Astellas Reports First Quarter FY2017 Financial Results

On July 28, 2017 Astellas Pharma Inc. (TSE: 4503, President and CEO: Yoshihiko Hatanaka, "Astellas") reported the financial results for the first quarter of fiscal year 2017 ("FY2017"), ending March 31, 2018 (Press release, Astellas, JUL 28, 2017, View Source [SID1234519921]).

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"Financial results for the first quarter of FY2017 were in line with our expectations and the previously announced consolidated forecasts. Although some development programs were discontinued, the rest of our development activities are progressing steadily, and the acquisition of Ogeda expanded Astellas’ late-stage clinical pipeline including fezolinetant," said Yoshihiko Hatanaka, president and CEO, Astellas. "We remain committed to creating innovative medical solutions and delivering value for patients and all stakeholders, as we continue to advance our strategic plan through maximizing the product value, creating innovation and pursuing operational excellence."

Consolidated Financial Results (April 1, 2017 – June 30, 2017) (core basis) (Millions of yen) Q1 FY2016 Q1 FY2017 Changes (%) Sales 337,752 322,571-15,182 (-4.5%) Core operating profit 93,951 65,124-28,827 (-30.7%) Core profit for the year 67,148 51,914-15,233 (-22.7%) Basic core earnings per share (yen) 31.60 25.14-6.46 (-20.4%)

Quarterly Revenue Highlights
Sales in the first three months of FY2017 decreased by 4.5% compared to those in the corresponding period of the previous fiscal year ("year-on-year") to ¥322.6 billion due to impacts such as the transfer of the global dermatology business in April 2016 and the transfer of long-listed products in Japan in April 2017.
 Oncology franchise
Sales of XTANDI increased by 5.8% year-on-year to ¥67.9 billion. Sales in the United States ("U.S.") decreased, but sales grew steadily in Japan, the Americas excluding the U.S., EMEA1, Asia and Oceania regions.

 Urology OAB franchise
Sales of Betanis / Myrbetriq / BETMIGA increased by 15.6% year-on-year to ¥27.2 billion. Sales increased in all regions: Japan, the Americas, EMEA, Asia and Oceania. Sales of Vesicare, however, decreased by 19.2% year-on-year to ¥24.6 billion.

 Transplantation franchise
Sales of Prograf (tacrolomis) remained largely unchanged year-on-year to ¥49.4 billion, and continued to grow in the EMEA, Asia and Oceania regions.

 Other new and key products
In the Japanese market, continued growth was achieved with products such as Celecox (celecoxib) for the treatment of inflammation and pain, Symbicort (budesonide and formoterol fumarate dihydrate) for the treatment of bronchial asthma, Suglat (ipragliflozin) for the treatment of type 2 diabetes, and Cimzia (certolizumab pegol) for the treatment of adult patients with rheumatoid arthritis. Accordingly total sales of these four products increased by 4.6% year-on-year to ¥27.7 billion. Meanwhile, we have been steadily working to penetrate the market with our launches of Repatha (evolocumab) for the treatment of hypercholesterolemia in April 2016 and of LINZESS (linaclotide) for the treatment of irritable bowel syndrome with constipation in March 2017. In the Americas, sales of azole antifungal CRESEMBA (isavuconazonium sulfate) grew.

(Billions of yen)
Q1 FY2016 Q1 FY2017 Change Oncology franchise 79.1 81.8 +3.4% XTANDI 64.2 67.9 +5.8% Urology OAB franchise 54.0 51.8-4.0% Vesicare 30.4 24.6-19.2% Betanis / Myrbetriq / BETMIGA 23.6 27.2 +15.6% Transplantation franchise 49.4 49.4 +0.0%

Sales by Region
Sales in Japan, the Americas and EMEA decreased, while sales in Asia and Oceania increased. As for the Japanese market, sales decreased by 7.5% year on year to ¥106.1 billion yen largely due to the impact of transferring 16 long-listed products in April 2017, and the introduction of generics for Micardis (telmisartan) for the treatment of hypertension during the first quarter of FY2017. Meanwhile in EMEA, sales decreased due to the impact of transferring the dermatology business in April 2016, yet sales showed an increase when calculated excluding this impact.

