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NCT05203835 · ClinicalTrials.gov registry record · Phase 2

Trial of Acebilustat for the Treatment of Upper Arm Lymphedema

A Phase 2 study of Lymphedema of Upper Arm, sponsored by Stanford University.

Active
Registry status
Phase 2
Development phase
40
Enrollment target
1
Study location

NCT05203835: Active Phase 2 study of Lymphedema of Upper Arm, sponsored by Stanford University.

NCT05203835 is a Phase 2 study of Lymphedema of Upper Arm that is active but no longer recruiting, run by Stanford University. The registered enrollment target is 40 participants, below the 151-participant average among 3 other Lymphedema of Upper Arm trials with a reported enrollment target (74% 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

NCT05203835, a Phase 2 study of Lymphedema of Upper Arm, is active but no longer recruiting, sponsored by Stanford University.

ACTIVE NOT RECRUITING
Registry status
Phase 2
Development phase
40 participants
Enrollment target
1
Study location

Study Summary

This study is designed to investigate the response of unilateral upper extremity (arm) lymphedema, during pharmacologic treatment of lymphedema with oral placebo and oral acebilustat. Participants will receive "study drug" (Acebilustat or placebo), for 9 months. For 3 of these months, the participant will receive placebo; for 6 of these months, the participant will receive active ingredient, acebilustat. The study is blinded which means that the participant will not be told which study pill they are taking.

Primary Outcome

Cutaneous thickness will be measured by skin calipers at three designated locations in the affected upper extremity.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG Acebilustat

Study Locations (1)

California

  • Stanford University - Palo Alto

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2022-07-27
Est. Completion 2026-03-31
Phase Phase 2
Stanford University

1,744 total trials

What the registry record for NCT05203835 still lists

NCT05203835 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 151-participant average among 3 other Lymphedema of Upper Arm trials with a reported enrollment target (74% lower).

The record links to 1 condition, with Lymphedema of Upper Arm appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT05203835 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT05203835 about?

NCT05203835 is a clinical study titled "Trial of Acebilustat for the Treatment of Upper Arm Lymphedema". This study is designed to investigate the response of unilateral upper extremity (arm) lymphedema, during pharmacologic treatment of lymphedema with oral placebo and oral acebilustat. Participants will receive "study drug" (Acebilustat or placebo), for 9 months. For 3 of these months, the participan...

What is the current status of trial NCT05203835?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 40 participants. The study started on 2022-07-27. Estimated completion is 2026-03-31.

What conditions does trial NCT05203835 study?

This clinical trial studies the following conditions: Lymphedema of Upper Arm.

What interventions are being tested in trial NCT05203835?

The interventions under investigation include: Placebo (DRUG), Acebilustat (DRUG).

Who is sponsoring clinical trial NCT05203835?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05203835 being conducted?

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

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Source: ClinicalTrials.gov NCT05203835, the US trial registry maintained by the National Library of Medicine. NCT05203835 (small enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.