[Press Release] Oncodesign: first-half 2020 results

On October 1, 2020 ONCODESIGN (Paris:ALONC) (ALONC – FR0011766229), a biopharmaceutical group specialized in precision medicine, reported its results for the first half of 2020 and issues a business update (Press release, Oncodesign, OCT 1, 2020, View Source [SID1234567894]).

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Philippe GENNE, Chairman and Chief Executive Officer of Oncodesign, says: "Within a context marked by an unprecedented global public health crisis in the first semester, Oncodesign has deployed a business continuity plan that has enabled to remain operational to serve clients, drive projects forward and continue the strategic development. The Group has shown resilience, with operating revenue of €18.1 million and a net profit at June 30, 2020. Our total revenue, on a like-for-like basis (excluding upfront and milestone payments), of €11.8 million in the first half of 2020 has held up, with a record cash position of €19.9 million. The first half was also marked by the success of our collaboration with Servier’s laboratories on the LRRK2 project that provided us with a €1 million milestone payment. The RIPK2 project with its First-in-class ODS 101 inhibitor, is following its development plan to the letter, and its IND is still scheduled for June 2021. We are now equipped to meet the targets we have set for 2023: i.e. pursue the clinical development of our drug candidates, support the development of Drug Discovery while consolidating our multi-year Drug Development service partnership offer (DDSA) and Integrated Drug Discovery (IDDS) offer to drive Service revenue and EBITDA growth. The Oncodesign teams and I are more than ever focusing on the Group’s future, as illustrated by the stakes recently acquired by members of the Company’s Senior Management team".

Arnaud LAFFORGUE, Chief Financial Officer of Oncodesign, continues: "From the start of the year, we implemented the growth plan for the next five years and structured our company into three Business Units. Lastly, despite this unprecedented context in which Business Development has been directly penalized, we have recorded a 14% increase in incoming orders compared to last year, to €11.6 million, driven by the signing of a number of multi-year contracts in Asia and Europe. Also, in the first half of the year, we have launched the integrated Drug Discovery service offer, DRIVE, including in partnership with Chinese company Hitgen, and a new service offer dedicated to COVID-19 in association with IDMIT, providing a response to the high level of demand on this market, the latter leading to a substantial order book with revenue prospects on this offer in the second half of 2020. In addition, for the first time, the income statements of 2 main BUs are presented, namely the Service BU and the Biotech BU for the first half of 2020 compared to the homogeneous figures for the first half of 2019 in order to better highlight the performance and challenges of its activities."

First-half 2020 financial results

The Group generated revenue of €11.8 million in the first half of 2020, down 16% compared with H1 2019, due to both the decrease in Biotech revenue, with a milestone payment of €1 million in H1 2020 versus an upfront of €3 million over the same period last year, and, for the Service revenue, resulting from the public health crisis.

Other operating revenue, which totaled €6.29 million in the first half, was up by 5.5% compared with the first half of 2019, and consisted primarily of the following:

the subsidy received from GSK, within the framework of the acquisition of the François Hyafil center, which amounted to €3.96 million in the first half of 2020 (6 months pro rata temporis). The final payment was carried out in January 2020;
the 12% increase in French and Canadian Research Tax Credit to €1.66 million, directly associated with investments in internal programs (RIPK2, MNK1/2) and on AI.
Operating expenses totaled €18.42 million, down because of the reduction in variable costs such as purchases of external subcontracting services and business trips because of the pandemic. Personnel expenses were stable at €9.2 million (+1.3%) as a result of the decision taken at the start of the year, given the first effects of the pandemic on the economy, to freeze all wage increases that normally take place at this time of the year. However, it is worth noting the effect of the full presence over the first half of the year of the new staff recruited during the second half of 2019, i.e. an additional 9 people.

Research & Development investments amounted to €5.41 million in the first half of 2020, versus €4.0 million at June 30, 2019. This acceleration in spending (+35%) was primarily associated with the RIPK2 program’s regulatory preclinical phase, entirely financed by Oncodesign.

