Research hero fallback

Curiosity fuels us,
collaboration shapes us.

Wonder Research advances mental healthcare through FDA Clinical Studies in psychedelic science, novel protocol development, and academic partnerships.

The Wondermed Pilot - Completed

Four years of clinical data powering the AI system

Wondermed’s 46-month telemedicine platform generated real-world data now embedded in Wonder Sciences’ AI systems and protocols.

  • 1,919 patients treated across real-world care settings
  • 24 U.S. states with active provider deployment
  • 40+ providers across a multi-state clinical network
Key Learnings:
  1. Mental healthcare needs a 360° AI operating system
  2. AI-native clinical operations generate exponential productivity
  3. One billion people are in need across a trillion-dollar market
  4. A chronic pain protocol would have the highest positive human impact
Results:

4 Advanced AI Utility Patents Filed, one unified, AI-native system with three integrated FDA products.

Wondermed

IRB Clinical Research Study with UCLA - Completed

Our clinical research paper:

“Sublingual Ketamine for Depression and Anxiety: A Retrospective Study of Real-World Clinical Outcomes”

UCLA IRB Study: 431 patients enrolled

Key Learnings:
  • 89% of patients with moderate to severe depression experienced clinically meaningful symptom improvement
  • 80% of patients with moderate to severe generalized anxiety disorder experienced clinically meaningful symptom improvement
  • 84% of patients with moderate to severe social anxiety disorder experienced clinically meaningful symptom improvement
Key Learnings:

Reengineer protocol focused on the science of Flow State - FDA 505(b)(2)

WonderFlow V1

A safer alternative to opioids for chronic pain

  • FDA 505(b)(2) Pathway
  • Leading Academic Partner
  • Study Launch: Q2 2027
  • Target NDA: 2030
  • 12-Week Virtual Protocol combining low-dose ketamine, supplements, CBT, mindfulness, and coaching
  • AI-Assisted opioid tapering with human-in-the-loop clinical oversight via WondermedAI
  • Continuous monitoring with real-time safety alerts via WondermedAI
  • Proprietary AI abuse surveillance designed for patient safety and regulatory compliance
  • Adaptive FDA Phase 2/3 design enabling accelerated clinical development
Wonder Relief

AI-guided protocol for anxiety and depression

FDA 505(b)(2) Pathway · Leading Academic Partner Study Launch: Q4 2027 · Target NDA: 2031
  • Flow State Protocol – Built on the neuroscience of flow to enhance neuroplasticity and therapeutic outcomes
  • Wonder Ketamine Lozenges – Proprietary formulation paired with cannabinoids to optimize efficacy and tolerability
  • WonderFlow Daily Supplement – Designed to support neuroplasticity, recovery, and treatment continuity
  • AI Personalization – Adaptive dosing, timing, and intervention pathways powered by patient response
  • Validated V1 Learnings – Refined from 1,500+ patients and IRB-backed clinical data
WonderFlow V2

The AI-native clinical OS for precision mental healthcare

FDA SaMD Submission: Q1 2028
Target FDA Approval: Q4 2028
  • WonderAI Pharmacology – Real-time prescribing intelligence and optimization across neuroplastic and psychiatric medications
  • WonderMate Copilot – Unified clinical support for prescribers and therapists
  • Wonder Cognitive (Cognitive Twin) – Continuous patient model across medication, therapy, and behavior
  • Continuous Monitoring – Always-on tracking, alerts, and adaptive care
  • AI-Native Infrastructure – One system connecting patients, providers, and protocols
Wondermed AI
Partner with Wonder Research
Curiosity fuels us,
collaboration shapes us.