|SanBio Co., Ltd. (4592)|
SanBio Company Limited
Mothers of Tokyo Stock Exchange
28th floor, St. Luke's Tower, 8-1 Akashi-cho, Chuo-ku, Tokyo
End of January
* The share price is the closing price on January 12, 2017. The number of shares issued and BPS were taken from the latest financial report.
This report outlines the financial results of the SanBio Group (SanBio Co., Ltd. and its subsidiary in the US, SanBio, Inc.) for the term ending January 2017 and so on.
HistoryPreviously, Mr. Keita Mori (currently the representative director and president of SanBio Company Limited) was an executive in research and development at Kirin Holdings, Ltd., but was eager to launch a new business in the biotechnology arena. He shared this goal with Mr. Toru Kawanishi, an old friend who had served as a consultant at The Boston Consulting Group, and was a cofounder and vice president of CareNet (2150, Mothers of Tokyo Stock Exchange), which assists pharmaceutical companies in sales activities.
They discussed various topics, including future directions and set a goal of "creating new products and markets in the biotech arena," as both of them had majored in biotechnology in the agricultural department at Tokyo University. They focused on "regenerative cell medicines," which appeared to be a new and promising field and established SanBio, Inc. in California in February 2001 with the objective of developing and commercializing these therapies.
At the time of the founding of the company, Messrs. Mori and Kawanishi became aware of the academic research of Professor Hideyuki Okano of Keio University, a leading expert in regenerative medicine and iPS research in the cranial nerve field, Dean of Keio Medical School, and Director of the Japanese Society for Regenerative Medicine. The two founders requested that Professor Okano collaborate in launching their business and ultimately reached agreement. In December 2002, following an introduction by Professor Okano, the intellectual property rights to certain technology required for producing SanBio's current products were transferred via Yokohama TLO Co., Ltd., an institution that licenses intellectual property of research conducted at national public and private universities in Kanagawa Prefecture to commercial enterprises. Since the founding of SanBio, Professor Okano has continued to consult to SanBio as a founding scientist. Meanwhile in the US, the company recruited advisors and top researchers in each discipline via its strong network in the regenerative medicine field, and pursued the development of both regenerative cell medicines and the production technologies necessary to scale them up for clinical use.
Following the development phase, SanBio sought partners among large pharmaceutical companies capable of bringing drug candidates through clinical trials and into widespread use. In December 2009, SanBio concluded a contract for licensing the development of the regenerative cell medicine SB623 for treating sufferers from chronic stroke disabilities with Teijin Ltd.. In May 2010, it received approval to conduct its first clinical trial from the US Food and Drug Administration (FDA). In September 2010, SanBio signed an option agreement for the treatment of disability resulting from stroke in the US and Canada with Sumitomo Dainippon Pharma Co., Ltd.
In January 2011, SanBio commenced a Phase 1/2a clinical trial of SB623 in the field of chronic stroke in the US, and in August 2013, the administration of SB623 to 18 patients was completed. There were no obvious product-related safety concerns, no dose-limiting toxicity, and statistically significant efficacy across multiple endpoints was observed.
During this same time period, the presence of Japan in the field of regenerative medicine became recognized internationally. Professor Shinya Yamanaka of Kyoto University received the Nobel Prize for his development of iPS cells in December 2012. And both an amended Pharmaceutical Affairs Act and a new law regarding regenerative medicines came into effect in November 2014, granting expedited approval for certain regenerative medicines. Considering this to be an historic opportunity, SanBio Company Limited was formed in Japan in February 2013, to establish global business operations, with R&D centered in its Silicon Valley laboratory, and management systems located in Japan. In January 2014, SanBio Company Limited in Japan became the parent company, and SanBio, Inc. in the US became a 100% owned subsidiary. Following this reorganization, SanBio Co. Ltd. filed its Initial Public Offering on the Mothers market of the Tokyo Stock Exchange in April 2015, raising 7.3 billion yen, one of the largest IPOs to date for a Japanese biotech venture.
SanBio Group and development systemsAs mentioned in the section on corporate history above, the SanBio Group is composed of SanBio Company Limited and its consolidated subsidiary, SanBio, Inc. (California, US).
Since the company's founding in 2001, the development and production teams of SanBio, Inc. in the US have engaged in the research and development of regenerative cell medicines. The SanBio Group is also establishing a network of contract research organizations (CROs) and collaborators in Japan to further its worldwide business operations.
Dr. Hideyuki Okano, a SanBio founding scientist, is a leading expert in regenerative medicine and iPS cell research in the brain. His work has been instrumental in overturning the conventional theory that "the brain does not regenerate." Dr. Okano has advised SanBio on scientific issues since the company was founded.
Dr. Donald Kennedy, the former FDA Commissioner, and president of Stanford University, and Dr. George Martin, the former Scientific Director of the National Institute on Aging at the National Institutes of Health (NIH), are also members of SanBio's Scientific Advisory Board.
SanBio also cooperates with leading US research institutes, including Stanford University, the University of Pittsburgh, New York University (NYU), the University of California Los Angeles (UCLA), and Northwestern University, which pursue cutting-edge medical care and form part of the Company's strong network of clinical researchers in the regenerative medicine field.
Dr. Damien Bates, SanBio's Chief Medical Officer and Head of Research, previously succeeded in obtaining the first approval for an "allogeneic" cell pharmaceutical product from US FDA. Prior to Dr. Bates' work, "autologous" transplantation had been approved in several cases, but not "allogeneic transplantation." ("Allogeneic transplantation" and "autologous transplantation" will be described later in the section titled "Business content and business model.")
SanBio's production executive, Dr. Michael McGrogan, is an innovator in the field of producing cells for therapeutic use, and obtained the first FDA approval for conducting trials with regenerative medicines. He has worked with SanBio for the past 10 years perfecting the methods needed to produce SB623 in quantities needed for clinical studies and later marketing. Many of these production processes and scale-up methods represent the proprietary information of SanBio.
Corporate missionThe mission of the SanBio Group is to develop treatments based on regenerative cell medicines for diseases that represent unmet medical needs*, such as chronic motor disability** secondary to stroke, traumatic brain injury, age-related macular degeneration, retinitis pigmentosa, Parkinson's disease, spinal cord injury, and Alzheimer's disease, and then use these innovative products to treat patients suffering from such diseases around the world.
*Unmet medical needs: Diseases for which no effective treatment methods have been developed.
**Chronic disability: Symptoms (e.g., weakness or paralysis of the limbs) persisting 6 months or more following brain injury such as stroke or traumatic brain injury.
Points in understanding SanBioThere are several major topics where basic facts are necessary in order to understand SanBio's business and competitive advantages, such as stem cells, brain regeneration, and regenerative medicine.
The human body has over 37 trillion cells and over 200 different kinds of cells.
The human body is produced from a single fertilized egg, which divides and multiplies repeatedly, changing into a variety of cells making up the adult body, including nerve, myocardial, and hepatic cells.
The human body consists of both fully-differentiated and incompletely differentiated cells. The former are called somatic cells and the latter, stem cells.
Stem cells include hematopoietic, adipose, neural, and mesenchymal stem cells. These cells have the capacity to change into various cell types within a limited range. For example, hematopoietic stem cells exist abundantly in bone marrow, and they produce all types of blood cells, including white blood cells and platelets, but they do not typically change into other types of cells.
During fetal life (about nine months from fertilization), the human brain contains neural stem cells, which are the origin of neurons, and produces new neurons through active cell division and differentiation. It was previously thought that this cell division ceases and that new neurons were no longer produced in adults.
Contrary to this view, recent research indicates that neural stem cells exist also in the adult brain, and that the adult brain has the capacity to produce new neurons and other types of brain cells.
Dr. Hideyuki Okano, a founding scientist of SanBio, was one of the first to discover this, and he succeeded in regenerating brain neurons.
ES and iPS Cells vs. MSC
Embryonic stem (ES) cells have a greater capacity to differentiate into different types of cells than adult stem cells. In theory, ES cells can differentiate into all of the types of cells in the body, including the heart muscle, nerves, liver, and blood.
While adult stem cells typically only develop into a limited range of cells, ES cells can differentiate into a much wider range of cells. This is a remarkable characteristic.
ES cells are produced from embryos used in treating infertility. Despite the fact that surplus embryos would otherwise be discarded, the use of fertilized eggs has raised ethical issues in many countries. In some cases, ES cells are derived from aborted fetuses, which is also considered ethically problematic by some. In 2007, Professor Shinya Yamanaka of Kyoto University invented a new cell called the "induced pluripotent stem cell (iPS cell)". iPS cells have similar characteristics to ES cells but do not require the use of embryonic or fetal cells. iPS cells are produced from human skin cells.
iPS cells have almost the same characteristics as ES cells in that they can change into various cells such as heart muscle, nerves, liver, and blood, and iPS cells are free from the ethical issues presented by ES cells. One drawback of iPS cells is the risk of causing cancer because iPS cells multiply without limit.
Mesenchymal Stem Cells (MSCs) are extracted from the bone marrow of healthy donors and have been used for many years for patients requiring complete replacement of their marrow and blood cells. There are no obvious ethical issues with the use of these cells, and they are not known to pose any risk of promoting cancer. While they can differentiate into other cell types, they usually persist for less than a month after injection or implantation. During this time, in vivo MSCs secrete growth factors that can influence other cell types and can be genetically manipulated (as demonstrated by SanBio) to further encourage nervous system recovery.
Regenerative MedicineRegenerative medicines are medicines designed to recover or revitalize organs that are not functioning normally by using cells, extracellular matrices, and growth factors. For example, the stem cells of a patient or a donor may be transplanted into a patient, and the transplanted cells induced to differentiate into desired cells or act on existing cells to treat diseases. Regenerative medicine is expected to enable innovative treatments that would have otherwise been impossible.
①What is regenerative medicine?
②The Japanese business environment is attracting attention from around the worldAccording to data released by the Ministry of Economy, Trade and Industry, the size of the regenerative medicine market was 9 billion yen in Japan and 100 billion yen outside Japan in 2012 and is projected to reach 2.5 trillion yen in Japan and 38 trillion yen outside Japan by 2050.
Research into regenerative medicines is very competitive. Professor Yamanaka produced epoch-making results regarding iPS cells in 2006 and 2007. Shortly thereafter, in 2009, US President Obama signed a bill lifting the ban on federal funding for ES cell research which had been prohibited under the Bush administration.
Later, in 2012 Japanese government officials stated that "systems based on the cooperation among government, industry, and academia are indispensable for surviving the fierce research competition and actualizing clinical technologies for patients" (Current situation and problems in regenerative cell medicine, Sep. 26, 2012; Research and Development Division, Health Policy Bureau, the Ministry of Health, Labour and Welfare), and "regenerative medicine" became one of the most important themes in the government's strategies for supporting the Japanese economy.
Consistent with this trend, the Pharmaceutical and Medical Device Act (the new title for the amended Pharmaceutical Affairs Act) and the Act for Securing the Safety of Regenerative Medicine, were enacted on November 25, 2014, and the legal framework for approving regenerative medicines was established. Most notably, an early approval system was adopted in the amended Pharmaceutical Affairs Act, which shortened the period for approval from 5-8 years to 3.5 years.
In addition, the outsourcing of cell culturing and processing was permitted through the Act for Securing the Safety of Regenerative Medicine. Following the legislative changes enacted by Japan, many overseas companies announced that they would enter the Japanese market through various alliances and agreements with Japanese companies. Clearly, the environment surrounding regenerative medicine in Japan is attracting global attention.
Business content and business modelSanBio develops, produces, and sells regenerative cell medicines for diseases that have unmet medical needs, such as chronic disability from stroke, chronic disability from traumatic brain injury, age-related macular degeneration, retinitis pigmentosa, Parkinson's disease, spinal cord injury, and Alzheimer's disease. All of these are related to brain neurons.
Regenerative Cell MedicinesSanBio's approach to treating these conditions is by administering regenerative cell medicines. These are pharmaceutical products that induce or promote the natural regeneration of cells and tissues responsible for physical functions lost due to loss of blood flow, injury, or aging. Regenerative medicines stimulate regeneration or recovery of cells responsible for functions such as mobility, speech, sight, and cognition.
① What are regenerative cell medicines?
