Accelerator Life Science Partners Launches Magnolia Neurosciences Corporation with $31 Million Series A to Develop Targeted Neuroprotective Therapies

NEW YORK, NY – August 13, 2018 – Accelerator Life Science Partners (Accelerator), a leading life science investment and management firm, today announced that it has launched Magnolia Neurosciences Corporation, a company developing a new class of neuroprotective medicines. Co-founded by Accelerator and The University of Texas MD Anderson Cancer Center (MD Anderson), the company will further develop discoveries made by scientists in MD Anderson’s Therapeutics Discovery division and the Neurodegeneration Consortium (NDC).

Investors participating in the $31 Million Series A financing include AbbVie Ventures, Alexandria Venture Investments, ARCH Venture Partners, Eli Lilly and Company, Innovate NY Fund, Johnson & Johnson Innovation – JJDC, Inc., the Partnership Fund for New York City, Pfizer Ventures, Watson Fund, L.P., WuXi AppTec’s Corporate Venture Fund and 180 Degree Capital Corp.

Neurodegenerative diseases and neuronal injury affect nearly 20 million individuals in the United States alone, and their incidence is expected to increase as the population ages. During embryonic development, excess neurons are eliminated by a process called programmed cell death. Research indicates that this tightly controlled process becomes re-activated in critical brain regions in Alzheimer’s disease and other neurological conditions. Blocking specific components of this process preserves brain tissue and leads to enhanced memory in animal models, suggesting that drugs targeting these key steps could maintain neural function.

“There is a critical need to develop medicines that slow or stop neuronal loss in these patients, and a growing body of data suggests that inhibition of these specific pathways has the potential to preserve neuron viability across a variety of disease states and pathological conditions,” said Jim Ray, PhD, director of Neurodegeneration Consortium. “Magnolia Neurosciences is focused on developing potent and highly selective neuroprotective therapies that have compelling preclinical pharmacologic profiles and for which clinical proof of concept can be obtained rapidly in order to address significant unmet patient needs.”

“The potential market for neuroprotective therapies is large and underserved, and we believe that Magnolia Neurosciences has the technology, intellectual property and scientific expertise to become a leader in the field,” said Thong Q. Le, chief executive officer at Magnolia Neurosciences Corporation and Accelerator Life Science Partners. “In launching Magnolia Neurosciences, we are pleased to be a catalyst for innovation that could improve the care and outcomes for millions of patients.”

Magnolia Neuroscience is built upon the expertise of scientists at MD Anderson, one of the world’s most respected cancer centers focused on patient care, research, education and prevention. With a comprehensive approach to improving patient care, scientists from MD Anderson and the NDC are focused on developing life-saving transformational medicines for patients in need of neuroprotective therapies, including those with Alzheimer’s disease and cancer.

“This investment in Magnolia Neurosciences exemplifies Pfizer’s commitment to funding neuroscience innovation and supporting cutting-edge translational neuroscience research,” said Laszlo Kiss, executive director, Worldwide Research & Development and principal at Pfizer Ventures. “Our new focus on neuroscience investing is designed to support entrepreneurs who are deciphering the molecular basis of neurologic disorders, and we believe that Magnolia

Neurosciences has the technology and scientific foundation on which to build an exciting portfolio of neuroprotective medicines.”

About Magnolia Neurosciences Corporation
Magnolia Neurosciences Corporation is a drug discovery and development company focused on the creation of a novel class of neuroprotective medicines. The company was launched by a $31 million Series A investment by Accelerator Life Science Partners in 2018 and was co- founded by world-class researchers at The University of Texas MD Anderson Cancer Center. The company endeavors to make life-changing medicines for the benefit of patients and their families suffering from serious CNS diseases. The company’s offices are located in the Alexandria Center for Life Science, New York City’s first and only premier life science campus. For more information, please visit www.magnolianeurosciences.com.

About Accelerator Life Science Partners
Accelerator Life Science Partners catalyzes the development and commercialization of breakthrough biotechnology innovations. Accelerator is a trusted partner that provides the complete business, scientific and financial toolkit necessary for successfully establishing and operating an early-stage biotechnology company. Accelerator nurtures its companies across all stages and in all facets of development, setting them on a path that offers the greatest chance for long-term success. Among these key resources are committed investment capital, experienced start-up management, world-class scientific expertise and state-of-the-art laboratories and shared facilities.

The company is uniquely positioned to provide this unprecedented collection of capabilities and resources through its partnership with top-tier investors, seasoned executive managers and world-class research institutions. The value of these collective resources has been validated over more than a decade of successful investing in life science companies that are helping to shape the rapidly evolving future of medicine and healthcare. For more information, please visit www.acceleratorlsp.com.

Media Contacts:

Rathbun Communications
Julie Rathbun
julie@rathbuncomm.com

Accelerator Life Science Partners
Jessica Burback
jburback@acceleratorlsp.com
T: 206-234-6481


Accelerator Life Science Partners Broadens its Leadership Teams and Expands its Geographic Operations to San Diego and the Greater Los Angeles Area

  • Newly formed Operating Partners group and Clinical and Scientific Advisory Board to provide critical insights to support portfolio companies’ success and guide investment strategies
  • Additional facility expected to catalyze the growth of innovative life science companies in Southern California

SEATTLE and NEW YORK – May 15, 2018 — Accelerator Life Science Partners (Accelerator), a leading life science investment and management firm, today announced that it has expanded its operations into San Diego and the Greater Los Angeles area with the opening of a new office at The Alexandria at Torrey Pines in San Diego. The firm also announced the formation of its Operating Partners group and Clinical and Scientific Advisory Board (CSAB). These strategic growth initiatives will better enable Accelerator to fulfill its dual missions of providing unique and compelling opportunities to its investors and partnering with cutting-edge life science companies to help achieve their near-term milestones and long-term visions.

“Accelerator is committed to supporting innovation wherever it takes place and without geographic limitation,” said David M. Schubert, chief operating partner at Accelerator. “Opening an office in San Diego, our third market, positions us to meet the needs of leading innovators throughout the vibrant San Diego and emerging Greater Los Angeles life science ecosystems. We have also brought together an experienced group of Operating Partners to support our ongoing efforts to identify new investment areas and specific company-building opportunities.”

