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NCT02470702 · ClinicalTrials.gov registry record · Phase 1

Multiple Oritavancin Doses on Safety, Tolerability, and Pharmacokinetics in Healthy Subjects

A Phase 1 study, sponsored by Melinta Therapeutics.

Completed
Registry status
Phase 1
Development phase
14
Enrollment target

NCT02470702: Completed Phase 1 study, sponsored by Melinta Therapeutics.

NCT02470702 is a Phase 1 study that has completed, run by Melinta Therapeutics. The registered enrollment target is 14 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02470702, a Phase 1 study, has completed, sponsored by Melinta Therapeutics.

COMPLETED
Registry status
Phase 1
Development phase
14 participants
Enrollment target

Study Summary

This protocol describes a double-blind study to evaluate the safety and pharmacokinetics of multiple IV doses of 1200 mg ORBACTIV (oritavancin) in healthy subjects.

Primary Outcome

a composite measure of the number and types of AEs/SAEs encountered and relationship to time of dosing

Interventions

  • DRUG Oritavancin
  • DRUG Placebo (D5W)

Trial Details

FieldValue
Enrollment Target 14 participants
Start Date 2015-06
Est. Completion 2015-10
Phase Phase 1
Melinta Therapeutics

31 total trials

What the finished NCT02470702 record still lists

NCT02470702 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 14 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (77% lower).

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

NCT02470702 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02470702 about?

NCT02470702 is a clinical study titled "Multiple Oritavancin Doses on Safety, Tolerability, and Pharmacokinetics in Healthy Subjects". This protocol describes a double-blind study to evaluate the safety and pharmacokinetics of multiple IV doses of 1200 mg ORBACTIV (oritavancin) in healthy subjects.

What is the current status of trial NCT02470702?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 14 participants. The study started on 2015-06. Estimated completion is 2015-10.

What interventions are being tested in trial NCT02470702?

The interventions under investigation include: Oritavancin (DRUG), Placebo (D5W) (DRUG).

Who is sponsoring clinical trial NCT02470702?

This trial is sponsored by Melinta Therapeutics, which has 31 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02470702's enrollment target sits among peer trials

14 1844th of 2000 higher than 154 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 NCT02470702, the US trial registry maintained by the National Library of Medicine. NCT02470702 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.