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NCT04898101 · ClinicalTrials.gov registry record · Phase 1

A Study to Evaluate the Effect of [14C]Acp-196 (Acalabrutinib) in Healthy Adult Participants

A Phase 1 study of Healthy Volunteers, sponsored by Acerta Pharma.

Completed
Registry status
Phase 1
Development phase
14
Enrollment target
1
Study location

NCT04898101: Completed Phase 1 study of Healthy Volunteers, sponsored by Acerta Pharma.

NCT04898101 is a Phase 1 study of Healthy Volunteers that has completed, run by Acerta Pharma. The registered enrollment target is 14 participants, below the 482-participant average among 283 other Healthy Volunteers trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04898101, a Phase 1 study of Healthy Volunteers, has completed, sponsored by Acerta Pharma.

COMPLETED
Registry status
Phase 1
Development phase
14 participants
Enrollment target
1
Study location

Study Summary

This study is to determine the absolute bioavailability of oral acalabrutinib and intravenous (IV) PK of \[14C\]ACP-196.

Conditions Studied

Interventions

  • DRUG Acalabrutinib
  • DRUG Microtracer [14C]ACP-196

Study Locations (1)

Wisconsin

  • Covance Clinical Research Unit, Inc. - Madison

Trial Details

FieldValue
Enrollment Target 14 participants
Start Date 2016-03-03
Est. Completion 2016-04-13
Phase Phase 1
Acerta Pharma

38 total trials

What the finished NCT04898101 record still lists

NCT04898101 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 14 participants, a relatively small participant target, below the 482-participant average among 283 other Healthy Volunteers trials with a reported enrollment target (97% lower).

The record links to 1 condition, with Healthy Volunteers appearing as the primary indexed condition, and to 2 interventions - of which Acalabrutinib is the first listed.

NCT04898101 reports a single indexed study location in Wisconsin.

Frequently Asked Questions

What is clinical trial NCT04898101 about?

NCT04898101 is a clinical study titled "A Study to Evaluate the Effect of [14C]Acp-196 (Acalabrutinib) in Healthy Adult Participants". This study is to determine the absolute bioavailability of oral acalabrutinib and intravenous (IV) PK of \[14C\]ACP-196.

What is the current status of trial NCT04898101?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 14 participants. The study started on 2016-03-03. Estimated completion is 2016-04-13.

What conditions does trial NCT04898101 study?

This clinical trial studies the following conditions: Healthy Volunteers.

What interventions are being tested in trial NCT04898101?

The interventions under investigation include: Acalabrutinib (DRUG), Microtracer [14C]ACP-196 (DRUG).

Who is sponsoring clinical trial NCT04898101?

This trial is sponsored by Acerta Pharma, which has 38 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04898101 being conducted?

This trial has 1 study location across Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Healthy Volunteers

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT04898101's enrollment target sits among peer trials

14 245th of 283 higher than 35 of 283 other Healthy Volunteers trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Healthy Volunteers 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 NCT04898101, the US trial registry maintained by the National Library of Medicine. NCT04898101 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.