Accelerator’s Operating Partners will assist with the evaluation of new business opportunities, support current (and future) Accelerator portfolio companies and serve in a variety of operating and board roles. The Operating Partners include:

  • Andrew Howard, Ph.D. (New York City, NY)
  • Wendy S. Johnson (San Diego, CA)
  • David L. Pompliano, Ph.D. (New York City, NY)
  • Francisco D. Salva (Philadelphia, PA)
  • John T. Santini, Jr., Ph.D. (Minneapolis, MN)
  • David M. Schubert  (New York City, NY)
  • Christopher T oombs, Ph.D. (Seattle, WA)
  • Court R. Turner, J.D. (San Diego, CA)

“Having state-of-the-art laboratories and world-class scientific leadership will help set our portfolio companies on a path to long-term success,” said Kendall Mohler, Ph.D., chief development officer at Accelerator. “We are excited to welcome our CSAB members to the Accelerator team. Advancing a groundbreaking scientific idea into and through clinical development takes not only robust data; it also requires critical insights into preclinical research, clinical trial design and strategy and keen understanding of the product approval pathway. Our CSAB members have demonstrated expertise in these areas, and we believe they will be an important asset as we partner with today’s most cutting-edge entrepreneurs.”

Accelerator’s CSAB Members:

  • Lee E. Babiss, Ph.D.
  • John Latham, Ph.D.
  • George L. McLendon, Ph.D.
  • Kendall M. Mohler, Ph.D.
  • Gerald T. Nepom, M.D., Ph.D.
  • Homer L. Pearce, Ph.D.
  • Anil K. Singhal, Ph.D.
  • James Tobin, Ph.D.

Additional information about the members of Accelerator’s Operating Partners and CSAB is available at: www.acceleratorlsp.com/our-team/.

About Accelerator Life Science Partners
Accelerator Life Science Partners catalyzes the development and commercialization of breakthrough biotechnology innovations. Accelerator is a trusted partner that provides the complete business, scientific and financial toolkit necessary for successfully establishing and operating an early-stage biotechnology company. Accelerator nurtures its companies across all stages and in all facets of development, setting them on a path that offers the greatest chance for long-term success. Among these key resources are committed investment capital, experienced start-up management, world-class scientific expertise and state-of-the-art laboratories and shared facilities.

The company is uniquely positioned to provide this unprecedented collection of capabilities and resources through its partnership with top-tier investors, seasoned executive managers and world-class research institutions. The value of these collective resources has been validated over more than a decade of successful investing in life science companies that are helping to shape the rapidly evolving future of medicine and healthcare. For more information, please visit www.acceleratorlsp.com

 

Media Contacts:

Rathbun Communications
Julie Rathbun
julie@rathbuncomm.com

Accelerator Life Science Partners
Jessica Burback
jburback@acceleratorlsp.com
T: 206-234-6481


Lodo Therapeutics Corporation Forms Multi-Target Strategic Collaboration with Genentech

  • Collaboration provides Genentech with access to Lodo Therapeutics’ proprietary metagenomics-based natural products drug discovery platform
  • Lodo to receive up to $969 million in upfront fees and milestone payments

New York, NY – May 9, 2018 – Lodo Therapeutics Corporation, a drug discovery and development company focused on identifying and producing unique, bioactive natural products directly from the microbial DNA sequence information contained in soil, today announced that it has formed a strategic drug discovery collaboration with Genentech, a member of the Roche Group.

Under the terms of the agreement, Genentech will utilize Lodo Therapeutics’ proprietary genome mining and biosynthetic cluster assembly platform to identify novel molecules with therapeutic potential against multiple disease-related targets of interest to Genentech. Lodo will receive an undisclosed upfront payment and is eligible to receive research, development and commercialization milestone payments up to $969 million based on achievement of certain predetermined milestones. In addition, Lodo is eligible to receive tiered-royalties on sales of certain products resulting from the collaboration.

“Lodo Therapeutics’ proprietary drug discovery platform is a powerful engine for identifying novel compounds with important therapeutic potential,” said Thong Q. Le, chief executive officer at Lodo Therapeutics and Accelerator Life Science Partners. “We are incredibly excited to work with Genentech, and we look forward to demonstrating the power and utility of Lodo’s unique technology for the benefit of global human health.”

Compounds derived from natural products comprise a significant proportion of the small molecule drugs used to treat cancer, infections and chronic illnesses such as Type 2 diabetes. Rather than relying on culturing known strains of bacteria, Lodo Therapeutics’ genome-based approach leverages the power of microbial evolution to identify novel, naturally occurring compounds that have therapeutic potential in the treatment of cancer and drug-resistant bacterial infections. This approach is expected to reduce the time and cost of drug discovery.

“Our ability to enter into a strategic collaboration with one of the leaders in innovating wholly new classes of drugs just two years after Lodo Therapeutics was founded reflects the potential of our proprietary platform to be a valuable resource to advance their drug discovery initiatives,” said David Pompliano, Ph.D., co-founder and chief scientific officer of Lodo Therapeutics.

“We are excited to work with Genentech in their quest to discover novel, next-generation natural products derived from the microbiome of the soil using this innovative platform developed by Lodo,” said Sean Brady, Ph.D., co-founder of Lodo Therapeutics and Associate Professor at The Rockefeller University.

James Sabry, M.D., Ph.D., senior vice president and global head of Genentech Partnering, commented, “Genentech is committed to accessing innovative technologies and we are excited to collaborate with Lodo Therapeutics to apply their Metagenomics Technology Platform to potentially discover therapeutics for difficult drug targets.”