Thanks to good management of operating expenses, down €1.1 million (-6%), there was an operating loss of -€320k, a controlled decrease of €830k compared with the first half of 2019 in view of the investment efforts undertaken over the period.

The net profit remained close to zero (+€40k), despite a financial income deteriorated due to the effect of exchange rate fluctuations (US$) for €125k. In addition, the restatement of goodwill, following the sell and lease-back of the Les Ulis building, enabled income of €500k to be recognized in consolidated accounts.

Cash position

The Company had cash and cash equivalents of €19.9 million at June 30, 2020, a substantial increase of +50% compared with June 30, 2019 (€13.3 million) despite the Group’s considerable R&D investments. This figure includes the €1.0 million milestone payment received from Servier, the €7.92 million GSK subsidy received for 2020 and the Research Tax Credit for 2018 (€3.5 million not redeemed at the end of 2019 and regularized in April 2020) and 2019, €3.2 million and usually received at the end of the following year. Lastly, it should be noted that this cash position was achieved without, as yet, incorporating the State-Guaranteed Loan.

First-half 2020 business update and outlook

Following completion of the new organization, the Service BU, which has 203 employees, realizes a total revenue of 14M€ by cumulating the "External" revenues corresponding to the sales realized with Oncodesign’s customers, and the "Internal" revenues1 carried out for the execution of work related to our therapeutic projects for the Biotech BU (RIPK2, LRRK2, MNK1/2). It is stable compared to last year at the same date (+260 K€).

External revenues amounted to €9.03 million over the period, a decrease of 10% in the first half of the year, following the economic slowdown associated with the global health crisis. Oncodesign SA (worldwide clients excluding the USA and Canada) recorded a 13.6% decrease in revenue to €7.71 million, while revenue generated in North America (USA and Canada) remained dynamic, increasing by 18.4% to €1.4 million. The latter’s growing weight – with it now accounting for 16% of revenue compared to 10% in 2019 – demonstrates its strategic role for the Service Business Unit, thus justifying its development over the coming years. Moreover, activity recorded in Asia (Japan and South Korea) has also grown rapidly over the last 3 years, with this region now accounting for 7% of total first-half 2020 revenue compared to just 2% in 2018. This international development reflects the substantial investments undertaken by the Company, and notably the strengthening of the sales teams.
Internal revenues increased by 30% to almost €5 million following the acceleration of our programs for the Biotech BU.
In terms of EBITDA, the BU achieves an increase of €1.8 million to reach €0.67 million in the first half of 2020, representing an improvement in EBITDA margin of 13.1% from -8.3% to +4.8% (thanks to good cost control and increased productivity as a result of the new BU organization). This performance illustrates the Service BU’s ability to improve its operational performance by optimizing its productivity and internal organization. These figures give us confidence in the Service BU’s ability to achieve its profitability objectives at term.

The objectives of the Service BU are to accelerate the development of the sale of integrated and long-term service contracts for growth in Service revenues and EBITDA.

A COVID-19 offer has been developed in association with IDMIT. This offer is seeing very high demand in the current context, particularly as few companies have the infrastructure and expertise to undertake this type of service. This offer has promising revenue potential, both for the short term in H2 and for the coming years.

Impact of the Covid pandemic: the activation of our Business Continuity Plan and the continuation of activity on our sites and in our laboratories allows us to undertake the work entrusted to us by our clients. To date, we have not recorded widespread order cancellations from our clients. The procurement of supplies is still possible for most of our consumables/raw materials; delivery times are occasionally longer but this isn’t blocking our work. Lastly, the nature of our portfolio of offers, notably multi-year programs, guarantees us a level of recurrent activity scheduled over the long term. In contrast, the booking of orders for one-off and non-recurrent offers could be penalized, with the cancellation of conferences and ongoing travel restrictions impeding the fieldwork of our sales staff, without us currently being able to assess the precise impact.

