Actively Recruiting
A Study to Evaluate HB0034 in Healthy Chinese Adult Participants
Led by Shanghai Huaota Biopharmaceutical Co., Ltd. · Updated on 2025-01-20
60
Participants Needed
1
Research Sites
49 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of this study is to investigate the safety and tolerability of HB0034 in healthy subjects following a single dose or multiple dose.
CONDITIONS
Official Title
A Study to Evaluate HB0034 in Healthy Chinese Adult Participants
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Healthy male or female subjects age �3E= 18 and �3C= 55 years
- Body Mass Index (BMI) �3E= 17.5 and �3C= 32 kg/m�B2
- Normal ECG, blood pressure, respiratory rate, temperature, and heart rate unless considered clinically insignificant by the investigator
- Signed and dated informed consent prior to study admission in accordance with GCP and local laws
You will not qualify if you...
- History of significant cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, hematological, psychiatric, or neurological disease
- Current or past malignancy
- Family history of premature Coronary Heart Disease (CHD)
- History of significant opportunistic infections such as invasive candidiasis or pneumocystis pneumonia
- Pregnant or breastfeeding women or those with a positive pregnancy test
- Additional exclusion criteria apply
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Central Hospital affiliated to Shandong First Medical University
Jinan, Shandong, China
Actively Recruiting
Research Team
Y
Yuan Tang
CONTACT
Q
Qiaoxia Qian
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
8
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