About Lodo Therapeutics
Lodo Therapeutics Corporation is a drug discovery and development company focused on the creation of novel therapeutics derived from nature that will impact patients around the world. The company was established to pursue the scientific vision of Dr. Sean Brady, head of The Rockefeller University’s Laboratory of Genetically Encoded Small Molecules. Lodo Therapeutics identifies and produces bioactive natural products directly from the microbial DNA sequence information contained in soil. Information encoded in bacterial genomes, not experimental serendipity, drives the company’s discovery of new medicines. Not constrained by traditional culture-based approaches to natural products drug discovery, Lodo Therapeutics has unlocked a vast trove of overlooked compounds evolutionarily selected for processes essential for life and with significant potential in the treatment of drug-resistant microbial infections and cancers

Lodo Therapeutics was formed by Accelerator Life Science Partners and is headquartered in New York City. The company’s lab and offices are located in the Alexandria Center for Life Science, New York City’s first and only premier life science campus.

 

Media Contact(s)

Rathbun Communications
Julie Rathbun
julie@rathbuncomm.com

Accelerator Life Science Partners
Jessica Burback
jburback@acceleratorlsp.com


Proniras Corporation Awarded Contract Worth Up to $89.5 Million from U.S. Biomedical Advanced Research and Development Authority to Develop Tezampanel as a Medical Countermeasure for Nerve Agent-Induced Seizures

SEATTLE, WA – April 27, 2018 – Proniras Corporation, an Accelerator Life Science Partners (Accelerator) portfolio company, today announced that it has been awarded a contract potentially worth $89.5 million from the U.S. Department of Health and Human Service’s Biomedical Advanced Research and Development Authority (BARDA) to develop tezampanel as a medical countermeasure for the treatment of nerve agent-induced seizures that are not stopped by current medications. Tezampanel (also known as LY-293,558) is a small molecule compound that previously had been evaluated in clinical trials as a potential therapy for acute migraine and other neurologic indications and has demonstrated an attractive safety and pharmacokinetic profile in more than 400 human subjects.

“As recent events have clearly demonstrated, the need for medical countermeasures that can effectively treat nerve agent exposure is sadly more than theoretical,” said Christopher Toombs, PhD, DABT, chief scientific officer at Proniras. “Tezampanel holds great potential as a solution to this serious challenge, having shown favorable safety and pharmacokinetic profiles in clinical trials for acute migraine and demonstrating efficacy in preclinical models of nerve agent-induced seizures. Proniras is pleased to have the opportunity to work with BARDA to improve our nation’s health and security preparedness.”

Under the terms of the contract, Proniras will be responsible for conducting preclinical studies, and the clinical development and manufacture of tezampanel. Payments totaling up to $89.5 million can be made upon attainment of pre-specified milestones over a five-year period. Given the inability to assess the safety and efficacy of tezampanel in humans with actual nerve agent exposure, tezampanel will be developed using the U.S. Food and Drug Administration’s (FDA) Animal Rule (21 CFR 314.600). Under this rule, the FDA can accept a New Drug Application for tezampanel based on efficacy data from a pivotal study in animal models of nerve agent-induced seizures and Phase 1 and 2 trials in human subjects with other relevant neurologic conditions, and adequate safety data from trials in healthy human volunteers.

Proniras expects to file an Investigational New Drug application with the FDA to initiate human trials as well as an application for an Orphan Drug designation in 2020 and anticipates receiving an NDA in 2022. The company may also evaluate continuing development of tezampanel in additional commercial indications following its approval as a medical countermeasure.

Tezampanel is a competitive, reversible receptor antagonist that inhibits glutamate signaling through the GluK1 receptor subunit. This is a novel mechanism of action that is distinct from currently approved seizure medications. Recent studies demonstrate that tezampanel is effective in arresting seizures in rodents exposed to the nerve agent, soman.1 Organophosphate nerve agents initiate seizures through cholinergic stimulation, and seizure activity can increase and be propagated by increasing glutamate signaling. While benzodiazepines are currently used for treatment of seizures caused by nerve agents, data show that, with time, seizures can become refractory to benzodiazepines, often returning and worsening in severity after a brief period of suppression. The superior efficacy of tezampanel, compared with benzodiazepines, in rodents exposed to soman may result in part from its direction inhibition of glutamate signaling, which plays a causal role in seizure activity.

“The robust body of human safety data and clinical, manufacturing and control data, coupled with the results of studies in a rodent model of nerve agent-induced seizures, is very compelling and should substantially reduce the development timeline, cost and risk of developing tezampanel as a medical countermeasure,” said David M. Schubert, chief operating officer at Proniras Corporation and chief operating partner at Accelerator Life Science Partners. “BARDA has a demonstrated track record of success in establishing public-private partnerships that support effective development of medical countermeasures. In addition to the funding provided under the contract, we expect that BARDA’s insight and expertise in the health preparedness arena will play a key role in the development of tezampanel.”

About Proniras Corporation
Proniras Corporation is a Seattle-based biopharmaceutical company focused on developing tezampanel as a medical countermeasure for nerve agent-induced seizures. The development of tezampanel in this indication is being funded in whole or in part with federal funds from the U.S. Department of Health and Human Services; Office of the Assistant Secretary for Preparedness and Response; Biomedical Advanced Research and Development Authority, under Contract No. HHSO100201800008C.

About Accelerator Life Science Partners
Accelerator Life Science Partners catalyzes the development and commercialization of breakthrough biotechnology innovations. Accelerator is a trusted partner that provides the complete business, scientific and financial toolkit necessary for successfully establishing and operating an early-stage biotechnology company. Accelerator nurtures its companies across all stages and in all facets of development, setting them on a path that offers the greatest chance for long-term success. Among these key resources are committed investment capital, experienced start-up management, world-class scientific expertise and state-of-the-art laboratories and shared facilities.

The company is uniquely positioned to provide this unprecedented collection of capabilities and resources through its partnership with top-tier investors, seasoned executive managers and world-class research institutions. The value of these collective resources has been validated over more than a decade of successful investing in life science companies that are helping to shape the rapidly evolving future of medicine and healthcare. For more information, please visit www.acceleratorlsp.com.

1 Apland, JP, Aroniadou-Anderjaska, V, Figueiredo, TH, Green, CE, Swezey, R, Yang, C, Qashu, F, and and Braga, MFM. Efficacy of the GluK1/AMPA receptor antagonist LY293558 against seizures and neuropathology in a soman-exposure model without pretreatment and its pharmacokinetics after intramuscular administration. JPET 2013: 344-133-140.

