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NCT03592264 · ClinicalTrials.gov registry record · Phase 1

A Phase I/II Study of OBI-3424 in Subjects with Advanced Solid Tumors

A Phase 1 study, sponsored by OBI Pharma.

Terminated
Registry status
Phase 1
Development phase
68
Enrollment target

NCT03592264: Clinical Trial Phase 1 study, sponsored by OBI Pharma.

NCT03592264 is a Phase 1 study that was terminated before completion, run by OBI Pharma. The registered enrollment target is 68 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (13% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03592264, a Phase 1 study, was terminated before completion, sponsored by OBI Pharma.

TERMINATED
Registry status
Phase 1
Development phase
68 participants
Enrollment target

Study Summary

A first-in-human open-label, Phase I/II study to evaluate the safety, tolerability, MTD/RP2D, PK, and preliminary efficacy of OBI-3424 administered as a single agent.

Primary Outcome

Adverse events will be graded according to the Common Toxicity Criteria for Adverse Events (CTCAE) version 5.0.

Interventions

  • DRUG OBI-3424

Trial Details

FieldValue
Enrollment Target 68 participants
Start Date 2018-07-02
Est. Completion 2024-03-21
Phase Phase 1
OBI Pharma

7 total trials

Why NCT03592264 stopped before completion

NCT03592264 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 68 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (13% higher).

The record links to 0 conditions, and to 1 intervention - of which OBI-3424 is the first listed.

NCT03592264 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03592264 about?

NCT03592264 is a clinical study titled "A Phase I/II Study of OBI-3424 in Subjects with Advanced Solid Tumors". A first-in-human open-label, Phase I/II study to evaluate the safety, tolerability, MTD/RP2D, PK, and preliminary efficacy of OBI-3424 administered as a single agent.

What is the current status of trial NCT03592264?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 68 participants. The study started on 2018-07-02. Estimated completion is 2024-03-21.

What interventions are being tested in trial NCT03592264?

The interventions under investigation include: OBI-3424 (DRUG).

Who is sponsoring clinical trial NCT03592264?

This trial is sponsored by OBI Pharma, which has 7 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03592264's enrollment target sits among peer trials

68 776th of 2000 higher than 1,219 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03592264, the US trial registry maintained by the National Library of Medicine. NCT03592264 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.