② Allogenic and Autologous CellsCells used in regenerative medicines typically fall into two categories: autologous and allogeneic. Autologous transplantation refers to the transplantation of cells that have been harvested from a patient and transplanted back into the same patient to treat the patient's own disease or disability.
The skeletal myoblast sheet produced by Terumo is an example of a regenerative medicine based on autologous transplantation. Muscular tissue is taken from the thigh of a patient. The skeletal myoblast portion of the tissue is cultured, a sheet of tissue is produced, and the sheet is transplanted back onto the heart of the patient to treat serious heart failure. An important advantage of this method is that, since cultured cells are autologous, they are theoretically free from immune rejection. However, processing and culturing of autologous cells is typically very time consuming and expensive, as it is performed on individual patients, and results may vary from individual to individual.
In contrast, allogeneic cells are taken from healthy adult donors and processed and cultured for large scale production. Because cells from one donor can potentially treat thousands of patients, allogeneic cell based treatments are inherently lower cost and easier to implement than autologous cell-based treatments. If issues related to immunological compatibility and safety are solved, allogeneic cell-based treatments will be the preferred method of regenerative medicine for many indications.
In order to fulfill the mission of the SanBio Group to develop new therapies for diseases that have unmet medical needs and to improve patients' physical functions by using cost effective regenerative cell medicines, the company has chosen to use allogeneic cell-based pharmaceutical products which are delivered to patients through existing distribution channels.
③ Mass-ProductionLarge scale production methods are needed in order to put regenerative cell medicines into practical use. SanBio has overcome this hurdle.
Very few companies have established the technology needed for mass-producing regenerative cell medicines. In the regenerative medicine business, in which medicines are more complex than conventional drugs, there exists a significant hurdle in order to achieve large scale production. This is sometimes called the "production valley of death", and must be faced before practical application. As SanBio has already surpassed this "valley of death", it is well ahead of potential competitors.
④ Regenerative Cell Medicine SB623SanBio's most advanced cell medicine is SB623 for treating chronic disability due to stroke and traumatic brain injury. For the time being, SanBio plans to concentrate on the expansion of indications for SB623. SanBio has also developed other cell medicines, known as SB618 and SB308, which are intended for other applications.
(1) Efficacy of SB623SB623 treatment has the potential to improve certain neurological functions and is aimed at facilitating the recovery processes of the body by stimulating the patient's own capacity for tissue regeneration. In the brain, this would ideally manifest itself by revitalizing the weakened functions of mobility, sight, speech, and cognition following brain injury. Its effects may include: neuronal growth and differentiation, neuro-protection, angiogenesis, and anti-inflammation. Research in the regenerative medicine field suggests that these effects may act synergistically.
Stroke, which is the first indication targeted for SB623, is a result of occlusion of blood vessels in the brain, preventing oxygen and nutrients from reaching neural tissue, causing loss of brain function or death. Thrombolytic agents are effective against stroke during the acute phase for several hours after onset, but after the acute phase, there are no treatment methods other than physical and speech therapy. Typically, physical and speech therapy benefits level off after the first 6-12 months following stroke.
In 2011, SanBio began a US-based two-year Phase 1/2a clinical trial to provide initial safety and efficacy data for SB623 in patients suffering chronic motor disability caused by ischemic stroke. In February 2014, the last patient in the Phase 1/2a study reached the 6 month follow up timepoint. There were no obvious product related safety concerns, no dose-limiting toxicity, and statistically significant efficacy results across multiple endpoints were observed. In June 2014, FDA approved SB623 to move to the next stage of clinical testing, Phase 2b and the clinical study is now ongoing.
The graph shows that the improvement in motor fuction sustained even 24 months after administration.
(2) SB623 AdministrationIn the case of SanBio's stroke study, the medicine is administered with local anesthesia in a stereotactic neurosurgical operation, which is a common method in this field.
(3) Progress of developmentAfter receiving the result of phase 1/2a clinical trial of "SB623" in the U.S. in Jun. 2014, SanBio obtained the FDA approval to move to the next phase 2b clinical trial. In Sep. 2014, Dainippon Sumitomo Pharma Co., Ltd., executed an option contract and started joint development of "SB623" to treat patients suffering from chronic motor disabilities caused by ischemic stroke in the U.S. and Canada.
