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COMPLETED Early Phase 1

A Study Comparing the Efficacy of TA103 and the Placebo Control in the Treatment of Interdigital Tinea Pedis.

NCT04883593 · View on ClinicalTrials.gov ↗

Study Summary

To evaluate and compare the safety and efficacy of TA103 in the treatment of tinea pedis.

Conditions Studied

Interventions

  • DRUG Placebo Control
  • DRUG TA103

Study Locations (1)

North Carolina

  • Catawba Research, LLC — Charlotte

Trial Details

FieldValue
Enrollment Target 160 participants
Start Date 2020-09-03
Est. Completion 2021-02-20
Phase Early Phase 1

Sponsor

Sun Pharmaceutical Industries

20 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04883593

The ClinicalTrials.gov registry entry for NCT04883593 describes a study currently listed as completed. It is categorized as Early Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 160 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Sun Pharmaceutical Industries, which has 20 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Tinea Pedis appearing as the primary indexed condition, and to 2 interventions — of which Placebo Control is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT04883593 reports 1 study location spanning 1 distinct geographic area — top geographies include North Carolina. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT04883593 about?

NCT04883593 is a clinical study titled "A Study Comparing the Efficacy of TA103 and the Placebo Control in the Treatment of Interdigital Tinea Pedis.". To evaluate and compare the safety and efficacy of TA103 in the treatment of tinea pedis.

What is the current status of trial NCT04883593?

This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 160 participants. The study started on 2020-09-03. Estimated completion is 2021-02-20.

What conditions does trial NCT04883593 study?

This clinical trial studies the following conditions: Tinea Pedis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04883593?

The interventions under investigation include: Placebo Control (DRUG), TA103 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04883593?

This trial is sponsored by Sun Pharmaceutical Industries, which has 20 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04883593 being conducted?

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

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial