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Observational Study for Patients at Risk for Chronic Graft-Versus-Host Disease

A Prospective, Observational Cohort Study of Participants at Risk for Chronic Graft-Versus-Host Disease in the United States (THRIVE)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05919511
Acronym
THRIVE
Enrollment
1500
Registered
2023-06-26
Start date
2023-08-01
Completion date
2027-10-15
Last updated
2026-08-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cGVHD

Keywords

chronic graft versus host disease, cGVHD, MA-GVHD-401, THRIVE, GVHD, chronic GVHD, allogenic stem cell transplant (alloSCT)

Brief summary

The purpose of this prospective observational study is to collect data from participants who have recently had an allogenic Stem Cell Transplant(alloSCT) and are at risk of Chronic Graft Versus Host Disease(cGVHD)

Interventions

OTHERNon-Interventional

This is an observational study

Sponsors

Incyte Corporation
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years inclusive at the time of signing the ICF * Allogeneic SCT 90 to 180 days prior to enrollment * Able to comprehend and willing to provide informed consent * Willing and able to complete participant-assessment questionnaires either alone or with minimal assistance from a caregiver and/or trained site personnel

Exclusion criteria

* There are no

Design outcomes

Primary

MeasureTime frame
Overall Burden of cGVHD diagnosis and severity36 months

Secondary

MeasureTime frame
To describe personal and healthcare resources associated with the management of cGVHD36 months
To describe changes in the proteomic, cytologic and molecular profile in blood, serum and saliva cGVHDUp to 36 months

Countries

United States

Contacts

CONTACTIncyte Corporation Call Center (US)
medinfo@incyte.com1.855.463.3463
CONTACTIncyte Corporation Call Center (ex-US)
eumedinfo@incyte.com+800 00027423

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 26, 2026