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NCT03113188 · ClinicalTrials.gov registry record · Phase 1

CBP501, Cisplatin and Nivolumab in Advanced Refractory Tumors

A Phase 1 study, sponsored by CanBas Co..

Completed
Registry status
Phase 1
Development phase
47
Enrollment target

NCT03113188: Completed Phase 1 study, sponsored by CanBas Co..

NCT03113188 is a Phase 1 study that has completed, run by CanBas Co.. The registered enrollment target is 47 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (22% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03113188, a Phase 1 study, has completed, sponsored by CanBas Co..

COMPLETED
Registry status
Phase 1
Development phase
47 participants
Enrollment target

Study Summary

This is a multicenter, open-label, phase 1b study of CBP501/cisplatin/nivolumab combination administered once every 21 days to patients with advanced solid tumors.

Primary Outcome

Define the recommended doses (RP2D) of CBP501, cisplatin and nivolumab when administered in combination once every 21 days in patients with previously treated advanced solid tumors

Interventions

  • DRUG CBP501

Trial Details

FieldValue
Enrollment Target 47 participants
Start Date 2017-10-25
Est. Completion 2021-02-15
Phase Phase 1
CanBas Co.

5 total trials

What the finished NCT03113188 record still lists

NCT03113188 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 47 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (22% lower).

The record links to 0 conditions, and to 1 intervention - of which CBP501 is the first listed.

NCT03113188 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03113188 about?

NCT03113188 is a clinical study titled "CBP501, Cisplatin and Nivolumab in Advanced Refractory Tumors". This is a multicenter, open-label, phase 1b study of CBP501/cisplatin/nivolumab combination administered once every 21 days to patients with advanced solid tumors.

What is the current status of trial NCT03113188?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 47 participants. The study started on 2017-10-25. Estimated completion is 2021-02-15.

What interventions are being tested in trial NCT03113188?

The interventions under investigation include: CBP501 (DRUG).

Who is sponsoring clinical trial NCT03113188?

This trial is sponsored by CanBas Co., which has 5 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03113188's enrollment target sits among peer trials

47 1053rd of 2000 higher than 943 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 NCT03113188, the US trial registry maintained by the National Library of Medicine. NCT03113188 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.