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Safety, Tolerability, and Pharmacokinetics/Pharmacodynamics of a Single Subcutaneous Injection of SHR-1703 in Patients With Asthma -- a Randomized, Double-blind, Dose-increasing, Placebo Controlled Phase I Clinical Study

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Trial Profile

Safety, Tolerability, and Pharmacokinetics/Pharmacodynamics of a Single Subcutaneous Injection of SHR-1703 in Patients With Asthma -- a Randomized, Double-blind, Dose-increasing, Placebo Controlled Phase I Clinical Study

Status: Active, no longer recruiting
Phase of Trial: Phase I

Latest Information Update: 06 Jun 2024

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At a glance

  • Drugs SHR-1703 (Primary)
  • Indications Asthma
  • Focus Adverse reactions
  • Sponsors Jiangsu Hengrui Medicine Co.

Most Recent Events

  • 24 Apr 2023 Status changed from recruiting to active, no longer recruiting.
  • 08 Jun 2022 Number of treatment arms has been increased from 2 to 4 by the addition of Placebo Comparator: Treatment group B and group D arms. Study design has been changed from open, non-randomized to double-blind, Randomized. Tolerability of adverse events of SHR-1703 is added as one more primary end-point.
  • 08 Jun 2022 Planned number of patients changed from 16 to 22.

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