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A randomized, placebo-controlled, single-administration, dose-escalation study to evaluate the safety, tolerability, pharmacokinetics and immunogenicity of LP-98 injection in healthy subjects in a first-in-human clinical study
Full description
The study was divided into two parts, Part A and Part B. The Part A and Part B studies were carried out separately according to the protocol flow, with the Part A study carried out first.
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Inclusion criteria
Subjects must meet all of the following inclusion criteria for study entry:
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
36 participants in 11 patient groups
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Central trial contact
xian Yu He, Doctor; Fan Wang
Data sourced from clinicaltrials.gov
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