FY2017 Guidance
The company’s business forecasts for FY2017 remain unchanged from the consolidated full-year business forecasts announced in April 2017.

Strategic Quarterly Highlights
Astellas continues to create sustainable growth over the mid-to-long term through the pursuit of three main strategies – "Maximizing the Product Value," " Creating Innovation" and "Pursuing Operational Excellence." The company achieved multiple accomplishments as outlined below.

Maximizing the Product Value
 Continued to maximize the growth of the Oncology franchise centered on XTANDI and the Urology OAB franchise including Vesicare and Betanis / Myrbetriq / BETMIGA with new launches across various countries and growth in sales.

Creating Innovation

 Completed the acquisition of Ogeda SA in May 2017.

 Announced the inauguration of "Alliance Station" with the aim of realizing advanced medical treatments with Kyoto University in June 2017.

The following lists the main development advances achieved during the first quarter of FY2017:

 Submitted an application for marketing approval of a combination drug of sitagliptin phosphate hydrate and ipragliflozin L-Proline for the treatment of type-2 diabetes in Japan in May 2017.

 Submitted a supplemental new drug application for mirabegron for the use in combination with solifenacin succinate for the treatment of OAB in the U.S. in June 2017.

NOTE: For further information on the results, please refer to the reference documents: Financial Results, Supplementary Documents, Overview of R&D Pipeline and Presentation Material for Information Meeting available on the Astellas website.

(1) EMEA: Europe, the Middle East and Africa
(2) Sales by Region: based on location of sellers

10-K – Annual report [Section 13 and 15(d), not S-K Item 405]

Champions Oncology has filed a 10-K – Annual report [Section 13 and 15(d), not S-K Item 405] with the U.S. Securities and Exchange Commission .

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Adaptive Biotechnologies Announces Translational Collaboration with National Cancer Institute

On July 27, 2017 Adaptive Biotechnologies, a pioneer in combining next-generation sequencing and expert bioinformatics to profile T-cell and B-cell receptors (TCRs and BCRs) of the adaptive immune system, reported a translational collaboration with the Cancer Therapy Evaluation Program (CTEP) of the National Cancer Institute (NCI), part of the National Institutes of Health (Press release, Adaptive Biotechnologies, JUL 27, 2017, View Source [SID1234519913]).

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Under this collaboration, the Adaptive immunoSEQ Platform will be used to more broadly incorporate TCR and BCR sequencing into select NCI-sponsored clinical trials. The goal is to apply this Platform to accurately measure and track immune repertoire dynamics that may drive response to different cancer immunotherapies.

In line with NCI efforts to implement novel correlative strategies across select clinical trials and tumor types, expanding the use of immunosequencing by NCI investigators may help better understand and potentially predict response to novel immuno-modulatory agents. Both Adaptive and NCI/CTEP are committed to accelerating the clinical validation and utility of novel immune-based molecular biomarkers from tissue and/or blood of cancer patients to better inform treatment decisions.

"We are delighted to announce our engagement with NCI," said Chad Robins, chief executive officer and founder at Adaptive Biotechnologies. "It’s our goal to support NCI investigators by enriching their research and expertise in immune correlative data generation with Adaptive’s immunoSEQ Platform, and to help expedite the development of new immune molecular biomarkers that inform the next wave of novel therapies and rational combinations."

Novocure Reports Second Quarter 2017 Financial Results and Provides Company Update

On July 27, 2017 Novocure (NASDAQ: NVCR) reported financial results for the three and six months ended June 30, 2017, highlighting year-over-year and sequential growth in active patients and net revenues (Press release, NovoCure, JUL 27, 2017, View Source [SID1234519914]). Novocure is an oncology company developing a profoundly different approach to cancer treatment utilizing a proprietary therapy called TTFields, the use of electric fields tuned to specific frequencies to disrupt solid tumor cancer cell division. TTFields is an approved treatment for adults with glioblastoma. We believe the mechanism of action of TTFields shows promise for a variety of solid tumors.

