CClinicalTrials.gg
Status unknownNCT04904315STAMP-2Updated May 27, 2021

Subjects Through the Application of the Mindera Kit Part 2

An observational study in Psoriasis, sponsored by Mindera Health. Status unknown. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2021-05-27.

Sponsored by Mindera Health · Observational

The sponsor has not verified this record recently (last verified May 2021), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
100
Ages
18 Years and older
Sex
All
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Study summary

A 16 week study to examine if baseline or on-therapy transcriptomics can be used to help predict selection of medications and provide new therapeutic targets for drug development in psoriasis subjects.

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Conditions studied

  • Psoriasis

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03

In context

Psoriasis

1,899 studies on the registry are indexed under Psoriasis; 233 are open to participants now.

This study's planned enrollment of 100 is below the median of 200 across 396 observational studies indexed under Psoriasis.

Browse Psoriasis studies →

Lead sponsor

Mindera Health is the lead sponsor of 2 studies on the registry; none are open to participants now.

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

Male and female subjects who are 18 years of age or older with a diagnosis of psoriasis.

Inclusion criteria

  1. Subject must have the ability to understand and sign written informed consent.
  2. Subject must be an adult male or female adult who is ≥ 18 years of age at the time of screening.
  3. Subject must be diagnosed with psoriasis by either a dermatologist or a rheumatologist, with the affected area of ≥ 2 centimeters in diameter.
  4. Subjects must be treated with anti-TNF-α (or biosimilar) therapy once enrolled in the study.A two-week period is required to washout of the previous biologic when switching therapies.

Exclusion criteria

Exclusion Criteria

  1. Subject is unable or unwilling to give written informed consent and/or to comply with study procedures.
  2. Subject has had usage of topical psoriasis treatments on study lesion within 2 weeks prior to baseline studyvisit and unwilling to washout.
  3. Subjects currently treated with Hydroxychloroquine (Plaquenil), unless otherwise approved by Sponsor
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
100 participants (estimated)
Patient registry
No

Interventions

  • OtherMindera Kit

    The entire duration of the study, including the screening period, will be approximately 16 weeks. Mindera Kit will be applied with applicator and left on the skin for 5 minutes, and once removed, the investigational product (IP) will be placed in a buffer solution, sealed, labeled and sent to Mindera for processing.

    Also known as: MK Patch, Microdermal Patch

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What researchers measure

Primary outcomes

  1. Observation of on therapy transcriptomics to potentially aid in new therapeutic targets

    To examine if baseline or on-therapy transcriptomics can be used to help predict selection of medications and provide new therapeutic targets for drug development in psoriasis subjects by collecting RNA and examining changes in PASI scores at the Week 4, 12, and 16 timepoints.

    Time frame: 16 weeks

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: No — In order to protect patient privacy genetic data will not be shared outside of the study without further patient consent to do so. If other researchers would like access to the data they must reach out to the patients themselves.

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 May 27, 2021, 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
NCT04904315
Lead sponsor
Mindera Health
Responsible party
Sponsor
First posted
May 27, 2021
Start date
Aug 1, 2021 (estimated)
Primary completion
Jan 1, 2022 (estimated)
Completion
May 30, 2022 (estimated)
Last update
May 27, 2021

Study contacts

Courtney Boyce
Contact
cboyce@minderadx.com
231-994-3848
Paul Montgomery
Contact
pmontgomery@minderadx.com
513-706-8614
Toby Dickerson
study chair · CSO

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 status unknown, as verified in May 2021. You cannot join it, but the record below documents what was studied.

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