ImStar Therapeutics Canada

ImStar Therapeutics is a private biotechnology company headquartered in Vancouver that is developing new approaches to treat patients with Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig's disease.

The company is developing compounds directed at a proprietary new therapeutic target for ALS discovered by co-founder Dr. Jean-Pierre Julien called TANA (i.e. TDP-43 Associated NF-kB Activation). The lead drug candidate, IMS-088, is a novel small molecule compound targeting the NF-kB activation pathway currently in preclinical development for ALS.

IMS-088 is the first in a series of novel compounds derived from withaferin A (WA), a natural withanolide isolated from the leaves of the winter cherry plant (withania somnifera).  In preclinical animal studies, WA showed promise but lacked suitable pharmacologic characteristics to be developed as a therapeutic drug.

Therapeutics targeting the TANA pathway could treat multiple neurodegenerative diseases expressing TDP-43 pathology such as ALS, Alzheimer's, Parkinson's and Dementia.

TAR DNA-binding protein 43 (TDP-43) was recently identified as a major disease-associated protein in ALS. Under normal conditions, TDP-43 regulates RNA and is predominantly localized in the nucleus. However, in ALS-affected neuronal cells the protein is misprocessed resulting in aggregation in the cytoplasm and a loss of motor function.

A recent discovery has shown that, in patients with ALS, TDP-43 unexpectedly associates with and activates nuclear factor-κB (NF-κB), an inflammation-regulating protein. This leads to exaggerated immune responses and motor neuron destruction. Inhibition of the pathway in an ALS disease model produced substantial improvements in disease and motor function illustrating this is an important new drug target.

Novel Withanolides

ImStar chemists have designed novel withanolides related to WA that have superior drug like properties. IMS-088 is the lead drug candidate in this series that is currently being developed for ALS. These compounds are covered by a new composition of matter patent filing.

TANA Inhibitors

ImStar is also developing various approaches to block TDP-43 activity and has identified novel single chain variable domain antibody fragments (scFv) that inhibit TDP-43 and block it's associated NF-kB activation. 

Website:
www.imstartx.com
Year Founded
2012
Biotech Phase of Development
Current Timeline
Anticipate initiating formal IND-enabling studies by mid 2015
Current Investors
Management and angel investors
IP Status
Worldwide PCT and provisional filings covering compositiona of matter, use and target
Recent Milestones
Preclinical POC using novel compounds in transgenic models of ALS
Management Team Highlights
Daniel Wattier President & CEO, Co-Founder Co-founded Valocor Therapeutics and led company as CEO until its acquisition by Dermira in 2011. Previously with QLT as President of QLT Specialty Medicine, and at J&J / Centocor, where he was responsible for the US launch of Remicade, achieving over $4B in annual sales. Jean-Pierre Julien, PhD Chief Scientific Officer, Co-Founder Canada Research Chair in Neurodegeneration at Laval University. Internationally recognized leader in ALS research. Member of: The Robert Packard Center for ALS at Johns Hopkins University, the Gairdner Medical Review Panel. Recipient of the prestigious Sheila Essey Award for ALS research from the American Academy of Neurology. Julia Levy, PhD Director and Chairman Co-founder & CEO of QLT. Recipient of many awards for achievements in business and science including: the Order of Canada, the Female Entrepreneur of the Year, the Friesen-Rygiel prize for medical research and the Prix Galien Canada research award. Chris Fibiger, PhD Director and Scientific Advisor CSO MedGenesis Therapeutix. Recently served as CSO of Biovail Corporation until its acquisition by Valeant. Previously VP & Global Therapeutic Area Head Neuroscience at Amgen and VP Neuroscience Discovery Research & Clinical Investigation at Lilly. Until 1998, Professor and Head of the Division of Neurological Sciences at UBC. Ian Massey, D.Phil, Chemistry Director and Scientific Advisor Co-founder & CEO of Synosia Therapeutics until its acquisition by Biotie Therapies Corp in 2011. Currently COO & President US Operations of Biotie. Previously Sr VP Head of Research & Preclinical Development at Roche Palo Alto and VP Head of Neurobiology Roche Bioscience. Prior VP Preclinical Research at Syntex
Daniel Wattier
Daniel Wattier
CEO 

Kairos Therapeutics Canada

Kairos Therapeutics has developed a proprietary next generation antibody-drug conjugate (ADC) platform based on novel toxin, linker and site-specific conjugation technology. Kairos has demonstrated superior pre-clinical in-vivo efficacy over T-DM1. Further pre-clinical studies demonstrate Kairos’ ADCs have superior tolerability and therapeutic index, compared to other leading platforms which may lead to greater clinical efficacy. Through key partnerships, Kairos is developing a novel therapeutic pipeline and is out-licensing its ADC platform to companies seeking access to state-of-the-art technology.  

