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

RECRUITING Phase 2

Utidelone Capsule Combined With Fluoropyrimidine- and Platinum-containing Therapy in First-line Treatment of Patients With Gastric or Gastroesophageal Junction Adenocarcinoma

NCT06841679 · View on ClinicalTrials.gov ↗

Study Summary

This is a multi-national, open-label, randomized, seamless phase II/III clinical study of UTD2 combined with fluoropyrimidine- and platinum-containing therapy to evaluate the efficacy and safety in patients with locally advanced or metastatic gastric or gastroesophageal junction adenocarcinoma untreated with systemic treatment in advanced setting.

Interventions

  • DRUG Oxaliplatin
  • DRUG Utidelone Capsule
  • DRUG Fluoropyrimidine- and Platinum-containing Therapy

Study Locations (10)

Other

  • AnYang Tumor Hospital — Anyang
  • Sun Yat-sen University Cancer Center — Guangzhou
  • Jinan Municipal Central Hospital — Jinan
  • Shandong First Medical University Affiliated Tumor Hospital — Jinan
  • Liaoning Cancer Hospital — Shenyang
  • Shanxi Cancer Hospital — Taiyuan
  • Tianjin Medical University Cancer Institute & Hospital — Tianjin
  • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology — Wuhan
  • Henan Cancer Hospital — Zhengzhou

Florida

  • Bioresearch Partner — Hialeah

Trial Details

FieldValue
Enrollment Target 778 participants
Start Date 2025-08-28
Est. Completion 2030-09-01
Phase Phase 2

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06841679

The ClinicalTrials.gov registry entry for NCT06841679 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 778 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Beijing Biostar Pharmaceuticals Co., 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 Gastric or Gastroesophageal Junction Adenocarcinoma appearing as the primary indexed condition, and to 3 interventions — of which Oxaliplatin 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: NCT06841679 reports 10 study locations spanning 2 distinct geographic areas — top geographies include Other, Florida. 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 NCT06841679 about?

NCT06841679 is a clinical study titled "Utidelone Capsule Combined With Fluoropyrimidine- and Platinum-containing Therapy in First-line Treatment of Patients With Gastric or Gastroesophageal Junction Adenocarcinoma". This is a multi-national, open-label, randomized, seamless phase II/III clinical study of UTD2 combined with fluoropyrimidine- and platinum-containing therapy to evaluate the efficacy and safety in patients with locally advanced or metastatic gastric or gastroesophageal junction adenocarcinoma untre...

What is the current status of trial NCT06841679?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 778 participants. The study started on 2025-08-28. Estimated completion is 2030-09-01.

What conditions does trial NCT06841679 study?

This clinical trial studies the following conditions: Gastric or Gastroesophageal Junction Adenocarcinoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06841679?

The interventions under investigation include: Oxaliplatin (DRUG), Utidelone Capsule (DRUG), Fluoropyrimidine- and Platinum-containing Therapy (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06841679?

This trial is sponsored by Beijing Biostar Pharmaceuticals Co., 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 NCT06841679 being conducted?

This trial has 10 study locations across Florida. 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