# Addressing Critical Knowledge Gaps in Early Diffuse Scleroderma Trial Design

> **NIH NIH R01** · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · 2020 · $206,580

## Abstract

Project Summary/Abstract
The overall goal of this proposal is to improve clinical trial design for early diffuse systemic
sclerosis (SSc) patients by using a clinical observational cohort to address three crucial gaps in
knowledge. These three critical knowledge gaps include 1) how disease duration should be
optimally defined as an inclusion criterion for trials using skin change as a primary outcome, 2) if
trial design or analysis should be stratified by SSc-associated autoantibody, and 3) the effect
size of mycophenolate mofetil (MMF) on skin thickness score in early diffuse SSc. Specific Aim
1 will determine the most appropriate definition of disease onset, first non-Raynaud symptom
compared to the first SSc-attributable symptom, by which to define disease duration as a clinical
trial inclusion criterion. Specific Aim 2 will then establish if clinical trials may be improved
through stratification of trial participants by SSc-associated autoantibody (anti-Scl70 or anti-RNA
polymerase 3). For Specific Aims 1 and 2, the already existing, prospectively collected clinical
observational cohort of the University of Pittsburgh Scleroderma Center will be used for
analysis. In Specific Aim 3 an observational cohort of early diffuse SSc patients treated with
MMF will be created and made available for future trial use with information on disease
characteristics, medication use and skin scores over a one year period. To accomplish this, the
pre-existing and prospectively followed cohort of early diffuse SSc patients treated with MMF in
the Pittsburgh database will be combined with a newly recruited additional cohort of early diffuse
SSc patients treated with MMF to form an observational hybrid cohort. The newly-recruited
patients will enrich the follow-up skin score data taken at 3-month time intervals and add
samples for skin gene expression. We will perform a matched analysis of the MMF-treated
hybrid cohort to our historical non-MMF treated early diffuse SSc patients and assess the effect
size of MMF on skin at 6 and 12 months of therapy. Potential applications of a MMF-treated
cohort are as a comparator or control group for future open label studies of potential
therapeutics for early diffuse SSc or to assess the effect of new investigational drugs in early
phase trials when MMF is allowed as ongoing background therapy. The knowledge gained from
each of the proposal Aims can be applied to both ongoing early diffuse SSc clinical trials and
trials in the planning stage.

## Key facts

- **NIH application ID:** 9685112
- **Project number:** 5R01AR069874-03
- **Recipient organization:** UNIVERSITY OF PITTSBURGH AT PITTSBURGH
- **Principal Investigator:** Robyn Therese Domsic
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $206,580
- **Award type:** 5
- **Project period:** 2017-04-01 → 2022-02-28

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/9685112

## Citation

> US National Institutes of Health, RePORTER application 9685112, Addressing Critical Knowledge Gaps in Early Diffuse Scleroderma Trial Design (5R01AR069874-03). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/9685112. Licensed CC0.

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