Goldman Sachs 47th Annual Global Healthcare Conference 2026
Logotype for Mineralys Therapeutics Inc

Mineralys Therapeutics (MLYS) Goldman Sachs 47th Annual Global Healthcare Conference 2026 summary

Event summary combining transcript, slides, and related documents.

Logotype for Mineralys Therapeutics Inc

Goldman Sachs 47th Annual Global Healthcare Conference 2026 summary

10 Jun, 2026

Strategic updates and financial transactions

  • NDA for lorundrostat was submitted late last year, with a PDUFA date set for December 6; preparations for launch are ongoing, including building out market access and medical affairs teams.

  • Acquired full IP and royalty rights to lorundrostat from Tanabe for $200M upfront and $100M in future milestones, expected to be offset by royalty savings.

  • Raised $150M in equity and secured a $500M debt facility, with $100M drawn upfront and additional tranches tied to FDA approval and commercial milestones.

  • The royalty buyback was opportunistic, driven by Bain Capital's acquisition of Tanabe and their desire to monetize non-core assets.

  • Leadership emphasized alignment of the royalty buyback with long-term value creation and business development strategy.

Clinical data and market positioning

  • LAUNCH-HTN post-hoc analysis showed lorundrostat reduced blood pressure effectively in both CKD and non-CKD patients, with a 55% reduction in albuminuria for those with baseline albuminuria.

  • Safety profile was favorable, with low incidence of hyperkalemia, and results were consistent with prior Explore-CKD data.

  • Data supports potential renal protection and de-risks future CKD development, with significant overlap between hypertension and CKD populations.

  • Physicians value blood pressure reduction, safety, and proteinuria benefit; lorundrostat addresses all three.

Market access, payer dynamics, and launch strategy

  • Initial market entry targeted at fourth-line hypertension, with anticipated rapid expansion to third-line based on demand and payer feedback.

  • Step edits for access will require evidence of prior use of three antihypertensive drugs, but not necessarily an MRA; process expected to be straightforward for most patients.

  • PBM reforms have shifted incentives, but clinical value and service-based fees remain important; parity access is the goal rather than exclusive contracts.

  • Sales force buildout is underway, with leadership and MSL teams in place; full sales force expected to be ready 90 days before PDUFA.

  • Baxfendy’s $500/month price aligns with payer research and is not expected to restrict access for the target population.

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