Oncodesign’s 2023 targets are notably, for the Service BU, to achieve revenue of €50 million and EBITDA of between 15% and 20%.

Biotech revenues consist mainly of the sale of partnerships and licensing resulting from Nanocyclix: so in the short term from Up-fronts / Milestones and the coverage of research costs of the Servier Partnership for LRRK2. Thus, its sales reached €2.8 million in the first half of 2020, versus last year’s figure of €4 million that included the initial €3 million payment by Servier, within the framework of the strategic partnership sealed in March 2019 to develop LRRK2 kinase inhibitors as a treatment for Parkinson’s Disease. Revenue relating to work on LRRK2 increased by +78% to €1.8 million and the program is progressing rapidly in accordance with its initial schedule.

Costs in the Biotech BU are under control thanks to our efforts to rationalize our expenses, in connection with the new allocation of scientific staff and the control of our purchases.

However, the medium-term trend of this BU, whose programs are progressing according to their development plan, should enable it to achieve milestones in the coming semesters.

The objectives of the Biotech BU are to continue to ensure the ramping up of our pipeline via the selection of, on the one hand, kinase inhibitor drug candidates resulting from Nanocyclix technology and, on the other hand, external opportunities on other targets.

Biotech’s prime focus is to develop the maturity of our therapeutic pipeline by taking our molecules to the clinical development stage: RIPK2, LRRK2 and MNK1/2 inhibitors in oncology.

At the end of 2019, the substantial investment efforts undertaken in R&D enabled Oncodesign to select a First-in-Class drug candidate, a RIPK2 kinase inhibitor, for autoimmune and inflammatory diseases, which represents a first step in the creation of expected value. As a reminder, Oncodesign initially planned to finance the development of ODS 101 up to the IND (significant risk-limiting step on the inhibitor by regulatory multi-species toxicity studies), programmed in June 2021, while looking for a Pharma partner.

In February 2020, Servier and Oncodesign announced that they had reached a major milestone several months ahead of schedule, within the framework of their strategic partnership in the research and development of drug candidates to treat Parkinson’s disease (LRRK2 program). Oncodesign received a first milestone payment of €1 million associated with the program’s first success.

Moreover, discussions are ongoing with new partners to enable the resumption of the clinical development of the mutated EGFR radiotracer. Regarding the partnership with Bristol-Myers Squibb (BMS), after the internalization of the program at the end of 2018, the company decided to stop the program for toxicity reasons related to the target. The intellectual property concerning the molecules has been returned to Oncodesign, which is free to exploit them. Lastly, the MNK1/2 program is continuing to move forward, the aim being to reach the pre-candidate stage by the end of 2020.

Impact of the Covid pandemic: for the Biotech Business Unit, as a result of our autonomy on work programs, the pandemic has had little impact on our activity or the ramping up of our pipeline. However, we are observing a slowing down of Big Pharma decision-making and therefore partner research processes for RIPK2.

Oncodesign is aiming to take 3 products to the clinical phase by 2023.

ARTIFICIAL INTELLIGENCE BU

The objective of the AI BU is to continue the development of our strategic technological pillars using AI: structure the Precision Medicine platform of the 21st century

On the basis of the OncosnipeTM project, whose launch 3 years ago initiated the application of AI technologies to the detection of new therapeutic targets and enabled the creation of an internal center of expertise on this subject, a third Business Unit dedicated to Artificial Intelligence was created in April 2020, under the direction of Stéphane Gérart.

Impact of the Covid pandemic: the OncosnipeTM project was penalized by the public health crisis in the first half, as it relies on a clinical trial whose patient enrollments had to be suspended during this period. In return, we opened 5 new clinical centers and received the associated BPI subsidy of €0.4 million at the end of June within the framework of the PSPC competitive cluster structuring project.

