoclax for Chronic Lymphocytic Leukemia or Acute Myeloid Leukemia". This is a phase I, dose-escalation, open-label clinical trial determining the safety and tolerability of adding Pitavastatin to Venetoclax in subjects with chronic lymphocytic leukemia (CLL) or acute myeloid leukemia (AML). These are subjects who are newly diagnosed subjects with AML who are ineligi...

What is the current status of trial NCT04512105?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 6 participants. The study started on 2020-12-02. Estimated completion is 2025-02-05.

What interventions are being tested in trial NCT04512105?

The interventions under investigation include: Venetoclax (DRUG), Pitavastatin (DRUG).

Who is sponsoring clinical trial NCT04512105?

This trial is sponsored by University of California, Irvine, which has 368 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04512105's enrollment target sits among peer trials

6 1974th of 2000 higher than 12 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 NCT04512105, the US trial registry maintained by the National Library of Medicine. NCT04512105 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.