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NCT03290079 · ClinicalTrials.gov registry record · Phase 2

Phase II Study of Pembrolizumab and Lenvatinib in Advanced Well-differentiated Neuroendocrine Tumors

A Phase 2 study, sponsored by H. Lee Moffitt Cancer Center and Research Institute.

Completed
Registry status
Phase 2
Development phase
20
Enrollment target

NCT03290079: Completed Phase 2 study, sponsored by H. Lee Moffitt Cancer Center and Research Institute.

NCT03290079 is a Phase 2 study that has completed, run by H. Lee Moffitt Cancer Center and Research Institute. The registered enrollment target is 20 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03290079, a Phase 2 study, has completed, sponsored by H. Lee Moffitt Cancer Center and Research Institute.

COMPLETED
Registry status
Phase 2
Development phase
20 participants
Enrollment target

Study Summary

The purpose of this study is to: * Assess overall radiographic response rate (ORR) * Assess progression-free survival (PFS) * Test the safety and tolerability of Pembrolizumab in combination with lenvatinib

Primary Outcome

Response Evaluation Criteria in Solid Tumors (RECIST) based response rate. Complete Response (CR): Disappearance of all extranodal target lesions. All pathological lymph nodes must have decreased to \<10 mm in short axis. Partial Response (PR): At least a 30% decrease in the sum of the longest diameter (SLD) of target lesions, taking as reference the baseline sum diameters. Progressive Disease (PD): SLD increased by at least 20% from the smallest value on study (including baseline, if that is th

Interventions

  • DRUG Pembrolizumab
  • DRUG Lenvatinib

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2017-12-15
Est. Completion 2024-05-13
Phase Phase 2

What the finished NCT03290079 record still lists

NCT03290079 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower).

The record links to 0 conditions, and to 2 interventions - of which Pembrolizumab is the first listed.

NCT03290079 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03290079 about?

NCT03290079 is a clinical study titled "Phase II Study of Pembrolizumab and Lenvatinib in Advanced Well-differentiated Neuroendocrine Tumors". The purpose of this study is to: * Assess overall radiographic response rate (ORR) * Assess progression-free survival (PFS) * Test the safety and tolerability of Pembrolizumab in combination with lenvatinib

What is the current status of trial NCT03290079?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 20 participants. The study started on 2017-12-15. Estimated completion is 2024-05-13.

What interventions are being tested in trial NCT03290079?

The interventions under investigation include: Pembrolizumab (DRUG), Lenvatinib (DRUG).

Who is sponsoring clinical trial NCT03290079?

This trial is sponsored by H. Lee Moffitt Cancer Center and Research Institute, which has 502 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03290079's enrollment target sits among peer trials

20 1805th of 2000 higher than 107 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT03290079, the US trial registry maintained by the National Library of Medicine. NCT03290079 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.