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

NCT04184869 · ClinicalTrials.gov registry record · Phase 1

Extension Study for Patients Who Had Not Met Criteria for Discontinuation in Previous Sponsored Belinostat Trials

A Phase 1 study, sponsored by Acrotech Biopharma.

Completed
Registry status
Phase 1
Development phase
8
Enrollment target

NCT04184869: Completed Phase 1 study, sponsored by Acrotech Biopharma.

NCT04184869 is a Phase 1 study that has completed, run by Acrotech Biopharma. The registered enrollment target is 8 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (87% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04184869, a Phase 1 study, has completed, sponsored by Acrotech Biopharma.

COMPLETED
Registry status
Phase 1
Development phase
8 participants
Enrollment target

Study Summary

This is an open-label, extension protocol designed to allow patients to continue to receive belinostat treatment after they have completed the protocol-specified assessments and procedures in a Spectrum sponsored belinostat study and have not met the criteria for treatment discontinuation in those studies. This extension of belinostat treatment allowance is not a part of the primary efficacy assessments for those trials. The extension is intended to provide all possible benefits to patients who are having a positive response to belinostat and must be under the Investigator's care. The additional treatment is optional and voluntary.

Primary Outcome

Frequency of adverse events (AEs \& serious adverse events (SAEs)

Interventions

  • DRUG Belinostat
  • DRUG Atazanavir

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2019-08-05
Est. Completion 2023-03-31
Phase Phase 1
Acrotech Biopharma

24 total trials

What the finished NCT04184869 record still lists

NCT04184869 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 8 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (87% lower).

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

NCT04184869 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04184869 about?

NCT04184869 is a clinical study titled "Extension Study for Patients Who Had Not Met Criteria for Discontinuation in Previous Sponsored Belinostat Trials". This is an open-label, extension protocol designed to allow patients to continue to receive belinostat treatment after they have completed the protocol-specified assessments and procedures in a Spectrum sponsored belinostat study and have not met the criteria for treatment discontinuation in those s...

What is the current status of trial NCT04184869?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 8 participants. The study started on 2019-08-05. Estimated completion is 2023-03-31.

What interventions are being tested in trial NCT04184869?

The interventions under investigation include: Belinostat (DRUG), Atazanavir (DRUG).

Who is sponsoring clinical trial NCT04184869?

This trial is sponsored by Acrotech Biopharma, which has 24 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04184869's enrollment target sits among peer trials

8 1959th of 2000 higher than 29 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT04184869, the US trial registry maintained by the National Library of Medicine. NCT04184869 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.