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Home
About Us
Our Core Values
Board of Directors
Senior Management
GI Clinical Advisory Board
Our Science
Our Technology
Our Lead Candidate
Our Pipeline
Clinical Trials & Publications
Expanded Access Program
Partnering
Investors
Investment Highlights
Events & Presentations
Stock Information
Stock Quote
Stock Chart
Analyst Coverage
Financials
Quarterly Results
SEC Filings
SEDAR Filings
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Governance Documents
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Information Request Form
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Investment Highlights
Home
About Us
Our Core Values
Board of Directors
Senior Management
GI Clinical Advisory Board
Our Science
Our Technology
Our Lead Candidate
Our Pipeline
Clinical Trials & Publications
Expanded Access Program
Partnering
Investors
Investment Highlights
Events & Presentations
Stock Information
Stock Quote
Stock Chart
Analyst Coverage
Financials
Quarterly Results
SEC Filings
SEDAR Filings
Governance
Governance Documents
Committee Composition
Resources
Investor FAQs
Information Request Form
Investor Email Alerts
Investor Contacts
News
Proprietary Diffusphere™ extended-release technology platform
High quantity of active drug delivered versus other polymer-based technologies
Patent protection for lead candidate (not including patent term extensions)
Global multi-billion dollar market for lead candidate in osteoarthritis
U.S. market for osteoarthritis valued at almost US$2 billion
Current global osteoarthritis treatments challenged by poor safety, limited efficacy, and/or limited duration
Pipeline of clinical and non-clinical candidates
Lead product candidate for treatment of OA symptoms is widely used corticosteroid with well-established systemic safety record
Additional non-clinical candidates in post-surgical pain, anti-infective and veterinary indications, and potentially in oncology
Compelling research results for lead candidate
Well tolerated with minimal local and systemic impact
Demonstrated immediate and sustained pain relief (WOMAC score)
Demonstrated no cartilage damage over 10-month period in non-clinical setting
Improvement in WOMAC function
Expected clear regulatory pathway for lead candidate
Lower risk approval pathway using U.S. 505(b)(2) application
Open IND with the FDA for Phase 2 study
Use of proceeds support completion of Phase 2 study
Manufacturing at initial commercial launch scale
Experienced management team and board
Extensive medical, life science and public company experience