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explore the clinical efficacy of Spicichibant in the treatment of perennial allergic rhinitis

explore the clinical efficacy of Spicichibant in the treatment of perennial allergic rhinitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114712
Enrollment
Unknown
Registered
2025-12-17
Start date
2025-12-18
Completion date
Unknown
Last updated
2026-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Allergic rhinitis

Interventions

Experimental Group:Received 8 weeks of treatment with the Sipucibin antibody biological agent combined with 4 weeks of conventional medication treatment

Sponsors

The Ninth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Applicants aged 18 to 60 (inclusive), with no gender restrictions; 2. The patient was diagnosed with moderate to severe chronic AR. Previous treatment with glucocorticoids had poor symptom control. 3. The patient tested positive for allergens (skin prick test or serum specific IgE test) (prick level >=++; sIgE level >= grade 2). 4. The patient can understand and sign the informed consent form; 5. The patient was able to actively comply with the protocol and accept follow-up.

Exclusion criteria

Exclusion criteria: 1. Patients with deviated nasal septum and other abnormal nasal structures, or those with a history of nasal surgery or trauma; 2. Combined with unstable asthma; 3. Women who are pregnant or breastfeeding; 4. Had an upper respiratory tract infection in the previous two weeks; Those with a history of severe systemic allergic reactions, immunosuppressive diseases (such as HIV infection history, etc.), malignant tumors, autoimmune diseases, tuberculosis, cardiovascular insufficiency or other serious organ system diseases as determined by the researcher. 5. Assess any other circumstances that are deemed unsuitable for participation in the trial.

Design outcomes

Primary

MeasureTime frame
The nasal mucosal ciliary transit time at baseline and 8 weeks of treatment were compared;The rhinitis symptom-medication combination scores at baseline and 8 weeks of treatment were compared;

Secondary

MeasureTime frame
The allergic rhinitis quality of life questionnaire was compared at baseline, 8 weeks of treatment, and 12 weeks after drug withdrawal;Olfactory function was compared at baseline, 8 weeks of treatment, and 12 weeks after drug withdrawal;The nasal mucociliary transit time (MTT) and rhinitis symptom-drug combination score were compared 12 weeks after drug withdrawal;

Countries

China

Contacts

Public ContactJiang Chenyan

The Ninth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine

13918529277@139.com+86 21 2327 1699

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026