Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02532140 · ClinicalTrials.gov registry record · Phase 1

Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of WCK 5107 Alone and in Combination With Cefepime

A Phase 1 study of Healthy, sponsored by Wockhardt.

Completed
Registry status
Phase 1
Development phase
88
Enrollment target
1
Study location

NCT02532140: Completed Phase 1 study of Healthy, sponsored by Wockhardt.

NCT02532140 is a Phase 1 study of Healthy that has completed, run by Wockhardt. The registered enrollment target is 88 participants, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (86% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02532140, a Phase 1 study of Healthy, has completed, sponsored by Wockhardt.

COMPLETED
Registry status
Phase 1
Development phase
88 participants
Enrollment target
1
Study location

Study Summary

• To evaluate the safety,tolerability and pharmacokinetics of single intravenous doses of WCK 5107 alone and in combination with cefepime in healthy adult human subjects.

Primary Outcome

To evaluate the safety of single intravenous doses of WCK 5107 alone and in combination with cefepime in healthy adult human subjects.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG WCK 5107 250 mg to 2000 mg
  • DRUG Cefepime 2000 mg
  • DRUG WCK 5107 1000/2000 mg with Cefepime 2000 mg combination

Study Locations (1)

Kansas

  • Quintiles - Overland Park

Trial Details

FieldValue
Enrollment Target 88 participants
Start Date 2015-08
Est. Completion 2015-12
Phase Phase 1
Wockhardt

27 total trials

What the finished NCT02532140 record still lists

NCT02532140 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 88 participants, a relatively small participant target, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (86% lower).

The record links to 1 condition, with Healthy appearing as the primary indexed condition, and to 4 interventions - of which Placebo is the first listed.

NCT02532140 reports a single indexed study location in Kansas.

Frequently Asked Questions

What is clinical trial NCT02532140 about?

NCT02532140 is a clinical study titled "Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of WCK 5107 Alone and in Combination With Cefepime". • To evaluate the safety,tolerability and pharmacokinetics of single intravenous doses of WCK 5107 alone and in combination with cefepime in healthy adult human subjects.

What is the current status of trial NCT02532140?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 88 participants. The study started on 2015-08. Estimated completion is 2015-12.

What conditions does trial NCT02532140 study?

This clinical trial studies the following conditions: Healthy.

What interventions are being tested in trial NCT02532140?

The interventions under investigation include: Placebo (DRUG), WCK 5107 250 mg to 2000 mg (DRUG), Cefepime 2000 mg (DRUG), WCK 5107 1000/2000 mg with Cefepime 2000 mg combination (DRUG).

Who is sponsoring clinical trial NCT02532140?

This trial is sponsored by Wockhardt, which has 27 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02532140 being conducted?

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

Similar trials for Healthy

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 NCT02532140's enrollment target sits among peer trials

88 259th of 1090 higher than 831 of 1,090 other Healthy trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Healthy 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

  • NCT03843463 · 88 participants · Phase 2

    Escitalopram and Language Intervention for Subacute Aphasia

  • NCT04066348 · 88 participants · Phase 2

    TNF-α Treatment of Blast-Induced Tinnitus

  • NCT04331704 · 88 participants · Phase 4

    ANCHORS Alcohol & Sexual Health Study: UH3 Project

  • NCT04536103 · 88 participants

    Multi-Vendor Multi-Site Novel Accelerated MRI Relaxometry

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02532140, the US trial registry maintained by the National Library of Medicine. NCT02532140 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.