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NCT02279719 · ClinicalTrials.gov registry record · Phase 1

A Study of BBI608 in Combination With Sorafenib, or BBI503 in Combination With Sorafenib in Adult Patients With Hepatocellular Carcinoma

A Phase 1 study, sponsored by Sumitomo Pharma America.

Completed
Registry status
Phase 1
Development phase
97
Enrollment target

NCT02279719: Completed Phase 1 study, sponsored by Sumitomo Pharma America.

NCT02279719 is a Phase 1 study that has completed, run by Sumitomo Pharma America. The registered enrollment target is 97 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (62% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02279719, a Phase 1 study, has completed, sponsored by Sumitomo Pharma America.

COMPLETED
Registry status
Phase 1
Development phase
97 participants
Enrollment target

Study Summary

This is an open label, three-arm, phase 1 dose escalation study and phase 2 study of BBI608 in combination with sorafenib, or BBI503 in combination with sorafenib. The study population is adult patients with advanced hepatocellular carcinoma who have not received systemic chemotherapy.

Primary Outcome

To assess the dose limiting toxicities for phase IB

Interventions

  • DRUG Sorafenib
  • DRUG BBI608
  • DRUG BBI503

Trial Details

FieldValue
Enrollment Target 97 participants
Start Date 2014-12
Est. Completion 2019-10
Phase Phase 1
Sumitomo Pharma America

168 total trials

What the finished NCT02279719 record still lists

NCT02279719 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 97 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (62% higher).

The record links to 0 conditions, and to 3 interventions - of which Sorafenib is the first listed.

NCT02279719 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02279719 about?

NCT02279719 is a clinical study titled "A Study of BBI608 in Combination With Sorafenib, or BBI503 in Combination With Sorafenib in Adult Patients With Hepatocellular Carcinoma". This is an open label, three-arm, phase 1 dose escalation study and phase 2 study of BBI608 in combination with sorafenib, or BBI503 in combination with sorafenib. The study population is adult patients with advanced hepatocellular carcinoma who have not received systemic chemotherapy.

What is the current status of trial NCT02279719?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 97 participants. The study started on 2014-12. Estimated completion is 2019-10.

What interventions are being tested in trial NCT02279719?

The interventions under investigation include: Sorafenib (DRUG), BBI608 (DRUG), BBI503 (DRUG).

Who is sponsoring clinical trial NCT02279719?

This trial is sponsored by Sumitomo Pharma America, which has 168 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02279719's enrollment target sits among peer trials

97 597th of 2000 higher than 1,401 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 NCT02279719, the US trial registry maintained by the National Library of Medicine. NCT02279719 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.