Year Founded
2014
Biotech Subsector
John Babcook
President & CSO 

Naegis Pharmaceuticals Inc. Canada

Naegis, based in Vancouver, British Columbia, is developing novel, small-molecule leukotirene synthesis inhibitors (LTSIs) for serious inflammatory conditions.  The Company is currently focused on two proprietary programs: 

topical and oral therapy for Uveitis, a condition that is responsible for 10% of legal blindness in the US and for which there are limited therapeutic options. 

o oral therapy for Chronic Obstructive Pulmonary Disease (COPD),  a serious lung disease with increasing rates of mortality.

Naegis has developed a large library of LTSIs that are potent inhibitors of either 5-LO or LTA4H.  The Company is currently identifying a lead compound for selection for futher development for ocular disease, in particular Uveitis.

The Company is also advancing a series of compounds that are novel structures and highly selective and potent inhibitors of LTA4H, which are expected to be developed as new therpaies for COPD

Naegis is seeking pharmaceutical partners and capital investment to advance more rapidly their novel programs.

Year Founded
2010
Biotech Subsector
Biotech Phase of Development
Technology Overview
Leukotrienes are key inflammatory mediators implicated in many diseases. There is growing evidence of their central role in Uveitis. 5-LO inhibitors have been shown to reduce the clinical signs of uveitis in animal models. Naegis is developing potent 5-LO inhibitors that are both topically and orally active, with unique structures that are not expected to have the limitations of earlier 5-LO inhibitors. In COPD recent evidence has demonstrated the critical role for LTA4H in the progression and persistence of the disease. However it has recently been shown that LTA4H has a dual role and functions as both a pro and anti-inflammatory. Thus it is necessary to identify compounds that are active only against the pro-inflammatory function of the enzyme, whilst sparing its anti-inflammatory effects. Naegis is developing highly specific inhibitors of LTA4H that inhibit only the anti-inflammatory activity of LTA4H.
Alliance & Collaborations
In discussion
Current Financing Needs
$500,000 - $1,000,000
Current Timeline
Lead
Current Investors
Private.
IP Status
Proprietary compounds
Management Team Highlights
CEO - Dr. David Burgoyne an experienced medicinal chemist who has developed compounds that are in current human clinical trials. Also on the Board are Dr. Philip Davies, formerly Executive Director of Research and Area Head of Immunology at Merck, New Jersey. Also Dr Julia Levy, founder of QLT and developer of the first effective therapy for macular degeneration.
Ian McBeath
Ian McBeath
Corporate Development 

National Research Council of Canada Canada

The National Research Council- Industrial Research Assistance Program (NRC-IRAP) is a Canadian federal government program that offers financial and advisory services to accelerate the growth of businesses through innovation and technology. Regarded worldwide as one of the most successful programs of its kind, NRC-IRAP is a vital component of Canada’s innovation system

 

Lesley Esford
Strategic Business Advisor 

Novelogics Biotechnology Inc. Canada

Novelogics Biotechnology Inc. has developed unique next generation antibody immunotherapies for treating multiple types of advanced cancers including colon and prostate cancers.  Immunotherapies for cancer are anticipated to be a $35B per year industry in the upcoming years.  

Cancer Drugs with Safety in Mind

From the beginning the novel and specific design of the therapeutic antibody drug minimizes the potential for autoimmune diseases or harming good cells with the bad.  We are dedicated to making cancer treatments that won't make you sick to get you better.

Unecumbered, Founder Owned

Novelogics has developed their assets in an unecumbered envriornment allowing investors to work directly with the team.  At this time the companyis 100% founder owned and undiluted.  Novelogics is anticipating an early exit and has begun discussions with pharmaceutical companies interested in this area.

In addition; a related Medical Device

In addition to the drug, Novelogics has a second PCT Patent pending for a related medical device with a readily available "go to" market in place. 

Year Founded
2013
Biotech Subsector
Medtech Subsector
Biotech Phase of Development
Medtech Phase of Development
Technology Overview
We have developed a panel of patent-protected monoclonal antibodies which bind members of the NKG2D ligand family for use as novel cancer immunotherapies. Studies have shown that cancer cells in part evade the immune system by releasing biologically active molecules, such as NKG2D ligands that interfere with immune cells ability to fight cancer. These ligands are capable of shutting down tumour killing immune effector cells by overwhelming the important activation-type NKG2D receptors, basically putting them to sleep, so tumors can continue to grow undetected. Using our specifically designed antibody drug, we now have the potential to clear out these ligands and restore the immune system in a more balanced way to destroy tumor cells without over-stimulating the immune system or causing adverse side effects.
Alliance & Collaborations
None
Supporting Metrics or Evidence
Proof of concept studies in progress
Current Financing Needs
$2M
Current Timeline
Within 2 years of IND
Current Investors
Founder Funded
IP Status
Two PCT patents pending
Recent Milestones
Have developed a panel of monoclonal antibodies,filed two PCT patents (pending), assembled management and scientific advisory team, completed preliminary invitro and invivo studies and will continue with further characterization before moving on to humanization of the Ab (antibody).
Management Team Highlights
Dr. Cheney, President & CSO has 26 years in R&D (10 years in oncology) including 16 years in drug discovery and has contributed to successful drugs that are either on the market or in late stage clinical trials. Co-Founder, Elaine Allison has 25+ years of corporate management experience.
Ms Elaine Allison
Ms Elaine Allison
LinkedIn logo VP, Business Development 

PlantForm Canada

PlantForm Corporation is a Canadian company formed in 2008 to commercialize a low-cost, plant-based manufacturing platform for monoclonal antibodies, protein drugs and vaccines for cancer and other critical illnesses.

The company’s technology platform provides several advantages over mammalian cell culture and other fermentation systems used to produce most biologic drugs on the market today: it’s fast, efficient, highly versatile (for new product development) and easily scalable. Best of all, it’s capable of reducing manufacturing costs for life-saving drugs by up to 90 per cent.

PlantForm licenses its technology from the University of Guelph, where it was developed by Dr. J. Christopher Hall, a PlantForm founder and the company’s Chief Scientific Officer. Dr. Hall held the Canada Research Chair in Recombinant Antibody Technology from 2002 to 2014 and is a leading authority in the field. All relevant intellectual property is protected by patent filings.

PlantForm’s pipeline features both innovator and biosimilar products, including:

• biosimilar trastuzumab, a plant-produced version of the $6-billion breast cancer drug Herceptin® (animal studies successfully completed, human clinical trials scheduled for 2014, market entry anticipated 2017)

• biosimilar versions of two additional oncology drugs with combined annual global sales of $11.4 billion (2010)

• innovator antibodies for HIV/AIDS, funded by the Government of Canada and the Bill & Melinda Gates Foundation

• recombinant butyrylcholinesterase (rBuChE), an enzyme used as preventative medicine for people vulnerable to attack by nerve agents, organophosphates or other stimulants ($1.8-million contract with the U.S. Defense Advanced Research Projects Agency and $800,00 contract with Defence Canada)

Year Founded
2008
Biotech Phase of Development
Technology Overview
Plant based disruptive platform technology enabling us to produce ultra-low cost drugs
Alliance & Collaborations
JV in Brazil
Current Financing Needs
Series A Round - $10 million
Current Timeline
pre-clinical and moving into clinical
Current Investors
Angels, Founders, Atlantic Asset Trust
IP Status
4 families of patents
Recent Milestones
Mfg. of material for Phase 1 clinical trial
Management Team Highlights
Experienced Industry and Business Professionals
David Cayea
David Cayea
COO 
Don Stewart
CEO 

Precision NanoSystems Canada

Precision NanoSystems Inc. (“PNI”) has developed proprietary technology (NanoAssemblr) and companion Reagent Kits (SUB9KITS) that enable the simple manufacture of novel nanoparticles that are used to delivery genetic and small molecule medicines (nanomedicines). Nanomedicines are the "FedEx" of the health-care industry and are used for cell-specific delivery of research tools, diagnostic imaging agents and drugs to study, diagnose and treat disease. PNI's products are commercialized and in high demand from many of leading RNA and small molecule therapeutic biotechnology and pharmaceutical companies.  http://www.precisionnanosystems.com/products/

Year Founded
2010
Biotech Phase of Development
Current Financing Needs
PNI is currently raising Series A financing.
Recent Milestones
PNI launched its flagship NanoAssemblr Benchtop and SUB9KIT products in H2 2013. Since that time, PNI has seen significant latent demand for its products and is rapid expanding product manufacturing to satisfy market need. Additionally, PNI has achieved important technical milestones in it's large-scale nanomedicine platform and SUB9KIT products.
Management Team Highlights
PNI’s management, directors & advisors have collectively contributed to over 100 patents and 500 papers, started over 20 biotech companies, raised over $1B in financing/deals and have brought 4 drugs to market. PNI’s CEO, Dr. James Taylor has over 10 years of experience in commercializing biotech and has lead PNI since invention. PNI’s COO, Dr. Euan Ramsay, has 13 years commercializing biotech, has secured over $40M in leveraged financing, and has developed nanomedicines to clinical trials.
James Taylor
CEO 
Euan Ramsay
COO 

Pulse Infoframe Inc. Canada

Pulse Infoframe Inc strives to improve workflow using computer-assisted capture of patient data for specialists – our cloud based software enables better local and global sharing of the data for those who need it to make decisions – our end-user driven tools analyze the data to advance knowledge and thus patient care. Data can be directly entered into our system, and because we sit on top of any EMR system we access additional data that is not otherwise easily accessible. Once accessed, the data is de-identified, aggregated and mined producing meaningful information for our end-users. 

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We have applied our solution in various clinical verticals including speciality clinics (Melanoma, Oncology, Neonatology, etc), Imaging and PACS systems (with INFINITT PACS, ClearCanvas, etc) and clinical trials (tracking prostate cancer, Pharmacovigilance, economics, etc). Modules are versatile and can be templated to be used in a variety of systems for achieving the best workflow possible.

Year Founded
2011
Main Sector
Medtech Phase of Development
Technology Overview
Our flagship product is a cloud-based clinical and informatics solution that acts either as a stand-alone system aggregator or is interoperable with existing EMRs. Our solution is a database-driven informatics tools can be used for creating, maintaining, organizing and modeling clinical and outcomes data. Our sophisticated analytics engine can access data so that end-users can dynamically conduct online analysis and reporting. All clinical, imaging and administrative data is aggregated from heterogeneous data sources and is organized for effortless analytics. Data is securely stored within our platform with full reporting or auditing abilities.
Dr Femida Gwadry-Sridhar
Dr Femida Gwadry-Sridhar
LinkedIn logo Co-Founder & CEO 
BIO

Dr. Femida Gwadry-Sridhar is the Co-Founder and CEO of Pulse Infoframe Inc. She is a pharmacist, epidemiologist and methodologist with over 25 years of experience in clinical trials, disease registries, knowledge translation, health analytics and clinical disease outcomes.

Fred Brown
COO 

Sitka Biopharma Inc. Canada

Sitka Biopharma is a preclinical stage company focused on developing a breakthrough nanoparticle platform technology designed to increase absorption of drugs in difficult-to-penetrate tissues. Initially targeting oncology indications, we are developing our lead candidate to address the absorption challenge of intravesical chemotherapy for bladder cancer, and later intraperitoneal delivery for ovarian cancer.

We have demonstrated preclinical proof-of-concept for our lead candidate using in vivo and ex vivo models for bladder cancer.
Our goal is to complete our IND in 2015 and begin a Phase 1/2a Proof-of-Concept clinical trial in nonmuscle-invasive bladder cancer in 2016.

Partnership Opportunities for Platform Technology:

Our nanoparticle platform technology offers unique benefits over other nano-delivery systems and has the potential to be combined with a variety of different drugs to improve absorption for therapeutic uses in both humans and animals.

Benefits of Sitka's HPG nanoparticle platform include:

  • unimolecular structure
  • small size (8-10 nm)
  • tailored for a high degree of localized drug bioavailability in large surface applications
  • potential utility with a wide variety of drugs and indications

We welcome opportunities to collaborate with biopharmaceutical companies that wish to take advantage of our platform technology.

Year Founded
2013
Biotech Phase of Development
Technology Overview
Our nanoparticle platform technology offers unique benefits over other nano-delivery systems and has the potential to be combined with a variety of different drugs to improve absorption for therapeutic uses in both humans and animals. Benefits of Sitka's HPG nanoparticle platform include: unimolecular structure; small size (8-10 nm) and low viscosity; tailored for a high degree of localized drug bioavailability in large surface applications; potential utility with a wide variety of drugs and indications
Current Financing Needs
Seed private investment of $500,000; can be leveraged 2:1 up to $1.5M via partnership with CVI founded Accel-Rx (www.accel-rx.com)
Current Timeline
IND/Entry into clinic in early 2016
Current Investors
CDRD Ventures Inc (www.cdrdventures.com)
Michael Parr
President & Chief Scientific Officer