◎ Chronic-phase stroke
The 2-year follow-up period of the phase 1/2a ended in Aug. 2015 and SanBio advanced to the phase 2b. The Company received a milestone payment of 5 million US dollars from a joint development partner for SB623 in North America, Sumitomo Dainippon Pharma, upon entering into an agreemnt with the first clinical site in Sep. 2015.
In Dec. 2015, SanBio started recruiting subjects for phase 2b (156 subjects, double blind study) in "patients suffering from chronic motor disabilities caused by ischemic stroke 6 months to 5 years after the onset of stroke", and the first subjects were enrolled on Mar. 8, 2016. SanBio received a milestone payment of 5 million US dollars from Dainippon Sumitomo Pharma for this.
SanBio is currently activating clinical sites of about 60 facilities throughout the US and also recruiting patients.
As of Mar. 2017, 13 surgical sites (18 sites planned) and 30 assessment sites (44 sites planned) are open and activated.
In Japan, development of SB623 for stroke is licensed out to Teijin Ltd.
◎ Traumatic brain injurySanBio is also developing SB623 for the treatment of motor disability caused by TBI, which is the next target indication for SB623 following stroke.
Traumatic brain injury results from a strong impact to the head (e.g., from a traffic accident or fall) and can be accompanied by serious permanent disorders, such as partial or complete paralysis, sensory impairment, memory loss, and higher cerebral dysfunction, which makes it difficult to control one's behavior and emotions. The period during
which physical therapy is effective is 6-12 months after onset, slightly longer than that of stroke; and after that period, there are no effective therapies. In the US, about 2.5 million patients receive emergency TBI medical treatment every year, and the number of patients with residual disability in the US is estimated to be 5.3 million.
For the clinical trials in the U.S., since traumatic brain injury is similar to stroke in damaged parts and symptoms and the administration method of SB623 is the same as that for stroke, it was regarded as an expanded indication of SB623. Therefore, in Apr. 2015, the FDA agreed that SanBio could skip phase 1 and start from phase 2, and the Company obtained approval to start the clinical trials from phase 2.
This phase 2 for traumatic brain injury is now being conducted as a Japan and U.S. global study for "patients with chronic motor disabilities, at least 12 months after the onset of traumatic brain injury" at about 30 clinical sites in the US and Japan and the number of patients enrolled will be 52 in total (double blind study).
In the U.S., the patient recruitment started in Oct. 2015, and the first subject was enrolled in Jul. 2016.
In Japan, with an approval for clinical trials by Pharmaceuticals and Medical Devices Agency (PMDA) in Apr. 2016, SanBio started a clinical trial in Sep. 2016 and enrolled the first subject in Oct. 2016.
As of Mar. 2017, 9 surgical sites (14 facilities planned) and 17 assessment sites (21 facilities planned) are activated in the US and Japan.
<Voices of SanBio staff>
Damien Bates, Chief Medical Officer and Head of Research
"SanBio's regenerative cell medicine SB623 appears to have the potential to improve the motor function of patients suffering from persistent disability post ischemic stroke. Furthermore, our non-clinical data support the the possibility that this medicine could also be effective for patients with persistent motor deficits secondary to TBI. We are now aggressively pursuing this hypothesis in both Japan and the US with our global Phase 2 clinical trial - the first of its kind in the world. With this gateway to clinical studies for our regenerative medicine product in Japan now open, we are actively exploring other target indications for SB623."
Takehiko Kaneko, Head of SanBio's Clinical Development Department Japan and Medical Director
"I'm delighted to see SB623 entering clinical development in Japan. We will conduct the clinical development of SB623 to treat patients with motor disorder as soon as possible."
◎ Age-related Macular DegenerationSince SB623 appears to have strong neuroregenerative activity, SanBio is exploring the possibility that it will prove effective against certain retinal disorders as well.
The macula is located at the center of the retina in the back of the eye. The macula is the most important part of the eye. It is the source of most optical information, including shape, size, colors, dimensions, and distance. As a person ages, the cells of the retina gradually die, and the function of the macula starts to decline. As a result, eyesight degrades, and the field of view is blurred. Such symptoms are called age-related macular degeneration (AMD). There is currently no effective treatment for the most common form of AMD - dry AMD.
Given the particularly large unmet medical need and growing market, SanBio is exploring dry AMD and retinitis pigmentosa as potential targets for SB623.
In January 2014, SanBio held a pre-pre-IND meeting with the US FDA to discuss its non-clinical data in animal models of retinal degeneration. Further to these discussions and guidance, SanBio is now completing additional non-clinical studies for IND approval, a prerequisite for FDA approval of clinical study initiation in the US.
<Business Model>After acquiring technologies from universities and internal development, SanBio performs preclinical studies and develops production methods for its products. Then, SanBio enters into license agreements with larger pharmaceutical companies to fund clinical studies and market products. In this business model, SanBio receives (1) upfront payments, (2) milestone payments, (3) fees for cooperation in development, (4) royalties, and (5) income related to supplying final product to the licensee.
SanBio performs research work both in-house and at university and contract laboratories. Production is typically contracted with firms specializing in cell harvesting and production.
In order to maximize value, the company verifies the safety and efficacy of products in human trials before considering out-licensing.
② Existing Pharmaceutical PartnershipsFor the development, production, and sale of SB623 for treating chronic motor deficit resulting from stroke, SanBio concluded contracts with Sumitomo Dainippon Pharma Co., Ltd. in the US and Canada, and Teijin Ltd. in Japan.
Characteristics and StrengthsThe target diseases of SanBio's regenerative cell medicines are mainly neurodegenerative diseases and other central nervous system disorders which have no effective therapies. These represent very large markets.
① Huge Target Markets
The number of stroke patients is said to be about 6.6 million in the US. According to the "Survey on Patients in 2014" by the Japanese Ministry of Health, Labour and Welfare (announced in December 2015), the estimated number of patients of cerebrovascular disease (stroke) in Japan in 2014 was 1.179 million, which is slightly smaller than the number (1.235 million) obtained in the previous survey (2011), but this accounts for about 1% of the population.
② Patent Strategies to Create Competitive AdvantagesSanBio's basic patent strategy is to acquire all of the necessary intellectual property for developing regenerative cell medicines, with the goal of maximizing income from the development and sale of products. SanBio has obtained all of the basic patents for its initial regenerative cell medicines, SB623, SB618, and SB308.
As seen below, SanBio has been issued basic patents in all major markets. The company plans to seek partnerships with leading pharmaceutical companies, such as Sumitomo Dainippon Pharma Co., Ltd. in the US and Canada, and Teijin Ltd. in Japan, and will develop a strong foundation for clinical trials, production process development, and product sale around the world.
Substance patents are for protecting substances themselves; they are the most important type of patents for pharmaceutical products, and they confer the broadest scope of rights. Accordingly, obtaining them requires significant cost and time. The owner of a substance patent is able to produce and sell developed products exclusively, for any use. Therefore, the SanBio Group is particularly focused on acquiring substance patents.
③ Securing of rights to supply productsCertain drug discovery ventures in-license drug candidates from other companies and develop them further - meaning that the licensor shares in any eventual royalty. Other ventures turn over the rights to produce drug products to their partner pharmaceutical companies; therefore, the income of the ventures is limited to royalties for product sale.
In the case of SanBio, regenerative cell medicines are not in-licensed from other companies but are the unique fruits of in-house research and development. In addition, SanBio engages in the production of regenerative cell medicines and does not turn over production rights to its partners. Therefore, SanBio receives all the royalties from product sale and also receives product supply revenue, resulting in a more complete and diversified set of revenues than that of many development companies.
④ Established mass-production technology and safety of regenerative cell medicinesAs mentioned above, SanBio has established technologies for formulation, production, storage, shipping, and administration and is able to mass-produce products for the market yielding a cost advantage. Another differentiating factor compared to companies focused on embryonic stem cells is that mesenchymal stem cells are considered to be safer and do not face obvious ethical issues. Mesenchymal cells are also considered safer than iPS cells with respect to tumorigenic risk. Therefore, SanBio's regenerative cell medicines are expected to be readily accepted in clinical practice.
|Fiscal Year January 2017 Earnings Results|
Operating loss posted due to R&DRevenue was 949 million yen, down 19.2% year on year. There were a milestone payment of 543 million yen, received upon the first patient enrolled at the Phase 2b clinical trial for stroke in the U.S. and development support revenue amounting to 406 million yen based on the joint development agreement of "SB623" with Sumitomo Dainippon Pharma in North America.