This BU is aiming to build, by 2023, a platform to identify and validate new therapeutic targets and to increase the Drug Discovery process’ reliability and reduce its development times, while developing revenue streams by providing research services to industry.

Oncodesign’s first-half 2020 financial report is available in French on the Company’s website:
www.oncodesign.com

Next investor meeting: Investir – Direct Dirigeants event in Paris on Tuesday October 6, 2020

Kyowa Kirin and MEI Pharma Announce First Patient Dosed in Japanese Pivotal Phase 2 Study of Zandelisib in Patients with Indolent B-cell non-Hodgkin’s Lymphoma

On October 1, 2020 Kyowa Kirin Co., Ltd. (Kyowa Kirin, TSE: 4151), a global specialty pharmaceutical company creating innovative medical solutions utilizing the latest biotechnology, and MEI Pharma, Inc. (NASDAQ: MEIP), a late-stage pharmaceutical company focused on advancing potential new therapies for cancer, reported the first patient has been dosed in the pivotal Phase 2 study of zandelisib (formerly called ME-401), an oral, once-daily, investigational drugcandidate selective for phosphatidylinositol 3-kinase delta (PI3Kδ) in patients with indolent B-cell nonHodgkin’s lymphoma (iNHL) without Small lymphocytic lymphoma, lymphoplasmacytic lymphoma (LPL), and Waldenström’s macroglobulinemia (WM) in Japan.

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This Phase 2, multicenter, open-label, single-arm clinical study is conducted by Kyowa Kirin to evaluate zandelisib as monotherapy for treatment of Japanese patients with relapsed or refractory iNHL with at least two prior systemic therapies.

Yoshifumi Torii, Ph.D., Vice President, Head of R&D Division of Kyowa Kirin, said "I am pleased that we have initiated the clinical study to seek regulatory approval in Japan. We are committed to delivering zandelisib as a new potential treatment option for Japanese patients and their physicians. And we continue to work closely with MEI Pharma to expand the global development program for zandelisib."

"The initiation of the Japanese Phase 2 pivotal study is an important addition to the zandelisib global development program," stated Richard Ghalie, M.D., senior vice president, clinical development of MEI Pharma. "We are excited to continue working diligently in close partnership with Kyowa Kirin to build on the potential for zandelisib inside and outside the U.S., and to expand development into indications beyond follicular lymphoma."

In April 2020, MEI and Kyowa Kirin entered a global license, development, and commercialization agreement to further develop and commercialize zandelisib. MEI and Kyowa Kirin will co-develop and co-promote zandelisib in the U.S., with MEI booking all revenue from the U.S. sales. Kyowa Kirin has exclusive commercialization rights outside of the U.S.


Indication iNHL* *SLL, WM and LPL are excluded
Phase Phase 2
Design Multicenter, open-label and single-arm study
Administration group Zandelisib monotherapy
Primary Endpoint Objective response rate (ORR)
Sample size 60
Estimated study completion September 2024
Countries/Regions Japan

About Zandelisib
Zandelisib (formerly called ME-401) is an investigational cancer treatment being developed as an oral, once-daily, selective PI3Kδ inhibitor for the treatment of B-cell malignancies. In March 2020 the U.S. FDA granted zandelisib Fast Track designation.

In April 2020, MEI and Kyowa Kirin entered a global license, development, and commercialization agreement to further develop and commercialize zandelisib. MEI and Kyowa Kirin will co-develop and co-promote zandelisib in the U.S., with MEI booking all revenue from the U.S. sales. Kyowa Kirin has exclusive commercialization rights outside of the U.S.

