Disclaimer

The alfapump® system is currently not approved in Canada for commercial use. DSR® therapy is still in development and is currently not approved in the United States or Canada. Any statements regarding safety and efficacy arise from ongoing pre-clinical and clinical investigations which have yet to be completed. Sequana Medical makes no claims of safety or effectiveness of the DSR® therapy in the U.S. or Canada. There is no link between the DSR® therapy and ongoing investigations with the alfapump® system in Europe, the United States or Canada.

Tag

Gereglementeerd
alfapump® – US FDA approval anticipated Q1 2025 and US launch planned for H2 2025; Strong progress with US reimbursement – CPT III codes issued & NTAP Application filed DSR® – Publication of RED DESERT and SAHARA data in peer-reviewed “European Journal of Heart Failure” highlights potential as treatment for Cardiorenal Syndrome;  Positive data from...
Read More
PRESS RELEASE REGULATED INFORMATION 9 August 2024, 07:00 CEST Ghent, Belgium – 9 August 2024 –Sequana Medical NV (Euronext Brussels: SEQUA) (the “Company” or “Sequana Medical“), a pioneer in the treatment of fluid overload in liver disease, heart failure and cancer, announces today that it received a transparency notification from the party listed below, notifying...
Read More
PRESS RELEASE REGULATED INFORMATION 5 August 2024, 06 pm CEST Ghent, Belgium – 5 August 2024 – Sequana Medical NV (Euronext Brussels: SEQUA) (the “Company” or “Sequana Medical“), a pioneer in the treatment of fluid overload in liver disease, heart failure and cancer, announces today that it received a transparency notification from the party listed...
Read More
PRESS RELEASE REGULATED INFORMATION 1 August 2024, 06:30 pm CEST Ghent, Belgium – 1 August 2024 – Sequana Medical NV (Euronext Brussels: SEQUA) (the “Company” or “Sequana Medical“), a pioneer in the treatment of fluid overload in liver disease, heart failure and cancer, announces today that it received a transparency notification from the parties listed...
Read More
Transparency Notifications from Shareholders Ghent, Belgium – 19 July 2024 – Sequana Medical NV (Euronext Brussels: SEQUA) (the “Company” or “Sequana Medical“), a pioneer in the treatment of fluid overload in liver disease, heart failure and cancer, announces today that it received a transparency notification from the shareholder listed below, notifying the number of voting...
Read More
PRESS RELEASE REGULATED INFORMATION 10 July 2024, 06:00 p.m. CEST Ghent, Belgium, 10 July 2024 – Sequana Medical NV (Euronext Brussels: SEQUA) (the “Company” or “Sequana Medical“), a pioneer in the treatment of fluid overload in liver disease, heart failure and cancer, announces today that in the context of the confirmation of the contribution in...
Read More
PRESS RELEASE REGULATED INFORMATION 5 July 2024, 06:00 p.m. CEST Ghent, Belgium, 5 July 2024 – Sequana Medical NV (Euronext Brussels: SEQUA) (the “Company” or “Sequana Medical“), a pioneer in the treatment of fluid overload in liver disease, heart failure and cancer, announces today that in the context of (i) a subscription to new shares...
Read More
PRESS RELEASE REGULATED INFORMATION 6 JUNE, 2024, 07.00 CEST Sequana Medical announces data on alfapump® safety and quality of life to be presented at EASL Congress 2024 “alfapump implantation significantly improved quality of life and showed similar safety outcomes compared to a contemporaneously enrolled refractory ascites cohort”;oral poster presentation by Dr. Bajaj Matched cohort analysis...
Read More
PRESS RELEASE REGULATED INFORMATION 23 May 2024, 06:00 pm CEST Ghent, Belgium – 23 May 2024 – Sequana Medical NV (Euronext Brussels: SEQUA) (the “Company” or “Sequana Medical“), a pioneer in the treatment of fluid overload in liver disease, heart failure and cancer, today announces that all proposed resolutions submitted to the Annual and Extraordinary...
Read More
PRESS RELEASE REGULATED INFORMATION – INSIDE INFORMATION 22 MAY 2024, 07:00 CEST Positive and collaborative meeting with FDA PMA substantive review complete;  No further new questions on clinical or pre-clinical data FDA Advisory Panel no longer expected FDA Marketing Approval now anticipated in Q1 2025 Planned US commercial launch remains H2 2025 Ghent, Belgium –...
Read More
1 2 3 4 9

PERSBERICHTEN

INSCHRIJVEN OP ONZE PERSBERICHTEN