Efficacy and Safety of LP-003 in Patients With CSU Who Remain Symptomatic Despite Antihistamine (H1) Treatment

Chronic Spontaneous Urticaria Clinical Trial

Official title:

Multi-center,Randomized,Double-blind Phase II Study to Evaluate the Efficacy and Safety of LP-003 in Patients With Chronic Spontaneous Urticaria (CSU) Who Remain Symptomatic Despite Antihistamine (H1) Treatment

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06228560
• Other study ID #: P10-LP003-03
• Status: Recruiting
• Phase: Phase 2
• Start date: January 25, 2024
• Est. completion date: January 30, 2025

Study information

• Verified date: January 2024
• Source: Longbio Pharma
• Contact: Hongzhou Yang
• Phone: 021-58372390
• Email: yanghz[@]longbio.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The study is a Phase II, multicenter, randomized, double-blind study to evaluatethe efficacy and safety of LP-003 administered subcutaneously as an add-on therapy for the treatment of adult patients aged 18-75 who have been diagnosed with refractory CSU and who remain symptomatic despitestandard-dose H1 antihistamine treatment.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 200
• Est. completion date: January 30, 2025
• Est. primary completion date: January 30, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Aged 18 to 75 years at the screening period.

2. Presence of wheals with itching for = 6 weeks prior to randomization. At the screening visit, subjects had taken double or more than the approved dose, or a combination of two or more H1 antihistamines for the treatment of chronic spontaneous urticaria for at least 2 weeks. Within the 7 days preceding randomization, the Urticaria Activity Score 7 (UAS7) was =16 (range 0-42), Itch Severity Score 7 (ISS7) was =8 (range 0-21), at least one UAS (range 0-6) was =4 on any screening visit day, and there must be a current record of medication use.

3. Subjects must not miss more than one diary record (morning or night) within 7 days prior to randomization (day 1), and are willing and able to complete daily symptom electronic diary records during the study period;

4. Male participants and their partners or female participants must agree to take one or more non pharmacological contraceptive measures (such as complete abstinence, contraceptive ring, partner ligation, etc.) during the trial period and within 6 months after the end of the trial and have no plans for sperm or egg donation.

5. Agree to participate in this clinical trial and voluntarily sign an informed consent form.

Exclusion Criteria:

1. The subject has a primary or sole trigger for chronic urticaria (chronic Induced urticaria), including artificial urticaria (symptomatic skin scratch disease), cold, heat, sun, pressure, delayed pressure, water, cholinergic, or contact urticaria;

2. Other medical conditions accompanied by symptoms of urticaria or angioedema including, but not limited to, urticarial vasculitis, pigmented urticaria, erythema multiforme, mastocytosis, hereditary urticaria, or drug-induced urticaria;

3. Any other dermatologic condition with chronic itching, such as atopic dermatitis, herpetic pemphigoid, herpetic dermatitis, senile itching, or psoriasis, which in the judgment of the Investigator may affect the evaluation of the study and the results of the study;

4. Subjects with clinically significant conditions such as (but not limited to) unstable ischemic heart disease, NYHA Class III/IV left ventricular failure, cardiac arrhythmias, uncontrolled hypertension, cerebrovascular disease, neurodegenerative, or other neurological disorders, uncontrolled hypothyroidism and hyperthyroidism and other autoimmune disorders, hypokalemia, hyper adrenergic state; past diagnosis of malignancy (other than basal cell carcinoma or squamous cell skin cancer); history of myocardial infarction within 12 months prior to screening;

5. Acute active infections requiring treatment at screening, including but not limited to, pulmonary infections, tuberculosis;

6. Positive hepatitis B surface antigen or hepatitis B core antibody (except for HBV-DNA testing below the lower limit of the research center's test) at screening; positive hepatitis C virus antibody, human immunodeficiency virus (HIV) antibody, and anti-syphilis helical antibody (TP-Ab) (except for those who are negative for RPR or TRUST);

7. Clinically significant cardiovascular, neurological, psychiatric, metabolic, hepatic, or other abnormalities identified during the Screening Period that may affect the interpretation of the study results and/or the safety of the subject;

