
For important risk and disclaimer information, Click here.
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Tamara Williams | Managing Director
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(385) 600-1871
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Gary Levy | Managing Director |
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(516) 457-0104 |
Overview

- Investor returns expected via asset monetization (licensing, JV, M&A, trade sale) or security trading in private/public markets
- Focused on high-burden conditions with limited or no effective pharmacotherapies
- Differentiation supported by peer-reviewed science, clinical and human tissue data, and a portfolio spanning AMPAkines, GABAkines, and a proprietary dronabinol formulation
- Non-dilutive support (grants, Australian R&D incentives) helps offset development risk and capital intensity
- Compelling statistically significant human safety and efficacy established for Ampakines (CX717, CX1739) with more than 250 human subjects and dronabinol, enabling further Phase II/III clinical development for SCI, ADHD and OSA
- Preclinical scientific validation includes multiple animal models in SCI and epilepsy
- Team includes experienced biotech founders, and seasoned CNS drug developers
Path to Value Creation and Monetization
- Strategy: RespireRx intends to monetize programs via licensing, JVs, asset sales, or M&A rather than direct commercialization; value increases as assets advance through preclinical and clinical milestones
- Partner Economics: Typical structures include upfront payments, milestone payments, and royalties (or profit share in JVs), with development costs borne or shared by partners
- ResolutionRx: Late-stage program with PK/PD study followed by one Phase 3 with proprietary dronabinol formulation for obstructive sleep apnea (large poorly met need); pursuing 505(b)(2) pathway; plan to out-license/JV/sell. Leveraging research and development tax incentive in Australia (43.5%)
- EndeavourRx – AMPAkines:
- CX1739 – Mid-stage for spinal cord injury (bladder function); DoD-funded Phase 2A/B via trial at Shirley Ryan AbilityLab (~$1.8M grant)
- CX717 – Phase 2B for ADHD; ~$2.8M NIH grant pending or investor funding
- EndeavourRx – GABAkines: Preclinical program for treatment-resistant epilepsy; ~$3M NIH grant awarded to fund preclinical toxicology program; Phase 1 safety studies planned

Management
Dr. Arnold S. Lippa
Executive Chairman, CEO, CSO
- Founder and CEO of DOV Pharmaceuticals (IPO in 2002)
- 50+ years in neuropharma R&D and venture creation
- Inventor on numerous patents, author of peer-reviewed publications
- A prolific inventor with numerous patents in the medical arena and an author or co-author of numerous peer-reviewed scientific publications
Jeff E. Margolis
SVP, CFO, Board Member
- Founder of Aurora Capital LLC (former FINRA-member firm)
- 30+ years in biotech capital markets
- Co-founder of life sciences investment entity with Dr. Lippa
Richard Purcell
SVP R&D
- 40 years of clinical development and commercialization experience
- Former EVP of NuGenerex Immuno-Oncology
- Active advisor and professor; led biotech/MedTech startups and M&A strategy
Senior Research Fellows
Dr. Jeffrey Witkin, PhD
Ex-Lilly; >250 publications; co-founder Gilgamesh Pharma; lead on GABAkines
Rok Cerne, MD, PhD
Senior Research Fellow 30+ years CNS R&D; key role in analgesic/antiepileptic drug discovery; principal instigator on GABAkines grant application
Daniel Radin, MD, PhD
Group Leader – AMPAKines
Specific Risks
- Regulatory & Clinical Risk: Early-stage programs; no guarantees of success
- Capital Risk: History of operating losses; RespireRx Inc. lacks sufficient authorized common shares (may use preferred or require shareholder vote)
- Execution Risk: Dependent on CROs, strategic vendors, license holders
- Strategic Partnering Risk: Partnerships may not materialize or may be on unfavorable terms
- Macro Risk: Market volatility and public sector budget cuts (NIH, DOD) could reduce grant availability
- Competition: Competing with better-funded peers for IP, talent, capital, and market share
- Private securities are speculative, illiquid, and carry a high degree of risk – including the loss of the entire investment