 

Media Contacts:

Rathbun Communications
Julie Rathbun
julie@rathbuncomm.com

Accelerator Life Science Partners
Jessica Burback
jburback@acceleratorlsp.com
T: 206-234-6481


Accelerator Life Science Partners Launches Proniras Corporation to Support Development of Tezampanel in the Treatment of Seizure Disorders

SEATTLE, WA – April 27, 2018 – Accelerator Life Science Partners (Accelerator), a leading life science investment and management firm, today announced that it has launched Proniras Corporation, a company developing tezampanel for the treatment of a variety of seizure disorders. Proniras has licensed exclusive global rights to tezampanel (LY-293,558), a small molecule compound that has been evaluated as a potential therapy for acute migraine in more than 400 patients to date, from Eli Lilly and Company. The launch of Proniras is supported by an initial financing from investors including Alexandria Venture Investments, ARCH Venture Partners, Eli Lilly and Company, Johnson & Johnson Innovation – JJDC, Inc., Watson Fund, L.P., WRF Capital and WuXi AppTec Corporate Ventures.

Recent studies demonstrate that tezampanel effectively arrests seizures in rodents exposed to the nerve agent soman1 and is potentially superior to benzodiazepines, which are the current standard of care for a variety of seizure disorders. Data from previous preclinical studies of tezampanel suggest that the compound elicits its central nervous system effects by antagonizing glutamate signaling.

“Treatment of seizures that result from either physiologic or pharmacologic stimuli is suboptimal for many patients,” said Christopher Toombs, PhD, DABT, co-founder and chief scientific officer at Proniras. “A robust body of clinical and preclinical data supports the potential utility of tezampanel as a novel therapy for seizures and seizure disorders. We believe that tezampanel could address significant unmet need for a safe, effective and durable seizure therapy.”

Dr. Toombs was most recently co-founder and chief scientific officer of Faraday Pharmaceuticals, a Seattle-based biotechnology company. Previously, he held senior leadership positions at Cylerus, Inc., Ikaria, Inc. and Amgen, Inc. Accelerator will manage the company’s executive operations.

“With tezampanel as its lead asset, Proniras is being established with a more advanced product development program than is typical for a start-up biopharmaceutical company,” said Thong Q. Le, chief executive officer at Accelerator. “As a result, we believe that Proniras has substantial near- and mid-term opportunities for value creation in an indication that has not seen significant innovation in many years.”

About Proniras Corporation
Proniras Corporation is a Seattle-based biopharmaceutical company focused on developing tezampanel as a medical countermeasure for nerve agent-induced seizures. The development of tezampanel in this indication is being funded in whole or in part with federal funds from the U.S. Department of Health and Human Services; Office of the Assistant Secretary for Preparedness and Response; Biomedical Advanced Research and Development Authority, under Contract No. HHSO100201800008C. For more information, please visit www.proniras.com.

About Accelerator Life Science Partners
Accelerator Life Science Partners catalyzes the development and commercialization of breakthrough biotechnology innovations. Accelerator is a trusted partner that provides the complete business, scientific and financial toolkit necessary for successfully establishing and operating an early-stage biotechnology company. Accelerator nurtures its companies across all stages and in all facets of development, setting them on a path that offers the greatest chance for long-term success. Among these key resources are committed investment capital, experienced start-up management, world-class scientific expertise and state-of-the-art laboratories and shared facilities.

The company is uniquely positioned to provide this unprecedented collection of capabilities and resources through its partnership with top-tier investors, seasoned executive managers and world-class research institutions. The value of these collective resources has been validated over more than a decade of successful investing in life science companies that are helping to shape the rapidly evolving future of medicine and healthcare. For more information, please visit www.acceleratorlsp.com.

1 Apland, JP, Aroniadou-Anderjaska, V, Figueiredo, TH, Green, CE, Swezey, R, Yang, C, Qashu, F, and and Braga, MFM. Efficacy of the GluK1/AMPA receptor antagonist LY293558 against seizures and neuropathology in a soman-exposure model without pretreatment and its pharmacokinetics after intramuscular administration. JPET 2013: 344-133-140.

 

Media Contacts:
Rathbun Communications
Julie Rathbun
julie@rathbuncomm.com

Accelerator Life Science Partners
Jessica Burback
jburback@acceleratorlsp.com
T: 206-234-6481


Accelerator Corporation Announces Key Senior Leadership Appointments and Name Change to Accelerator Life Science Partners

  • Biotechnology industry veterans bring decades of experience in working collaboratively to innovate breakthrough life science products

SEATTLE, Wash. and NEW YORK – December 13, 2017 — Accelerator Corporation a leading life science investment and management firm, today announced the appointments of Kendall Mohler, Ph.D., to the newly created position of chief development officer, and Ian Howes to chief financial officer. The firm also announced that it has changed its name to Accelerator Life Science Partners. The new name reflects Accelerator’s commitment to developing robust, long-term partnerships with its portfolio companies and to nurturing innovation and entrepreneurship within the life science community. This commitment is shared by Accelerator’s current investors, including AbbVie, Alexandria Venture Investments, ARCH Venture Partners, Eli Lilly and Company, Johnson & Johnson Innovation – JJDC, Inc., the Partnership Fund for New York City, Pfizer Venture Investments, Watson Fund, WRF Capital, WuXi AppTec and 180 Degree Capital Corp.

“Innovation takes great ideas, and the translation of ideas into transformative life science products doesn’t occur in a vacuum,” said Thong Q. Le, chief executive officer at Accelerator. “We believe that fostering innovation requires more than providing capital and lab space. It also requires a shared passion for advancing human health and an understanding of how to navigate the complex landscape that such advances often require. The additions of Ken and Ian to our executive team enhances our ability to make that journey — for the benefit of our investors, our portfolio companies and the talented entrepreneurs we work with, and ultimately for patients in need.”

