Delivering Genetic Medicines Beyond Biological Barriers

Building a future where patients with genetic diseases have access to medicines that address the root causes of their conditions—not just the symptoms

Delivering Genetic Medicines Beyond Biological Barriers

Building a future where patients with genetic diseases have access to medicines that address the root causes of their conditions—not just the symptoms

Our Vision

At QurCan, we are working to overcome the biological barriers that prevent genetic medicines from reaching the brain. By combining advanced materials science, molecular engineering, and translational biology, we aim to translate breakthrough science into practical RNA medicines that preserve neurological function, improve independence, and deliver lasting benefits for patients and their families.

Through our internal pipeline and partnered programs, we are advancing transformative medicines for genetically driven diseases with significant unmet needs.

Our Vision

At QurCan, we are working to overcome the biological barriers that prevent genetic medicines from reaching the brain. By combining advanced materials science, molecular engineering, and translational biology, we aim to translate breakthrough science into practical RNA medicines that preserve neurological function, improve independence, and deliver lasting benefits for patients and their families.

Through our internal pipeline and partnered programs, we are advancing transformative medicines for genetically driven diseases with significant unmet needs.

Our Approach: TERP™ Technology

RNA and DNA medicines can precisely target disease biology,
but their success depends on safe and efficient delivery to the
right tissues and cells.

This is especially challenging in neurological diseases,
where the blood–brain barrier restricts access to the brain.

Existing approaches also face limitations: viral vectors may
constrain repeat dosing and payload capacity, while direct
administration into the brain or cerebrospinal fluid is invasive.

Our Approach: TERP™ Technology

RNA and DNA medicines can precisely target disease biology, but their success depends on safe and efficient delivery to the right tissues and cells.

This is especially challenging in neurological diseases, where the blood–brain barrier restricts access to the brain.

Existing approaches also face limitations: viral vectors may constrain repeat dosing and payload capacity, while direct administration into the brain or cerebrospinal fluid is invasive.

TERP Payloads

Our Science

TERP™—Target-Engineered Responsive Polymer—is QurCan’s proprietary next-generation polymer–lipid nanoparticle platform. It is designed for systemic, non-viral, and repeat-dosable delivery of genetic medicines to targeted tissues and cells. Through a proprietary library of components, TERP formulations can be customized for:

  • Selective tissue and cellular targeting
  • Compatibility with different therapeutic payloads
  • Responsive intracellular payload release
  • Reproducible and scalable manufacturing

TERP Payloads

Our Science

TERP™—Target-Engineered Responsive Polymer—is QurCan’s proprietary next-generation polymer–lipid nanoparticle platform. It is designed for systemic, non-viral, and repeat-dosable delivery of genetic medicines to targeted tissues and cells. Through a proprietary library of components, TERP formulations can be customized for:

  • Selective tissue and cellular targeting
  • Compatibility with different therapeutic payloads
  • Responsive intracellular payload release
  • Reproducible and scalable manufacturing
Brain

The CNS-penetrating TERP technology (C-TERP) is designed to facilitate active blood–brain–barrier (BBB) penetration via dual-specific transport pathways.

Blood–brain barrier cross-section
Brain
Blood–brain barrier cross-section

The CNS-penetrating TERP technology (C-TERP) is designed to facilitate active blood–brain–barrier (BBB) penetration via dual-specific transport pathways.

The C-TERP platform offers:

Systemic CNS Delivery

TERP is engineered to transport genetic medicines across the blood–brain barrier following systemic administration, with the goal of achieving broad distribution across functionally important and deep brain regions.

Repeat-Dosable by Design

The non-viral and biocompatible properties of TERP are designed to support repeat administration, flexible dose titration, and treatment adjustment over time.

Broad Payload Versatility

TERP supports diverse therapeutic payloads, creating opportunities for gene silencing, protein replacement, gene regulation, and genome-editing strategies.

The C-TERP platform offers:

Systemic CNS Delivery

TERP is engineered to transport genetic medicines across the blood–brain barrier following systemic administration, with the goal of achieving broad distribution across functionally important and deep brain regions.

Repeat-Dosable by Design

The non-viral and biocompatible properties of TERP are designed to support repeat administration, flexible dose titration, and treatment adjustment over time.

Broad Payload Versatility

TERP supports diverse therapeutic payloads, creating opportunities for gene silencing, protein replacement, gene regulation, and genome-editing strategies.

Leadership Team

Dr. Mohammad Ali Amini

Dr. Mohammad Ali Amini

CEO

Chief Executive Officer & Co-Founder

DVM, PhD

Dr. Amini is an experienced entrepreneur with strong business leadership and is experienced in various aspects of business formation, operation, and management. He is a veterinary doctor with several years of clinical practice and is also a PhD in Pharmaceutics from the University of Toronto. He possesses extensive experience in leading and managing teams and projects in this field. He co-founded QurCan Therapeutics (formerly known as Nanology Labs) in 2018 and has been successful in establishing strategic relations with leading healthcare organizations in Canada, as well as internationally. He is the recipient of several prestigious international entrepreneurship awards, including the LabCentral Ignite Golden Ticket and MaRS HealthKick.

Dr. Shirley Wu

Dr. Shirley Wu

CSO

Chief Scientific Officer & Co-Founder

PhD, Professor, FAAPS

Dr. Shirley Wu is the Director of the Advanced Pharmaceutics Laboratory at the Leslie Dan Faculty of Pharmacy, University of Toronto. She has over 27 years of experience and expertise in developing innovative drug delivery systems and pharmaceutical formulations for unmet medical needs, including cancer. She is a co-inventor of 14 issued and 6 pending patents worldwide.

Dr. John Reid

Dr. John Reid

CBO

Chief Business Officer

PhD, MBA

Dr. Reid brings over 25 years of experience in business development, pharmaceutical drug discovery, technology transfer, and biotech operations to the opportunity and challenge of developing new therapeutics based on innovative medical research. Prior to joining QurCan Therapeutics in 2020, he was Director of Technology Development and Commercialization at the University Health Network, Director of Strategic Partnering and Business Development at AstraZeneca, and Director of Molecular Sciences at AstraZeneca. He holds a PhD from the University of California (Berkeley), an MBA from LeBow-Drexel, and Executive Education from Wharton.

Dr. Azhar Z. Abbasi

Dr. Azhar Z. Abbasi

EVP of R&D

Executive VP of R&D

PhD

Dr. Abbasi is one of the founding members of QurCan Therapeutics and leads the R&D activities. In this role, he oversees the development of manufacturing processes, analytical methods, quality control, and new product design to support the QurCan Therapeutics portfolio. He brings over 15 years of experience in nanoparticle-based drug product development, their pre-clinical screening, and CMC-related regulatory requirements from early to post-IND stage. Prior to joining QurCan Therapeutics, he worked in the R&D of Apotex Inc. Dr. Abbasi holds a PhD in nanomedicine from the University of Marburg, Germany.

Dr. Chanson He

Dr. Chanson He

EVP of Operations

Executive VP of Operations

PhD

Dr. He is one of the founding members of QurCan Therapeutics and leads the operations of the company in support of its goals. He has several years of experience in the pharmaceutical industry and more than 10 years of experience in nano-formulations development, scale-up, and drug product quality control. His expertise covers preclinical, nonclinical studies, and IND-enabling studies. Dr. He received his PhD degree from the East China University of Science and Technology, Shanghai, China.

Strategic Partnership

Eli Lilly & Company

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Toronto, ON M5G 0B7, Canada

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