The Company posted an operating loss, due to operating expenses that are composed of mainly R&D cost. R&D cost was 1.8 billion yen smaller than the estimated amount. This is because, as mentioned in the previous report, the expense plans which included clinical trial expenses had many uncertainties, and their expected maximum amounts incorporated during planning were too conservative. As development progressed, the Company increased the number of R&D staff by 6 and other staff by 9, that is, the number of all staff rose by 15.
In addition, an exchange loss of 199 million was posted in non-operating expenses, due to the fluctuations in the exchange market.
Net assets dropped 1,771 million yen from the end of the previous term to 4,594 million yen, due to further decline in retained earnings.
As a result, equity ratio decreased 4.2 points from 77.0% at the end of the previous term to 72.8%.
(3) TopicsThe results of the phase 1/2a clinical trial of SB623 was published in the medical journal "Stroke" of American Heart Association and this publication received the third prize for the 2016 Stroke Progress and Innovation Award.
◎ Received Innovation Award from American Heart Association
"Stroke" is a leading scientific journal addressing the diagnosis and treatment of cerebrovascular diseases, jointly published by the American Heart Association and American Stroke Association. The previous award winners have established important standards of therapeutic agents and therapies, including "acute stage therapeutic agent, Activase, for stroke" which was the first award for Genentech, which has grown to be a world class bio-venture company, and "cerebral hypothermia" which has a reputation for preventing further development of dysfunction when the brain is damaged, and was awarded for its unconventional and innovative studies.
SB623's publication was chosen among several hundreds of publications, and SanBio deem the reasons that this award was given are "innovation and efficacy: clinically significant efficacy" and "simple administration method: direct administration and stereotaxic surgery" that have "the possibilities to change the conventional treatments for stroke"
Dr. Damien Bates, Chief Medical Officer and Research Head of the SanBio group, commented "This prize from the American Heart Association recognizes the innovation of our stem cell treatment, SB623, and its potential to treat patients suffering from chronic physical impairments following ischemic stroke. The results of this study are encouraging to all those suffering from the long-term effects of stroke as well as the medical community working to advance treatment options."
◎ Progress and projection of developmentAs mentioned above, 13 surgical sites (18 facilities planned) and 30 assessment sites (44 facilities planned) are open and activated as of Mar. 2017.
1) Chronic stroke
SanBio aims to complete the patient enrollment (156 subjects) by Mar. 2018, 24 months after the first patient enrollment in Mar. 2016.
2) Traumatic brain injuryAs of Mar. 2017, 9 surgical sites (14 facilities planned) and 17 assessment sites (21 facilities planned) are activated in total, in the U.S and Japan.
After the enrollment of 52 subjects (the schedule is undisclosed), SanBio aims to obtain the first marketing approval in Japan by utilizing the early approval system for regenerative medicine products in Japan.
|Fiscal Year January 2018 Earnings Estimates|
To proceed with development with the aim of completing enrollment in phase 2Revenue is estimated to be 662 million yen, down 30.2% year on year, with an expected income from development support fee under the joint development agreement with Sumitomo Dainippon Pharma.
The company plans to proceed with development with the aim of completing enrollment in the phase 2b for stroke and the phase 2 for traumatic brain injury. Operating loss is expected to augment 2 billion yen year on year, including 1.8 billion yen of the R&D cost that was not used in the previous term.
The personnel necessary for development have been already secured, and so personnel cost will be flat.
and the global clinical trials for traumatic brain injury conducted in the US and Japan, as well as the development of stroke program in Japan.
|<Reference: Regarding corporate governance>|
◎ Corporate Governance ReportLast update: October 18, 2016.
◎ Reasons for Non-compliance with the Principles of the Corporate Governance CodeThe report mentions "Our company implements all of the basic principles of the corporate governance code, and so there are no items to be written in this blank."
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