Dr. Mohler has more than two decades of experience in the biopharmaceutical industry, including several years leading scientific research and development teams in the areas of autoimmune disease, inflammation and oncology. He was chief scientific officer and, most recently, senior vice president of research at Juno Therapeutics, Inc. (NASDAQ: JUNO), a clinical-stage cell immunotherapy company focused on re-engaging the body’s immune system to treat cancer. Prior to Juno, Dr. Mohler co-founded Trubion Pharmaceuticals Inc., a biopharmaceutical company focused on the development of novel protein therapeutics to treat autoimmune and inflammatory diseases and cancer. While at Trubion, Dr. Mohler served as the company’s chief scientific officer and senior vice president, and oversaw the development of several first-in-class product candidates and supported several partnerships with global pharmaceutical companies. Dr. Mohler also previously served as vice president of biological sciences at Immunex Corporation, where he played critical roles in the development and approval of Enbrel (etanercept), a multi-billion dollar product for the treatment of several autoimmune diseases. Dr. Mohler has published more than 35 manuscripts and has four issued patents and six pending patent applications. He received a Ph.D. in Immunology from the University of Texas Health Science Center and a B.S. from the University of Kansas.

Mr. Howes has over 20 years of experience in senior financial roles developing early-stage life sciences companies, including the successful completion of numerous rounds of private and public equity and debt transactions and two initial public offerings. He also managed multiple M&A transactions, including the sale of Scioderm to Amicus Therapeutics and the sale of Serenex to Pfizer. Most recently, Mr. Howes served as CFO of Heart Metabolics, a venture-backed pharmaceutical company developing an innovative therapy for the treatment of hypertrophic cardiomyopathy. Previously, he was CFO of Scioderm, a pediatric orphan disease company; CFO for Akebia Therapeutics (NASDAQ: AKBA), a biotechnology company developing pharmaceutical drugs for anemia and ophthalmology; CFO and senior vice president of corporate development at Serenex, an integrated discovery and development oncology company; and CFO and vice president of operations at Paradigm Genetics (NASDAQ: PDGM). Mr. Howes began his professional career with Coopers & Lybrand in London. He is a Chartered Accountant and has an M.B.A. from the Kenan-Flagler Business School at the University of North Carolina at Chapel Hill.

About Accelerator Life Science Partners
Accelerator Life Science Partners catalyzes the development and commercialization of breakthrough biotechnology innovations. Accelerator is a trusted partner that provides the complete business, scientific and financial toolkit necessary for successfully establishing and operating an early-stage biotechnology company. Accelerator nurtures its companies across all stages and in all facets of development, setting them on a path that offers the greatest chance for long-term success. Among these key resources are committed investment capital, experienced start-up management, world-class scientific expertise and state-of-the-art laboratories and shared facilities.

The company is uniquely positioned to provide this unprecedented collection of capabilities and resources through its partnership with top-tier investors, seasoned executive managers and world-class research institutions. The value of these collective resources has been validated over more than a decade of successful investing in life science companies that are helping to shape the rapidly evolving future of medicine and healthcare. For more information, please visit www.acceleratorlsp.com.

 

Media Contacts:

Rathbun Communications
Julie Rathbun
julie@rathbuncomm.com

Accelerator Corporation
Jessica Burback
jburback@acceleratorcorp.com
T: 206-234-6481


Accelerator Corporation Announces Series A Financing in Rodeo Therapeutics to Focus on Small-Molecule Regenerative Therapies

  • Novel Approach to Tissue Repair Holds Promise in Diverse Disease Indications

SEATTLE, WA – July 25, 2017 – Accelerator Corporation, a leading life science investment and management firm, today announced a $5.9 million Series A financing in Rodeo Therapeutics Corporation, a company developing small-molecule therapies designed to promote regeneration and repair of multiple tissue types. Investors participating in the financing include AbbVie Ventures, Alexandria Venture Investments, ARCH Venture Partners, Eli Lilly and Company, Johnson & Johnson Innovation – JJDC, Inc., Watson Fund, L.P., WRF Capital and WuXi AppTec.

“Tissue damage and degradation play critical roles in the development and progression of a broad array of disease indications, including a variety of inflammatory diseases,” said Sanford Markowitz, M.D., Ph.D., the Markowitz-Ingalls Professor of Cancer Genetics and Distinguished University Professor at Case Western Reserve University School of Medicine and a founder of Rodeo Therapeutics. “The ability to stimulate the body’s natural processes for tissue regeneration and repair has broad therapeutic potential in disease settings such as ulcerative colitis and in hemopoietic recovery following bone marrow transplantation. Rodeo Therapeutics is focused on developing small-molecule therapies that stimulate these processes and enable new approaches to address serious medical conditions that today have a substantial unmet medical need.”

“Rodeo Therapeutics’ founding scientists have achieved a level of biology and medicinal chemistry for their lead product candidate that is advanced beyond what we would typically see in an academic setting,” said David M. Schubert, chief operating officer of Accelerator Corporation. “We believe that this Series A investment will provide the financial resources to rapidly advance the company’s development program toward human trials, which will open the door to an exciting new therapeutic approach that has significant clinical and commercial potential.”

Rodeo Therapeutics’ scientific approach is based on research conducted by world-renowned scientists at Case Western Reserve University and the University of Texas Southwestern Medical Center (UT Southwestern). In addition to Dr. Markowitz, the company’s founding scientists are Stanton Gerson, M.D., and Joseph Ready, Ph.D.

  • Dr. Markowitz is an NCI Outstanding Investigator Awardee and principal investigator of the Case GI SPORE, one of five NCI centers awarded nationally for excellence in gastrointestinal cancer research. He has conducted seminal research in the genetic causes of colon cancer and was instrumental in the development of a novel stool DNA test that has won FDA approval for the early detection of colon cancer. His contributions have been recognized with the Hamdan Award for Medical Research Excellence from the government of Dubai and a Top 10 Award from the Clinical Research Forum.
  • Dr. Gerson is director of the Case Comprehensive Cancer Center, the Asa and Patricia Shiverick–Jane Shiverick (Tripp) Professor of Hematological Oncology and founding director of the Ohio Wright Center for Stem Cell and Regenerative Medicine, now called the National Center for Regenerative Medicine. Dr. Gerson has extensive expertise in stem cell research and has led the development of both cell and gene therapies that promote tissue and DNA repair. His research has generated 12 patents in the area of gene therapy and cancer drug development that have been licensed to three companies.
  • Dr. Ready is a professor in the Department of Biochemistry at University of Texas Southwestern Medical Center and the director of the Medicinal Chemistry Laboratory. His research focuses on synthetic and medicinal chemistry in the areas of regenerative medicine, neurodegeneration and oncology. Three previous research projects from his group have been licensed by pharmaceutical companies for further development.