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Second quarter 2017 highlights include:


Three months ended Six months ended
June 30, June 30,
2017 2016 % Change 2017 2016 % Change

Non-financial
Prescriptions received in period(1) 1,059 657 61 % 1,953 1,412 38 %
Active patients at period end(2) 1,460 891 64 %

Financial, in millions
Net revenues $ 38.4 $ 17.9 114 % $ 73.3 $ 31.0 137 %
Net loss $ (21.2 ) $ (40.6 ) 48 % $ (39.2 ) $ (76.0 ) 48 %

Cash and cash equivalents at the end of period $ 80.2 $ 80.9
Short-term investments at the end of period
$ 104.2 $ 120.0

(1) A "prescription received" is a commercial order for Optune that is received from a physician certified to treat patients with Optune for a patient not previously on Optune. Orders to renew or extend treatment are not included in this total.
(2) An "active patient" is a patient who is on Optune under a commercial prescription order as of the measurement date, including patients who may be on a temporary break from treatment and who plan to resume treatment in less than 60 days.

"The second quarter of 2017 was a period of steady growth across all key commercial metrics in all key markets. At the end of the quarter, we had 1,460 active patients on therapy," said Asaf Danziger, Novocure’s Chief Executive Officer. "We believe second quarter growth benefitted from our ongoing emphasis on building prescriber confidence in Optune for the treatment of GBM, including the presentation of our EF-14 five-year survival data at AACR (Free AACR Whitepaper)."

"With 204 million U.S. lives under positive coverage polices as of June 30, 2017, more than 93 percent of Americans with private insurance now have access to Optune," added Mr. Danziger. "We continue to be reimbursed on a case-by-case basis in Germany and are in a constructive dialogue with government payers in the United States, Switzerland and Japan. Our second quarter 2017 revenues of $38.4 million represent 114 percent growth versus the second quarter 2016."

"While we continue to focus on bringing Optune to patients with GBM, we also remain steadfast in our commitment to advancing TTFields as a possible treatment for additional solid tumor indications," said William Doyle, Novocure’s Executive Chairman. "We are recruiting for phase 3 pivotal trials in non-small cell lung cancer and brain metastases. In April, we presented data from our phase 2 pilot trials in advanced pancreatic cancer and recurrent ovarian cancer suggesting improved patient outcomes when TTFields is added to existing standards of care. We plan to move both indications into phase 3 pivotal trials based on the strength of the pilot data."

"In May, our TTFields delivery system received a humanitarian use device (HUD) designation from the FDA for treatment of pleural mesothelioma, an initial step towards a Humanitarian Device Exemption (HDE) approval in the United States. In July, we announced a clinical trial collaboration with Celgene to study marizomib and temozolomide in combination with Optune for the treatment of GBM," continued Mr. Doyle. "We are encouraged to see increased interest in TTFields by independent parties and continue to believe the mechanism of action shows promise for the treatment of a variety of solid tumor types in indications with significant unmet medical needs."

Second quarter 2017 Operating Statistics and Financial Update

There were 1,460 active patients on Optune at June 30, 2017, an increase of 569 active patients, or 64 percent, compared to June 30, 2016. The increase in active patients was driven primarily by prescription growth. The proportion of Optune prescriptions written for newly diagnosed GBM continued to be more than 55 percent in the second quarter 2017.

In the United States, there were 1,083 active patients on Optune at June 30, 2017, an increase of 347 active patients, or 47 percent, compared to June 30, 2016.
In Germany and other EMEA markets, there were 376 active patients on Optune at June 30, 2017, an increase of 221 active patients, or 143 percent, compared to June 30, 2016.
In Japan, there was 1 active patient on Optune at June 30, 2017. There were no active patients on Optune in Japan during the same period in 2016.
Additionally, 1,059 prescriptions were received in the quarter ended June 30, 2017, an increase of 402 prescriptions, or 61 percent, compared to the same period in 2016. The increase in prescriptions was driven primarily by commercial activities in our currently active markets.

