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Not listed No phase listed Observational

Chemotherapy Induced Peripheral Neuropathy Natural History Study (EPIPHANY)

ClinicalTrials.gov ID: NCT03997981

Public ClinicalTrials.gov record NCT03997981. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 5:52 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a prospective natural history study of CIPN in approximately 200 participants receiving taxanes (paclitaxel, docetaxel) for breast cancer, bortezomib for multiple myeloma, oxaliplatin-based regimens for colorectal cancer, or vincristine for lymphoma.. Demographic data, medical history, electronic PROs, ClinROs blood biomarkers including NF-L, PGx DNA analyses and Bedside-QST will be assessed at Baseline. The Observation Period will initiate with the first dose of chemotherapy and conclude with the last dose of chemotherapy. During the Observation Period, participants will be evaluated for the development of CIPN using PROs and ClinROs. Blood biomarkers and Bedside-QST will be measured at various timepoints corresponding with treatment regimen schedules throughout the observation period. The Post Chemotherapy Follow-up Period will begin with the first visit after the last dose of chemotherapy and conclude 6 months after the last dose of chemotherapy. During the Post Chemotherapy Follow-up Period, participants will be evaluated for CIPN using PROs and ClinROs. Blood biomarkers and Bedside-QST will also be measured at the beginning and at the end of the Post-Chemotherapy Follow-up Period. PROs will be assessed electronically on a monthly basis.

Study identification

NCT ID
NCT03997981
Recruitment status
Not listed
Study type
Observational
Phase
Not listed
Lead sponsor
Disarm Therapeutics
Industry
Enrollment
200 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 2, 2019
Primary completion
Mar 30, 2024
Completion
Apr 8, 2024
Last update posted
Feb 29, 2024

2019 – 2024

United States locations

U.S. sites
10
U.S. states
9
U.S. cities
9
Facility City State ZIP Site status
Alpha Oncology Research LLC DeBary Florida 32713 Completed
University of Maryland School of Medicine Baltimore Maryland 21201-1544 Recruiting
Johns Hopkins University School of Medicine Baltimore Maryland 21287 Not yet recruiting
University of Michigan Ann Arbor Michigan 48109-0400 Recruiting
Mayo Clinic Rochester Minnesota 55905-0002 Completed
Washington University Medical School St Louis Missouri 63110 Completed
Ohio State University Columbus Ohio 43212 Completed
University of Pensylvania Hospital Philadelphia Pennsylvania 19104 Recruiting
University of Vermont Medical Center Burlington Vermont 05401 Recruiting
VCU Medical Center Richmond Virginia 23298 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03997981, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 29, 2024 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03997981 live on ClinicalTrials.gov.

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