We’re evaluating whether an investigational combination of two long-approved medications can help restore healthy brain energy signaling in PTSD. This IRB oversight study provides active medication — no placebo, clinical monitoring, and personalized dose optimization.
Emerging research suggests PTSD involves disrupted astrocyte-neuron energy support and dysregulated cellular “energy switches.” HB-01 is designed to address these pathways by combining two established medicines to support energy production and coordination. Use in PTSD is investigational and is being evaluated in this trial.
improve mitochondrial output and fuel routing to key circuits.
Normalize astrocyte signaling to reduce “energy crisis” states.
Cognitive, functional, and safety assessments at each visit.
A long-approved medication hypothesized to help shift astrocytes from “conserve” to “support” mode and bolster mitochondrial efficiency. Safety monitored throughout.
A well-established medicine hypothesized to stabilize astrocyte activity and reduce inefficient over-excitation in stress networks.
A confidential phone screen determines fit and answers your questions.
Under stress, astrocytes may prioritize conservation over support, reducing efficient fuel delivery to circuits that govern cognition and emotion.
AMPK/mTOR signaling helps cells balance survival vs. performance; dysregulation is an active research focus in stress-related disorders.
Astrocyte calcium activity coordinates local networks; instability can impair synchrony and resilience under stress.
“It felt like someone turned the lights back on. I could think clearly and be present again.”
-Study participant, Week 8 (individual experience; results vary)
Our research team will answer questions and discuss eligibility.
Cost? There is no cost for study medication or study visits.
Placebo? This protocol uses active medication for all enrolled participants.
Voluntary? Participation is voluntary; you may withdraw at any time.
Important Information & Disclaimers
HB-01 combines two FDA-approved medications for other conditions. Its safety and efficacy for PTSD are investigational and are being evaluated in this IRB oversight clinical study. The information above is not medical advice. You will receive and should review the informed consent documents before deciding whether to participate.
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