In the United States, 803 prescriptions were received in the quarter ended June 30, 2017, an increase of 256 prescriptions, or 47 percent, compared to the same period in 2016.
In Germany and other EMEA markets, 255 prescriptions were received in the quarter ended June 30, 2017, an increase of 145 prescriptions, or 132 percent, compared to the same period in 2016.
In Japan, there was 1 prescription received in the quarter ended June 30, 2017. There were no prescriptions received in Japan during the same period in 2016.
We continued to work with payers in the United States to expand coverage of Optune for the treatment of both newly diagnosed and recurrent GBM. As of June 30, 2017, payers administering plans for more than 204 million lives had issued positive coverage policies stating that Optune is approved for the treatment of newly diagnosed and/or recurrent GBM, an increase of approximately 17.8 million lives since March 31, 2017, including new policies with Health Care Services Corporation and Blue Cross Blue Shield of Florida.

For the three months ended June 30, 2017, net revenues increased to $38.4 million compared to $17.9 million for the same period in 2016, representing 114 percent growth. This growth was primarily driven by increased Optune adoption and the transition to accrual-based revenue recognition for a portion of our billings.

For the three months ended June 30, 2017, cost of revenues increased to $13.2 million compared to $9.8 million for the same period in 2016, representing an increase of 34 percent. This was primarily driven by an increase in active Optune patients, resulting in increased transducer array shipments and increased field equipment depreciation expenses, as well as increased personnel costs to establish infrastructure necessary to support an increasing volume of shipments to patients.

Research, development and clinical trials expenses for the three months ended June 30, 2017, were $9.4 million compared to $11.3 million for the same period in 2016, representing a decrease of 17 percent. This was primarily due to a decrease in clinical trial expenses resulting from the conclusion of our EF-14 phase 3 pivotal trial in newly diagnosed GBM.

Sales and marketing expenses for the three months ended June 30, 2017, were $16.4 million compared to $14.6 million for the same period in 2016, representing an increase of 12 percent. This was primarily due to increased personnel and shipping costs, reflecting our expanding commercial operations in the U.S. and Germany, partially offset by a decrease in advertising and professional services related to the launch of second generation Optune and the communication of Optune’s inclusion in the updated National Comprehensive Cancer (NCCN) Clinical Practice Guidelines In Oncology (NCCN Guidelines) for Central Nervous System Cancers.

General and administrative expenses for the three months ended June 30, 2017, were $15.0 million compared to $13.0 million for the same period in 2016, representing an increase of 15 percent compared to the same period in 2016. This was primarily due to increased personnel costs partially offset by a decrease in professional services and other expenses.

Personnel costs for the three months ended June 30, 2017, included $7.6 million in non-cash share-based compensation expenses, comprised of $0.1 million in cost of revenues; $0.8 million in research, development and clinical trials; $1.7 million in sales and marketing; and $4.9 million in general and administrative expenses. Total non-cash share-based compensation expenses for the second quarter 2016 were $5.6 million.

Net losses for the three months ended June 30, 2017, were $21.2 million compared to net losses of $40.6 million for the same period in 2016.

Financial Update for the Six Months ended June 30, 2017

For the six months ended June 30, 2017, net revenues increased to $73.3 million compared to $31.0 million for the same period in 2016, representing 137 percent growth. This growth was primarily driven by increased Optune adoption and the transition to accrual-based revenue recognition for a portion of our billings.

For the six months ended June 30, 2017, cost of revenues increased to $24.8 million compared to $17.8 million for the same period in 2016, representing an increase of 40 percent. This was primarily driven by an increase in active Optune patients, resulting in increased transducer array shipments and increased field equipment depreciation expenses, as well as increased personnel costs to establish infrastructure necessary to support an increasing volume of shipments to patients.

Research, development and clinical trials expenses for the six months ended June 30, 2017, were $18.8 million compared to $22.8 million for the same period in 2016, representing a decrease of 17 percent. This was primarily due to a decrease in clinical trial expenses resulting from the conclusion of our EF-14 phase 3 pivotal trial in newly diagnosed GBM.

Sales and marketing expenses for the six months ended June 30, 2017, were $31.1 million compared to $27.9 million for the same period in 2016, representing an increase of 12 percent. This was primarily due to increased personnel and shipping costs, reflecting our expanding commercial operations in the U.S. and Germany, partially offset by a decrease in advertising and professional services related to the launch of second generation Optune and the communication of our inclusion in NCCN Guidelines.

