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

RECRUITING Phase 2

A Study Evaluating TRIV-509 in Atopic Dermatitis

NCT07167758 · View on ClinicalTrials.gov ↗

Study Summary

The goal of this interventional study is to learn if TRIV-509 works to treat moderate to severe atopic dermatitis in adults. It will also evaluate the safety of TRIV-509. Participants will receive 4 doses of the study intervention that they are randomized to (TRIV-509 or placebo), and at Week 16 will cross over and receive 4 doses of the other study intervention. The study duration for individual participants is up to 57 weeks, including a Screening period of up to 30 days.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG TRIV-509

Study Locations (20)

Florida

  • Triveni Bio Site #3 — Miami
  • Triveni Bio Site #7 — Tampa
  • Triveni Bio Site #9 — Tampa

Texas

  • Triveni Bio Site #16 — Bellaire
  • Triveni Bio Site #5 — Dallas
  • Triveni Bio Site #2 — Dallas

Other

  • Triveni Bio Site #32 — Lovech
  • Triveni Bio Site #38 — Pleven
  • Triveni Bio Site #39 — Sofia

California

  • Triveni Bio Site #11 — Fountain Valley
  • Triveni Bio Site #4 — San Diego

Indiana

  • Triveni Bio Site #6 — Indianapolis
  • Triveni Bio Site #10 — South Bend

Pennsylvania

  • Triveni Bio Site #1 — Camp Hill
  • Triveni Bio Site #20 — Pittsburgh

Sofia-Grad

  • Triveni Bio Site #35 — Sofia
  • Triveni Bio Site #36 — Sofia

Utah

  • Triveni Bio Site #14 — Springville

Trial Details

FieldValue
Enrollment Target 90 participants
Start Date 2025-08-26
Est. Completion 2027-06
Phase Phase 2

Sponsor

Triveni Bio

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07167758

The ClinicalTrials.gov registry entry for NCT07167758 describes a study currently listed as recruiting. 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 90 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Triveni Bio, which has 1 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 Atopic Dermatitis appearing as the primary indexed condition, and to 2 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: NCT07167758 reports 20 study locations spanning 10 distinct geographic areas — top geographies include Florida, Texas, Other. 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 NCT07167758 about?

NCT07167758 is a clinical study titled "A Study Evaluating TRIV-509 in Atopic Dermatitis". The goal of this interventional study is to learn if TRIV-509 works to treat moderate to severe atopic dermatitis in adults. It will also evaluate the safety of TRIV-509. Participants will receive 4 doses of the study intervention that they are randomized to (TRIV-509 or placebo), and at Week 16 wi...

What is the current status of trial NCT07167758?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 90 participants. The study started on 2025-08-26. Estimated completion is 2027-06.

What conditions does trial NCT07167758 study?

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

What interventions are being tested in trial NCT07167758?

The interventions under investigation include: Placebo (DRUG), TRIV-509 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07167758?

This trial is sponsored by Triveni Bio, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07167758 being conducted?

This trial has 20 study locations across California, Florida, Indiana, Pennsylvania, Texas. 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