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COMPLETED Phase 2

Efficacy and Safety Study of SUNPG1623

NCT02980692 · View on ClinicalTrials.gov ↗

Study Summary

This is a randomized, double-blind, placebo-controlled, multiple-dose, phase 2b study to demonstrate the safety and efficacy of SUNPG1623

Conditions Studied

Interventions

  • DRUG PLACEBO
  • DRUG SUNPG1623 I
  • DRUG SUNPG1623 II
  • DRUG SUNPG1623 III
  • DRUG SUNPG1623 IV

Study Locations (1)

Ohio

  • SPARC Site 1 — Middleburg Heights

Trial Details

FieldValue
Enrollment Target 391 participants
Start Date 2017-04-19
Est. Completion 2019-09-24
Phase Phase 2

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02980692

The ClinicalTrials.gov registry entry for NCT02980692 describes a study currently listed as completed. It is categorized as Phase 2, 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 391 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Sun Pharmaceutical Industries Limited, which has 13 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 Active Psoriatic Arthritis appearing as the primary indexed condition, and to 5 interventions — of which PLACEBO 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: NCT02980692 reports 1 study location spanning 1 distinct geographic area — top geographies include Ohio. 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 NCT02980692 about?

NCT02980692 is a clinical study titled "Efficacy and Safety Study of SUNPG1623". This is a randomized, double-blind, placebo-controlled, multiple-dose, phase 2b study to demonstrate the safety and efficacy of SUNPG1623

What is the current status of trial NCT02980692?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 391 participants. The study started on 2017-04-19. Estimated completion is 2019-09-24.

What conditions does trial NCT02980692 study?

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

What interventions are being tested in trial NCT02980692?

The interventions under investigation include: PLACEBO (DRUG), SUNPG1623 I (DRUG), SUNPG1623 II (DRUG), SUNPG1623 III (DRUG), SUNPG1623 IV (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02980692?

This trial is sponsored by Sun Pharmaceutical Industries Limited, which has 13 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02980692 being conducted?

This trial has 1 study location across Ohio. 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