Marco Aurélio Gomes Veado
4 min read
•
November 28, 2025
For decades, families affected by dementia have waited for meaningful breakthroughs, treatments that go beyond temporary symptom relief and instead offer neuroprotection, slowed progression, or even prevention.
Yet the scientific landscape is full of promising discoveries that never seem to reach clinical practice.
This article explores the structural, economic, and scientific pressures that may delay or suppress innovation, not through conspiracy theories, but through well-documented systemic issues that affect how drugs are researched, approved, and commercialized.
Our goal at MCI and Beyond is to empower caregivers and families with information, advocate for transparency, and promote evidence-based hope.

Pharmaceutical companies face enormous financial pressure. Bringing a new drug to market can cost over $2 billion and take more than 10–12 years. Because of this, companies often prioritize medications that:
This is one reason why drugs targeting progressive, chronic conditions, like Alzheimer’s and other dementias, receive more investment than preventive therapies or low-cost interventions that cannot be patented.
Studies have shown that research dollars frequently shift toward treatments offering incremental improvements, not radical breakthroughs, because the latter carry high financial risk. That does not mean better treatments are intentionally hidden, but it does suggest that the most promising innovations may not align with corporate incentives.
Many scientifically credible approaches have been historically underfunded, including:
Neuroprotective strategies involving sleep, diet, exercise, vascular health, stress reduction, and cognitive training produce measurable benefits, yet they lack the commercial appeal of medications. As a result, they remain under-promoted.
Drugs like metformin, lithium, melatonin, or anti-inflammatory agents have shown potential in early dementia research. But because they are inexpensive and off-patent, companies have little motivation to invest in large clinical trials.
AI-based (read our article on technology for dementia care) early detection, brain stimulation therapies, and digital cognitive support tools are advancing rapidly. However, they compete for attention in a market dominated by drug-centered solutions (read our article on: Are We Overmedicating Dementia Patients? The Silent Role of Big Pharma).
Even when novel therapies show promise, regulatory agencies and approval pathways are slow and conservative. This caution protects patients, but it can also delay access to innovations for years (ambiguous issue).
As a result, dozens of therapies stall in clinical trials, not because they fail, but because the infrastructure for testing them is inadequate.
Hopefully, it is not intentional. But systemic forces (profit models, rigid regulations, lack of funding for non-drug solutions, and slow scientific pipelines) can functionally keep better options away from families.
A more accurate framing would be:
Better treatments exist, but the current system makes it hard for them to reach the people who need them, especially those in low-income communities.
What Caregivers and Families Can Do Now? While we push for change, families can take meaningful steps.
First of all, always stay informed through trusted sources, as we do here at MCI and Beyond, where we advocate for equitable access, early detection, community education, and low-cost preventive strategies that empower families today, not years from now.
Ultimately, change comes from awareness, advocacy, and community action—not waiting for a miracle drug.
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