About Rodeo Therapeutics
Rodeo Therapeutics is focused on developing small-molecule therapies that increase tissue levels of prostaglandin PGE2. Preclinical studies published in Science have shown that increasing PGE2 through inhibition of a prostaglandin-degrading enzyme (15-PGDH) accelerates hematopoietic stem cell reconstitution following bone marrow transplant, protects against colitis and promotes liver regeneration in a variety of animal models.1 The company will initially focus on developing 15-PGDH inhibitors for the treatment of inflammatory bowel disease and promoting blood cell reconstitution following bone marrow transplant.

1 Zhang Y et al. Science. 2015;348(6240):aaa2340. doi: 10.1126/science.aaa2340


Accelerator Corporation Announces $7M Series A Investment in ApoGen Biotechnologies to Develop a New Class of Drugs Targeting Resistance to Cancer Therapy

  • Third Accelerator Corporation-Backed Startup Launched in 2016

SEATTLE, WA – December 12, 2016 – Accelerator Corporation, a leading life science investment and management firm, today announced an investment in ApoGen Biotechnologies, Inc., a company developing a new class of drugs that target the underlying mechanisms that cause genomic mutations to interrupt the development of drug resistance by cancer cells. The investors participating in the $7 million Series A financing include AbbVie Ventures, Alexandria Venture Investments, ARCH Venture Partners, Eli Lilly and Company, Johnson & Johnson Innovation – JJDC, Inc., Watson Fund, L.P., WRF Capital and WuXi PharmaTech.

“One of the great challenges in treating cancer is that it evolves over time and develops resistance to therapy,” said Thong Q. Le, chief executive officer of Accelerator. “ApoGen’s drug discovery and development efforts are focused on the development of highly selective and potent small molecule inhibitors that aim to slow or stop cancer mutation and the development of drug resistance. The company is also working to develop companion diagnostics to identify the patients likely to get the most benefit from these therapies. We are excited to invest Accelerator’s unique startup resources to potentially develop these promising technologies for cancer patients in need.”

ApoGen’s scientific approach is based on discoveries made at the University of Minnesota (U of M). The company’s founders include two researchers at the U of M and an experienced life science serial entrepreneur:

  • Reuben S. Harris, Ph.D., investigator of the Howard Hughes Medical Institute (HHMI); professor of biochemistry, molecular biology and biophysics at the U of M; associate director of the U of M’s Institute for Molecular Virology
  • Daniel A. Harki, Ph.D., associate professor of medicinal chemistry at the U of M
  • John T. Santini, Jr., Ph.D., president and CEO of Vergent Bioscience, a protease-focused biotech company located in Minneapolis, Minn.; co-founder of MicroCHIPS, Inc.; former CEO of four life science companies. Dr. Santini will serve as a member of ApoGen’s board of directors.

ApoGen will initially focus its drug development efforts on an antiviral component of the human innate immune system – the APOBEC cytidine deaminases – which have been implicated as a prominent source of mutations in cancers. Dr. Harris, along with his colleagues at the U of M, have observed that mutations induced by APOBEC occur throughout the genome in many tumorous cells. By targeting this mechanism, ApoGen hopes to interrupt a cancer cell’s ability to develop drug therapy resistance. ApoGen has obtained a worldwide, exclusive license from the U of M related to a portfolio of APOBEC technologies developed by Drs. Harris and Harki.

ApoGen’s scientific advisory board is comprised of a highly respected panel of world-class investigators in the areas of chemical biology, cancer genomics, drug development and clinical research:

  • José Baselga, M.D., Ph.D., physician-in-chief at Memorial Sloan Kettering Cancer Center (MSKCC); professor of medicine, Weill Cornell Medical College
  • Peter B. Dervan, Ph.D., Bren Professor of Chemistry at California Institute of Technology
  • Charles Swanton, M.D., Ph.D., senior clinical research fellow and group leader, Translational Cancer Therapeutics, , Francis Crick Institute; chief investigator, CRUK TRACERx study; co-director, CRUK Lung Cancer Centre of Excellence and Thoracic Medical Oncologist at UCL Hospitals
  • Douglas Yee, M.D., director, Masonic Cancer Center, University of Minnesota; professor, departments of Medicine and Pharmacology, University of Minnesota

“I have been working with Drs. Harris and Harki to move ApoGen’s science toward clinical and commercial development, and I am thrilled to now partner with Accelerator Corporation,” said Dr. Santini. “We believe that we have assembled the ideal team to advance our therapeutic technologies to slow or stop tumor evolution, which has the potential to yield a significant clinical impact for cancer patients.”

About ApoGen Biotechnologies
ApoGen Biotechnologies, Inc. is a biotechnology company focused on the development of a new class of therapeutics targeting drivers of cancer genomic mutation. ApoGen is building upon technologies developed at the University of Minnesota to develop drugs that block a key pathway that causes drug resistance. ApoGen’s drug discovery and development efforts are directed toward highly selective and potent small molecule inhibitors of the APOBEC family of enzymes, which are DNA cytosine deaminases and an important endogenous source of DNA mutation in cancer. For more information, visit www.apogenbiotech.com.

About Accelerator Corporation
Accelerator Corporation, established in 2003, is a biotechnology investment and management company with operations in Seattle and New York City. Formed by a syndicate of top-tier venture capital investors and the Institute for Systems Biology, Accelerator identifies, evaluates, finances and manages the development of emerging biotechnology opportunities. Accelerator has built a unique solution that addresses many of the key problems associated with investing in early-stage biotechnology by providing access to venture capital, management, scientific expertise and facilities.

