A Study of BBT001 in Healthy Volunteers (HVs) and in Adult Patients With Moderate to Severe Atopic Dermatitis (AD)
Recruiting · NCT07239947 · Interventional (participants receive a specific treatment) · Lead sponsor: Bambusa Therapeutics
View the official record on ClinicalTrials.gov →Interventions studied
BBT001Placebo
What this trial is about
This is a Phase 1, randomized, blinded, placebo controlled, single ascending dose (SAD) study of BBT001 in healthy volunteers (HVs) and adult patients with moderate to severe Atopic Dermatitis (AD).
Who can take part
Age range
18 Years to 65 Years
Sex
All (male and female)
Healthy volunteers
Yes - healthy volunteers may be accepted
Phase
Phase 1
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Part A and B):
- Age of 18-65 years.
- Body mass index between 18-28 kg/m², capped at 120 kg.
- Negative pregnancy tests for women of childbearing potential.
- Willingness to refrain from alcohol consumption for 24 hours prior to each study visit.
- Non-smokers, healthy current smokers (≤5 cigarettes/day), or ex-smokers.
- Adequate contraception use (for men and women of childbearing potential).
- No clinically significant abnormalities or history of relevant diseases.
- Key Inclusion Criteria (Part B only):
- Must have dermatologist-confirmed chronic atopic dermatitis (≥12 months). Inadequate response to topical treatments or where they are medically inadvisable.
- Moderate to severe atopic dermatitis
- Validated investigator's global assessment for atopic dermatitis (vIGA-ADTM) score ≥3
- Atopic lesions cover ≥10% of body surface area (BSA)
- Average peak pruritus numeric rating scale (PP-NRS) score ≥4 in the 7 days before randomization.
- Eczema Area and Severity Index (EASI) score ≥16 at screening and randomization visits.
- (for biologic/JAKi experienced subjects) Patients with prior systemic exposure to the following agents are eligible for enrollment: biologics targeting IL-4/IL-13 or IL-31 pathway or JAK inhibitors.
- Key
Exclusion criteria
- for (Part A\&B)
- Significant health issues, such as: diabetes, positive tests for human immunodeficiency virus (HIV), hepatitis C virus (HCV), or hepatitis B surface antigen (HBsAg), immunodeficiencies, autoimmune diseases, or cancer, history of conditions predisposing to infections.
- History of major metabolic, dermatological, liver, kidney, hematological, or other significant disorders.
- Clinically relevant abnormal lab results, including low blood counts, liver issues, or abnormal kidney function.
- Positive drug/alcohol tests or abnormal vital signs at screening or Day -1.
- Abnormal Electrocardiogram (ECG) findings
- History of drug/alcohol abuse in the past 2 years.
- Donated \>500mL blood within 2 months of screening.
- History of severe allergic reactions or hypersensitivity.
- Key Exclusion Criteria for (Part B only)
- Skin diseases other than atopic dermatitis, significant tattoos, or scarring.
- Receipt of immunoglobulin or blood products within 30 days.
- Atopic dermatitis with ocular symptoms or chronic ocular steroid use.
- Chronic pruritus from conditions other than atopic dermatitis.
- Acute/treated infections or chronic skin infections.
- Current use of sedating antihistamines or corticosteroids.
Where it is running
10 locations listed.
- The Second Hospital of Anhui Medical Univesity - Hefei, Anhui, China
- The Second Affiliated Hospital of Wannan Medical College - Wuhu, Anhui, China
- Peking University People's Hospital - Beijing, Beijing Municipality, China
- Dermatology Hospital of Southern Medical University - Guangzhou, Guangdong, China
- The Second Xiangya Hospital of Central South University - Changsha, Hunan, China
- Wuxi Second People's Hospital - Wuxi, Jiangsu, China
- Jiangsu University Affiliated Hospital - Zhenjiang, Jiangsu, China
- Jiangxi Provincial Dermatology Hospital - Nanchang, Jiangxi, China
- Shandong Provincial Hospital for Skin Diseases - Jinan, Shandong, China
- Shanghai Dermatology Hospital - Shanghai, Shanghai Municipality, China