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David Young

President of Research and Development at Processa Pharmaceuticals
Executive
Board

About David Young

Dr. David Young (age 72) is Founder and President of Research & Development at Processa Pharmaceuticals and a director since 2017. He served as CEO (Oct 4, 2017–Aug 7, 2023) and Chairman until July 11, 2022, and transitioned to President, R&D on Aug 8, 2023 . He holds a B.S. in Physiology, M.S. in Medical Physics, and Pharm.D.-Ph.D. in pharmacokinetics-pharmacodynamics; he has met with FDA over 100 times and been a key member on more than 30 FDA indication approvals, with prior roles on FDA Advisory Committees and NIH grant review committees . Pay-versus-performance disclosure shows TSR deterioration through 2024 and continued net losses, underscoring a capital-constrained environment for pay design and retention: TSR value of $100 investment fell from $74 (2021) to $17 (2022), $5 (2023), and $1 (2024); net loss was $(11,427)k (2021), $(27,474)k (2022), $(11,122)k (2023), $(11,850)k (2024) .

Past Roles

OrganizationRoleYearsStrategic Impact
Processa PharmaceuticalsChief Executive Officer2017–2023Led regulatory science approach; transitioned leadership to CEO George Ng in Aug 2023 .
Processa PharmaceuticalsChairman of the BoardUntil Jul 11, 2022Oversight of strategy and governance; role separated from CEO to strengthen independence .
Processa PharmaceuticalsPresident, Research & DevelopmentSince Aug 8, 2023Leads Next Generation Chemotherapy (NGC) portfolio and regulatory strategy .
Questcor PharmaceuticalsBoard Member; later Chief Scientific Officer2006–2014Worked with FDA on sNDA approval of Acthar for infantile spasms; company sold for $5.7B in 2014 .

External Roles

OrganizationRoleYearsStrategic Impact
FDA Advisory CommitteesMemberContributed to guidance and review processes; foundation of Processa’s regulatory science approach .
NIH Grant Review CommitteesMemberSupported scientific rigor in oncology and rare disease programs .
World Orphan Drug Congress USA 2025Speaker (“Applying Principles of FDA’s Project Optimus…”)Apr 24, 2025Advocated dose-optimization principles for rare disease approvals aligned with Processa’s regulatory strategy .

Fixed Compensation

Metric202320242025 (Agreement Terms)
Base Salary ($)$160,200 $290,940 (incl. $181,733 voluntarily deferred) $387,920 (per Mar 19, 2025 agreement)
Target Bonus (%)40% of base salary
Actual Bonus Paid ($)— (not disclosed) — (not disclosed) — (no payout disclosed to date)

Performance Compensation

Incentive TypeGrant DateMetricTargetActualPayoutVesting/Distribution
RSUs (6,466 sh)Jun 28, 2024Service-basedTenure over 3 yearsOngoingRSUs vest over schedule3,233 sh vest Jan 1, 2025; 2,425 sh vest 1/3 on Jan 1, 2025 and monthly thereafter .
RSUs (event-based)Jun 28, 2024Nasdaq bid price compliance regainedEvent achievedAchieved Oct 2, 2024404 sh vestedDistribution per plan requirements .
RSUs (event-based)Jun 28, 2024First patient dosed in Phase 2 (NGC-Cap)Event achievedAchieved Oct 2, 2024404 sh vestedDistribution per plan requirements .
RSUsJan 1, 2023Service-basedAnnual vestingOngoingRSUs vest annually1,202 sh vest annually on Jan 1, 2024–2026 .
RSUs (event-based)Jul 1, 2021Capital raise milestoneCumulative $30M raisedPending/ongoing215 sh vest at eventDistribution at milestone; earlier tranches under 2021 grant also covered interim analyses .

Notes: Dr. Young reallocated a portion of his shortfall RSUs (10,500 sh originally granted) to other employees in 2023, evidencing team retention focus .

Equity Ownership & Alignment

MetricApr 22, 2024May 1, 2025Aug 7, 2025
Total Beneficial Ownership (sh)159,176 475,734 470,661
Ownership (%) of Outstanding Shares5.5% (O/S 2,856,104) 3.9% (O/S 11,884,356) <1% (O/S 50,349,149)
Direct/Common Shares (sh)80,544 205,405 217,332
Warrants (sh)186,750186,750
Family Entities (sh)18,851 18,851 18,851
CorLyst, LLC (sh)41,464 (disclaimed portion) 41,464 (disclaimed portion) 41,464 (22,920 on behalf of entities controlled; 18,544 other holders)
RSUs Issuable within 60 Days (sh)18,317 23,264 6,264
Pledged/Hedged SharesNo pledging or hedging disclosedNo pledging or hedging disclosedNo pledging or hedging disclosed .
Ownership Guidelines ComplianceNot disclosedNot disclosedNot disclosed .