Ongoing studies evaluating zandelisib include TIDAL (Trials of PI3K DeltA in Non-Hodgkin’s Lymphoma) a Phase 2 clinical trial evaluating zandelisib as a monotherapy for the treatment of adults with follicular lymphoma after failure of at least two prior systemic therapies including chemotherapy and an antiCD20 antibody. Subject to the results, upon completion TIDAL is intended to be submitted to FDA to support an accelerated approval marketing application under 21 CFR Part 314.500, Subpart H. Ongoing zandelisib studies also include a Japanese Phase 2 pivotal study in patients with iNHL without Small lymphocytic lymphoma, LPL and WM being conducted by Kyowa Kirin. (Press release, Kyowa Hakko Kirin, OCT 1, 2020, View Source [SID1234567893])

Entry into a Material Definitive Agreement

On October 1, 2020, Protalix BioTherapeutics, Inc., a Delaware corporation (the "Company"), reported that it entered into an ATM Equity OfferingSM Sales Agreement (the "Sales Agreement") with BofA Securities, Inc., as the Company’s sales agent (the "Agent") (Filing, 8-K, Protalix, OCT 1, 2020, View Source [SID1234567892]). Pursuant to the terms of the Sales Agreement, the Company may sell from time to time through the Agent shares of the Company’s common stock having an aggregate offering price of up to $30 million (the "Shares"). The Shares will be issued pursuant to the Company’s shelf registration statement on Form S-3 (Registration No. 333-230604). The Company intends to use the net proceeds from the offering, after deducting the Agent’s commissions and the Company’s offering expenses, for general corporate purposes.

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In accordance with the terms of the Sales Agreement, the Company may offer and sell the Shares at any time and from time to time through the Agent. Sales of the Shares, if any, will be made by means of transactions that are deemed to be "at the market" offerings as defined in Rule 415 under the Securities Act of 1933, as amended, including block trades and sales made in ordinary brokers’ transactions on the NYSE American or otherwise at market prices prevailing at the time of the sale, at prices related to prevailing market prices or at negotiated prices. Under the terms of the Sales Agreement, the Company may also sell Shares to the Agent as principal for its own account at a price to be agreed upon at the time of sale. Any sale of Shares to the Agent as principal would be pursuant to the terms of a separate terms agreement between the Company and the Agent.

The foregoing description of the Sales Agreement in this report does not purport to be complete and is qualified by reference to the full text of the Sales Agreement, which is filed as Exhibit 1.1 hereto. The legal opinion and consent relating to the Shares are included as Exhibits 5.1 and 23.1, respectively, hereto.

This Current Report on Form 8-K shall not constitute an offer to sell or the solicitation of an offer to buy any Shares, nor shall there be any sale of Shares in any state or other jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such state or other jurisdiction.

Delcath Strengthens Executive Team with Appointment of Gerard Michel as Chief Executive Officer

On October 1, 2020 Delcath Systems, Inc. (NASDAQ: DCTH) reported that the Board of Directors appointed Gerard Michel as Chief Executive Officer, effective October 1, 2020 (Press release, Delcath Systems, OCT 1, 2020, View Source [SID1234567891]). Mr. Michel will also serve as a member of the Delcath Systems Board of Directors. In his most recent role, Mr. Michel was the Chief Financial Officer and Vice President of Corporate Development at Vericel Corporation. Mr. Michel was a key member of the executive team that successfully restructured Vericel enabling it to become a commercial leader in the fields of advanced Cell Therapy and specialty Biologics.

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In addition to Mr. Michel’s appointment as CEO, John Purpura, was appointed as Chief Operating Officer. Mr. Purpura’s leadership and operational excellence in areas of regulatory affairs, manufacturing and distribution have been a critical component of preparing Delcath for its planned New Drug Application (NDA) resubmission to the FDA in mid-2021.

"Following an intensive process, the Board determined that Gerard is the right leader for Delcath at this critical juncture," said Dr. Roger Stoll, Chairman, Delcath Systems. "He is uniquely qualified to take on this role given his track record of success and experience across therapeutics classes. Gerard’s extensive experience in strategy, operations, commercialization, business development and capital markets will be a tremendous asset." Dr. Stoll added, "We thank John for successfully guiding Delcath as interim CEO over recent months. On behalf of the Board, I congratulate him on his appointment to COO."

