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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.
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
| Field | Value |
|---|---|
| Enrollment Target | 22 participants |
| Start Date | 2021-01-14 |
| Est. Completion | 2023-02-28 |
| Phase | Phase 1 |
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.
Learn More About Clinical Trials
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
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