8. Comorbid neurological or psychiatric disorders that prevent or prevent cooperation; patients with disabilities as defined by law (blindness, deafness, mute, mental retardation, psychiatric disorders, etc.);

9. Major surgery within 8 weeks prior to screening or surgery planned during the study period;

10. Evidence of historical or ongoing alcohol or substance abuse in the 6 months prior to screening;

11. Poor compliance, such as low medication adherence, inability to accurately complete a diary card, or use of prohibited medications;

12. Pregnant women, nursing mothers, or those with recent birth plans;

13. Patients who have participated in clinical trials of other drugs within the last 3 months;

14. Those who are considered by the investigator to be unfit to participate in the clinical trial.

Related Conditions & MeSH terms

• Chronic Spontaneous Urticaria
• Chronic Urticaria
• Urticaria

Intervention

Biological:
• LP-003
Liquid in vial
• Placebo
Liquid in vial
• Omalizumab
Liquid in vial

Locations

Country	Name	City	State
China	Beijing Friendship Hospital, Capital Medical University	Beijing	Beijing
China	Peking Union Medical College Hospital, Chinese Academy of Medical Sciences	Beijing	Beijing
China	Peking University Third Hospital	Beijing	Beijing
China	The First Affiliated Hospital of China Medical University	Beijing	Beijing
China	The First Hospital of Peking University	Beijing	Beijing
China	The Second XiangYa Hospital of Central South University	Changsha	Hunan
China	The First Affiliated Hospital of PLA Army Medical University	Chongqing	Chongqing
China	Fujian Medical University Union Hospital	Fuzhou	Fujian
China	Dermatology Hospital of Southern Medical University	Guangzhou	Guangdong
China	The Second Affiliated Hospital of Guangzhou Medical University	Guangzhou	Guangdong
China	Hospital of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College	Nanjing	Jiangsu
China	Ruijin Hospital Affiliated to Shanghai Jiaotong University School of Medicine	Shanghai	Shanghai
China	Shanghai Skin Disease Hospital	Shanghai	Shanghai
China	Shengjing Hospital of China Medical University	Shenyang	Liaoning
China	Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology	Wuhan	Hubei
China	the Second Affiliated Hospital of Xi'an Jiaotong University	Xi'an	Shanxi

Sponsors (1)

Lead Sponsor	Collaborator
Longbio Pharma

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The proportion of participants achieving complete absence of wheals and itching (UAS7 = 0) at week 12		Week 12
Secondary	The incidence of adverse events during the study		40 weeks
Secondary	The proportion of participants with no hives (HSS7 = 0) at week 4, 8, 12, 16, 20, 24, 32, and 40		Week 4, 8, 12, 16, 20, 24, 32, and 40
Secondary	The proportion of participants achieving complete absence of wheals and itching (UAS7 = 0) at week 4, 8, 16, 20, 24, 32, and 40		Week 4, 8, 16, 20, 24, 32, and 40
Secondary	The proportion of participants achieving complete absence of angioedema (AAS7 = 0) at week 4, 8, 12, 16, 20, 24, 32, and 40		Week 4, 8, 12, 16, 20, 24, 32, and 40
Secondary	The proportion of participants with controlled disease activity (UAS7 = 6) at week 4, 8, 12, 16, 20, 24, 32, and 40		Week 4, 8, 12, 16, 20, 24, 32, and 40
Secondary	Change From Baseline in UAS7, HSS7, ISS7, AAS7 at week 4, 8, 12, 16, 20, 24, 32, and 40		Baseline and week 4, 8, 12, 16, 20, 24, 32, and 40
Secondary	Change From Baseline in Chronic Urticaria Quality of Life Questionnaire (CU-Q2oL) at week 4, 8, 12, 16, 20, 24, 32, and 40		Baseline and week 4, 8, 12, 16, 20, 24, 32, and 40
Secondary	Blood concentrations of LP-003, free IgE, total IgE, anti-drug antibodies (ADA), and neutralizing antibodies (Nab) during the study		40 weeks