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NCT02955459 · ClinicalTrials.gov registry record · Phase 1

VNRX-5133 SAD/MAD Safety and PK in Healthy Adult Volunteers

A Phase 1 study, sponsored by Venatorx Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
84
Enrollment target

NCT02955459: Completed Phase 1 study, sponsored by Venatorx Pharmaceuticals.

NCT02955459 is a Phase 1 study that has completed, run by Venatorx Pharmaceuticals. The registered enrollment target is 84 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (40% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02955459, a Phase 1 study, has completed, sponsored by Venatorx Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
84 participants
Enrollment target

Study Summary

This is a 2-part, first-in-human dose-ranging study to evaluate the safety, tolerability and pharmacokinetics of escalating doses of VNRX-5133 administered via intravenous (IV) infusion in healthy subjects. In part 1, subjects will receive a single dose of VNRX-5133; in part 2 subjects will receive VNRX-5133 for 7 days.

Interventions

  • DRUG Placebo
  • DRUG VNRX-5133

Trial Details

FieldValue
Enrollment Target 84 participants
Start Date 2016-11
Est. Completion 2017-06
Phase Phase 1
Venatorx Pharmaceuticals

6 total trials

What the finished NCT02955459 record still lists

NCT02955459 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 84 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (40% higher).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT02955459 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02955459 about?

NCT02955459 is a clinical study titled "VNRX-5133 SAD/MAD Safety and PK in Healthy Adult Volunteers". This is a 2-part, first-in-human dose-ranging study to evaluate the safety, tolerability and pharmacokinetics of escalating doses of VNRX-5133 administered via intravenous (IV) infusion in healthy subjects. In part 1, subjects will receive a single dose of VNRX-5133; in part 2 subjects will receive ...

What is the current status of trial NCT02955459?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 84 participants. The study started on 2016-11. Estimated completion is 2017-06.

What interventions are being tested in trial NCT02955459?

The interventions under investigation include: Placebo (DRUG), VNRX-5133 (DRUG).

Who is sponsoring clinical trial NCT02955459?

This trial is sponsored by Venatorx Pharmaceuticals, which has 6 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02955459's enrollment target sits among peer trials

84 659th of 2000 higher than 1,336 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 NCT02955459, the US trial registry maintained by the National Library of Medicine. NCT02955459 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.