Scientific Program
Scientific Program
Scientific agenda
Last update: March 15, 2024
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Last update: March 15, 2024 ✍️
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Friday, March 15, 2024
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Arrival to the Embassy of France
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By Course Director Professor Patrick Rossignol (Monaco, MON) on behalf of the scientific committee
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Moderators: George Bakris (Chicago, USA) & Glenn Chertow (Stanford, USA)
Speakers (10 minutes each):
Investigator’s perspective: Hiddo Heerspink Lambers (Groningen, NED)
Discussants (5 minutes each):
Statistician’s perspective: Tom Greene (Salt Lake City, USA)
Investigator’s perspective: Matt Weir (Baltimore, USA)
Investigator’s perspective: Marc Froissart (Lausanne, SUI)
Statistician’s perspective: Tim Friede (Göttingen, GER)
Industry perspective: Jerome Rossert (AstraZeneca, USA), Maria Borentain (Bayer, USA) & Svenja Seide (Boehringer Ingelheim, GER)
Regulators’ perspective: Kiyoshiro Tanaka (PMDA, JPN) & Frank Holtkamp (EMA, NED)
Panel discussion with all of the above
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In the lobby of the Maison Française
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Moderator: Christoph Wanner (Würzburg, GER) & Meg Jardine (Sydney, AUS)
Which is/are the most suitable triple/quadruple combination therapy for CKD patients (with or without diabetes) acknowledging the two/three recommended pillars (ACEI/ARB, SGLT2i, +/- nsMRA, to be initiated simultaneously vs sequentially ?), and new molecules /targets being developed (GLP1 RA, ASI, nsMRAs, endothelin antagonists): which sponsors (industry vs. academia) and trial design consideration (registration vs pragmatic trials, potentially embedded in registries) to ultimately change guidelines and medical practices ?
Speakers (10 minutes each):
Investigator viewpoint : Vlado Perkovic (Sydney, AUS)
Investigator viewpoint: George Bakris (Chicago, USA)
Discussants (5 minutes each):
Funder’s perspective: Harold Feldman (PCORI, USA)
Industry perspective: Jerome Rossert (AstraZeneca, USA), Maria Borentain (Bayer, USA), Fred Yang (KBP Biosciences, USA) & Ekaterina Sokareva (Novo Nordisk, DEN)
Regulator’s perspective: Toshiyuki Takahashi (PMDA, JPN)
Panel discussion with all the above
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In the lobby of the Maison Française
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Moderator: Vlado Perkovic (Sydney, AUS)
Capitalysing on several positive trials, how to best define a therapeutic strategy and next trials?
Speakers (10 minutes each):
Investigator’s perspective: Jürgen Floege (Aachen, GER)
Investigator’s perspective: Jonathan Barratt (Leicester, GBR)
Discussants (5 minutes each):
Investigator’s perspective: Dana Rizk (Birmingham, USA )
Industry perspective: Radko Komers (Travere, USA), Kerry Cooper (Vera Therapeutics, USA), Jeffrey Hafkin (Otsuka US)
Regulators’ perspective: Yaa Oppong (FDA, USA), Toshiyuki Takahashi (PMDA, JPN) & Frank Holtkamp (EMA, NED)
Panel discussion with all the above
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In the lobby of the Maison Française
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Moderator: Hiddo Heerspink Lambers (Groningen, NED)
Speakers (10 minutes each):
Investigator’s perspective: Joseph Bonventre (Boston, USA)
Discussants (5 minutes each):
Investigator’s perspective: Mathias Kretzler (Ann Arbor, USA)
NIDDK perspective: Ivonne Schulmann (NIDDK, USA)
Industry perspective: Paul Hockings (Antaros Medical, SWE) & Erwin Berthier (Tasso Inc, USA)
Panel discussion with all the above
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Moderator: Meg Jardine (Sydney, AUS)
Speakers (10 minutes each):
Investigator’s perspective: Glenn Chertow (Stanford, USA)
IRB’s perspective: Andrew McLachlan (Sydney, Australia)
Investigator’s perspective: Amanda Siriwardana (Sydney, AUS)
Discussants (5 minutes each):
Investigator’s perspective: Amit Garg (London, CAN)
KHI perspective: Uptal Patel (KHI, USA)
NHLBI perspective: Yves Rosenberg (NHLBI, USA)
