drugset / Trial / NCT05179265
Recombinant Human Serum Albumin in Healthy Subjects
RandomizedParallel-groupDouble-blindTreatment
Summary
This trial adopts a single-center, randomized, double-blind, dose-escalation, placebo-controlled design to evaluate the safety, tolerability, pharmacokinetics, and efficacy of a single administration of recombinant human serum albumin in healthy subjects Kinetics and anti-drug antibody characteristics. Qualified healthy subjects (both male and female) were screened and enrolled to the four dose levels of 2 g, 5 g, 10 g, and 20 g according to the principle of dose escalation, and 6 out of 8 subjects in each dose group One patient received the test drug, and two received a placebo.
Timeline
- Start
- 2021-03-29
- Primary completion
- 2022-07-07
- Completion
- 2022-07-07
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | HUMAN SERUM ALBUMIN, RECOMBINANT RICE-DERIVED | Protein / enzyme biologic | 2 g | Intravenous |
| Subject | HUMAN SERUM ALBUMIN, RECOMBINANT RICE-DERIVED | Protein / enzyme biologic | 5 g | Intravenous |
| Subject | HUMAN SERUM ALBUMIN, RECOMBINANT RICE-DERIVED | Protein / enzyme biologic | 10 g | Intravenous |
| Subject | HUMAN SERUM ALBUMIN, RECOMBINANT RICE-DERIVED | Protein / enzyme biologic | 20 g | Intravenous |
Indications
No indication recorded.