From Vitrisa to Drive — A Decade of Aptamer Innovation
Drive Therapeutics was founded in 2019 by Matt Levy and 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 D28P001 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 three co-founders represent a rare combination: the scientist who discovered the aptamers, the chemist who knows how to make them at scale, and the CEO who has taken aptamer therapeutics into the clinic before.
Headquartered in Research Triangle Park, 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. Chris Courts leads $260M in total equity financings.
Core team reassembles at Vitrisa Therapeutics. Matt Levy discovers anti-VEGF and anti-IL-8 aptamers. Ryan Quick manufactures 1,500+ compounds.
Drive Therapeutics founded. Matt Levy and Ryan Quick acquire aptamer IP from Vitrisa. D28P001 bispecific construct program begins.
Doug Gooding joins as CEO. NSF SBIR Phase I grant awarded. SynOligo continues manufacturing process optimization. Preclinical characterization of candidate bispecific constructs advances.
NSF SBIR Phase II awarded ($1.825M non-dilutive, July 2025 – June 2027) to advance D28P001 preclinical development. $2.1M raised to date.
Formulation viscosity and biophysical characterization completed across the PEG-architecture panel. NSF Interim Report 1 filed. D28P001 safety package drafted, drawing on the Vitrisa nonclinical precedent and >11,000-patient class clinical precedent in aptamers of the same chemistry.
Series A fundraise ($7–10M) to advance D28P001 through IND-enabling studies and into clinical development.