Scientific Evidence

Research-Guided
Botanical Formulations

Quality Standards & Botanical Research

Our botanical formulations are developed following quality standards and guided by published research into wellness support

Our Research Foundation

EPI1's scientific approach is built on decades of research into immunology, the endocannabinoid system, and nutritional therapeutics

Scientific Methodology

Our research methodology combines traditional clinical science with cutting-edge AI analytics through AI powered Clinical Research. This integration allows us to:

  • Analyze complex immunological pathways with unprecedented precision
  • Track real-time patient outcomes and biomarker changes
  • Continuously refine formulations based on data feedback
  • Identify molecular synergies between compounds

Validation Approach

EPI1 employs multi-tiered validation to ensure safety, efficacy, and reproducibility:

  • In vitro studies: Cellular response and cytokine modulation
  • Blood assay validation: Quantitative biomarker analysis
  • Clinical observation: Real-world patient outcomes
  • Peer review: Publication in scientific journals
30+
Years of Research
150+
Patients Studied
15+
Countries
Multiple
Patents Filed

Clinical Research Areas

Our research focuses on conditions with significant unmet medical needs and shared immunological mechanisms

Long COVID &
Post-Viral Recovery

Market Size
$10B+
Growing rapidly

Research Focus:

Cytokine dysregulation and persistent inflammation (elevated IL-6, TNF-α, IFN-γ)

Mitochondrial dysfunction and cellular energy depletion

Endocannabinoid system modulation for neuro-immune balance

Microbiome restoration and gut-immune axis healing

Early Results: Patients report significant reduction in fatigue, brain fog, and inflammation markers within 4-8 weeks

Autoimmune
Modulation

Market Size
$120B+
Multiple conditions

Research Focus:

Immune homeostasis restoration without suppression

T-regulatory cell enhancement and balance

Anti-inflammatory pathway activation (CB2, PPAR-γ)

Oxidative stress reduction and cellular protection

Conditions Studied: Rheumatoid arthritis, lupus, inflammatory bowel disease, psoriasis, multiple sclerosis

Oncology
Support Therapy

Market Size
$400B+
By 2028

Research Focus:

Chemotherapy-induced peripheral neuropathy (CIPN) management

Cancer-related fatigue and inflammation reduction

Quality of life improvements during treatment

Immune resilience and recovery enhancement

Adjunctive Approach: Designed to complement standard cancer treatments, not replace them

Regenerative
Medicine

Market Size
$30B+
By 2030

Research Focus:

Stem cell therapy enhancement through immune modulation

Bioactive sutures for accelerated wound healing

Tissue regeneration and cellular repair mechanisms

Integration with AI-driven personalized protocols

Innovation: Combining cellular therapies with immunomodulation for synergistic healing

Evidence Base

Customer Feedback

Feedback from customers using our botanical formulations as part of their wellness routine

Key Biomarkers Tracked

Inflammatory Cytokines
IL-6, TNF-α, IFN-γ, IL-1β levels
Oxidative Stress Markers
MDA, 8-OHdG, glutathione ratios
Immune Cell Profiles
T-cell subsets, NK cell activity
Metabolic Function
Mitochondrial markers, ATP production
Endocannabinoid Levels
Anandamide, 2-AG, receptor expression

Patient-Reported Outcomes

Fatigue Reduction
Validated fatigue severity scales
Cognitive Function
Memory, focus, brain fog assessment
Pain & Inflammation
Visual analog scales, joint mobility
Quality of Life
SF-36, daily activity levels
Sleep Quality
Duration, efficiency, restorative sleep

Preliminary Clinical Observations

70%+
Patients Report Improvement
Fatigue and inflammation reduction
4-8
Weeks to Notable Results
Average response timeline
95%+
Safety Profile
Minimal adverse events reported

* Results based on observational studies. Formal clinical trials in progress. Individual results may vary.

Strategic Research Partnerships

Collaborating with leading institutions to advance clinical validation and regulatory pathways

UAGM Partnership

Universidad Ana G. Méndez

  • School of Naturopathy access
  • Multiple lab facilities
  • Toxicology testing
  • Chromatography analysis

PRCCI Collaboration

Puerto Rico Clinical & Translational Research Consortium

  • Early-phase trials
  • Clinical study design
  • FDA-aligned protocols
  • Data quality assurance

Inteco Partnership

Research & Development Institute

  • Post-market studies
  • Animal model research
  • Bioavailability testing
  • Quality control validation

NIH Grant Pathways

EPI1 is actively pursuing funding through NIH translational research programs to support clinical validation and accelerate regulatory approval pathways.

Our research aligns with NIH priorities including Long COVID recovery, autoimmune disease management, and precision medicine approaches.

NCCIH Programs
Complementary & integrative health research
NIAID Initiatives
Post-viral syndrome & immune recovery
NCI Support
Cancer supportive care research
SBIR/STTR Grants
Small business innovation pathways

Future Research Initiatives

Planned studies and expansion of our clinical research program

1

Randomized Controlled Trials

2024-2025

  • Double-blind, placebo-controlled Long COVID study (n=150)
  • Safety and efficacy assessment in autoimmune conditions
  • Dose optimization and pharmacokinetic profiling
  • Multi-center trial design with academic partners
2

Expanded Biomarker Studies

Ongoing

  • Comprehensive cytokine panel analysis (20+ markers)
  • Metabolomic profiling and pathway analysis
  • Microbiome sequencing and diversity assessment
  • Endocannabinoid receptor expression studies
3

Oncology Support Research

2025-2026

  • CIPN management pilot study with cancer centers
  • Quality of life assessments during chemotherapy
  • Immune resilience markers in cancer patients
  • Safety data collection in oncology population
4

Regenerative Medicine Trials

2026+

  • Stem cell therapy enhancement protocols
  • Bioactive suture clinical validation
  • Wound healing acceleration studies
  • Combination therapy efficacy assessment

Research Timeline

2022
Phase I Safety Studies
2025
Randomized Controlled Trials
2026
Phase II Efficacy Studies
2027+
Regulatory Submissions

Join Our Research Journey

Whether you're a patient interested in participating in clinical studies, a researcher seeking collaboration, or an institution looking for partnership opportunities — we welcome your inquiry.

4
Clinical Areas
3
Research Partners
150+
Patients Studied
20+
Biomarkers Tracked

All research conducted under IRB approval and FDA-aligned protocols. Patient safety and data privacy are our highest priorities.