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11:35 – 11:45 CuRAGE presented by: Ihor Terleckyj, CEO & Founder
Based on research from the lab of Drs. Lynne Johnson and Yared Tekabe, Columbia University
Department of Medicine
Patients with peripheral artery disease (PAD) experience a low quality of life. The hallmark clinical
feature is reduced blood flow to the legs and arms due to narrowing of the arteries. With time, the
ability to walk is impaired, patients can develop skin ulcers, and gangrene that may require limb
amputation. Currently, there is no therapy that restores blood flow, alleviates symptoms and impacts
disease progression. In the US, close to 8 million patients suffer with PAD. Of these, 40-50% are diabetic.
CuRAGE is developing CR-3, and anti-RAGE monoclonal antibody, for use in PAD. Activation of RAGE
(receptor for advanced glycation endproducts) by specific immunomodulators, such as AGEs, triggers a
deleterious inflammatory response and reduces the ability to generate new vessels. Diabetics are more
prone to the effects of RAGE activity owing to the high levels of AGEs produced in this disease. In 2
different experimental models of diabetic PAD, CR-3 has demonstrated the ability to restore blood flow
to major muscle groups and to stimulate regeneration of blood vessels. The current US market size is
estimated at $8B, and projected to reach $10B by 2024. Through multiple rounds, CuRAGE is seeking a
total of $27M for human proof-of-concept. Additional disease states associated with high RAGE activity
include ovarian cancer, which may provide a second indication for CR-3.
11:45– 11:55 TEMPRES TECHNOLOGIES Presented by: Chathuranga (Chat) De Silva, CEO
Based on research from the lab of Dr. Jefferey Koberstein, Chemical Engineering at Columbia University
Pancreatic cancer (PDAC), is one of the most aggressive and lethal cancers found in humans. It is the
fourth leading cause of cancer deaths in the US (45,000 annually) and only 1-6% of patients contracting
the disease survive past five years. Chemotherapy remains the primary option in treating metastatic
PDAC ($1.7 billion market size) but its effectiveness is only palliative and has minimal impact on survival.
The poor efficacy is attributed to inefficient delivery of chemotherapeutic agents to the pancreas and
their rapid clearance. In other words, it is difficult to get drugs to reach the pancreas. Once there, they
clear rapidly, and are not taken up well by the tumor due to poor hypovasculature. Our team has
developed a drug-carrier, Gemzin (Gemcitabine conjugate) that is intended for use with a promising new
method of drug delivery, direct injection of tumors by endoscopic ultrasound fine needle injection (EUS-
FNI). In EUS-FNI, therapeutics are injected directly into PDAC tumors by a fine needle guided through the
stomach and into the tumor by ultrasound imaging. Gemzin carriers are expected to meet two
important criteria: they physically retain gemcitabine in the pancreas after injection and provide
controlled release over an extended period of time. These features would result in the reduction of side-
effects typically associated with chemotherapy and improved clinical outcomes. In the next 12-months,
we plan complete work to demonstrate these primary end-points in mouse models and file for an
Investigation New Drug (IND) application for this treatment.
11:55 – 12:05 POMEREX THERAPEUTICS Presented by: Brent Stockwell
Based on research from the lab of Dr. Brent Stockwell, Columbia Departments of Biological Sciences and
Chemistry
Many disease-causing proteins are difficult to inhibit directly with biologics and small molecules.
However, new advances allow for the control of the abundance of proteins using small molecules,
providing a path to medicines that selectively control protein stability. Pomerex Therapeutics is building
a platform for the systematic discovery of small molecules that control the stability of disease-modifying
proteins. We have developed novel compounds that can cause the destruction of otherwise
undruggable but crucial protein targets, including those driving the genesis and survival of aggressive
cancers. We are seeking funds to expand our platform and develop our lead oncology programs.
12:05 – 1:30 NETWORKING & LUNCH
2018 Columbia and Harvard Pitch Day Agenda
8:00 – 8:30 REGISTRATION & BREAKFAST
8:30 – 9:00 Opening Remarks by Orin Herskowitz, Executive Director of CTV and Sr. VP of Intellectual Property &
Tech Transfer at Columbia University; Sam Liss, Executive Director for Strategic Partnerships at Harvard
University’s Office of Technology Development; and Stephen Davis, Partner at Goodwin Procter LLP.