About this trial
The primary purpose of this study is to evaluate the safety and tolerability of H021 tablets following oral administration of single and multiple ascending doses in healthy participants.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Male or female, non-smoker (no use of tobacco or nicotine products within 3 months prior to screening), greater than and equal to (>=) 18 and less than and equal to (<=) 55 years of age, with body mass index (BMI) greater than (>)18.5 and less than (<) 32.0 kilograms per square meter (kg/m²).
the absence of clinically significant illness and surgery within 4 weeks prior to study drug administration.
the absence of clinically significant history of neurological, endocrine, cardiovascular, respiratory, hematological, immunological, psychiatric, gastrointestinal, renal, hepatic, and metabolic disease.
post-menopausal (spontaneous amenorrhea for at least 12 months prior to dosing) with confirmation by documented follicle-stimulating hormone (FSH) levels >=40 milli-international units per milliliter (mIU/mL); or
Disqualifiers
Any clinically significant abnormal finding at physical examination.
Clinically significant abnormal laboratory test results including biochemistry, hematology, urinalysis, and coagulation results, or positive serology test results for hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibody, or human immunodeficiency virus (HIV) antigen and antibody, or QuantiFERON®-TB test at screening.
Positive pregnancy test or lactating female participant.
Positive urine drug screen, urine cotinine test, or alcohol breath test at screening or Day -1.
Trial design
Parallel
Treatments tested in this trial
H021
DrugH021 oral tablet.
H021 Placebo
DrugH021 placebo oral tablet.
Treatment groups
10
Treatment groupsSee each treatment group below.
Trial outcomes
Primary outcomes
Number of Participants with Adverse Events (AEs)
An AE is defined as any untoward medical occurrence in a participant or clinical trial participant administered a pharmaceutical product and which does not necessarily have a causal relationship with the treatment. An AE can, therefore, be any unfavorable and unintended sign (including an abnormal laboratory finding, for example), symptom, or disease temporally associated with the use of a medicinal (investigational) product, whether or not considered related to the medicinal (investigational) product. Any clinically significant changes in vital signs, electrocardiogram (ECG) measurement, physical examination and clinical laboratory parameters will be recorded as AE.
Secondary outcomes
SAD Part: Area under the concentration-time curve from time zero until the last observed concentration (AUC0-t) of H021
AUC0-t is an area under the concentration-time curve from time zero (pre-dose) to time of last observed concentration.
SAD Part: Area under the concentration-time curve from time zero to infinity (AUC0-infinity) of H021
AUC0-infinity is an area under the concentration-time curve from time zero to infinity (extrapolated).
SAD Part: Maximal observed concentration (Cmax) of H021
Cmax is a measure of the maximum amount of drug in the plasma after the dose was given.
SAD Part: Time to Reach Cmax (Tmax) of H021
Tmax is a measure of the time to reach the maximum concentration in the plasma after the dose was given.
Other outcomes
MAD Part: Change From Baseline in Micro-RNA-124 (miR-124) Expression in Peripheral Blood Mononuclear Cells (PBMCs)
Change from baseline in miR-124 expression in PBMCs will be assessed.
MAD Part: Change From Baseline in Interleukin (IL)-6, Tumor Necrosis Factor Alpha (TNF-α), IL-17A, and Interferon Gamma (IFN-γ) in Blood Serum
Change from baseline in IL-6, TNF-α, IL-17A, and IFN-γ in blood serum will be assessed.
Sponsors and contacts
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