Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02306850 · ClinicalTrials.gov registry record · Phase 2

Neoadjuvant Pembrolizumab for Unresectable Stage III and Unresectable Stage IV Melanoma

A Phase 2 study, sponsored by St. Louis University.

Completed
Registry status
Phase 2
Development phase
10
Enrollment target

NCT02306850: Completed Phase 2 study, sponsored by St. Louis University.

NCT02306850 is a Phase 2 study that has completed, run by St. Louis University. The registered enrollment target is 10 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02306850, a Phase 2 study, has completed, sponsored by St. Louis University.

COMPLETED
Registry status
Phase 2
Development phase
10 participants
Enrollment target

Study Summary

This study is being done to see if using the study drug, pembrolizumab, can shrink down melanoma tumors enough so that they will be small enough to cut out, so that there will be no cancer left in the body. Eligible participants include those who have not received any systemic melanoma therapies (i.e. participants do not have to fail ipilimumab or BRAF inhibitor) and those who have failed all available systemic options (if the participant meets other inclusion / exclusion criteria).

Primary Outcome

'Resectability rate' is defined as the proportion of subjects in the trial that were unresectable at baseline who after treatment with pembrolizumab are now eligible for curative resection with complete metastectomy. The primary endpoint "resectability rate" is merely a novel statistical approach; it has no bearing on the duration of treatment that an individual patient may receive during the trial.

Interventions

  • DRUG Pembrolizumab

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2015-01
Est. Completion 2018-06-08
Phase Phase 2
St. Louis University

107 total trials

What the finished NCT02306850 record still lists

NCT02306850 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower).

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

NCT02306850 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02306850 about?

NCT02306850 is a clinical study titled "Neoadjuvant Pembrolizumab for Unresectable Stage III and Unresectable Stage IV Melanoma". This study is being done to see if using the study drug, pembrolizumab, can shrink down melanoma tumors enough so that they will be small enough to cut out, so that there will be no cancer left in the body. Eligible participants include those who have not received any systemic melanoma therapies (i...

What is the current status of trial NCT02306850?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 10 participants. The study started on 2015-01. Estimated completion is 2018-06-08.

What interventions are being tested in trial NCT02306850?

The interventions under investigation include: Pembrolizumab (DRUG).

Who is sponsoring clinical trial NCT02306850?

This trial is sponsored by St. Louis University, which has 107 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02306850's enrollment target sits among peer trials

10 1968th of 2000 higher than 12 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00623389 · 10 participants · NA

    Evaluation of an Advanced Lower Extremity Neuroprostheses

  • NCT01241864 · 10 participants · Phase 2

    Islet Transplantation in Type 1 Diabetic Kidney Allograft

  • NCT01293214 · 10 participants · NA

    Vascularized Composite Allotransplantation for Multiple Extremity Amputations

  • NCT01474148 · 10 participants · NA

    A Neuroprosthesis for Seated Posture and Balance

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02306850, the US trial registry maintained by the National Library of Medicine. NCT02306850 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.