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NCT04593784 · ClinicalTrials.gov registry record · Phase 2

Study of Ciraparantag for Reversal of Anticoagulation Induced by Edoxaban, Apixaban or Rivaroxaban in Healthy Adults

A Phase 2 study, sponsored by AMAG Pharmaceuticals.

Terminated
Registry status
Phase 2
Development phase
41
Enrollment target

NCT04593784: Clinical Trial Phase 2 study, sponsored by AMAG Pharmaceuticals.

NCT04593784 is a Phase 2 study that was terminated before completion, run by AMAG Pharmaceuticals. The registered enrollment target is 41 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (69% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04593784, a Phase 2 study, was terminated before completion, sponsored by AMAG Pharmaceuticals.

TERMINATED
Registry status
Phase 2
Development phase
41 participants
Enrollment target

Study Summary

A randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of ciraparantag for reversal of anticoagulation induced by different anticoagulant drugs in generally healthy adults as measured primarily by an automated coagulometer device.

Primary Outcome

The primary efficacy endpoint is achieving a WBCT (measured by PoC coagulometer) ≤ 120% of baseline within 1 hour after administration of ciraparantag/PBO, which is subsequently sustained after 1 hour through at least 6 hours after ciraparantag/PBO dosing (Responder).

Interventions

  • DRUG Placebo
  • DRUG Ciraparantag
  • DEVICE Point-of-Care Coagulometer (investigational device)

Trial Details

FieldValue
Enrollment Target 41 participants
Start Date 2021-10-13
Est. Completion 2023-08-26
Phase Phase 2
AMAG Pharmaceuticals

23 total trials

Why NCT04593784 stopped before completion

NCT04593784 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 41 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (69% lower).

The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.

NCT04593784 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04593784 about?

NCT04593784 is a clinical study titled "Study of Ciraparantag for Reversal of Anticoagulation Induced by Edoxaban, Apixaban or Rivaroxaban in Healthy Adults". A randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of ciraparantag for reversal of anticoagulation induced by different anticoagulant drugs in generally healthy adults as measured primarily by an automated coagulometer device.

What is the current status of trial NCT04593784?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 41 participants. The study started on 2021-10-13. Estimated completion is 2023-08-26.

What interventions are being tested in trial NCT04593784?

The interventions under investigation include: Placebo (DRUG), Ciraparantag (DRUG), Point-of-Care Coagulometer (investigational device) (DEVICE).

Who is sponsoring clinical trial NCT04593784?

This trial is sponsored by AMAG Pharmaceuticals, which has 23 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04593784's enrollment target sits among peer trials

41 1352nd of 2000 higher than 639 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT04593784, the US trial registry maintained by the National Library of Medicine. NCT04593784 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.