ZG-801 Phase III Trial - Randomized, Double-blind, Placebo-controlled Trial of ZG-801 in Patients With Hyperkalemia -
Latest Information Update: 30 Sep 2024
At a glance
- Drugs Patiromer (Primary)
- Indications Hyperkalaemia
- Focus Therapeutic Use
- Sponsors Zeria
- 24 Sep 2024 According to a CSL media release, CSL Vifor granted Zeria the exclusive right to develop and market Veltassa in Japan, in 2018. Zeria expects to begin the marketing following National Health Insurance price listing. Veltassa has now received marketing authorizations in 41 countries worldwide, including US and EU.
- 24 Sep 2024 According to a CSL media release, CLS's partner Zeria Pharmaceutical Co., Ltd. (Zeria) has received marketing authorization approval for Veltassa from the Japan's Ministry of Health and Labor Welfare (MHLW) for the treatment of adult patients with hyperkalemia. The approval is based on Zeria's MA application supported by positive clinical data from the Japanese clinical development program of ZG-801conducted in patients with hyperkalemia in Japan.
- 18 Apr 2023 Status changed from active, no longer recruiting to completed.