Since its inception, Accelerator has raised more than $100 million in capital commitments to invest in innovative early stage life science companies. Accelerator has assembled a team of talented professionals with deep investment, operational and scientific expertise to build high-quality life science startup companies and will continue to seek out the most exciting and potentially valuable emerging biotechnologies. Earlier this year, Accelerator announced the launch of Petra Pharma Corporation with $48 million in Series A financing commitments and Lodo Therapeutics with $17 million in Series A financing commitments. Both companies were formed from early-stage research originally developed by two of its New York City institution partners.

 

Contact:

Dan Budwick
Pure Communications, Inc.
973-271-6085
dan@purecommunicationsinc.com


Accelerator Corporation Expands Operations with New Research Institution Partners

  • Expanded Operations Provide New Resources for Seattle and Greater Northwest Region Portfolio
  • Dr. Bruce Carter Appointed to Board of Directors

SEATTLE – October 20, 2016 – Accelerator Corporation, a leading life science investment and management firm, today announced it has expanded operations with three new institution partners: CoMotion at the University of Washington, Fred Hutchinson Cancer Research Center and Oregon Health & Science University. In conjunction with these additions, Accelerator also announced the appointment of life science veteran Bruce L.A. Carter, Ph.D., to its board of directors.

“It has been a momentous year for Accelerator. Earlier this year, we launched our first two startups from our New York City portfolio, Petra Pharma and Lodo Therapeutics. Today, we’ve debuted the expansion of our strategic resources in the Seattle region with the addition of three leading research institution partners and the appointment of Dr. Bruce Carter – a true life science veteran – to our board,” said Thong Q. Le, chief executive officer of Accelerator. “These milestones reflect our mission to carefully and thoughtfully curate high-quality startups backed by promising research. It is through this kind of close collaboration with academia and industry that we are able to continue to fund and form the next generation of innovative companies poised to transform patient care.”

Founded in 2003 in Seattle, Accelerator uses a unique model of investing in life science companies. As part of its model, Accelerator provides its portfolio companies with an exclusive set of startup resources in the form of a complete business, scientific and financial toolkit necessary for running an early-stage biotechnology company. With resources like world-class institution partners, committed investment capital, experienced startup management and scientific expertise, and state-of-the-art laboratories and shared facilities, Accelerator’s portfolio companies have ground-up support that position them for long-term success.

New Institution Partners
CoMotion at the University of Washington, Fred Hutchinson Cancer Research Center and Oregon Health & Science University have joined Accelerator’s current syndicate of institution partners in the Pacific Northwest, bringing its total to 19 institution partnerships nationwide. By partnering with leading research institutions, Accelerator gains access to innovative global technologies and potential commercial opportunities. In turn, these institutions lend their broad expertise to Accelerator’s portfolio companies, providing them with integrated technology, research and development capabilities.

“Accelerator has played a critical role in establishing Seattle and the greater northwest region as a rapidly growing hub of life science innovation,” said Nicole (Niki) Robinson, Ph.D., vice president of business development and industry relations at Fred Hutchinson Cancer Research Center. “Accelerator has a differentiated model that aims to spur creation of startup companies that have built-in resources and support from the life science ecosystem continuum from day one. This collaboration combines the Fred Hutch’s own expertise and research efforts with Accelerator’s deep therapeutic development capabilities to bring forward new oncology medicines for patients in need.”

“Accelerator brings an impressive track record to investments in life science opportunities, with more than 14 startup companies formed to date,” said Vikram Jandhyala, vice president for innovation strategy at the University of Washington (UW) and executive director of CoMotion. “We have worked with Accelerator to create new startup companies based on research developed by our faculty, and we look forward to leveraging Accelerator’s network and expertise in life science management and investment as a way to add value to UW researchers and CoMotion’s programs, including CoMotion Labs.”

“Collaboration is necessary to drive innovation in therapeutic development, and Oregon Health & Science University is excited to join Accelerator to bring together a broad set of experts and opportunities to support new life science startups,” said Brendan Rauw, M.B.A., CLP, vice president of technology transfer and business development at Oregon Health & Science University.

Dr. Bruce Carter Joins Board of Directors
Dr. Carter brings extensive experience in the pharmaceutical and biotechnology industries. For the past 30 years, Dr. Carter has been an affiliate professor in the Department of Biochemistry at the University of Washington. In November 2009, he joined Immune Design Corp., where he served as executive chairman of the board until 2011. Prior to joining Immune Design, Dr. Carter was a member of the management team at ZymoGenetics, Inc., where he held various positions – including CEO – from 1986 to 2009. In 1988, Novo Nordisk A/S acquired ZymoGenetics and, in 1994, Dr. Carter was appointed corporate executive vice president and chief scientific officer for Novo Nordisk. In 2000, Dr. Carter helped establish ZymoGenetics as an independent company from Novo Nordisk. He is the chairman of the boards at Xencor and the Infectious Disease Research Institute in Seattle, and currently serves on the board of directors of Enanta Pharmaceuticals, Mirati Therapeutics, TB Alliance and Dr. Reddy’s Laboratories. Dr. Carter holds a B.Sc. with honors in botany from the University of Nottingham, England, and a Ph.D. in microbiology from Queen Elizabeth College, University of London.

About Accelerator Corporation
Accelerator Corporation, established in 2003 in Seattle, is a biotechnology investment and management company with operations in Seattle and New York City. Formed by a syndicate of top-tier venture capital investors and a world-class research institution, Accelerator identifies, evaluates, finances and manages the development of emerging biotechnology opportunities. Accelerator has built a unique solution that addresses many of the key problems associated with investing in early-stage biotechnology by providing access to venture capital, management, scientific expertise and facilities.

Since its inception, Accelerator has raised more than $100 million in capital commitments to invest in innovative life science companies. Accelerator has assembled a team of talented professionals with deep investment, operational and scientific expertise to build high-quality life science startup companies and will continue to seek out the most exciting and potentially valuable emerging biotechnologies. Earlier this year, Accelerator announced the launch of Petra Pharma Corporation with $48 million in Series A financing commitments and Lodo Therapeutics with $17 million in Series A financing commitments. Both companies were formed from early-stage research originally developed by two of its New York City institution partners. For more information, please go to: www.acceleratorcorp.com.

