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Diffuse Scleroderma clinical trials at UCLA

10 in progress, 4 open to eligible people

Showing trials for
  • Belimumab in Adults With Systemic Sclerosis Associated Interstitial Lung Disease

    open to eligible people ages 18 years and up

    This study investigates the efficacy and safety of belimumab compared to placebo, in addition to standard therapy, for the treatment of participants with systemic sclerosis associated interstitial lung disease (SSc-ILD). The study will evaluate the effect of belimumab treatment on lung function as well as on extra-pulmonary disease manifestations, including skin thickening and general symptoms, such as fatigue, that impact quality of life (QoL).

    Los Angeles, California and other locations

  • EncompaSSc: Evaluation of MTX-474 in Participants With Diffuse Cutaneous Systemic Sclerosis (dcSSc)

    open to eligible people ages 18 years and up

    A Phase 2 Randomized, Double-blind, Placebo-Controlled Study of the Safety and Efficacy of MTX-474 in Participants with Diffuse Cutaneous Systemic Sclerosis (dcSSc)

    Newport Beach, California and other locations

  • Evaluate Ianalumab in Participants With Diffuse Cutaneous Systemic Sclerosis

    open to eligible people ages 18-70

    The purpose of this study is to evaluate efficacy, safety and tolerability of s.c. ianalumab administered in participants with diffuse cutaneous systemic sclerosis relative to placebo

    Los Angeles, California and other locations

  • Rapcabtagene Autoleucel in Participants With Diffuse Cutaneous Systemic Sclerosis

    open to eligible people ages 18-70

    The purpose of this study is to evaluate the efficacy, safety and tolerability of rapcabtagene autoleucel (administered once following lymphodepletion) in participants with severe refractory diffuse cutaneous systemic sclerosis relative to rituximab.

    Los Angeles, California and other locations

  • BMS-986278 in Participants With Progressive Pulmonary Fibrosis

    Sorry, in progress, not accepting new patients

    The purpose of this study is to evaluate the efficacy, safety, and tolerability of BMS-986278 in Participants with Progressive Pulmonary Fibrosis.

    Los Angeles, California and other locations

  • Determine Effectiveness of Anifrolumab In SYstemic Sclerosis (DAISY)

    Sorry, in progress, not accepting new patients

    The purpose of this study is to evaluate the efficacy and safety of treatment with subcutaneous anifrolumab versus placebo in adult participants with systemic sclerosis. The target population for this study includes patients who meet the 2013 American College of Rheumatology/European League Against Rheumatism (ACR/EULAR) classification for systemic sclerosis, either limited or diffuse cutaneous subsets, with a disease duration of less than 6 years from first non-Raynaud's phenomenon symptom.

    Los Angeles, California and other locations

  • Oral Ifetroban to Treat Diffuse Cutaneous Systemic Sclerosis (SSc) or SSc-associated Pulmonary Arterial Hypertension

    Sorry, in progress, not accepting new patients

    The purpose of this phase 2 multicenter, randomized, double-blind, placebo-controlled, study is to assess the safety and efficacy of ifetroban in patients with diffuse cutaneous systemic SSc (dcSSc) or SSc-associated pulmonary arterial hypertension (SSc-PAH).

    Los Angeles, California and other locations

  • Preliminary Efficacy of EHP-101 in Diffuse Cutaneous Systemic Sclerosis

    Sorry, currently not accepting new patients, but might later

    The purpose of this trial is to evaluate the safety, tolerability, pharmacokinetics, and preliminary efficacy of EHP-101 in adult subjects with diffuse cutaneous Systemic Sclerosis (dcSSc).

    Los Angeles, California and other locations

  • Tibulizumab Systemic Sclerosis Understanding and Response Evaluation (TibuSURE)

    Sorry, in progress, not accepting new patients

    The study is a Phase 2, multi-center, randomized, double-blind, placebo-controlled study to evaluate the effects of tibulizumab over 24 weeks (Period 1) in adult participants with systemic sclerosis, followed by an open-label extension period where all active participants will receive tibulizumab and will be evaluated for an additional 28 weeks (Period 2)

    Los Angeles, California and other locations

  • Tulisokibart (MK-7240/PRA023) in Subjects With Systemic Sclerosis Associated With Interstitial Lung Disease (SSc-ILD) (MK-7240-007)

    Sorry, in progress, not accepting new patients

    The purpose of this study is to assess the safety and efficacy of tulisokibart in participants with SSc-ILD.

    Los Angeles, California and other locations

Our lead scientists for Diffuse Scleroderma research studies include .

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