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

NCT04338659 · ClinicalTrials.gov registry record · Phase 1

A Phase 1a Study Evaluating the Safety, Tolerability, and Efficacy of IBI322 in Subjects With Advanced Cancers

A Phase 1 study, sponsored by Innovent Biologics (Suzhou) Co..

Completed
Registry status
Phase 1
Development phase
22
Enrollment target

NCT04338659: Completed Phase 1 study, sponsored by Innovent Biologics (Suzhou) Co..

NCT04338659 is a Phase 1 study that has completed, run by Innovent Biologics (Suzhou) Co.. The registered enrollment target is 22 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (63% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04338659, a Phase 1 study, has completed, sponsored by Innovent Biologics (Suzhou) Co..

COMPLETED
Registry status
Phase 1
Development phase
22 participants
Enrollment target

Study Summary

This is a phase I study evaluating the safety, tolerability and preliminary efficacy of IBI322 in cancer subjects who failed standard treatment.

Interventions

  • BIOLOGICAL IBI322 Recombinant anti-human CD47/PD-L1 bispecific antibody injection

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2021-01-14
Est. Completion 2023-02-28
Phase Phase 1
Innovent Biologics (Suzhou) Co.

7 total trials

What the finished NCT04338659 record still lists

NCT04338659 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 22 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (63% lower).

The record links to 0 conditions, and to 1 intervention - of which IBI322 Recombinant anti-human CD47/PD-L1 bispecific antibody injection is the first listed.

NCT04338659 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04338659 about?

NCT04338659 is a clinical study titled "A Phase 1a Study Evaluating the Safety, Tolerability, and Efficacy of IBI322 in Subjects With Advanced Cancers". This is a phase I study evaluating the safety, tolerability and preliminary efficacy of IBI322 in cancer subjects who failed standard treatment.

What is the current status of trial NCT04338659?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 22 participants. The study started on 2021-01-14. Estimated completion is 2023-02-28.

What interventions are being tested in trial NCT04338659?

The interventions under investigation include: IBI322 Recombinant anti-human CD47/PD-L1 bispecific antibody injection (BIOLOGICAL).

Who is sponsoring clinical trial NCT04338659?

This trial is sponsored by Innovent Biologics (Suzhou) Co., which has 7 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04338659's enrollment target sits among peer trials

22 1601st of 2000 higher than 386 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02508038 · 22 participants · Phase 1

    Alpha/Beta CD19+ Depleted Haploidentical Transplantation + Zometa for Pediatric Hematologic Malignancies and Solid Tumors

  • NCT03099356 · 22 participants · Phase 2

    Cyclophosphamide and Sirolimus for the Treatment of Metastatic, RAI-refractory, Differentiated Thyroid Cancer

  • NCT03676647 · 22 participants

    Diagnostic DNA Methylation Signature in Diagnosing Thyroid Cancer After Fine-Needle Aspiration in Patients With Thyroid Nodules

  • NCT04569591 · 22 participants · NA

    DDAVP for Pituitary Adenoma

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT04338659, the US trial registry maintained by the National Library of Medicine. NCT04338659 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.