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NCT07523282: AID

Safety and Preliminary Efficacy of HN2302 in Patients With Autoimmune Diseases

Not yet recruiting Phase 1 Last updated 14 April 2026
What this trial tests

Phase 1 trial testing HN2302 Injection in Autoimmune Disease in 12 participants. Not yet recruiting.

Timeline
28 April 2026
Primary endpoint
31 December 2027
30 June 2028

Quick facts

Lead sponsorShenzhen MagicRNA Biotechnology Co., Ltd
PhasePhase 1
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment12
Start date28 April 2026
Primary completion31 December 2027
Estimated completion30 June 2028
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Shenzhen MagicRNA Biotechnology Co., Ltd — full company profile →

Who can join

Adults 18 to 69, any sex, with Autoimmune Disease or Systemic Lupus Erythematosus. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is an open-label, single-arm study designed to evaluate the safety and preliminary efficacy of HN2302 in patients with autoimmune diseases, including systemic lupus erythematosus (SLE) and systemic sclerosis (SSc).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Autoimmune Disease

Currently open trials in the same condition.

Other Shenzhen MagicRNA Biotechnology Co., Ltd 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/NCT07523282.

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