Primary Cutaneous Amyloidosis

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Review clinical trials related to Primary Cutaneous Amyloidosis. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Efficacy and Safety of Stapokibart for Primary Cutaneous Amyloidosis

This trial is planned to investigate the efficacy and safety of Stapokibart (an IL-4 receptor antagonist) in patients with PCA.

Participants needed: 40
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: First Affiliated Hospital of Chongqing Medical UniversityUpdated: Aug 27, 2025
Eligibility criteria

Males or females aged 18 to 75 years, with a diagnosis of PCA confirmed by skin... [+6]

Use of any of the following treatments within 4 weeks prior to randomization: a.... [+22]

Status: Recruiting

A Prospective Cohort Study on Primary Cutaneous Amyloidosis

The aim of this clinical trial is to find out whether the combination of tocilizumab tablets and acitretin capsules is more effective than acitretin capsules alone in treating primary cutaneous amyloidosis. It will also investigate the safety of the combination of tocilizumab tablets and acitretin capsules. The main questions it aims to answer are: 1. Does the combination of tocilizumab tablets and acitretin capsules relieve the pruritus symptoms of the participants faster and reduce the pruritus score more than acitretin capsules alone? 2. What medical problems will the participants encounter when taking tocilizumab tablets combined with acitretin capsules? The researchers compared the combination of tocilizumab tablets and acitretin capsules with acitretin capsules alone to see if the combination could better treat primary cutaneous amyloidosis without causing serious adverse reactions. Participants will: 1. Take the combination of tocilizumab tablets and acitretin capsules or acitretin capsules alone every day for 16 weeks. 2. Visit the clinic once every 4 weeks for checkups and tests. 3. Observe participants at 4 weeks, 12 weeks and 24 weeks after discontinuation of medication to determine the recurrence status. 4. Collect the visual analogue scale (VAS) scores for pruritus, symptom severity (SCORAD) scores , rash area and severity, treatment response (EASI) scores, dermatological quality of life index (DLQI), and insomnia severity index (ISI) of participants before and after treatment.

Participants needed: 56
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Army Medical University, ChinaUpdated: Aug 13, 2025Locations: 1
Eligibility criteria

Age ≥ 18 years old, without infectious diseases such as "hepatitis B" and "tuber... [+4]

Nodular amyloidosis or combined with other types of amyloidosis (such as systemi... [+2]