NCT06589752Completed
Replication of the NefIgArd Trial of TRF-budesonide in Primary IgAN
Replication of the NefIgArd Trial of Effectiveness and Safety of a Targeted-release Formulation of Budesonide in Patients With Primary IgA Nephropathy
Source: ClinicalTrials.gov · Last updated 19 Sept 2024
Brief summary (registry, in English)
This replication of the NefIgArd trial of TRF-budesonide aims to use real-world data to evaluate the efficiency and safety of TRF-budesonide in the treatment of IgA nephropathy, from completing real-world research to providing real-world evidence.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 200 (actual)
- First submitted
- 21 Jul 2024
- Start date
- 24 Apr 2023
- Primary completion date
- 5 Sept 2024
- Lead sponsor
- Ruijin Hospital
- Diseases
- IgA nephropathy
- NCT number
- NCT06589752
What you commit to
- Study type: Observational
- Participants enrolled: 200
- From 24 Apr 2023 to the primary completion date, 5 Sept 2024
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients who have received kidney transplants;
- Patients who are allergic to budesonide or any component of the investigational drug formulation;
- Patients who have previously had a severe adverse reaction to steroids;
- Have received any systemic glucocorticoid therapy within 3 months prior to medication;
- Received immunosuppressants or biologics within 3 months prior to medication;
- Patients taking potent inhibitors of the cytochrome P450 3A4 enzyme (CYP3A4);
- Current or former (within the last 2 years) alcohol or drug abuse;
Other illness
- Systemic diseases that may cause interstitial IgA deposition, including but not limited to anaphylactoid purpura, systemic lupus erythematosus, herpetic dermatitis, and ankylosing spondylitis;
- Those with other glomerular diseases (such as C3 glomerular disease or diabetic nephropathy) and nephrotic syndrome;
- Patients with acute, chronic, or latent infectious diseases, including hepatitis, tuberculosis (TB), human immunodeficiency virus (HIV), and chronic urinary tract infections;
- Patients with cirrhosis or severe liver function impairment, as assessed by the investigator;
- Patients diagnosed with poorly controlled type 1 or type 2 diabetes;
- Patients with a history of unstable angina, grade III or IV congestive heart failure, and/or arrhythmia as assessed by the investigator;
- Patients diagnosed with malignancy within the last 5 years, with the exception of treated basal cell carcinoma of the skin, curably resected squamous cell carcinoma of the skin, polyps of the colon, or carcinoma in situ of the cervix;
- Patients with known glaucoma, known history of cataract and/or cataract surgery that may interfere with study drug action or release (such as peptic ulcer disease, inflammatory bowel disease, and chronic diarrhea);
Age
- Life expectancy \<5 years;
Other
- Patients with poorly controlled blood pressure with systolic or diastolic blood pressure ≥140mmHg or 90mmHg. At least one blood pressure measurement should be in the above range (based on up to three measurements, 1 minute apart, taken after resting in the supine position for at least 5 minutes);
- Patients with osteoporosis who are known to be at moderate or high risk. Chinese patients are defined according to the Asian Osteoporosis Self-Assessment Tool (OSTA) Index;
- Patients with psychotic symptoms;
- Patients who are unwilling or unable to meet program requirements;
- Women who are pregnant, nursing, or unwilling to use contraception during treatment.
Who the study is looking for
- Male or female patients aged ≥18 years;
- Primary IgA nephropathy confirmed by renal biopsy;
- Stable use of RAS blockers;
- 24-hour urine albumin quantitation ≥1g/day, or urine protein/creatinine ratio ≥0.8g/g (≥90 mg/mmol);
- eGFR ≥30 mL/min/1.73m².
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Ruijin hospital Coordinator of this site? Confirm its status | Shanghai | China | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.