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Predicting Medication Response for Autoimmune Disease (REEF)

C

Coral Genomics

Status

Terminated

Conditions

Psoriasis
Ulcerative Colitis
Crohn's Disease
Rheumatoid Arthritis

Treatments

Diagnostic Test: Coral FRS test

Study type

Observational

Funder types

Industry
NIH

Identifiers

NCT04995783
2R44HG010445-02 (U.S. NIH Grant/Contract)
20201349

Details and patient eligibility

About

Coral is conducting a large study comparing and predicting the relative effectiveness of different medications for autoimmune patients.

Patients with Inflammatory Bowel Disease (IBD) who have been diagnosed with either Ulcerative Colitis or Crohn's Disease and are undergoing treatment are eligible to participate.

Patients with Rheumatoid Arthritis (RA) and Psoriasis (Ps) will also be enrolled.

A novel clinical test will be performed to predict the responsiveness of a particular patient to different immune modulating therapies used in these conditions.

Enrollment

200 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Ulcerative Colitis, Crohn's Disease, Rheumatoid Arthritis, Psoriasis diagnosis
  • On or about to begin a treatment for condition above

Trial design

200 participants in 5 patient groups

Ulcerative Colitis
Treatment:
Diagnostic Test: Coral FRS test
Crohn's Disease
Treatment:
Diagnostic Test: Coral FRS test
Rheumatoid Arthritis
Treatment:
Diagnostic Test: Coral FRS test
Psoriasis
Treatment:
Diagnostic Test: Coral FRS test
Control

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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