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NCT06340347 · ClinicalTrials.gov registry record · Phase 1

A Study to Learn How the Body Processes the Study Medicine Called Osivelotor (PF-07940367) in People With Loss of Liver Function

A Phase 1 study, sponsored by Pfizer.

Completed
Registry status
Phase 1
Development phase
8
Enrollment target

NCT06340347: Completed Phase 1 study, sponsored by Pfizer.

NCT06340347 is a Phase 1 study that has completed, run by Pfizer. 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.

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The verdict

NCT06340347, a Phase 1 study, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 1
Development phase
8 participants
Enrollment target

Study Summary

The purpose of this study is to understand how Osivelotor is processed in people with loss of liver function. This study is seeking participants that are: * stable loss of liver function with mild or moderate severity * none of underlying conditions possibly affecting the study medicine being absorbed by the body All participants will receive one amount of Osivelotor by mouth before breakfast on the first day at the study clinic. A number of blood samples will be collected to understand how Osivelotor is changed and removed from the body. Participants will also have to undergo physical examination and other tests. This will help to understand if Osivelotor is safe. Participants will take part in the study for a maximum of 112 days. During this time, participants will have to stay onsite for 5 days. There will be 5 study visits at the study clinic.

Interventions

  • DRUG Osivelotor

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2024-04-30
Est. Completion 2024-09-18
Phase Phase 1
Pfizer

1,845 total trials

What the finished NCT06340347 record still lists

NCT06340347 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 1 intervention - of which Osivelotor is the first listed.

NCT06340347 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06340347 about?

NCT06340347 is a clinical study titled "A Study to Learn How the Body Processes the Study Medicine Called Osivelotor (PF-07940367) in People With Loss of Liver Function". The purpose of this study is to understand how Osivelotor is processed in people with loss of liver function. This study is seeking participants that are: * stable loss of liver function with mild or moderate severity * none of underlying conditions possibly affecting the study medicine being abso...

What is the current status of trial NCT06340347?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 8 participants. The study started on 2024-04-30. Estimated completion is 2024-09-18.

What interventions are being tested in trial NCT06340347?

The interventions under investigation include: Osivelotor (DRUG).

Who is sponsoring clinical trial NCT06340347?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06340347'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

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Source: ClinicalTrials.gov NCT06340347, the US trial registry maintained by the National Library of Medicine. NCT06340347 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.