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RECRUITING Phase 3

Phase 3 Study of Taletrectinib vs Placebo as an Adjuvant Therapy in ROS1 Positive NSCLC (TRUST-IV)

NCT07154706 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this phase 3 multicenter double-blind randomized study is to assess the use of taletrectinib in the early-stage non-small cell lung cancer (NSCLC). The study compares taletrectinib (study drug) versus placebo (sugar pill) in patients with ROS1-fusion positive stage IB, II, IIIA NSCLC. The study will evaluate if taletrectinib is better than placebo at preventing the participant's disease from coming back after the participant's lung tumor was removed.

Interventions

  • DRUG Placebo
  • DRUG Taletrectinib

Study Locations (10)

Texas

  • Sarah Cannon Research Institute (SCRI) - Texas Oncology-Central South — Austin
  • MD Anderson — Houston

California

  • UCLA — Los Angeles

District of Columbia

  • Georgetown University Medical Cener (GUMC) — Washington D.C.

Idaho

  • Saint Alphonsus Health System — Boise

Massachusetts

  • Dana Farber Cancer Institute — Boston

Minnesota

  • Mayo Clinic — Rochester

New York

  • Memorial Sloan Kettering Cancer Center — New York

Virginia

  • Virginia Cancer Specialists — Fairfax

Trial Details

FieldValue
Enrollment Target 180 participants
Start Date 2025-08-21
Est. Completion 2033-08-30
Phase Phase 3

Sponsor

Nuvation Bio

5 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07154706

The ClinicalTrials.gov registry entry for NCT07154706 describes a study currently listed as recruiting. It is categorized as Phase 3, 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 180 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Nuvation Bio, which has 5 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 Non-small Cell Lung Cancer (NSCLC) 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: NCT07154706 reports 10 study locations spanning 9 distinct geographic areas — top geographies include Texas, California, District of Columbia. 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 NCT07154706 about?

NCT07154706 is a clinical study titled "Phase 3 Study of Taletrectinib vs Placebo as an Adjuvant Therapy in ROS1 Positive NSCLC (TRUST-IV)". The purpose of this phase 3 multicenter double-blind randomized study is to assess the use of taletrectinib in the early-stage non-small cell lung cancer (NSCLC). The study compares taletrectinib (study drug) versus placebo (sugar pill) in patients with ROS1-fusion positive stage IB, II, IIIA NSCLC....

What is the current status of trial NCT07154706?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 180 participants. The study started on 2025-08-21. Estimated completion is 2033-08-30.

What conditions does trial NCT07154706 study?

This clinical trial studies the following conditions: Non-small Cell Lung Cancer (NSCLC). These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07154706?

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

Who is sponsoring clinical trial NCT07154706?

This trial is sponsored by Nuvation Bio, which has 5 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07154706 being conducted?

This trial has 10 study locations across California, District of Columbia, Idaho, Massachusetts, Minnesota. 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