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

NCT01711684 · ClinicalTrials.gov registry record · Phase 1

Treatment of Cutaneous Metastases With Diphenylcyclopropenone (DPCP)

A Phase 1 study, sponsored by Rockefeller University.

Completed
Registry status
Phase 1
Development phase
6
Enrollment target

NCT01711684: Completed Phase 1 study, sponsored by Rockefeller University.

NCT01711684 is a Phase 1 study that has completed, run by Rockefeller University. The registered enrollment target is 6 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01711684, a Phase 1 study, has completed, sponsored by Rockefeller University.

COMPLETED
Registry status
Phase 1
Development phase
6 participants
Enrollment target

Study Summary

Melanoma is a life-threatening cancer which poses a significant health burden, especially when metastatic or spreading to areas other than the original tumor growth. Although various treatment options are currently available for melanoma, melanomas that have metastasized widely to the skin pose a significant clinical challenge as the available therapies have limited effect. This study proposes the use of a topically applied compound named diphenylcyclopropenone (DPCP) which has been shown to be effective in treating melanoma patients whose diseases have spread widely throughout the skin. DPCP works by having a patient's own immune system, which is usually used to fight infections, attack cancerous cells. This compound has commonly been used to treat other conditions such as warts and hair loss throughout the world for many years and is known to cause limited side effects. Altering a patient's own immune system through topical treatments has also been shown to benefit patients with other cancers that have metastasized to skin such as breast cancer. In this study, the investigators will use DPCP to treat cutaneous metastases of various cancers including melanoma. Our overall intention is to get a better understanding of effective immune responses in the skin that may mediate metastatic cancer regression or cure.

Interventions

  • DRUG Diphenylcyclopropenone (DPCP)

Trial Details

FieldValue
Enrollment Target 6 participants
Start Date 2012-10-16
Est. Completion 2015-06-22
Phase Phase 1
Rockefeller University

117 total trials

What the finished NCT01711684 record still lists

NCT01711684 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 6 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (90% lower).

The record links to 0 conditions, and to 1 intervention - of which Diphenylcyclopropenone (DPCP) is the first listed.

NCT01711684 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01711684 about?

NCT01711684 is a clinical study titled "Treatment of Cutaneous Metastases With Diphenylcyclopropenone (DPCP)". Melanoma is a life-threatening cancer which poses a significant health burden, especially when metastatic or spreading to areas other than the original tumor growth. Although various treatment options are currently available for melanoma, melanomas that have metastasized widely to the skin pose a si...

What is the current status of trial NCT01711684?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 6 participants. The study started on 2012-10-16. Estimated completion is 2015-06-22.

What interventions are being tested in trial NCT01711684?

The interventions under investigation include: Diphenylcyclopropenone (DPCP) (DRUG).

Who is sponsoring clinical trial NCT01711684?

This trial is sponsored by Rockefeller University, which has 117 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01711684's enrollment target sits among peer trials

6 1974th of 2000 higher than 12 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

Nationwide trials with similar profiles

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

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT01711684, the US trial registry maintained by the National Library of Medicine. NCT01711684 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.