CRO perspective: Cassandra Kennedy (Fortrea, USA)
Industry perspective: Dustin Little (AstraZeneca, USA)
Panel discussion with all the above
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In the lobby of la Maison Française
Saturday, March 16, 2024
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In the Lobby of la Maison Française
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Moderators: Prabir Roy-Chaudhury (Chapel Hill, USA) & Patrick Rossignol (Monaco, MON)
Speakers (8 minutes each):
Lessons from the latest major outcome randomized trials in hemodialysis (challenges and opportunities)
Insights from Convince (Device) Peter Blankestijn (Utrecht, NED)
Insights from Alchemist (drug) Patrick Rossignol (Monaco, MON)
Creating an Innovation Substrate for ESKD: Phaneth Keo (Fresenius Medical Care, USA)
Discussants (4 minutes each):
Investigator’s perspective: My ideal patient for Hemodiafiltration and Next Steps Needed: Michel Jadoul (Brussels, BEL)
Investigator’s perspective: Is there a role for MRA’s in Hemodialysis Patients and Next Steps Needed: Jule Pinter (Würzburg, GER)
Industry perspective: Endo AVFs and DCBs: Why-Who-When-What : Lindsay Downing (Becton Dickinson, USA)
Industry perspective: Patient Centered Innovation: What does it Really Mean?: Despina Rüssmann (CSL Vifor, SUI)
NIDDK perspective: Creating an Innovation Substrate for Dialysis and Vascular Access: Dany Gossett (NIDDK, USA)
Regulator's perspective: Optimizing the Regulatory Substrate for the Next Generation of Dialysis and Vascular Access Products: Robert Lee (FDA, USA)
Patient's perspective: A Patients Perspective on Quality in Dialysis and Vascular Access: Vanessa Evans (Boston, USA)
Value Based Care Perspective: Discovery and Process of Care Innovation as Drivers of Value Based Care: Rajiv Poduval (Panoramic Health, USA)
Panel discussion with all of the above
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In the lobby of la Maison Française
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Moderator: Vlado Perkovic (Sydney, AUS)
Speakers (10 minutes each):
Investigator’s perspective: Peter Rossing (Copenhagen, DEN)
Discussants (5 minutes each):
Industry perspective: Thomas Idorn (Novo Nordisk, DEN)
Panel discussion with all the above
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In the lobby of la Maison Française
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Moderators: Mathieu Legrand (San Francisco, USA) & (Patrick Rossignol, Monaco, MON)
Speakers (10 minutes each):
Lessons from the latest major outcome randomized trials in AKI:
The ADQI meeting on clinical trials endpoints: Guiding principles: Marlies Ostermann (London, GBR)
Insights from STARRT-AKI trial: Sean Bagshaw (Edmonton, CAN)
Discussants (5 minutes each):
Investigator’s perspective: Sradha Kotwal (Sydney, AUS)
Investigator’s perspective: Amit Garg (London, CAN)
90-day redmissions with the NIH ongoing trial: Chirag Parikh (Baltimore, USA)
Patient’s perspective: D’Arcy Duquette (Calgary, CAN)
Industry perspective: NEUTRALIZE-AKI: Kevin Chung (SeaStar Medical, USA) & Juliane Bernholz (AM-Pharma, NED)
Regulator’s perspective: Frank Holtkamp (EMA, NED)
Payer’s perspective: Abigail Ryan (CMS, USA)
Panel discussion with all of the above
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In the lobby of the Maison Française
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Moderators: Dana Fuhrman (Pittsburgh, USA) & Sean Bagshaw (Edmonton, CAN)
Speakers (10 minutes each):
Identification of Core Outcome Domains for future COS in AKI:
Methodology for COS generation: Bruno Garcia (Brussels, BEL)
Domains that matter: Natalje Stanski (Cincinatti, USA)
Discussants (5 minutes each):
Repair domain/biomarkers for AKI in transplant: Chirag Parikh (Baltimore, USA)
Investigator’s perspective: Jay Koyner (Chicago, USA)
Patient’s perspective: D’Arcy Duquette (Calgary, CAN)
Industry perspective: Vadim Paluy (Novartis, USA) & Christine Solinsky (Alexion, USA),
Payer’s perspective: Abigail Ryan (CMS, USA)
Panel discussion with all of the above
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Final words by Professor Patrick Rossignol and co-directors, and adjourn