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NCT03289273 · ClinicalTrials.gov registry record

Observational Study to Evaluate, Under Real-world Practice Conditions, the Safety and Effectiveness of Regorafenib in Patients Diagnosed With Unresectable Hepatocellular Carcinoma (uHCC)

A clinical trial, sponsored by Bayer.

Completed
Registry status
1,010
Enrollment target

NCT03289273: Completed study, sponsored by Bayer.

NCT03289273 is a clinical trial that has completed, run by Bayer. The registered enrollment target is 1,010 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03289273 has completed, sponsored by Bayer.

COMPLETED
Registry status
1,010 participants
Enrollment target

Study Summary

Observational study to evaluate, under real-world practice conditions, the safety and effectiveness of regorafenib in patients diagnosed with unresectable hepatocellular carcinoma (uHCC)

Primary Outcome

The primary endpoint is the safety of regorafenib in patients with uHCC, defined as the frequency of documented TEAEs, including serious adverse events (SAEs). Safety will be assessed in all patients who receive at least one dose of regorafenib regardless of prior treatment.

Interventions

  • DRUG Regorafenib (Stivarga, BAY73-4506)

Trial Details

FieldValue
Enrollment Target 1,010 participants
Start Date 2017-09-13
Est. Completion 2022-06-21
Bayer

591 total trials

What the finished NCT03289273 record still lists

NCT03289273 is an observational study that tracks outcomes without assigning an intervention. Its 1,010 participants enrollment target places it among the larger protocols in the corpus.

The record links to 0 conditions, and to 1 intervention - of which Regorafenib (Stivarga, BAY73-4506) is the first listed.

NCT03289273 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03289273 about?

NCT03289273 is a clinical study titled "Observational Study to Evaluate, Under Real-world Practice Conditions, the Safety and Effectiveness of Regorafenib in Patients Diagnosed With Unresectable Hepatocellular Carcinoma (uHCC)". Observational study to evaluate, under real-world practice conditions, the safety and effectiveness of regorafenib in patients diagnosed with unresectable hepatocellular carcinoma (uHCC)

What is the current status of trial NCT03289273?

This trial is currently completed. The enrollment target is 1,010 participants. The study started on 2017-09-13. Estimated completion is 2022-06-21.

What interventions are being tested in trial NCT03289273?

The interventions under investigation include: Regorafenib (Stivarga, BAY73-4506) (DRUG).

Who is sponsoring clinical trial NCT03289273?

This trial is sponsored by Bayer, which has 591 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT03289273, the US trial registry maintained by the National Library of Medicine. NCT03289273 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.