Full Press Release Details
Cancer Therapeutics VAL - 083: Validated DNA - targeting Agent for Multiple Drug Resistant Solid Tumor Indications August 2019
that do not describe historical facts may constitute forward - looking statements as that term is defined in the Private Securities
Litigation Reform Act of 1995. Any forward - looking statements contained herein or made in the course of the presentation are
based on current expectations, but are subject to a number of risks and uncertainties. The factors that could cause actual future
results to differ materially from current expectations include, but are not limited to, risks and uncertainties relating to the
Company's ability to develop, market and sell products based on its technology; the expected benefits and efficacy of the Company's
products and technology; the availability of substantial additional funding for the Company to continue its operations and to
conduct research and development, clinical studies and future product commercialization; and, the Company's business, research,
product development, regulatory approval, marketing and distribution plans and strategies. These and other factors are identified
and described in more detail in the Company's filings with the SEC, including its current reports on Form 8 - K's,
Form 10 - Q's and most recent Form 10 - K. DelMar Pharmaceuticals does not undertake to update these forward - looking statements
Demonstrated Efficacy - Validated biological and tumor effecting activity - Biomarker enriched patient population Well
Characterized Safety Profile - Large historical safety database of over 1,000 patients Mature Manufacturing Status - CMC
advanced to Phase 3 / commercial stage Efficient Capital Management - Low quarterly burn - Funded through full enrollment
for all three Phase 2 study arms Executing Clinical Development through expert centers - Phase 2 studies being conducted
by M.D. Anderson Cancer Center (MDACC) and Sun Yat - sen University Cancer Center (SYSUCC) - Supported by world class Scientific
Stage Phase 2 Programs
molecule, DNA - targeting agent - Established and unique mechanism of action - Proven to cross the blood - brain barrier
Lead indication - Biomarker - driven, MGMT - unmethylated glioblastoma multiforme (GBM) - Three distinct GBM patient populations
in Phase 2 studies 505(b)(2) path allows use of prior toxicology and clinical data from National Cancer Institute (exclusively
authorized to DelMar - 1 ) and other studies to support FDA filings Fast Track Designation and Orphan Drug Designations
(US and EU) 1. Letter of Authorization November 3, 2010
Previous work at National Cancer Institute (NCI) demonstrated efficacy of compound - Randomized trial in 42 patients: Radiation
only patients mOS of 35 weeks Radiation and VAL - 083 mOS of 67 weeks - 1 VAL - 083 Effectively Crosses Blood -
Brain Barrier - Established in previous NCI work - 2 - Further demonstrated through PK data from ongoing Phase 2 clinical trial
at SYSUCC - 3 Myelosuppression is consistent with other successful approved chemotherapy treatments VAL - 083's
unique mechanism of action creates inter - strand DNA cross - links at the N7 position of guanine, resulting in double - strand
Activity of VAL - 083 1. Eagan 1979 JAMA 2. Eckhardt 1977 Cancer Treat Rep 3. Chen AACR Poster 2019 4. Fouse 2014 Neuro Oncol
Enriched Patient Population MGMT - unmethylated GBM Patients Have Very Limited Treatment Options Across All Disease Stages - 1
Evaluating MGMT promoter methylation has become standard practice in GBM diagnosis, treatment, and outcomes September
2017 NCCN guidelines highlight limited effectiveness of temozolomide (TMZ) for patients with MGMT - unmethylated tumors - 1 -
TMZ monotherapy [for patients with KPS<60] in only recommended if tumor is MGMT - methylated - Clinical benefit from TMZ is
likely to be lower in patients whose tumors are MGMT - unmethylated MGMT testing is a commercially available diagnostic
Enriched Patient Population VAL - 083 is Equipotent Independent of MGMT Promoter Methylation Status - 1 U251 MGMT - Methylated
patients with glioblastoma with unmethylated MGMT promoter is particularly challenging. These tumors are inherently resistant
to the temozolomide, which alkylates DNA at the O - 6 position of methylguanine, and is readily repaired by MGMT. VAL - 083 has
been shown to be safe and may provide a valuable treatment option for these patients" - 1 "We agree that we desperately
need something better to offer our patients and we feel that VAL - 083 has some promise and potential" - 2 Copyright 2019,
Department of Neuro - Oncology at MD Anderson Cancer Center Principal Investigator on DelMar rGBM and Adjuvant arm trial 2. Dr.
