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Lupus Trials

​The Division of Rheumatology strives to understand more about lupus through research.  Please see the list below, which summarizes the st​udies available to individuals interested in advancing our understanding and treatment of rheumatic disease. 

Study Name/IRB​#/PIBrief Description​Basic Eligibility​ Criteria°ä´Ç²Ô³Ù²¹³¦³Ù​

AstraZeneca (Lavendar)

Kristen Demoruelle, MD, PhD

Evaluate the Efficacy and Safety of Anifrolumab in adults with chronic and/or subacute cutaneous lupus erythematosus who are refractory adn/or intolerant to antimalarial therapy.  Each study stage will have a randomized, double-blind, placebo-controlled design, followed by an open label treatment period. 

1. Adult women or men (ages 18-70) and a body weight of >=40.0 kg.

2. Confirmed diagnosis of chronic CLE (including discoid CLE adn other subtypes) and/or subacute CLE with or without systemic manifestation.

3. Either a BILAG A in one organ or a BILAG B in two organs

4. Must have current autoantibody positivity (ANA or dsDNA or anti-Smith) and low complement (C3 OR C4 OR CH50) at screening

Chong Pedrick

303-724-7518

Chong.Pedrick@cuanschutz.edu

 

Najeeb Arishi

303-724-7512

Najeeb.Arishi@cuanschutz.edu

 

TOPAZ

IRB# 22-0670

Christopher Striebich, MD, PhD
A multicenter, randomized, placebo-controlled, phase 3 study to evaluate the efficacy and safety of BIIB059 in adult participants with active SLE receiving background non-biologic standard of care treatment. 

Participants must be at least 18 years old and diagnosed with SLE at least 24 weeks prior, meeting 2019 EULAR/ACR classification criteria for SLE.

Disease activity will be determined by modified SLEDAI-2K and BILAG scores at screening.

-Must have a modified clinical SLEDAI 2K score of at least 4 (excluding anti-dsDNA, low complement, alopecia, fever, headache and organic brain syndrome)

 

And

-Must have a BILAG2004 level A disease in ≥ 1 organ system or BILAG2004 level B disease in ≥ 2 organ systems

Chong Pedrick

303-724-7518

Chong.Pedrick@cuanschutz.edu

 

Najeeb Arishi

303-724-7512

Najeeb.Arishi@cuanschutz.edu

COSMIC

IRB# 23-1287

Christopher Striebich, MD, PhD

Proof of concept study to evaluate the efficacy, safety, and tolerability of GS-5718 in participants with Cutaneous Lupus Erythematosus (CLE)

To review the clinical trials.gov info click

-Active cutaneous lupus (either SLE or CLE) affecting more than one area

-Willingness to undergo skin punch biopsy at 2 timepoints

Chong Pedrick

303-724-7518

Chong.Pedrick@cuanschutz.edu

Najeeb Arishi

303-724-7512

Najeeb.Arishi@cuanschutz.edu

Novartis SIRIUS

IRB #23-1961

Christopher Striebich, MD, PhD

The trial will evaluate efficacy, safety and tolerability of two regimens of ianalumab compared to placebo, given as monthly or quarterly subcutaneous injection on top of standard-of-care treatment in participants with active systemic lupus erythematosus (SLE)

To review the clinical trials.gov info click

Eligibility:

  • 18 and older
  • Diagnosis of SLE meeting criteria for at least 6 months prior to screening

Chong Pedrick

303-724-7518

Chong.Pedrick@cuanschutz.edu

Najeeb Arishi

303-724-7512

Najeeb.Arishi@cuanschutz.edu

IDORSIA

IRB #22-1370

Christopher Striebich, MD, PhD

The goal of this clinical trial is to see how well cenerimod is in reducing symptoms of Systemic Lupus Erythematous in adult patients with moderate to severe symptoms.

