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NCT07143864

Efficacy and Safety of Stapokibart for Primary Cutaneous Amyloidosis

Not yet recruiting NA Last updated 27 August 2025
What this trial tests

NA trial testing Stapokibart in Primary Cutaneous Amyloidosis in 40 participants. Not yet recruiting.

Timeline
15 September 2025
Primary endpoint
31 December 2026
31 December 2026

Quick facts

Lead sponsorFirst Affiliated Hospital of Chongqing Medical University
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment40
Start date15 September 2025
Primary completion31 December 2026
Estimated completion31 December 2026

Drugs / interventions tested

Conditions studied

Sponsor

First Affiliated Hospital of Chongqing Medical University

Who can join

Adults 18 to 75, any sex, with Primary Cutaneous Amyloidosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Stapokibart

Trials testing the same drug.

Other First Affiliated Hospital of Chongqing Medical University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07143864.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing