Beruflich Dokumente
Kultur Dokumente
V: DXD
This presentation contains forward-looking information within the meaning of applicable Forward-looking information is also subject to numerous risks and uncertainties, including:
securities laws in Canada, including statements about 3D Signatures business and corporate 3D Signatures short operating history; the possibility that 3D Signatures may never receive
strategy, product utility, development and performance, regulatory matters, manufacturing any product sales revenue or achieve profitability; risks involved in completing the clinical
plans and intellectual property plans and the expected development of 3D Signatures development of, and receiving regulatory approval for, our product candidates; uncertainties
business, trials, products, projects and partnerships. Particularly, information regarding our related to whether our product candidates under development will become effective
expectations of future results, performance, achievements, prospects or opportunities is diagnostics; as well as those risks and uncertainties discussed under Part 1 - Risk Factors in
forward-looking information. In some cases, forward-looking information can be identified by 3Ds Filing Statement, dated August 22, 2016 and available on the Companys SEDAR profile at
the use of forward-looking terminology such as may, will, expect, intend, estimate, www.sedar.com. Although we have attempted to identify important risk factors that could cause
anticipate, believe, continue, plans or variations of such words. In addition, any actual results to differ materially from those contained in the forward-looking information in this
statements that refer to expectations, intentions, projections or other characterizations of future presentation, there may be other risk factors not presently known to us, or that we presently
events or circumstances contain forward-looking information. For this purpose, any statement believe are not material, that could also cause actual results or future events to differ materially
that is not a statement of historical fact should be considered forward-looking information. from those expressed in the forward-looking information in this presentation.
Forward-looking information contained in this presentation is based on our opinions, estimates There can be no assurance that the forward-looking information in this presentation will prove
and assumptions in light of our experience and perception of historical trends, current to be accurate, as actual results and future events could differ materially from those anticipated
conditions and expected future developments, as well as other factors that we currently believe in such information. The forward-looking information contained in this presentation represents
are appropriate and reasonable in the circumstances. Despite a careful process to prepare and our expectations as of the date of this presentation or the date indicated, regardless of the time
review the forward-looking information, there can be no assurance that the underlying opinions, of delivery of the presentation. 3D Signatures undertakes no obligation to update the forward-
estimates and assumptions will prove to be correct. looking information in this presentation except as required by applicable law. All of the forward-
looking information contained in this presentation is expressly qualified by the foregoing
cautionary statements.
2
Unlike most diagnostic
companies, our proprietary
imaging software goes beyond
identifying whether a patient
suffers from a specific disease
or condition.
14 2,000+
patients
20
clinical studies
diseases
(Cancer & Alzheimers)
4
3D TELOMERE ANALYSIS
AN ENTIRELY NEW CLASS OF BIOMARKERS
3D Telomere Analysis is a
disruptive technology
based on a universal
structural biomarker 55
3D TELOMERE
ANALYSIS
3D telomere
organization
is a highly
DNA is packaged into Using fluorescent The 3D organization of accurate,
chromosomes. markers and
high resolution
telomeres within a given
cell is highly predictive
universal
At the tips of each microscopes, the of the disease status of biomarker.
chromosome are location of each the patient.
protective regions of telomere within a
DNA called telomeres. cell nucleus can be
visualized and
digitally analyzed.
6
ENABLING TRULY
PERSONALIZED MEDICINE
Who has a
particular disease DIAGNOSTIC
7
PUBLICATION SUMMARY
HODGKINS LYMPHOMA PROSTATE CANCER ALZHEIMERS
1. Knecht H, Mai S. The use of 3D telomere FISH for the characterization of the nuclear aarchitecture in 1. Wark L, Thomas Klonisch T, Quon H, Mai S. Three dimensional telomere signature dynamics in 1. Garcia A, Huang D, Righolt A, Kalaw MC, Mathur S, McAvon E, derson J, Luedke A, Itorralba J, Mai
EBV-positive Hodgkins lymphoma. (Invited manuscript). Methods Mol Biol 2016 (e-pub November 25) circulating tumor cells of early follow-up high-risk prostate cancer patients undergoing androgen- S. Super-resolution structure of DNA significantly differs in buccal cells of controls an Alzheimers
2017, 1532:93-104. deprivation and radiation therapy. Urol Oncol. 2016 Dec 9. pii: S1078-1439(16)30332-5. patients. Journal of Cell Physiol. Dec 2016 Accepted
2. Righolt CH, Knecht H, Mai S. DNA Superresolution Structure of Reed-Sternberg Cells Differs Between 2. Adebayo Awe J, Saranchuk J, Drachenberg D, Mai S. Filtration-based enrichment of circulating tumor 2. Garcia A, Mathur S, Kalaw MC, McAvoy E, Anderson J, Luedke A, Itorralba J, Mai S. Quantitative 3D
Long-Lasting Remission Versus Relapsing Hodgkins Lymphoma Patients. J Cell Biochem. 2016 cells from all prostate cancer risk groups. Urol Oncol. 2016 Accepted telomeric imaging of buccal cells reveals Alzheimers disease-specific signatures. J of Alzheimers
Jul;117(7):1633-7 Disease. Nov 2016 Submitted
3. Alsaadi A, Awe JA, Wark L, Saranchuk JW, Drachenberg D, and Mai S. Enumeration and Morphological
3. Lajoie V, Lemieux B, Sawan B, Lichtensztejn D, Lichtensztejn Z, Wellinger R, Mai S, Knecht H. LMP1 Features of CTCs in all Risk Groups of Localized and Metastatic Prostate Cancer Using Size-Based 3. Mai S. Editorial: Towards New Approaches in Alzheimers Research and Alzheimers Disease. Curr
mediates multinuclearity through downregulation of shelterin proteins and formation of telomeric Filtration. Urol Oncol. 2016 Submitted Alzheimer Res. 2016;13(7):728-9
aggregates. Blood. 2015 Jan 7. pii: blood-2014-08-594176.
4. Awe JA, Xu MC, Wechsler J, Benali-Furet N, Cayre YE, Saranchuk J, Drachenberg D, Mai S. 3D 4. Mathur S, Glogowska A, McAvoy E, Righolt C, Rutherford C, Willing C, Banik U, Ruthirakuban M, Mai
4. Kongruttanachok N, Cayre YE, Knecht H, Mai S. Rapid separation of mononuclear Hodgkin from telomeric analysis of isolated circulating tumor cells (CTCs) defines CTC subpopulations. Translational S, Garcia A. Three-dimensional quantitative imaging of telomeres in buccal cells identifies mild,
multinuclear reed-Sternberg cells. Lab Hematol. 2014 Mar 1;20(1):2-6. Oncology. 2013 2013 Feb;6(1):51-65. moderate and severe Alzheimer patients. J of Alzheimers Disease. 2014 Jan 1;39(1):35-48.
5. Righolt CH, Guffei A, Knecht H, Young IT, Stallinga S, van Vliet L, Mai S. Differences in nuclear DNA 5. Rak M, Gough K, Del Bigio MR, Mai S, Westaway D. In Situ FTIR Spectromicroscopy of Brain Tissue
organization between lymphocytes, Hodgkin and Reed-Sternberg cells revealed by structured from a Transgenic Mouse Model of Alzheimer Disease. Vibr Spectrosc 38, 133-141. 2005.
illumination. J Cell Biochem. 2014 Mar 4. MULTIPLE MYELOMA
6. Knecht H, Righolt C, Mai S. Genomic Instability: The Driving Force behind Refractory /Relapsing 1. Sathitruangsak C, Righolt CH, Klewes L, Chang DT, Kotb R, Mai S. Distinct and shared three-
Hodgkins Lymphoma. Cancers. 2013, 5(2), 714-725. dimensional chromosome organization patterns in lymohocytes, monocloncal gammopathy of
7. Knecht H, Kongruttanachok N, Sawan B, Brossard J, Prevost S, Turcotte E, Lichtensztejn Z, undetermined significance and multiple myeloma. Int J Cancer. 2016. Accepted for publication.
Lichtensztejn D, Mai, S. 3D telomere signatures of Hodgkin- and Reed-Sternberg cells at diagnosis 2. Taylor-Kashton C, Lichtensztejn D, Baloglu E, Senapedis W, Shacham S, Kauffman MG, Kotb R, Mai S.
indicate refractory/relapsing Hodgkins lymphoma. Translational Oncology. Aug;5(4):269-77. 2012. XPO1 Inhibition Preferentially Disrupts the 3D Nuclear Organization of Telomeres in Tumor Cells. J Cell
8. Knecht H, Mai S. 3D imaging of telomeres and nuclear architecture: an emerging tool of 3D nano- Physiol. 2016 Dec;231(12):2711-9.
morphology based diagnosis. J Cell Physiol. 2011 Apr;226(4):859-67. 3. Martin LD, Harizanova J, Mai S, Belch AR, Pilarski LM. FGFR3 preferentially colocalizes with IGH in the
9. Knecht H, Brderlein S, Wegener S, Lichtensztejn D, Lichtensztejn Z, Mller P and Mai S. 3D nuclear interphase nucleus of multiple myeloma patient B-cells when FGFR3 is located outside of CT4. Genes
organization of telomeres in the Hodgkin cell lines U-HO1 and U-HO1-PTPN1: PTPN1 expression Chromosomes Cancer. 2016 Dec;55(12):962-974.
prevents the formation of very short telomeres including t-stumps. BMC Cell Biology. 2010 Dec 4. Sathitruangsak C, Righolt CH, Klewes L, Tammur P, Ilus T, Tamm A, Punab M, Olujohungbe A, Mai S.
14;11(1):99. BMC Cell Biology cover image of the month. Quantitative Superresolution Microscopy Reveals Differences in Nuclear DNA Organization of Multiple
10. Guffei A, Sarkar R, Klewes R, Righolt C, Knecht H, Mai S. Dynamic chromosomal rearrangements Myeloma and Monoclonal Gammopathy of Undetermined Significance. J Cell Biochem 2014 Dec 10.
in Hodgkins lymphoma are due to ongoing 3D nuclear remodeling and breakage-bridge-fusions. 5. Klewes L, Vallente R, Dupas E, Brand C, Grn D, Guffei A, Sathitruangsak C, Awe JA, Kuzyk A,
Haematologica. 2010 Dec;95(12):2038-46. Lichtensztejn D, Tammur P, Ilus T, Tamm A, Rubinger M, Olujohungbe A, Mai S. 3D nuclear telomere
11. Knecht H, Brderlein S, Mai S, Mller P, Sawan B. 3D structural and functional characterization of the organization in multiple myeloma. Translational Oncology 2013 6(6): 749756.
transition from Hodgkin to Reed-Sternberg cells. Ann Anat. 2010 Sep 20;192(5):302-8. Article and 6. Martin LD, Harizanova J, Righolt CH, Zhu G, Mai S, Belch AR, Pilarski LM. Differential nuclear
journal cover. organization of translocation-prone genes in nonmalignant B cells from patients with t(14;16) as
12. Knecht H, Sawan B, Lichtensztejn Z, Lichtenstejn D, Mai S. 3D Telomere FISH defines LMP1 compared with t(4;14) or t(11;14) myeloma. Genes Chromosomes Cancer. 2013 Jun;52(6):523-37.
expressing Reed-Sternberg Cells as End-Stage Cells with Telomere-poor Ghost Nuclei and very short 7. Martin LD, Harizanova J, Zhu G, Righolt C, Belch A, Mai S, Pilarski L. Lineage-specific repositioning and
Telomeres. Lab Invest. 2010 Apr;90(4):611-9. increased proximity of translocation-prone genes in normal B-cells from multiple myeloma patients.
13. Knecht H, Sawan B, Lichtensztejn D, Lemieux B, Wellinger RJ, Mai S. The 3D nuclear organization Genes Chromosomes Cancer 2012 Aug;51(8):727-42.
of telomeres marks the transition from Hodgkin to Reed-Sternberg cells. Leukemia. 2009
Mar;23(3):565-73.
8
OPPORTUNITY
WELL-PROTECTED
NORTH AMERICA AND EUROPE
9
OPPORTUNITY
WELL-PROTECTED
NORTH AMERICA AND EUROPE
Diagnostic Methods for Prognostic and risk predictive Canada National Phase; 2760873
Hematological Disorders test for blood cancers USA National Phase; 692645
Methods for Evaluating Alzheimers Prognostic and risk predictive test for Canada National Phase; 2856419
Disease and Disease Severity Alzheimers disease patients USA National Phase; 14/491,996
Method for Characterizing and Isolating Circulating Prognostic and risk predictive Canada National Phase; 2775315
Tumour Cell Subpopulations (Prostate Cancer) test for Prostate Cancer patients USA National Phase; 13/869797
Diagnostic Methods Prognostic, risk predictive and monitoring for several cancers
USA National Phase; 14/852143
Using Granulometry by examining DNA-occupied territories inside the cell/nucleus
10
WHAT WE DO
SCREENING
Who has a particular disease
DIAGNOSIS
TELOVIEW SCORING What kind of disease/cancer PERSONALIZED MEDICAL
IMAGE ANALYSIS MODEL REPORT TO CLINICIAN
PROGNOSIS
How stable or aggressive
is the disease/cancer
PREDICTING
1. Number of telomere signals Scoring model based How will the patient respond Personalized medical
to a specific treatment
2.Signal intensities on the parameters report to clinician
3. Number of telomere aggregates generated by TeloView and clear information
MONITORING
4.Distribution of telomeres
image analysis Whether the patient is stable over for the patient/family
within nuclei the course of treatment/disease
13
UNIVERSAL
STRUCTURAL BIOMARKER
Hodgkins Lymphoma
Prostate Cancer
Multiple Myeloma
Alzheimers Unique 3D telomere
Thyroid Cancer
MDS/ML
signatures found to
Glioblastoma correlate with various
Cholangiocarcinoma
Breast Cancer (TNBC)
stages and forms of
Ependymoma the disease
Esophageal Cancer
Neuroblastoma
NSC Lung Cancer 14
PRIORITY
PIPELINE
Alzheimers 3D Telo-AD
15
HODGKINS LYMPHOMA
PROOF OF CONCEPT
8,500
new cases in 2016
respond to standard
0.5%
of all new cancer cases are chemotherapy and
diagnosed as Hodgkins Lymphoma
enter long-term remission
or not respond and
relapse, usually
Median age at diagnosis is
39 years old
within 24 months.
~$400,000
cost per relapsing patient vs
US market only. ~$90,000 cost per non-relapsing patient*
Source: 2016 US NIH, SEER (http://seer.cancer.gov/statfacts/html/hodg.html) 16
http://www.melissabeatslymphoma.com/2014/01/how-much-does-cancer-cost.html
*Source: 2014 ASCO Annual Meeting
ADVANCED
PROGNOSTIC TARGETS
HODGKINS LYMPHOMA
20%
These patients can receive optimized treatments
at the outset, resulting in:
of patients with
Hodgkins Lymphoma New Treatment
Options
Reduced
Complications
Significant
Cost Savings
Shortened
Treatment Cycles
will not respond to
standard chemotherapy
17
PROSTATE
CANCER ~30 million
men are screened for
prostate cancer each year
~$15B
spent annually diagnosing
and treating prostate cancer
18
US market only. Source: 2016 US NIH, SEER (http://seer.cancer.gov/statfacts/html/prost.html)
GAME CHANGER
INFORMING A DIFFICULT CHOICE
11% 2%
BOWEL URGENCY active surveillance or
pursuing treatment that
BOWEL
BOWEL 14% 34%
FUNCTION
DYSFUNCTION
FREQUENT BOWEL MOVEMENTS, PAIN, URGENCY
1 DISRUPTIVE
TECHNOLOGY
4 5 6
EXPERT TEAM WITH
SUCCESSFUL TRACK RECORD EXCEPTIONAL TIMING AHEAD FISCAL
IN BIOMEDICAL MARKET OF IMPORTANT CATALYSTS MANAGEMENT
Accomplished leadership with Steady stream of positive news Drive growth through strategic
ability to develop and commercialize flow expected including talent allocation of capital.
new products and secure strategic acquisition, clinical trial progress Control expenses through sensible
partnerships. and new business developments. fiscal management and streamlined
operations.
21
BOARD
GORDON MCCAULEY
DIRECTOR
President and CEO of Viable Healthworks Corp. and Chairman of
Life Sciences BC. Co-founder and former President and COO of
Neuro Discovery Inc. (NDI Capital). Past President and CEO of
Allon Therapeutics.
22
MANAGEMENT
DR. SABINE MAI, PhD DIRECTOR AND CHAIR, CLINICAL AND SCIENTIFIC ADVISORY BOARD
Kenneth C. Anderson, MD
Dr. Anderson is the Kraft Family Professor of Medicine at Harvard Medical School, as well as Director of the Lebow Institute for Myeloma Therapeutics
and Jerome Lipper Multiple Myeloma Center at Dana-Farber Cancer Institute. He is a Doris Duke Distinguished Clinical Research Scientist and American
Cancer Society Clinical Research Professor. After graduating from Johns Hopkins Medical School, he trained in internal medicine at Johns Hopkins Hospital,
and then completed hematology, medical oncology, and tumor immunology training at the Dana-Farber Cancer Institute. Over the last three decades,
he has focused his laboratory and clinical research studies on multiple myeloma. He has developed laboratory and animal models of the tumor in it is
microenvironment which have allowed for both identification of novel targets and validation of novel targeted therapies, and has then rapidly translated these
studies to clinical trials culminating in FDA approval of novel targeted therapies. His paradigm for identifying and validating targets in the tumor cell and its
milieu has transformed myeloma therapy and markedly improved patient outcome.
Laurence Klotz, MD
Dr. Klotz is internationally recognized for his contributions to the treatment of prostate cancer, notably for pioneering the adoption of Active Surveillance as
a standard aspect of patient care. Dr. Klotz obtained his medical degree and residency training from the University of Toronto with a special fellowship in
uro-oncology and tumour biology at Memorial Sloan Kettering Cancer Centre, New York. He is a widely published uro-oncologist who serves on the board
or heads many medical/scientific organizations. He is a Professor, Department of Surgery, University of Toronto, past Chief of Urology, Sunnybrook Health
Sciences Centre, Toronto, and Chairman, World Uro-Oncology Federation. Dr. Klotz was awarded the Order of Canada in 2014 for his contribution to
prostate cancer treatment.
Hans Knecht, MD
Dr. Knecht established himself as a prominent haematologist through his ground-breaking translational research on lymphoma biology. His current focus
is on the molecular events leading to the transition from the mononuclear Hodgkin to the multinuclear Reed-Sternberg cell and the impact of 3D nuclear
telomere organization on this transformation. Dr. Knecht received his medical degree from the University of Zurich, Switzerland with post-graduate work
under both Maxime Seligmann (Haematology) and Karl Lennert (Haematopathology) in Paris and Kiel, respectively. Dr. Knecht is currently a Professor of
Medicine and Chief, Division of Haematology at McGill University and Jewish General Hospital, Montreal. 24
CLINICAL AND SCIENTIFIC
ADVISORY BOARD
Darrel Drachenberg, MD
Dr. Drachenberg is a urologic oncologist and researcher and strong proponent of Active Surveillance for prostate cancer patients. Dr. Drachenberg attended medical
school at the University of British Columbia and urology residency at Dalhousie University. He is an American Foundation of Urology Scholar with fellowship training
in urologic oncology at the National Cancer Institute in Bethesda, Maryland. He founded the laparoscopic urology program and prostate brachytherapy, cryotherapy,
and HIFU programs at the University of Manitoba where he works as assistant professor of surgery and director of research for the Manitoba Prostate Center and
Section of Urology and Chair of the Genito-Urinary disease site group, CancerCare Manitoba.
Rami Kotb, MD
Dr. Kotb completed his medical residency training in Paris, France, and then became a staff member at Paris XI University. He joined the Hematology-Oncology team
at Sherbrooke University (QC, Canada) in 2005 as an Assistant, then Associate Professor. He also worked as the Director of Hematology undergraduate education,
Head of the supra-regional team of Hematological Neoplasia and Head of the Institutional Oncology Quality Sub-committee. Late 2011, he moved to British Columbia
to work at the BC Cancer Agency as an Oncologist/Hematologist, Associate Professor at the University of British Columbia and affiliate Professor at the University of
Victoria. He joined the team at CancerCare Manitoba in September 2014. His practice and research activity will be focused on lymphoid neoplasia, primarily myeloma
and lymphoma.
Thomas Cremer, MD
Dr. Cremer is an internationally-recognized scientist specializing in the studies of nuclear architecture. He is one of the pioneers of interphase cytogenetics
and comparative genomic hybridization (CGH). These methods have become widely used tools for cytogenetic analyses of chromosomal imbalances.
He is a corresponding member of the Heidelberg Academy for Sciences and Humanities since 2000, a member of Germanys National Academy of Sciences
Leopoldina since 2006, an honorary member of both the European Cytogenetics Association (ECA) and the German Society of Human Genetics since 2011,
as well as the recipient of the medal of Honor of this Society. Dr. Cremer is an independent expert to 3DS.
Nigel Terrett
companies, and the acquisition of ProXeon by ThermoFisher and the acquisition of Halo Genomics by Agilent.
As chairman of the board of Excelleris Technologies, Mr. Terrett led the creation of the largest integrated patient and physician diagnostic database
in Canada. During his tenure as chief strategic officer of LifeLabs, he created innovative collaborative programs with health institutions, provincial
governments and health providers to improve health care while reducing costs. As senior vice-president and general manager of Life Labs British
Columbia, Mr. Terrett was responsible for 900 operational staff, 90 branch locations and two state-of-the-art medical laboratories providing over
15 million medical results per year. As chief information officer of MDS Diagnostics, he led the restructuring of information technology services that
resulted in multimillion-dollar savings for the company. During his tenure as vice-president of information technology at MDS Diagnostics, Mr. Terrett
led a North American team that increased operating income by over 50 per cent. 26
PRO-FORMA
CAPITAL STRUCTURE
Warrants 7,624,838
Options 5,121,081
28
Genomic imaging for TSX.V: DXD