EU approves label update for AZ’ Lokelma
Update provides dosing regimen specifically for hyperkalaemia in patients with end-stage renal disease on stable haemodialysis
Read Moreby Selina McKee | May 4, 2020 | News | 0
Update provides dosing regimen specifically for hyperkalaemia in patients with end-stage renal disease on stable haemodialysis
Read Moreby Selina McKee | Apr 27, 2020 | News | 0
The drug’s label now includes a dosing regimen specifically to treat hyperkalaemia in patients with end-stage renal disease on stable hemodialysis
Read Moreby Selina McKee | Dec 16, 2019 | News | 0
The drug will be funded on the NHS to treat hyperkalaemia
Read Moreby Selina McKee | Oct 29, 2018 | News | 0
Preliminary guidelines released by the National Institute for Health and Care Excellence do not recommend NHS funding for hyperkalaemia treatments Lokelma and Veltassa.
Read Moreby Selina McKee | May 21, 2018 | News | 0
US regulators have finally issued a green light for AstraZeneca’s Lokelma as a treatment for hyperkalaemia – elevated potassium levels in the blood – in adult patients.
Read Moreby Selina McKee | Mar 23, 2018 | News | 0
AstraZeneca’s Lokelma has been approved in Europe to treat hyperkalaemia in adult patients.
Read Moreby Selina McKee | Jul 21, 2017 | News | 0
European regulators have approved Vifor Pharma’s new potassium binder Veltassa to treat hyperkalaemia in adult patients.
Read Moreby Selina McKee | Mar 20, 2017 | News | 0
AstraZeneca’s hyperkalaemia treatment ZS-9 has suffered another setback on the path to US approval having been rejected by regulators for the second time. The drug giant also unveiled a US-based partnership with Circassia for development and commercialisation of COPD drugs Turdoza and Duaklir.
Read Moreby Selina McKee | Oct 19, 2016 | News | 0
US regulators have accepted AstraZeneca unit ZS Pharma’s resubmission of ZS-9, a potassium-binding compound being developed for hyperkalaemia.
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