To observe the safety and tolerability of a single subcutaneous injection of pegylated recombinant human granulocyte colony stimulating factor injection in healthy subjects, evaluate the safe dosage range of the drug, investigate the pharmacokinetic and pharmacodynamic characteristics of this product in healthy subjects, determine the maximum tolerated dose in healthy subjects, and provide a basis for the later clinical research of this product.
The statistics for drugs in the Pipeline is the current organization and its subsidiaries are counted as organizations,Early Phase 1 is incorporated into Phase 1, Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3
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