From Vitrisa to Drive — A Decade of Aptamer Innovation
Drive Therapeutics was founded in 2019 by Ryan Quick through the acquisition of intellectual property assets developed at Vitrisa Therapeutics. The anti-VEGF and anti-IL-8 aptamers that form the core of D28L001 were discovered by the same team that had pioneered aptamer development across two prior companies — Regado Biosciences and Vitrisa.
Doug Gooding joined as CEO in 2020, bringing a track record of building aptamer companies from pre-clinical discovery to clinical testing and public markets. Together, the co-founders pair the chemist who knows how to make aptamers at scale with the CEO who has taken aptamer therapeutics into the clinic before.
Headquartered in Morrisville, North Carolina, Drive has assembled a network of world-class advisors, CDMOs, and collaborators to support its mission of developing a first-in-class bispecific aptamer therapeutic for diseases driven by dual angiogenesis and inflammation.
Regado Biosciences co-founded by Doug Gooding and Chris Rusconi. Aptamer team forms in Durham, NC.
Regado advances aptamer anticoagulant through Phase 2a. Conducts largest commercial aptamer synthesis (600 mmol). Team members collaborate across discovery, CMC, and clinical operations.
Regado IPOs on NASDAQ.
Core team reassembles at Vitrisa Therapeutics. The anti-VEGF and anti-IL-8 aptamers are discovered. Ryan Quick manufactures 1,900+ compounds.
Drive Therapeutics founded. Ryan Quick acquires aptamer IP from Vitrisa. D28L001 bispecific construct program begins.
Doug Gooding joins as CEO. NSF SBIR Phase I grant awarded. Manufacturing process optimization continues. Preclinical characterization of candidate bispecific constructs advances.
NSF SBIR Phase II awarded ($990,477, July 2025 – June 2027) to advance D28L001 preclinical development; $1.32M in competitively awarded non-dilutive grant capital to date.
Formulation viscosity and biophysical characterization completed across the PEG-carrier panel; two co-finalist candidates carried forward to the rabbit PK study that selects the lead. Two US composition patents issued and the bispecific application allowed. NSF interim reports filed.
$10M Seed round to take D28L001 through the porcine PVR study and IND-enabling work to an IND.