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Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Immunogenicity Study Following Multiple Subcutaneous Injections of SHR-1222 in Postmenopausal Osteoporosis Patients

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Trial Profile

Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Immunogenicity Study Following Multiple Subcutaneous Injections of SHR-1222 in Postmenopausal Osteoporosis Patients

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 10 Jul 2023

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At a glance

  • Drugs SHR 1222 (Primary)
  • Indications Postmenopausal osteoporosis
  • Focus Adverse reactions
  • Sponsors Jiangsu Hengrui Medicine Co.

    • Most Recent Events

    • 03 Jul 2023 Status changed from active, no longer recruiting to completed.
    • 05 Jan 2022 New cohort "SHR-1222 dosage 5 every 2 months for 6 months" added. Dose frequency of cohort 4 and 6 amended.
    • 05 Jan 2022 Planned End Date changed from 31 Dec 2020 to 31 Dec 2022.

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