 

Media Contact:

Pure Communications, Inc.
Katie Engleman
Katie@purecommunicationsinc.com
910-509-3977


Accelerator Corporation Launches Lodo Therapeutics with $17 Million Series A to Develop Therapies Derived from Natural Products

  • Second Startup in Accelerator’s New York City Portfolio

NEW YORK CITY – January 11, 2016 – Accelerator Corporation, a leading life science investment and management firm, today announced the formation of Lodo Therapeutics Corporation to develop novel therapeutics derived from the company’s metagenomics-based small molecule discovery platform. The investors participating in the $17 million Series A financing include Accelerator New York’s investment syndicate partners: AbbVie, Alexandria Venture Investments, ARCH Venture Partners, Eli Lilly and Company, Harris & Harris Group, Inc., Innovate NY Fund, Johnson & Johnson Innovation – JJDC, Inc., The Partnership Fund for New York City, Pfizer Venture Investments, Watson Fund and WuXi PharmaTech. The financing also includes investment participation by the Bill & Melinda Gates Foundation.

Lodo Therapeutics seeks to realize the vision of researcher and Lodo Therapeutics co- founder Sean Brady, Ph.D., head of The Rockefeller University’s Laboratory of Genetically Encoded Small Molecules. Dr. Brady’s research centers on the discovery, biosynthesis and characterization of new, genetically-encoded small molecules from microbial sources, with a special focus on those produced by uncultured soil bacteria and the human microbiome. Veteran drug hunter and Lodo Therapeutics co-founder David Pompliano, Ph.D., will join the company as interim chief scientific officer. Dr. Pompliano is a well-established and internationally known scientist with extensive experience in the discovery and early development of anti-infective and oncology drugs within both large pharmaceutical companies and small biotechnology firms.

“More than half of all small molecule drugs for cancer, infections and Type 2 diabetes today are derived from natural products, representing significant promise of this approach for patients. Our genome-based, culture-independent approach exploits the power of microbial evolution to identify therapeutically valuable natural products,” stated Dr. Brady. “With the support of Accelerator, we can tap this rich, natural source of small molecule diversity to develop new therapies for emerging bacteria and drug resistant bacteria, critical needs in today’s global healthcare environment.”

Lodo Therapeutics has entered into a license agreement with The Rockefeller University to practice and expand upon this technology platform and approach to developing therapeutics for unmet medical needs in both the developed and developing world. Since 2014, The Bill & Melinda Gates Foundation has sponsored research in the laboratory of Dr. Brady to support this drug discovery platform. Dr. Brady’s broad-based work at The Rockefeller University initially focused on antibiotics, but has since expanded to focus on uncovering improved therapeutics for a variety of diseases that affect patients in the world’s poorest countries. Lodo Therapeutics, in partnership with The Bill & Melinda Gates Foundation, will work to bring these drug candidates toward the initiation of human clinical trials. Lodo will continue to develop Dr. Brady’s platform, not only for a broad range of infectious diseases like tuberculosis, but also in additional areas including oncology, metabolic disorders and rare diseases.

“Tuberculosis is a leading cause of preventable death in the world’s poorest countries, yet current drug regimens are lengthy, expensive and often ineffective,” said Trevor Mundel, president of Global Health at the Bill & Melinda Gates Foundation. “We are thrilled to partner with Lodo Therapeutics to support the development of novel technologies to find new and better drugs to treat tuberculosis and combat the problem of drug resistant infectious disease more generally.”

“As the second company that Accelerator has launched in New York City this month, we are well on our way to building the next generation of successful biotechnology and life science companies that may make a huge impact in the lives of patients,” said David M. Schubert, chief operating officer of Accelerator.

“Sean Brady’s approach to developing new therapeutics based on microbes from soil has the potential to make a tremendous impact on human health, and I am enormously pleased that this work will advance beyond the walls of academia,” said Marc Tessier- Lavigne, Ph.D., president of The Rockefeller University. “We have the best hope of advancing science and creating new medicines when bright, dedicated scientists from basic research labs join forces with their counterparts in industry. The formation of Lodo Therapeutics represents not only the advancement of medicinal science, but also the continuing development of New York City’s rich biotechnology ecosystem.”

Under Accelerator’s unique and proven investment and operations management model, the early operations of Lodo Therapeutics will be overseen by Accelerator’s core management team. By leveraging Accelerator’s capabilities, Lodo Therapeutics will be highly focused on achieving key value-building scientific milestones, while the Accelerator management team handles all aspects of business management and scientific oversight. In addition to leveraging Accelerator’s management capabilities, Lodo Therapeutics will also utilize highly talented and capable consultants in areas of chemistry, biology and early preclinical development.

Lodo Therapeutics’ office and lab headquarters will be located within Accelerator’s facilities at the Alexandria Center for Life Science, New York City’s first and only premier life science park. Since its establishment, The Alexandria Center for Life Science has become the leading commercial destination in New York City for world-class life science entities to translate innovative discoveries into breakthrough products for patients with significant unmet medical needs.

About Accelerator Corporation
Accelerator Corporation, established in 2003 with operations in Seattle and New York City, is a biotechnology investment and management company. Formed by a syndicate of top-tier venture capital investors and a world-class research institution, Accelerator identifies, evaluates, finances, and manages the development of emerging biotechnology opportunities. Accelerator has built a unique solution that addresses many of the key problems associated with investing in early-stage biotechnology by providing access to venture capital, management, scientific expertise, and facilities. For more information, please go to: www.acceleratorcorp.com.

Since its inception, Accelerator has raised more than $100 million in capital commitments to invest in innovative life science companies. Accelerator has assembled a team of talented professionals with deep investment, operational and scientific expertise to build high-quality life science startup companies and will continue to seek out the most exciting and potentially valuable emerging biotechnologies. Earlier this year, Accelerator announced the launch of Petra Pharma Corporation with $48 million in Series A financing commitments to develop novel, small molecule therapeutics for the treatment of cancer and metabolic diseases.

 

Media Contact:

Pure Communications, Inc.
Katie Engleman Katie@purecommunicationsinc.com 910-509-3977

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