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

NCT01602757 · ClinicalTrials.gov registry record · Phase 1

Pharmacokinetic Study of Synera in Healthy Volunteers

A Phase 1 study of Healthy, sponsored by ZARS Pharma.

Completed
Registry status
Phase 1
Development phase
12
Enrollment target
1
Study location

NCT01602757: Completed Phase 1 study of Healthy, sponsored by ZARS Pharma.

NCT01602757 is a Phase 1 study of Healthy that has completed, run by ZARS Pharma. The registered enrollment target is 12 participants, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (98% 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

NCT01602757, a Phase 1 study of Healthy, has completed, sponsored by ZARS Pharma.

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

Study Summary

This study will measure the amount of lidocaine and tetracaine in the blood after 2-, 4-, and 12-hour application of 4 Synera patches and a 4 hour application of 4 patches without heat.

Primary Outcome

Peak plasma concentration of Synera after application of 4 patches for 2-, 4- and 12-hours

Conditions Studied

Interventions

  • DRUG Synera

Study Locations (1)

North Dakota

  • Cetero Research - Fargo

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2010-02
Est. Completion 2010-03
Phase Phase 1
ZARS Pharma

23 total trials

What the finished NCT01602757 record still lists

NCT01602757 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (98% lower).

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

NCT01602757 reports a single indexed study location in North Dakota.

Frequently Asked Questions

What is clinical trial NCT01602757 about?

NCT01602757 is a clinical study titled "Pharmacokinetic Study of Synera in Healthy Volunteers". This study will measure the amount of lidocaine and tetracaine in the blood after 2-, 4-, and 12-hour application of 4 Synera patches and a 4 hour application of 4 patches without heat.

What is the current status of trial NCT01602757?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 12 participants. The study started on 2010-02. Estimated completion is 2010-03.

What conditions does trial NCT01602757 study?

This clinical trial studies the following conditions: Healthy.

What interventions are being tested in trial NCT01602757?

The interventions under investigation include: Synera (DRUG).

Who is sponsoring clinical trial NCT01602757?

This trial is sponsored by ZARS Pharma, which has 23 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01602757 being conducted?

This trial has 1 study location across North Dakota. 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 NCT01602757's enrollment target sits among peer trials

12 996th of 1090 higher than 61 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

  • NCT02602769 · 12 participants

    Whole Transcriptome Profiling and Metabolic Phenotyping in Children With ROHHAD Syndrome

  • NCT02605421 · 12 participants · Phase 2

    Myeloablative Consolidation Therapy and Tandem Autologous Stem Cell Rescue in Patients With High-Risk Neuroblastoma

  • NCT02619448 · 12 participants · Early Phase 1

    Concurrent Chemotherapy Plus HFR Radiation Therapy in Inoperable NSCLC

  • NCT03311503 · 12 participants · Phase 1

    Phase I/II Trial of Lentiviral Gene Transfer for SCID-X1 With Low Dose Targeted Busulfan Conditioning

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 NCT01602757, the US trial registry maintained by the National Library of Medicine. NCT01602757 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.