Mr. Michel commented, "I am excited to join the talented Delcath team ahead of a transformational year as we prepare to report phase 3 FOCUS trial data in metastatic ocular melanoma (mOM) in early 2021. I am committed to leading the organization towards its goal of making Melphalan/HDS the first product specifically labeled for metastatic ocular melanoma patients, a population which currently has limited therapeutic options."

Mr. Michel added, "Interventional oncology is a rapidly growing segment of comprehensive oncology care. Within that segment Melphalan/HDS is a clinically differentiated, high-value platform with the potential to address multiple cancer indications of high-unmet medical need. I look forward to building value both through the successful commercialization of Melphalan/HDS in mOM and initiating additional targeted clinical programs to expand the market opportunity of this platform technology."

Mr. Michel joins Delcath Systems with over 30 years of experience in the pharmaceutical and medical technology industries across multiple functional areas. Prior to Delcath, he was Chief Financial Officer of Vericel since June 2014 where he was a key member of the management team which integrated a transformative acquisition and revised the company’s business model from a research focused company to a fully integrated, profitable commercial business. Mr. Michel also served as Chief Financial Officer and Vice President, Corporate Development of Biodel from November 2007 to May 2014, and Chief Financial Officer and Vice President of Corporate Development of NPS Pharmaceuticals Inc. from August 2002 to November 2007. Prior to that, Mr. Michel was a Principal at Booz Allen and held a variety of commercial roles at both Lederle Labs and Wyeth Labs. Mr. Michel holds a M.S in Microbiology from the University of Rochester School of Medicine, an M.B.A. from the Simon School of Business, and a B.S. in both Biology and Geology from the University of Rochester.

Inducement Grant Under NASDAQ Listing Rule 5635(c)(4)

The Company also announced the grant of an option award to Mr. Michel, which was approved by the Board on August 31, 2020 as an inducement material to his entering employment with the Company in accordance with NASDAQ Listing Rule 5635(c)(4). The inducement award was approved subject to his commencement of employment with the Company on October 1, 2020 and consists of an option to purchase up to 498,000 shares of the Company’s common stock. The option will be exercisable at a price of $11.67 per share (the closing price on October 1, 2020) as to the first 396,000 shares to vest, (ii) 1.5 times the closing trading price per share of the Company’s common stock on October 1, 2020 as to the next 51,000 shares to vest and (iii) 2.0 times the closing trading price per share of the Company’s common stock on October 1, 2020 as to the remaining 51,000 shares to vest and will vest ratably over thirty-six months, provided that he remains employed by Delcath on each vesting date.

Quest Diagnostics To Release Third Quarter 2020 Financial Results On October 22

On October 1, 2020 Quest Diagnostics Incorporated (NYSE: DGX), the world’s leading provider of diagnostic information services, reported that it will report third quarter 2020 results on Thursday, October 22, 2020, before the market opens (Press release, Quest Diagnostics, OCT 1, 2020, View Source [SID1234567890]). It will hold its quarterly conference call to discuss the results beginning at 8:30 a.m. Eastern Time on that day.

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The conference call can be accessed by dialing 888-455-0391 within the U.S. and Canada, or 773-756-0467 internationally, using the passcode: "7895081." The earnings release and live webcast will be posted on www.QuestDiagnostics.com/investor. The company suggests participants dial in approximately 10 minutes before the call.

A replay of the call may be accessed online at www.QuestDiagnostics.com/investor or by phone at 800-337-6568 for domestic callers or 402-220-9660 for international callers; no passcode is required. Telephone replays will be available from approximately 10:30 a.m. Eastern Time on October 22, 2020 until midnight Eastern Time on November 5, 2020.

Anyone listening to the call is encouraged to read the company’s periodic reports on file with the Securities and Exchange Commission, including the discussion of risk factors and historical results of operations and financial condition in those reports.