David Reardon, Clinical Director of the Center for Neuro - Oncology at the Dana - Farber Cancer Institute Dr. John de Groot, Chairman,
ad interim of the Department of Neuro - Oncology at MD Anderson Cancer Center Members, DelMar Scientific Advisory Board
DelMar's GBM program builds on previous work from the National Cancer Institute - ~40 Phase 1 and Phase 2 clinical trials
in multiple indications as well as significant preclinical work - More than 1,000 patient historical safety database Safety
database augmented by completed and ongoing DelMar clinical trials with addition of over 100 patients to date Consistent
with prior NCI data, myelosuppression has been the most common adverse event (AE); AEs have generally resolved spontaneously Copyright
VAL - 083 Drug Substance (DS) manufactured by STA Pharmaceutical Co., Ltd. (STA), a WuXi AppTech company - STA focused on late
stage and commercial DS manufacturing - Engineering and GMP lots manufactured; strong stability results VAL - 083 Drug
Product (DP) manufactured by Chemi Pharma (subsidiary of Italfarmaco) - Chemi Pharma is focused on late stage and commercial DP
manufacturing - Robust process built on lyophilization temperature - Engineering and GMP lots manufactured; strong purity and
11 Advanced Manufacturing Status
Only $38.8M in shareholder capital spent to establish multiple clinical programs (through March 31, 2019) Low quarterly
burn - Efficient internal operations and low fixed costs - Exceptional value from clinical partners at MDACC and SYSUCC
12 Efficient Capital Management
- 083 Clinical Development Program VAL - 083 Preclinical IND Phase 1 Phase 2 Phase 3 Recurrent MGMT - unmethylated GBM Newly -
diagnosed MGMT - unmethylated GBM P l a t i nu m - R es i s t a n t Ovarian Cancer Other Solid T u m o r s Adjuvant MGMT - unmethylated
Validate VAL - 083 in recurrent, Avastin - na ve MGMT - unmethylated GBM patients post TMZ failure - Primary endpoint is
Median Overall Survival compared to historical control of Lomustine at 7.2 months - Conducted at MDACC (NCT02717962) 56
of 83 planned recurrent patients have been enrolled - 1 47 patients have received assessment at end of cycle 2 - 2 - 13/47
(28%) patients have been assessed as Stable Disease Consistent with prior studies, myelosuppression is the most common
- Jul - 2019 2. Data cut - off 5 - May - 2019 Assessment based on Investigator's clinical and radiologic assessment according
Validate VAL - 083 in adjuvant GBM MGMT - unmethylated patients post radiation - Primary endpoint is Progression Free Survival
compared to historical control of TMZ at 6.9 months - Conducted at MDACC (NCT02717962) First of 24 planned adjuvant patients
Validate VAL - 083 in newly - diagnosed MGMT - unmethylated GBM patients - Primary endpoint is Progression Free Survival compared
to historical control of TMZ at 6.9 months - Conducted at SYSUCC (NCT03050736) Copyright 2019, DelMar Pharmaceuticals All rights
reserved 18 20 of 30 planned newly - diagnosed patients have been enrolled - 1 17 patients have received at least
one assessment - 2 - 9/17 (53%) assessed as Complete Response - 7/17 (41%) assessed as Stable Disease - One patient assessed as
Disease Progression (6%); two patients not on study long enough to be assessed; one patient died before first assessment time
point - "For a tumor such as GBM, which is intrinsically infiltrative and destructive in the brain, stabilization of disease
is an important achievement." - 3 - Consistent with prior studies, myelosuppression is the most common adverse event VAL
- 083 Newly - Diagnosed Study Arm 1. Data cut - off 1 - Aug - 2019 2. Best Overall Response based on Investigator's clinical
and radiologic assessment according to RANO criteria 3. Dr. David Reardon, Clinical Director of the Center for Neuro - Oncology
at the Dana - Farber Cancer Institute
GBM is the most common adult brain tumor with annual incidence ~29,000 new cases in US and EU - 1 >17,000 Newly - diagnosed
and adjuvant MGMT - unmethylated patients annually - 2 >12,000 Recurrent MGMT - unmethylated patients annually - 3
2005, N Eng J Med 3. Brandes 2009, J Clin Onc
Dr. Napoleone Ferrara - World renowned scientist and Distinguished Professor of Pathology and a Distinguished Adjunct Professor
of Ophthalmology and Pharmacology at the University of California, San Diego Dr. John de Groot - Chairman, ad interim
of the Department of Neuro - Oncology at MD Anderson Cancer Center Dr. David Reardon - Clinical Director of the Center
for Neuro - Oncology at the Dana - Farber Cancer Institute and Professor of Medicine at the Harvard Medical School Dr.
Timothy Cloughesy - Professor of neurology at David Geffen School of Medicine at the UCLA and member of UCLA Brain Research Institute
and Jonsson Comprehensive Cancer Center Dr. Nicholas Butowski - Neuro - oncologist practicing at UCSF Medical Center and
Director of translational research in neuro - oncology and a researcher at the Brain Tumor Center Copyright 2019, DelMar Pharmaceuticals
Highly De - Risked Late Phase 2 Program - Demonstrated Efficacy - Well Characterized Safety Profile - Mature Manufacturing Status
- Efficient Capital Management - Executing Clinical Development through expert and highly regarded centers Opportunities
in biomarker - enriched patient population across all GBM disease stages - Newly - diagnosed patients (1st line) - Adjuvant patients
(Post initial cycle with radiation therapy) - Recurrent patients (2nd line) Fast Track and Orphan Drug Designations Copyright
Cancer Therapeutics NASDAQ: DMPI Corporate Headquarters Suite 720 - 999 W. Broadway Vancouver BC V5Z 1K5 Canada Clinical Operations
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