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RECRUITING Phase 1

A Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Efficacy of TT125-802 in Subjects With Advanced Solid Tumors

NCT06403436 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to test the safety and therapeutic effect of TT125-802 (single agent) in subjects with advanced solid tumors.

Interventions

  • DRUG TT125-802

Study Locations (7)

Other

  • NEXT Oncology Barcelona — Barcelona
  • Vall d'Hebron Institute of Oncology — Barcelona
  • NEXT Oncology Madrid — Madrid
  • Ente Ospedaliero Cantonale — Bellinzona
  • Centre Hospitalier Universitaire Vaudois — Lausanne

Tennessee

  • Sarah Cannon Research Institute Oncology Partners — Nashville

Virginia

  • NEXT Oncology Virginia — Fairfax

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2023-11-07
Est. Completion 2026-12
Phase Phase 1

Sponsor

TOLREMO therapeutics

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06403436

The ClinicalTrials.gov registry entry for NCT06403436 describes a study currently listed as recruiting. It is categorized as 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 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is TOLREMO therapeutics, 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 8 conditions, with Cancer appearing as the primary indexed condition, and to 1 intervention — of which TT125-802 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: NCT06403436 reports 7 study locations spanning 3 distinct geographic areas — top geographies include Other, Tennessee, Virginia. 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 NCT06403436 about?

NCT06403436 is a clinical study titled "A Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Efficacy of TT125-802 in Subjects With Advanced Solid Tumors". The purpose of this study is to test the safety and therapeutic effect of TT125-802 (single agent) in subjects with advanced solid tumors.

What is the current status of trial NCT06403436?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 50 participants. The study started on 2023-11-07. Estimated completion is 2026-12.

What conditions does trial NCT06403436 study?

This clinical trial studies the following conditions: Cancer, Advanced Solid Tumor, NSCLC, KRAS G12C, Squamous Cell Lung Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06403436?

The interventions under investigation include: TT125-802 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06403436?

This trial is sponsored by TOLREMO therapeutics, 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 NCT06403436 being conducted?

This trial has 7 study locations across Tennessee, Virginia. 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