Related-party note: CorLyst reimbursed Processa ~$112k (2023) and ~$110k (2024) for shared costs; Dr. Young is CorLyst’s CEO/Managing Member and disclaims beneficial ownership of a portion of CorLyst shares .

Employment Terms

ProvisionDr. Young Agreement (Mar 19, 2025)
Term/RolePresident, R&D; employment at-will under agreement .
Base Salary$387,920; reviewed annually .
Target Bonus40% of base salary via executive bonus pool .
Severance (termination by Company without cause or resignation for good reason)One year of base salary; 12 months of continued health coverage; full vesting of all time-based RSUs/equity then outstanding; subject to release .
“Good Reason” (examples)>5% decrease in base or target bonus (except broad temporary reductions) or material decrease in authority/responsibilities .
Non-Compete/Non-SolicitStandard employee non-compete and non-solicit for 1 year post-termination; confidentiality indefinite .
Change-of-Control (equity plan)Double trigger: if awards are assumed, unvested equity accelerates on termination without cause/for good reason within 24 months post-CoC; if not assumed, broad vesting/cash-out prior to CoC .

Board Governance

AttributeDetail
Board ServiceDirector since 2017; executive (non-independent) director .
Committee RolesNone (audit, compensation, nominating committees are independent-only) .
Chairman/LeadershipChairman is Justin Yorke (since Jul 11, 2022); CEO+Chair roles separated to bolster independence .
Meeting Attendance (2024)Board met 20 times; Dr. Young missed 2 meetings .
Independence StatusNon-independent (executive) .

Compensation Structure Analysis

  • Heavy equity mix and salary shortfall RSUs reflect cash conservation and alignment with milestones (Nasdaq compliance, clinical first-patient dosing), indicating event-based pay levers rather than pure financial KPIs (revenue/EBITDA) in a pre-revenue biotech context .
  • Plans prohibit option/SAR repricing and gross-ups; double-trigger equity acceleration limits “single-trigger” windfalls, supporting shareholder-friendly governance .
  • Year-over-year, Dr. Young’s cash salary increased from $160,200 (2023) to $290,940 (2024), with significant deferrals in 2024 ($181,733), and an updated 2025 agreement establishing $387,920 base and 40% target bonus—suggesting a pivot from pure equity-heavy comp towards competitive fixed pay for retention amid scale-up .

Related Party Transactions

  • CorLyst reimbursements: ~$112,000 (2023) and ~$110,000 (2024) for shared costs (payroll, health insurance, rent). Dr. Young is CEO and Managing Member of CorLyst; CorLyst held 56,467 PCSA shares as of Apr 22, 2024/May 1, 2025. Dr. Young disclaims beneficial ownership of a portion of CorLyst shares .

Risk Indicators & Red Flags

  • Ongoing net losses and TSR decline (2021–2024) increase retention risk and pressure to tie incentives to clinical and capital milestones rather than financial metrics .
  • Nasdaq bid-price compliance regained in 2024 via milestone; multiple reverse splits and large authorized share increases/dilution proposals signal financing risk and potential investor pushback on equity overhang (reverse split approvals in 2023 and proposals in 2025, plus authorization increase and plan evergreen) .
  • Plan protections (no repricing, double trigger) mitigate governance concerns; no pledging/hedging disclosed .

Say-on-Pay & Peer Group

  • Advisory say-on-pay presented in 2024 and 2025 proxies; peer group and vote outcomes not disclosed. Compensation Committee comprises independent directors (Chair: Geraldine Pannu; members: Khoso Baluch, James Neal), without consultant conflicts disclosed .

Expertise & Qualifications

  • Advanced degrees (Pharm.D.-Ph.D.) with extensive FDA engagement (>100 meetings) and >30 indication approvals; prior CSO role at Questcor tied to Acthar sNDA approval; speaking/publishing on dose optimization principles (Project Optimus) in rare disease drug development .

Investment Implications

  • Alignment: Event-based RSUs (Nasdaq compliance; Phase 2 first-patient dosing) create tangible execution incentives; 2025 agreement adds competitive fixed pay and 40% target bonus for retention .
  • Selling pressure: Warrants (186,750 sh) and RSUs vesting cadence could create periodic supply; larger corporate authorizations and plan evergreen dilute alignment but reflect capital needs typical of small-cap biotech .
  • Governance: Separation of CEO/Chair, independent committees, double-trigger CoC and no-repricing provisions are shareholder-friendly; related-party CorLyst reimbursements are modest and disclosed .
  • Execution risk: TSR and net losses emphasize reliance on clinical milestones and financing; compensation levers tied to operational KPIs are appropriate but require sustained delivery (trial progress, partnerships, capital access) .