Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT06640920 · ClinicalTrials.gov registry record · Phase 1
A Study to Investigate Efficacy and Safety of NSI-8226 in Healthy Participants
A Phase 1 study, sponsored by Uniquity One (UNI).
- Completed
- Registry status
- Phase 1
- Development phase
- 48
- Enrollment target
NCT06640920: Completed Phase 1 study, sponsored by Uniquity One (UNI).
NCT06640920 is a Phase 1 study that has completed, run by Uniquity One (UNI). The registered enrollment target is 48 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (20% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06640920, a Phase 1 study, has completed, sponsored by Uniquity One (UNI).
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 48 participants
- Enrollment target
Study Summary
A Phase 1 Randomized, Double-Blind Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Bioavailability of NSI-8226 in Healthy Participants.
Primary Outcome
To evaluate the incidence of treatment emergent adverse events of NSI-8826 in healthy participants according to Common Terminology Criteria for Adverse Events (CTCAE) V4.0
Interventions
- BIOLOGICAL Cohort A
- BIOLOGICAL Cohort B
- BIOLOGICAL Cohort C
- BIOLOGICAL Cohort D
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 48 participants |
| Start Date | 2024-04-29 |
| Est. Completion | 2024-10-29 |
| Phase | Phase 1 |
What the finished NCT06640920 record still lists
NCT06640920 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 48 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (20% lower).
The record links to 0 conditions, and to 4 interventions - of which Cohort A is the first listed.
NCT06640920 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT06640920 about?
NCT06640920 is a clinical study titled "A Study to Investigate Efficacy and Safety of NSI-8226 in Healthy Participants". A Phase 1 Randomized, Double-Blind Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Bioavailability of NSI-8226 in Healthy Participants.
What is the current status of trial NCT06640920?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 48 participants. The study started on 2024-04-29. Estimated completion is 2024-10-29.
What interventions are being tested in trial NCT06640920?
The interventions under investigation include: Cohort A (BIOLOGICAL), Cohort B (BIOLOGICAL), Cohort C (BIOLOGICAL), Cohort D (BIOLOGICAL).
Who is sponsoring clinical trial NCT06640920?
This trial is sponsored by Uniquity One (UNI), which has 4 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT06640920's enrollment target sits among peer trials
48 1025th of 2000 higher than 948 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
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT01765777 · 48 participants · NA
Efficacy of Osteopathic Manipulative Medicine (OMM) and Phototherapy for Patients With Chronic Lower Back Pain
- NCT03073343 · 48 participants · NA
A Prospective, Randomized, Open Label Trial of Two Doses of Oral Betaine
- NCT03431064 · 48 participants
Lung Recruitment Maneuver as a Potential Predictor of Fluid Responsiveness in Mechanically Ventilated Pediatric Patients
- NCT03514602 · 48 participants · NA
Maternal Smoking Cessation and Pediatric Obesity Prevention
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI