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

NCT02010333 · ClinicalTrials.gov registry record · Phase 2

A Pediatric Safety and Pharmacokinetics Study of Ha44 Gel Administered Topically for Treatment of Head Lice Infestation

A Phase 2 study of Head Lice Infestation, sponsored by Dr. Reddy's Laboratories Limited.

Completed
Registry status
Phase 2
Development phase
22
Enrollment target
2
Study locations

NCT02010333: Completed Phase 2 study of Head Lice Infestation, sponsored by Dr. Reddy's Laboratories Limited.

NCT02010333 is a Phase 2 study of Head Lice Infestation that has completed, run by Dr. Reddy's Laboratories Limited. The registered enrollment target is 22 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (83% lower). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02010333, a Phase 2 study of Head Lice Infestation, has completed, sponsored by Dr. Reddy's Laboratories Limited.

COMPLETED
Registry status
Phase 2
Development phase
22 participants
Enrollment target
2
Study locations

Study Summary

The primary purpose of the study is to evaluate safety and tolerability of a single application of Ha44 Gel 0.74% w/w for the treatment of head lice. Secondary purpose is to evaluate PK of Ha44 and benzyl alcohol under conditions of maximal exposure in pediatric population.

Primary Outcome

Clinically significant changes in Physical Examinations, vital signs, safety laboratory tests and assessments of scalp and eye irritation and Electrocardiogram. The frequency and severity of Adverse Events.

Conditions Studied

Interventions

  • DRUG Ha44 Gel 0.74% w/w

Study Locations (2)

California

  • Universal Biopharma Research Institute - Dinuba
  • Axis Clinical Trials - Los Angeles

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2013-04
Est. Completion 2014-08
Phase Phase 2
Dr. Reddy's Laboratories Limited

52 total trials

What the finished NCT02010333 record still lists

NCT02010333 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 22 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (83% lower).

The record links to 1 condition, with Head Lice Infestation appearing as the primary indexed condition, and to 1 intervention - of which Ha44 Gel 0.74% w/w is the first listed.

NCT02010333 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT02010333 about?

NCT02010333 is a clinical study titled "A Pediatric Safety and Pharmacokinetics Study of Ha44 Gel Administered Topically for Treatment of Head Lice Infestation". The primary purpose of the study is to evaluate safety and tolerability of a single application of Ha44 Gel 0.74% w/w for the treatment of head lice. Secondary purpose is to evaluate PK of Ha44 and benzyl alcohol under conditions of maximal exposure in pediatric population.

What is the current status of trial NCT02010333?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 22 participants. The study started on 2013-04. Estimated completion is 2014-08.

What conditions does trial NCT02010333 study?

This clinical trial studies the following conditions: Head Lice Infestation.

What interventions are being tested in trial NCT02010333?

The interventions under investigation include: Ha44 Gel 0.74% w/w (DRUG).

Who is sponsoring clinical trial NCT02010333?

This trial is sponsored by Dr. Reddy's Laboratories Limited, which has 52 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02010333 being conducted?

This trial has 2 study locations across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT02010333's enrollment target sits among peer trials

22 1790th of 2000 higher than 207 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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

  • NCT02508038 · 22 participants · Phase 1

    Alpha/Beta CD19+ Depleted Haploidentical Transplantation + Zometa for Pediatric Hematologic Malignancies and Solid Tumors

  • NCT03099356 · 22 participants · Phase 2

    Cyclophosphamide and Sirolimus for the Treatment of Metastatic, RAI-refractory, Differentiated Thyroid Cancer

  • NCT03676647 · 22 participants

    Diagnostic DNA Methylation Signature in Diagnosing Thyroid Cancer After Fine-Needle Aspiration in Patients With Thyroid Nodules

  • NCT04569591 · 22 participants · NA

    DDAVP for Pituitary Adenoma

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 NCT02010333, the US trial registry maintained by the National Library of Medicine. NCT02010333 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.