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NCT06662097 · ClinicalTrials.gov registry record · Phase 2

A Study of Bevonescein in Patients Undergoing Abdominopelvic Surgery

A Phase 2 study of Surgery and Nerve Injury, sponsored by Alume Biosciences.

Recruiting
Registry status
Phase 2
Development phase
64
Enrollment target
1
Study location

NCT06662097: Recruiting Phase 2 study of Surgery and Nerve Injury, sponsored by Alume Biosciences.

NCT06662097 is a Phase 2 study of Surgery and Nerve Injury that is actively recruiting participants, run by Alume Biosciences. The registered enrollment target is 64 participants, below the 52,851-participant average among 120 other Surgery trials with a reported enrollment target (100% 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

NCT06662097, a Phase 2 study of Surgery and Nerve Injury, is actively recruiting participants, sponsored by Alume Biosciences.

RECRUITING
Registry status
Phase 2
Development phase
64 participants
Enrollment target
1
Study location

Study Summary

Feasibility study of Bevonescein to highlight Nerves and Ureter in patients undergoing Minimally Invasive Surgery

Primary Outcome

To assess the feasibility of the Fluorescence System in each of the identified Minimally Invasive Surgery settings.

Interventions

  • DRUG Bevonescein

Study Locations (1)

California

  • University of California San Diego - San Diego

Trial Details

FieldValue
Enrollment Target 64 participants
Start Date 2024-10-16
Est. Completion 2025-09
Phase Phase 2
Alume Biosciences

4 total trials

What NCT06662097 shows while recruiting

NCT06662097 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 64 participants, a relatively small participant target, below the 52,851-participant average among 120 other Surgery trials with a reported enrollment target (100% lower).

The record links to 3 conditions, with Surgery appearing as the primary indexed condition, and to 1 intervention - of which Bevonescein is the first listed.

NCT06662097 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT06662097 about?

NCT06662097 is a clinical study titled "A Study of Bevonescein in Patients Undergoing Abdominopelvic Surgery". Feasibility study of Bevonescein to highlight Nerves and Ureter in patients undergoing Minimally Invasive Surgery

What is the current status of trial NCT06662097?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 64 participants. The study started on 2024-10-16. Estimated completion is 2025-09.

What conditions does trial NCT06662097 study?

This clinical trial studies the following conditions: Surgery, Nerve Injury, Imaging.

What interventions are being tested in trial NCT06662097?

The interventions under investigation include: Bevonescein (DRUG).

Who is sponsoring clinical trial NCT06662097?

This trial is sponsored by Alume Biosciences, which has 4 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06662097 being conducted?

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

Similar trials for Surgery

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 NCT06662097's enrollment target sits among peer trials

64 79th of 120 higher than 41 of 120 other Surgery trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Surgery 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 NCT06662097, the US trial registry maintained by the National Library of Medicine. NCT06662097 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.