Queen's University

Overview
Founded in 1841, Queen’s University in Kingston, Ontario is one of Canada’s leading research-intensive institutions, combining quality and intensity in research with excellence in undergraduate and graduate education.
Research is a core component of the mission of Queen’s University. A member of the U15, a group of Canada’s leading research-intensive universities, Queen’s ranks highly in terms of research funding and research intensity amongst universities nationally.
Their commitment to research excellence is evident in the many exceptional national and international accolades awarded to their researchers, most recently Queen’s Professor Emeritus Dr. Arthur B. McDonald was awarded the 2015 Nobel Prize in Physics – with co-recipient Takaaki Kajita of Japan – in Stockholm, Sweden.
This excellence, found across disciplines – from health care, the environment, materials, energy, law, economics, culture, and many others – attracts the best students, the best faculty, and the best collaborators from local and global communities, other institutions, government, and industry.
Through their diverse programs, Queen’s university promotes social innovation, fosters creative expression, and explores how societies work best. And it’s this culture of excellence that has made Queen’s one of Canada’s leading research universities.
Queen’s Partnerships and Innovation
The Queen’s Partnerships and Innovation (QPI) team supports the advancement of partnerships, research collaborations, and knowledge mobilization as well as innovation, entrepreneurship, and economic development. The QPI team develops and facilitates partnerships with industry, governments, not-for-profit organizations, and other academic institutions to advance the research enterprise at Queen’s and the commercialization of inventions, and to strengthen the regional innovation ecosystem in Kingston and Eastern Ontario. 
With support from external funding, the QPI team offers numerous services, resources and programs to support entrepreneurs, including those from Queen’s, and to accelerate the growth of startups and small to medium-sized enterprises (SMEs) within Kingston and Eastern Ontario. The team has transformed more than 1,000 invention disclosures into hundreds of technologies covered by at least one patent; additionally, the team has supported the founding and-or acceleration of hundreds of startups and SMEs in the Kingston region.

<h1 id="background">Background</h1>
Von Willebrand factor (vWF) is a multimeric blood glycoprotein with a monomeric size of ~250 kilodaltons. vWF plays a major role in hemostasis. It exerts its function by binding to other proteins, in particular factor VIII, and it is important in platelet adhesion to wound sites. Factor VIII is bound to vWF in the circulation with a half-life of up to 12 hours but without this binding it is rapidly degraded with a reduced half-life of 1-2 hours.
Defects in vWF lead to the bleeding disorder von Willebrand disease (VWD), which is characterized by mucosa-associated bleeding and bleeding due to trauma or surgery. VWD is is subdivided into types 1, 2, and 3. Patients with type 1 VWD have blood levels of vWF of 20%-50% of normal and represent upto 80% of all VWD patients. Symptoms are mild. Type 2 VWD patients have functional defects in vWF due to missense mutations and represent between 15%-30% of all VWD patients. Type 2 is broken down into four subtypes: type 2A, type 2B, type 2M and type 2N, depending on the presence and behaviour of multimers, molecular chains of VWF. Symptoms are mild to moderate. Finally, type 3 VWD is a severe deficiency and is usually caused by genetic defects in the vWF gene leading to homozygous or compound heterozygous vWF null alleles. Type 3 patients represent &lt;5% of all VWD patients. Symptoms are typically severe, and include spontaneous bleeding episodes, often into their joints and muscles. According to Orphanet annual incidence of type 3 VWD varies between countries ranging from 1/2,000,000 to 1/350,000 in Europe and the USA and with estimates of around 1/500,000 in countries where consanguinity is more frequent.
<h1 id="technology-overview">Technology Overview</h1>
Unlike other vWD patients – those with type 3 VWD do not respond to desmopressin and therefore substitution therapy with vWF is necessary. Historically this has been accomplished with plasma-derived vWF-containing concentrates. These concentrates have evolved from crude preparations of plasma proteins to plasma-derived concentrates containing both vWF and factor VIII.
However, some patients (7.5-9.5% of cases) develop alloantibodies against vWF rendering the substitution treatment ineffective and resulting in an anaphylactic response associated with the formation of immune complexes. In these cases, alternative treatments, such as continuous infusion of recombinant factor VIII or recombinant activated factor VII, are considered. Furthermore, the varying amounts and quality of these vWF concentrates, including the varying content of Factor VIII, have contributed to the lack of a standardized approach to replacement therapy. To try to overcome this lack of standardization a recombinant vWF drug, Vonvendi, was approved by the FDA in 2015. It has predicted global sales of $400-500 million USD.
<img src="https://s3-eu-west-1.amazonaws.com/assets.in-part.com/figures/LjUVLrclRFmXBwnkIsrL_VON1.png" alt="Figure 1: Plasmid Injection Into vWF Deficient Mice Rescues Factor VIII" />
Queen’s researchers have developed novel recombinant vWF and Factor VIII using ancestral sequence reconstruction. These proteins have a number of functional improvements over existing vWFs and will translate into improved therapy for both vWD and haemophilia patients. For example, clearance data in rodents indicates these novel AnvWF proteins remain in the circulation twice as long as native vWF. In addition, these AnvWF have higher affinity for Factor VIII than native human vWF forms. This additional benefit in forming a complex should provide improved treatment for haemophilia and reduce rate of infusions needed. Thus, AnvWF could be provided alone, as a recombinant protein complex with Factor VIII, or via gene therapy.
<img src="https://s3-eu-west-1.amazonaws.com/assets.in-part.com/figures/gwXSWnpBTRaAQGVO3RPz_VON2.png" alt="Figure 2: Clearance Studies of Ancestral vWFs in Mice" />
As an example, one of the AnvWFs (An-70, <img src="https://s3-eu-west-1.amazonaws.com/assets.in-part.com/figures/Zb5QvbPcS9m2ampOIA6u_von3.png" alt="Figure 3" />) appears to be the equivalent to Factor IX-Padua. This AnvWF has:
<ul>
<li>Has a higher specific activity than human vWF</li>
<li>Possesses higher collagen binding as well as improved Factor VIII rescue in vivo as demonstrated by gene therapy experiments</li>
<li>Surface plasmon resonance (SPR) data shows that that the An-70 protein binds Factor VIII molecules with greater affinity than other vWF molecules.</li>
<li>Has a 3-fold enhanced half-life over human vWF</li>
<li>Thus An-70 appears to be a good drug candidate but also could be used to design and modify a new hybrid.</li>
</ul>
Only the D’D3 domains of vWF are necessary to stabilize Factor VIII in vivo. With the enhanced affinity and circulation time of AnvWFs for human FVIII, a single injection of a FVIII-VWF fragment protein complex may provide more time in the normal range of FVIII coverage and also more protection/higher trough levels following conventional dosing for extended half-life products.
Please see 2021 Publication in Blood Advances: <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876868/">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876868/</a>
<h1 id="benefits">Benefits</h1>
<ol>
<li>Biochemical improvements as listed above will translate into a longer lasting more efficacious vWF therapy</li>
<li>Potential to add to Factor VIII for improved treatment of hemophilia A</li>
<li>Flexible treatment modalities - can be given as a recombinant protein therapeutic or as a gene therapy</li>
</ol>
<h1 id="applications">Applications</h1>
<ol>
<li>Von Willebrand Disease: type I, III and 2N VWD</li>
<li>Potentially Hemophilia</li>
</ol>
<h1 id="opportunity">Opportunity</h1>
Preclinical Development/seeking exclusive licensee, research collaborator or venture investment