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NCT06480240 · ClinicalTrials.gov registry record · Phase 1

A Phase 1/2 Study of OBI-992 in Subjects With Advanced Solid Tumors

A Phase 1 study of Advanced Solid Tumor, sponsored by OBI Pharma.

Active
Registry status
Phase 1
Development phase
117
Enrollment target
8
Study locations

NCT06480240 is a Phase 1 study of Advanced Solid Tumor that is active but no longer recruiting, run by OBI Pharma. The registered enrollment target is 117 participants, below the 192-participant average among 189 other Advanced Solid Tumor trials with a reported enrollment target (39% lower). The trial reports 8 study locations across 6 states.

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The verdict

NCT06480240, a Phase 1 study of Advanced Solid Tumor, is active but no longer recruiting, sponsored by OBI Pharma.

ACTIVE NOT RECRUITING
Registry status
Phase 1
Development phase
117 participants
Enrollment target
8
Study locations

Study Summary

This is a 2-part trial: Part A (Dose Escalation) is designed to establish the maximum tolerated dose (MTD) and recommended phase 2 dose (RP2D) of OBI-992 (Anti-TROP2 antibody drug conjugate, anti-TROP2 monoclonal antibody-cleavable peptide linker-exatecan) as monotherapy. Part B (Cohort Expansion) is intended to further characterize the safety and preliminary clinical activity profile of the RP2D of OBI-992 in subjects with advanced solid tumors.

Conditions Studied

Interventions

  • DRUG OBI-992

Study Locations (8)

California

  • California Clinical Trials Medical Group (CCTMG) - Glendale
  • Scripps Green Hospital - La Jolla

Texas

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

Michigan

  • Karmanos Cancer Institute - Detroit

Virginia

  • NEXT Virginia - Fairfax

Xindian District

  • Taipei Tzu Chi Hospital - New Taipei City

Zhonghe District

  • Taipei Medical University - Shuang Ho Hospital - New Taipei City

Trial Details

FieldValue
Enrollment Target 117 participants
Start Date 2024-06-12
Est. Completion 2027-06
Phase Phase 1

Sponsor

OBI Pharma

7 total trials

What the Registry Record Tells You About NCT06480240

The ClinicalTrials.gov registry entry for NCT06480240 describes a study currently listed as active not recruiting, categorized as Phase 1. The registered enrollment target is 117 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 192-participant average among 189 other Advanced Solid Tumor trials with a reported enrollment target (39% lower). The listed sponsor is OBI Pharma, which has 7 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Advanced Solid Tumor appearing as the primary indexed condition, and to 1 intervention - of which OBI-992 is the first listed.

NCT06480240 reports 8 study locations spanning 6 distinct geographic areas - top geographies include California, Texas, Michigan.

Frequently Asked Questions

What is clinical trial NCT06480240 about?

NCT06480240 is a clinical study titled "A Phase 1/2 Study of OBI-992 in Subjects With Advanced Solid Tumors". This is a 2-part trial: Part A (Dose Escalation) is designed to establish the maximum tolerated dose (MTD) and recommended phase 2 dose (RP2D) of OBI-992 (Anti-TROP2 antibody drug conjugate, anti-TROP2 monoclonal antibody-cleavable peptide linker-exatecan) as monotherapy. Part B (Cohort Expansion) i...

What is the current status of trial NCT06480240?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 117 participants. The study started on 2024-06-12. Estimated completion is 2027-06.

What conditions does trial NCT06480240 study?

This clinical trial studies the following conditions: Advanced Solid Tumor.

What interventions are being tested in trial NCT06480240?

The interventions under investigation include: OBI-992 (DRUG).

Who is sponsoring clinical trial NCT06480240?

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

Where is trial NCT06480240 being conducted?

This trial has 8 study locations across California, Michigan, Texas, Virginia, Xindian District. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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