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Relypsa Announces Presentation of New Clinical and Real-World Analyses of Veltassa® at AMCP Nexus 2018
22 oct. 2018 08h00 HE | Relypsa, Inc.
REDWOOD CITY, Calif., Oct. 22, 2018 (GLOBE NEWSWIRE) -- Relypsa, Inc., a Vifor Pharma Group company, will present new data on Veltassa® (patiromer) at the Academy of Managed Care Pharmacy’s AMCP...
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Relypsa Announces Presentation of New Clinical and Real-World Analyses of Veltassa® at ASN Kidney Week 2018
09 oct. 2018 16h00 HE | Relypsa, Inc.
REDWOOD CITY, Calif., Oct. 09, 2018 (GLOBE NEWSWIRE) -- Relypsa, Inc., a Vifor Pharma Group company, will present new data on Veltassa® (patiromer) at the American Society of Nephrology (ASN) Kidney...
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Relypsa Announces Appointment of Patrick Treanor as President
01 oct. 2018 08h00 HE | Relypsa, Inc.
REDWOOD CITY, Calif., Oct. 01, 2018 (GLOBE NEWSWIRE) -- Relypsa, Inc., a Vifor Pharma Group company, today announced the appointment of Patrick Treanor as president on an interim basis, effective...
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Relypsa Announces FDA Approval of Supplemental New Drug Application to Enable the Usage of Veltassa® (patiromer) With or Without Food
08 mai 2018 08h00 HE | Relypsa, Inc.
REDWOOD CITY, Calif., May 08, 2018 (GLOBE NEWSWIRE) -- Relypsa, Inc., a Vifor Pharma Group company, today announced that the United States (U.S) Food and Drug Administration (FDA) approved a...
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Relypsa Funds Three Innovative Research Projects on Hyperkalemia and Associated Disorders
16 avr. 2018 16h00 HE | Relypsa, Inc.
REDWOOD CITY, Calif., April 16, 2018 (GLOBE NEWSWIRE) -- Relypsa, Inc., a Vifor Pharma Group company, today announced that it has awarded three research grants to supplement institutional funding...
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Relypsa Presents Patiromer Clinical Trial Data on Serum Potassium in Patients with Hyperkalemia at the National Kidney Foundation 2018 Spring Clinical Meetings
11 avr. 2018 08h00 HE | Relypsa, Inc.
REDWOOD CITY, Calif., April 11, 2018 (GLOBE NEWSWIRE) -- Relypsa, Inc., a Vifor Pharma Group company, today announced results from a pooled analysis of three clinical trials evaluating the effects...
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Relypsa Announces Presentation of New Clinical and Real-World Analyses of Veltassa® at ASN Kidney Week 2017
03 nov. 2017 17h30 HE | Relypsa, Inc.
REDWOOD CITY, Calif., Nov. 03, 2017 (GLOBE NEWSWIRE) -- Relypsa, Inc., a Vifor Pharma Group company, today announced results from a prespecified analysis of data from the Phase 4 TOURMALINE study of...
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Relypsa Announces European Approval of Veltassa® to Treat Adult Patients with Hyperkalemia (Elevated Blood Potassium Levels)
21 juil. 2017 08h00 HE | Relypsa, Inc.
Today’s European Commission approval is the second worldwide; in the U.S., more than 33,000 patients have been treated with Veltassa since it was approved by the FDA in 2015Patients with advanced...
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Relypsa Presents Veltassa® Phase 4 Data Showing Consistent Efficacy and Safety Whether Taken With or Without Food in Patients with Hyperkalemia
19 avr. 2017 18h00 HE | Relypsa, Inc.
In the study, Veltassa, the first new medicine approved by the FDA for hyperkalemia in more than 50 years, showed a consistent potassium-lowering effect and safety profile whether taken with or...
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Relypsa Announces Publication of Results of Veltassa Drug-Drug Interaction Studies in Journal of Cardiovascular Pharmacology and Therapeutics
13 févr. 2017 16h30 HE | Relypsa, Inc.
Phase 1 studies with 12 oral medications commonly used in hyperkalemic patients with chronic kidney disease showed minimal risk for drug-drug interactions with Veltassa when other oral drugs are...