PaTHway CHINA TRIAL: A Trial to Investigating the Safety, Tolerability and Efficacy of TransCon PTH in Adults With Hypoparathyroidism
PaTHway CHINA TRIAL: A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Trial, With an Open-Label Extension, Investigating the Safety, Tolerability and Efficacy of TransCon PTH Administered Subcutaneously Daily in Adults With Hypoparathyroidism
Sponsor: Visen Pharmaceuticals (Shanghai) Co., Ltd.
This PHASE3 trial investigates Endocrine System Diseases and Hypoparathyroidism and is currently completed. Visen Pharmaceuticals (Shanghai) Co., Ltd. leads this study, which shows 4 recorded versions since 2021 — indicating limited longitudinal coverage. The change history captured here reflects the iterative nature of clinical trial conduct.
Status Flow
Change History
4 versions recorded-
Feb 2026 — Present [monthly]
Completed PHASE3
Status: Recruiting → Completed
-
Sep 2024 — Feb 2026 [monthly]
Recruiting PHASE3
-
Jul 2024 — Sep 2024 [monthly]
Recruiting PHASE3
-
Jun 2022 — Jul 2024 [monthly]
Recruiting PHASE3
First recorded
Jul 2021
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Visen Pharmaceuticals (Shanghai) Co., Ltd.
For direct contact, visit the study record on ClinicalTrials.gov .