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Active, not recruitingNCT03728842Updated Oct 27, 2025

Spontaneous Regression in Metastatic Melanoma and Renal Cell Carcinoma

An observational study in Melanoma; Renal Cell Carcinoma, sponsored by Indiana University. Active, not recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-10-27.

Sponsored by Indiana University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
19
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to collect blood and clinical data from patients with metastatic melanoma and renal cell cancer who have experienced spontaneous regression for studies of immune response and other factors that may influence these occurrences.

Read the detailed description

Spontaneous regression in patients with metastatic cancer is an incredibly rare event. It has been described after infection in cancer patients and also rarely in patients with renal cell cancer (usually after resection of the renal primary) and, less commonly, in patients with metastatic melanoma.

Primary Objective To collect peripheral blood from patients with metastatic melanoma and renal cell cancer and spontaneous regression for studies of immune response and other studies.

Secondary Objective To collect clinical data from subjects registered to this study. Clinical data collection will include demographics and cancer characteristics, history and treatment.

02

Conditions studied

  • Melanoma; Renal Cell Carcinoma

Keywords

  • metastatic disease
  • spontaneous regression
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In context

Melanoma

3,006 studies on the registry are indexed under Melanoma; 520 are open to participants now.

This study's enrollment of 19 is below the median of 182 across 438 observational studies indexed under Melanoma.

Browse Melanoma studies →

Lead sponsor

Indiana University is the lead sponsor of 958 studies on the registry; 200 are open to participants now.

Of its 142 completed or terminated interventional studies of FDA-regulated products, 112 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with metastatic melanoma and renal cell cancer and spontaneous regression.

Inclusion criteria

  1. ≥ 18 years old at the time of informed consent
  2. Ability to provide written informed consent and HIPAA authorization
  3. Patients must have metastatic melanoma or renal cell cancer with spontaneous regression.
  4. Willingness to undergo phlebotomy for research blood samples

Exclusion criteria

Exclusion Criteria

  1. Concurrent disease or condition that would make the patient inappropriate for study participation or any serious medical or psychiatric disorder that would interfere with the subject's safety
  2. Dementia, altered mental status, or any psychiatric condition that would prohibit the understanding or rendering of informed consent
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
19 participants (actual)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Spontaneous regression

    Patients must have metastatic melanoma or renal cell cancer with spontaneous regression.

    Other: Blood collection for laboratory studies · Other: Data collection from medical record

Interventions

  • OtherBlood collection for laboratory studies

    Peripheral whole blood will be collected

  • OtherData collection from medical record

    Clinical data such as demographics and cancer characteristics, history and treatment will be collected

06

What researchers measure

Primary outcomes

  1. Number of blood samples collected

    samples collected from metastatic melanoma and renal cell cancer patients

    Time frame: 1 year

07

Study locations

1 site
  • Indiana University Simon Cancer Center
    Indianapolis, Indiana 46202, United States
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 27, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03728842
Lead sponsor
Indiana University
Responsible party
Theodore Logan (Associate Professor of Medicine, Indiana University) — Principal investigator
First posted
Nov 2, 2018
Start date
Jan 4, 2004
Primary completion
Mar 1, 2027 (estimated)
Completion
Mar 1, 2027 (estimated)
Last update
Oct 27, 2025

Study contacts

Theodore Logan, MD
principal investigator · Indiana University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Oct 2025. You cannot join it, but the record below documents what was studied.

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