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Manila Times Business

Mineralys Therapeutics Presents New Lorundrostat Data in Participants with Hypertension and Chronic Kidney Disease at ASN Kidney Week 2026

In the large, pivotal Phase 3 Launch-HTN trial, lorundrostat achieved similar significant blood pressure reductions in participants with and without CKD, with consistent reductions across Stages 1-3 CKD In participants with CKD, lorundrostat also reduced albuminuria by 52% versus placebo, validating similar findings in a prior trial in participants with established CKD RADNOR, Pa., Oct. 22, 2026 (GLOBE NEWSWIRE) -- Mineralys Therapeutics, Inc. (Nasdaq: MLYS), a biopharmaceutical company focused

Context & Analysis

Hypertension and chronic kidney disease are not distant problems for Filipino families. They are among the leading causes of death and long-term disability in the country, and they carry one of the heaviest financial burdens on households and on PhilHealth. Dialysis alone consumes a significant share of the national health insurance budget, and many patients still cannot access regular treatment. Any drug that can slow or prevent kidney damage in hypertensive patients therefore represents a potential relief valve for a system under constant strain.

Lorundrostat is still in clinical trials, so no Filipino patient will be prescribed it anytime soon. But the story matters for several audiences here. For Filipino investors who track Nasdaq-listed biotech stocks, Phase 3 success is a meaningful signal that the company is moving closer to commercialization, which in turn affects the broader sector's risk appetite. Mineralys Therapeutics is a small-cap biopharma play, and its progress adds to a growing investor thesis that aldosterone-targeted therapies — a mechanism distinct from the ACE inhibitors and calcium channel blockers that dominate Philippine pharmacies — represent a viable next wave of cardiovascular treatment.

For the Philippine pharmaceutical industry, the relevance is more indirect but still real. The country imports the vast majority of its finished drugs, and new-to-market therapies typically arrive through multinational distributors after US or EU approval. The gap between a Phase 3 readout and actual availability in a local pharmacy can stretch five to seven years, factoring in FDA Philippines registration, pricing negotiations, and PhilHealth formulary inclusion. That timeline matters for local distributors and hospital procurement teams who need to plan ahead.

What to watch next is whether Mineralys secures FDA approval in the US and how the pricing conversation plays out. A drug that reduces albuminuria by the magnitude reported here could, in theory, delay dialysis onset and lower long-term healthcare costs. But if it enters the market at a premium price point typical of novel biologics and targeted therapies, Philippine insurers may be slow to cover it, leaving out-of-pocket costs as the primary barrier. For now, this is a promising data point that sits comfortably in the "watch list" category for Filipino healthcare stakeholders — significant enough to track, too early to bank on.

Analysis by IJE Software — original commentary on the story above.

This is an excerpt. Read the full article at the original source:

Source: manilatimes.net

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