To review the clinical trials.gov info click

Eligibility

  • Ages: 18 Years to 75 
  • Diagnosis of (SLE) made at least 6 months prior to screening

Chong Pedrick

303-724-7518

Chong.Pedrick@cuanschutz.edu

Najeeb Arishi

303-724-7512

Najeeb.Arishi@cuanschutz.edu

CAR-T study in SLE, IIM and SSc

24-0289

Melissa Griffith, MD
A Phase 1, Multicenter, Open-Label Study Of CC-97540 (BMS-986353), CD19-Targeted Nex-T Chimeric Antigen Receptor (CAR) T Cells, in Participants with Severe, Refractory Autoimmune Diseases: Systemic Lupus Erythematosus, idiopathic Inflammatory Myopathy or Systemic Sclerosis
  • Adult women or men (age 18 and above) with confirmed, active SLE, IIM, SSc
  • Fulfilling the 2019 (EULAR/ACR) classification criteria of SLE.
  • presence of anti-dsDNA, anti-histone, anti-chromatin, anti-Ro (anti-SS-A), anti-La (anti-SS-B), or anti-Sm antibodies at screening.
  • Active disease at screening, with recent ≥ 1 major organ system with  (BILAG A) score or class III or IV Lupus nephritis
  • Inadequate response to glucocorticoids and to at least 2 of the following treatments, used for at least 3 months each: cyclophosphamide, mycophenolic acid or its derivatives, belimumab, azathioprine, anifrolumab, methotrexate, rituximab, obinutuzumab, cyclosporin, tacrolimus or voclosporin
  • SLE only, not drug-induced, not overlapping autoimmune diseases like (MS, Psoriasis, IBD)

Chong Pedrick

303-724-7518

Chong.Pedrick@cuanschutz.edu

 

Najeeb Arishi

303-724-7512

Najeeb.Arishi@cuanschutz.edu

 

Mario Farag

303-724-6438

Mario.Farag@cuanschutz.edu

Immunovant

Elena Weinstein, MD

To evaluate the efficacy of IMVT-1402 compared to placebo in participants with CLE as assessed by changes in cutaneous lupus erythematosus disease area and severity index activity (CLASI-A) score.

Eligibility

  • Age >= 18 who have active SCLE/CCLE with detectable autoantibody with or without systemic manifestations
  • Have a total CLASI-A score of >=10 at screening and day 1. A CLASI-A score of >=8 and <10 eligible if the score does not include alopecia and/or mucous membrane lesions
  • Positive for at least one of the following at screening - ANA, anti-dsDNA, anti-Ro/SSA, anti-La/SSB, anti-Sm, or anti-RNP710 g positive direct immunofluorescence confirming IgG deposition in a skin biopsy.

Chong Pedrick

303-724-7518

Chong.Pedrick@cuanschutz.edu

Najeeb Arishi

303-724-7512

Najeeb.Arishi@cuanschutz.edu

SELECT-SLE (Abbvie)

Christopher Striebich, MD/PhD

Study to evaluate the safety and efficacy of JAK inhibitor Upadacitinib (Rinvoq) in individuals with moderat to severe active SLE.
  • Age 18-63 years of age
  • Clinical diagnosis of SLE at least 24 weeks prior to screening
  • At screening must be positive for at least one of the following - ANA (titer >=1:80), anti-dsDNA, anti-Smith.

Chong Pedrick

303-724-7518

Chong.Pedrick@cuanschutz.edu

Najeeb Arishi

303-724-7512

Najeeb.Arishi@cuanschutz.edu

 

Please note that study status changes frequently and therefore, a listed study may not be actively enrolling. Also, the complete list of inclusion and exclusion criteria for a given study is often not listed due to its length.  A visit to determine an individuals eligibility may be required.  A placebo is an inactive substance or treatment that looks the same as, and is given the same way as, an active drug or treatment being tested. The effects of the active drug or treatment are compared to the effects of the placebo.

Rheumatology (SOM)

CU Anschutz

Barbara Davis Center for Diabetes

1775 North Aurora Court

3102

Aurora, CO 80045


303-724-7605

 

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