General and administrative expenses for the six months ended June 30, 2017, were $27.4 million compared to $25.3 million for the same period in 2016, representing an increase of 9 percent compared to the same period in 2016. This was primarily due to increased personnel costs partially offset by a decrease in professional services and other expenses.

Personnel costs for the six months ended June 30, 2017, included $12.1 million in non-cash share-based compensation expenses, comprised of $0.3 million in cost of revenues; $1.7 million in research, development and clinical trials; $2.4 million in sales and marketing; and $7.8 million in general and administrative expenses. Total non-cash share-based compensation expenses for the six months ended June 30, 2016 were $11.1 million.

Net losses for the six months ended June 30, 2017, were $39.2 million compared to net losses of $76.0 million for the same period in 2016.

At June 30, 2017, we had $80.2 million in cash and cash equivalents and $104.2 million in short-term investments, for a total balance of $184.4 million in cash, cash equivalents and short-term investments. At June 30, 2017, we had $100.0 million of principal indebtedness outstanding under our Loan and Security Agreement with Biopharma Secured Investments III Holdings Cayman LP.

Anticipated clinical milestones

Trial initiations:

Phase 3 pivotal trial in locally advanced pancreatic cancer (2H 2017)
Phase 3 pivotal trial in recurrent ovarian cancer (2018)
Top-line data readouts:

Phase 2 pilot STELLAR trial in mesothelioma (2018)
Phase 3 pivotal METIS trial in brain metastases (2020)
Phase 3 pivotal LUNAR trial in non-small cell lung cancer (2021)

Champions Oncology Reports 38% Revenue Growth for Fiscal Year Ended April 30, 2017

On July 27, 2017 Champions Oncology, Inc. (Nasdaq: CSBR), engaged in the development of advanced technology solutions and services to personalize the development and use of oncology drugs, reported its financial results for the fourth quarter and year ended April 30, 2017 (Filing, Annual, Champions Oncology, 2016, JUL 27, 2017, View Source [SID1234519916]).

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Fourth Quarter and Recent Business Highlights:

•
Record annual revenue of $15.4M, a 38% year over year increase
•
Record TOS segment revenue of $13.7M, a 49% year-over-year increase
•
Record annual TOS bookings, a 51% year over year increase
•
Opened new lab facility in Rockville, Maryland, doubling capacity, expanding revenue generating opportunities and reducing costs
•
Forecast for fiscal 2018 of at least 20% revenue growth and positive cash flow

Ronnie Morris, CEO of Champions, commented, "We delivered significant gains in revenue and bookings and narrowed our net loss, positioning the company for consistent profitability as we continue to grow in our next fiscal year. Demand for our products and services continues to expand as evidenced by fourth quarter revenue growth of 31%, annual revenue growth of 38%, and annual TOS revenue growth of 49%. At 38%, our revenue growth has far outpaced the minimal 3.2% growth in our largely fixed base of costs as we continue to manage our costs aggressively, reducing our full year operating loss by 50%. Additionally, we recently moved into our new lab facility which we expect will further reduce lab costs. As we look ahead, we are confident revenue will grow by at least 20% in fiscal 2018, setting the stage for continued rapid growth and cash flow positive results".

Financial Results

For the fourth quarter of fiscal 2017, revenue was $3.7 million, as compared to $2.8 million for the fourth quarter 2016, an increase of 31.1%. Total operating expenses for the fourth quarter fiscal 2017 and 2016 was $6.1 million and $5.4 million, respectively, an increase of $700,000 or 12.9%. Revenue was $15.4 million and $11.2 million for the twelve months ended April 30, 2017 and 2016, respectively, an increase of $4.2 million or 37.8%.

For the fourth quarter of fiscal 2017 and 2016, Champions reported a loss from operations of $2.4 million and $2.6 million, respectively, a decrease of $200,000 or (7.3%). Excluding stock-based compensation of $761,000 and $509,000 for the three months ended April 30, 2017 and 2016,

Exhibit 99.1

respectively, Champions recognized a loss from operations of $1.6 million and $2.1 million for fourth quarter 2017 and 2016, respectively.

