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

RECRUITING Phase 1

A Study Evaluating OBI-902 in Participants With Advanced Solid Tumors

NCT07124117 · View on ClinicalTrials.gov ↗

Study Summary

This is a 3-part study. Phase 1a (dose escalation) is designed to assess the safety and tolerability and to determine the maximum tolerated dose (MTD) and putative recommended phase 2 dose (RP2D) of study drug as monotherapy. Phase 1b (Cohort Expansion) is intended to further characterize the safety and preliminary antitumor activity of the putative RP2D of OBI-902 in selected tumor types. Phase 2 (Randomized Dose Optimization Cohorts) is intended to determine the optimal RP2D of OBI-902 in selected tumor types, before advancing to larger Phase 3 trials.

Conditions Studied

Interventions

  • DRUG OBI-902

Study Locations (6)

Texas

  • The University of Texas MD Anderson Cancer Center — Houston
  • NEXT Oncology — San Antonio

California

  • Scripps Green Hospital — La Jolla

Wenshan

  • Wan Fan Hospital — Taipei

Zhonghe

  • Shuang Ho Hospital — Taipei

Other

  • China Medical University Hospital — Taichung

Trial Details

FieldValue
Enrollment Target 147 participants
Start Date 2025-08-04
Est. Completion 2029-02-08
Phase Phase 1

Sponsor

OBI Pharma

4 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07124117

The ClinicalTrials.gov registry entry for NCT07124117 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 147 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is OBI Pharma, which has 4 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 Advanced Solid Tumor appearing as the primary indexed condition, and to 1 intervention — of which OBI-902 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: NCT07124117 reports 6 study locations spanning 5 distinct geographic areas — top geographies include Texas, California, Wenshan. 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 NCT07124117 about?

NCT07124117 is a clinical study titled "A Study Evaluating OBI-902 in Participants With Advanced Solid Tumors". This is a 3-part study. Phase 1a (dose escalation) is designed to assess the safety and tolerability and to determine the maximum tolerated dose (MTD) and putative recommended phase 2 dose (RP2D) of study drug as monotherapy. Phase 1b (Cohort Expansion) is intended to further characterize the safety...

What is the current status of trial NCT07124117?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 147 participants. The study started on 2025-08-04. Estimated completion is 2029-02-08.

What conditions does trial NCT07124117 study?

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

What interventions are being tested in trial NCT07124117?

The interventions under investigation include: OBI-902 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07124117?

This trial is sponsored by OBI Pharma, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07124117 being conducted?

This trial has 6 study locations across California, Texas, Wenshan, Zhonghe. 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