PaTHway CHINA TRIAL: A Trial to Investigating the Safety, Tolerability and Efficacy of TransCon PTH in Adults With Hypoparathyroidism

PHASE3RecruitingINTERVENTIONAL
Enrollment

76

Participants

Timeline

Start Date

July 28, 2021

Primary Completion Date

December 31, 2022

Study Completion Date

December 31, 2025

Conditions
HypoparathyroidismParathyroid Hormone DeficiencyEndocrine System DiseasesParathyroid Diseases
Interventions
DRUG

TransCon PTH

TransCon PTH is supplied as a solution with a concentration of 0.3 mg PTH(1-34)/mL in a single-patient-use prefilled pen intended for SC injection.

DRUG

placebo

Placebo is supplied as a solution containing the formulation buffer for TransCon PTH in a single-patient-use prefilled pen intended for subcutaneous injection.

Trial Locations (1)

100730

RECRUITING

Peking Union Medical College Hospital, Beijing

All Listed Sponsors
lead

Visen Pharmaceuticals (Shanghai) Co., Ltd.

INDUSTRY