For the twelve months ended April 30, 2017 and 2016, Champions reported a loss from operations of $6.8 million and $10.3 million, respectively, a decrease of $3.5 million or (34.2%). Excluding stock-based compensation of $2.7 million and $2.6 million for the twelve months ended April 30, 2017 and 2016, Champions recognized loss from operations of $4.1 million and $7.7 million, respectively.

Net cash used in operations was $2.8 million and $6.4 million for the twelve months ended April 30, 2017 and 2016, respectively, a decrease of $3.6 million or (55.7%). The reduction in cash burn is the result of revenue growth and aggressive expense management.

The company ended the quarter with $3.3 million of cash and cash equivalents on the balance sheet.

Translational Oncology Services (TOS) revenue was $3.4 million and $2.3 million for the three months ended April 30, 2017 and 2016, respectively, an increase of $1.1 million or 48.9%. TOS revenue was $13.7 million and $9.2 million for the twelve months ended April 30, 2017 and 2016, respectively, an increase of $4.5 million or 48.7%. The increase is due to bookings growth in prior quarters, both in the number and size of the studies.

TOS cost of sales was $2.3 million and $1.9 million for the three months ended April 30, 2017 and 2016, respectively, an increase of $400,000, or 21.3%. TOS cost of sales was $8.3 million and $6.6 million for the twelve months ended April 30, 2017 and 2016, respectively, an increase of $1.7 million or 25.6%. For the three months ended April 30, 2017 and 2016, gross margin for TOS was 31.3% and 15.6%, respectively. For the twelve months ended April 30, 2017 and 2016, gross margin was 39.6% and 28.5%, respectively. The increase in TOS cost of sales was due to an increase in TOS studies. The improvement in gross margin was due to higher TOS revenue leveraged off the fixed cost component of the lab and effective management of the variable lab costs. Gross margin varies based on timing differences between expense and revenue recognition. While the gross margin improved, there are expenses incurred in advance of future revenue.

Personalized Oncology Services (POS) revenue was $366,000 and $585,000 for the three months ended April 30, 2017 and 2016, respectively, a decrease of $219,000 or (37.4%). POS revenue was $1.7 million and $2.0 million for the twelve months ended April 30 , 2017 and 2016, respectively, a decrease of $300,000 or (12.%). The decrease is primarily the result of the decline in implant and drug panel revenue of offset by an increase in sequencing revenue.

POS cost of sales was $266,000 and $441,000 for the three months ended April 30, 2017 and 2016, respectively, a decrease of $175,000, or (39.7%). POS cost of sales was $1.4 million and $2.1 million for the twelve months ended April 30, 2017 and 2016, respectively, a decrease of $700,000 or (31.8%). For the three months ended April 30, 2017 and 2016, gross margin for POS was 27.3% and 24.6%, respectively. For the twelve months ended April 30, 2017 and 2016, gross margin for POS was 16.7%.and negative (6.6%). The improvement is attributed to the increase in higher margin sequencing revenue and aggressively managing our lab costs.

Research and development expense was $1.0 million and $1.2 million for the three months ended April 30, 2017 and 2016, respectively, a decrease of $200,000, or (8.5%). Research and development expense was $4.3 million and $4.2 million for the years ended April 30, 2017 and 2016, respectively an increase of $100,000, or 2.4%. Sales and marketing expense for the three months ended April 30, 2017 and 2016 was $892,000 and $757,000 respectively, an increase of $135,000, or 17.8%.

Exhibit 99.1

The increase is due to commissions earned in the fourth quarter of fiscal 2017. Sales and marketing expense was $3.3 million and $3.4 million for the years ended April 30 2017 and 2016, respectively a decrease of $100,000, or (5.3%). General and administrative expense was $1.6 million and $1.1 million for the three months ended April 30, 2017 and 2016, respectively, an increase of $500,000 or 41.3%). The increase is due to a one time charge, resulting from an option grant modification, to stock based compensation. General and administrative expense was $5.0 million and $5.2 million for the years ended April 30, 2017 and 2016 respectively, a decrease of $200,000 or (4.1%). The decrease is primarily due to aggressive cost management.