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NCT06963281 · ClinicalTrials.gov registry record · Phase 1

Study of IBI3020 Treatment in Participants With Late-Stage Solid Tumors

A Phase 1 study of Solid Tumors, sponsored by Innovent Biopharmaceutical Technology (Hangzhou) Co..

Recruiting
Registry status
Phase 1
Development phase
285
Enrollment target
9
Study locations

NCT06963281 is a Phase 1 study of Solid Tumors that is actively recruiting participants, run by Innovent Biopharmaceutical Technology (Hangzhou) Co.. The registered enrollment target is 285 participants, roughly in line with the 282-participant average among 125 other Solid Tumors trials with a reported enrollment target. The trial reports 9 study locations across 8 states.

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The verdict

NCT06963281, a Phase 1 study of Solid Tumors, is actively recruiting participants, sponsored by Innovent Biopharmaceutical Technology (Hangzhou) Co..

RECRUITING
Registry status
Phase 1
Development phase
285 participants
Enrollment target
9
Study locations

Study Summary

The main purpose of this study is to evaluate the safety and tolerability of IBI3020 and to determine the maximum tolerated dose (MTD) and/or the recommended dose for expansion (RP2D) of IBI3020.

Conditions Studied

Interventions

  • DRUG IBI3020

Study Locations (9)

Texas

  • NEXT Houston - Houston
  • NEXT Dallas - Irving

Arizona

  • Mayo Clinic - Arizona - Pheonix

Florida

  • Mayo Clinic - Florida - Jacksonville

Minnesota

  • Mayo Clinic - Rochester - Rochester

New York

  • Montefiore Cancer Center - New York

Guangdong

  • The sixth affiliated hospital, Sun Yat-sen University - Guangzhou

Shandong

  • Shandong Cancer Hospital - Jinan

Shanxi

  • Shanxi Cancer Hospital - Taiyuan

Trial Details

FieldValue
Enrollment Target 285 participants
Start Date 2025-04-29
Est. Completion 2028-03-31
Phase Phase 1

What the Registry Record Tells You About NCT06963281

The ClinicalTrials.gov registry entry for NCT06963281 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 285 participants, a figure that helps gauge the scale of data the investigators plan to collect, roughly in line with the 282-participant average among 125 other Solid Tumors trials with a reported enrollment target. The listed sponsor is Innovent Biopharmaceutical Technology (Hangzhou) Co., which has 1 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Solid Tumors appearing as the primary indexed condition, and to 1 intervention - of which IBI3020 is the first listed.

NCT06963281 reports 9 study locations spanning 8 distinct geographic areas - top geographies include Texas, Arizona, Florida.

Frequently Asked Questions

What is clinical trial NCT06963281 about?

NCT06963281 is a clinical study titled "Study of IBI3020 Treatment in Participants With Late-Stage Solid Tumors". The main purpose of this study is to evaluate the safety and tolerability of IBI3020 and to determine the maximum tolerated dose (MTD) and/or the recommended dose for expansion (RP2D) of IBI3020.

What is the current status of trial NCT06963281?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 285 participants. The study started on 2025-04-29. Estimated completion is 2028-03-31.

What conditions does trial NCT06963281 study?

This clinical trial studies the following conditions: Solid Tumors.

What interventions are being tested in trial NCT06963281?

The interventions under investigation include: IBI3020 (DRUG).

Who is sponsoring clinical trial NCT06963281?

This trial is sponsored by Innovent Biopharmaceutical Technology (Hangzhou) Co., which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06963281 being conducted?

This trial has 9 study locations across Arizona, Florida, Minnesota, New York, Texas. 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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.