← Back to Search

Immunosuppressant

Cyclosporine for Interstitial Cystitis (CIC Trial)

Phase 2
Waitlist Available
Led By Daniel Shoskes, M.D.
Research Sponsored by The Cleveland Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 months
Awards & highlights

Summary

This is a study for patients that have a condition called Interstitial Cystitis, also known as Painful Bladder Syndrome. Patients would have tried at least two different therapies, unsuccessfully,(eg. medications, pelvic floor physical therapy) The purpose of this research project is to study the immunosuppressive drug Cyclosporine in patients with Interstitial Cystitis to assess how well it works, what the side effects are and what is its mechanism of action. Cyclosporine is a drug that is FDA-approved to prevent organ rejection after kidney, liver, and heart transplant but is not approved by the FDA for Interstitial Cystitis. Several research studies have been published showing that Cyclosporine can improve the symptoms of Interstitial Cystitis, that it works better than a placebo ("sugar pill" or inert treatment) and that it works more effectively than Pentosan Polysulfate (Elmiron), which is an FDA approved therapy. The dose of Cyclosporine used in these studies on Interstitial Cystitis are much lower that the doses used to prevent rejection in transplant patients. Based on these studies, the American Urological Association has recently published treatment guidelines that recommend Cyclosporine therapy for Interstitial Cystitis after the failure of other more conservative therapies and medications. Nevertheless, much is not known about using Cyclosporine therapy for Interstitial Cystitis including the mechanism of action, the ideal dose, how best to monitor for side effects and in particular whether kidney damage can occur at the low doses used in these studies. In this study, to examine the mechanism of action, blood and urine samples will be collected before, during and after therapy to look at "biomarkers", chemical substances that can be associated with inflammation and tissue injury. We will also test effects of therapy on skin sensation and pain perception because the molecule which Cyclosporine binds to (calcineurin) is also found in nerves that conduct pain signals. This study is only being done at the Cleveland Clinic and will involve about 30 patients with Interstitial Cystitis.

Eligible Conditions
  • Interstitial Cystitis

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 3 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Symptom Improvement of Interstitial Cystitis

Side effects data

From 2019 Phase 3 trial • 446 Patients • NCT01820572
21%
Diarrhoea
20%
Nasopharyngitis
17%
Urinary tract infection
14%
Cough
13%
Hypertension
12%
Headache
10%
Fatigue
10%
Oedema peripheral
10%
Bronchitis
10%
Arthralgia
9%
Kidney transplant rejection
9%
Pyrexia
9%
Blood creatinine increased
8%
Upper respiratory tract infection
8%
Back pain
7%
Nausea
7%
Dizziness
5%
Pain in extremity
5%
Vomiting
5%
Oropharyngeal pain
5%
Abdominal pain
5%
Basal cell carcinoma
4%
Insomnia
3%
Tremor
3%
Urosepsis
2%
Musculoskeletal pain
2%
Squamous cell carcinoma of skin
2%
Acute kidney injury
2%
Sepsis
2%
Pneumonia
1%
Bowen's disease
1%
Congenital cystic kidney disease
1%
Chest pain
1%
Herpes zoster
1%
Extremity necrosis
1%
Pancreatitis
1%
Bacterial pyelonephritis
1%
Influenza
1%
Osteomyelitis
1%
Deep vein thrombosis
1%
Overdose
1%
Squamous cell carcinoma
1%
Proteinuria
1%
Osteoarthritis
1%
Acute myocardial infarction
1%
Atrial fibrillation
1%
Coronary artery disease
1%
Myocardial infarction
1%
Renal graft infection
1%
Hypotension
100%
80%
60%
40%
20%
0%
Study treatment Arm
Belatacept
CNI-Based Regimen

Trial Design

1Treatment groups
Experimental Treatment
Group I: CyclosporineExperimental Treatment1 Intervention
Drug: Cyclosporine, Pill form, dosage calculated upon patient study visit, frequency - twice daily, duration - 3 months.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Cyclosporine
FDA approved

Find a Location

Who is running the clinical trial?

The Cleveland ClinicLead Sponsor
1,049 Previous Clinical Trials
1,370,718 Total Patients Enrolled
1 Trials studying Interstitial Cystitis
200 Patients Enrolled for Interstitial Cystitis
Daniel Shoskes, M.D.Principal InvestigatorThe Cleveland Clinic
~2 spots leftby Oct 2025