On August 30, 2017 FUJIFILM Corporation (President: Kenji Sukeno) reported that it has decided to start clinical trials in the United States in 2018 for its anti-cancer agent FF-10832 to assess it as a potential treatment for advanced solid tumors (Press release, Fujifilm, AUG 30, 2017, View Source [SID1234520339]). FF-10832 is a liposome-based agent which harnesses the advanced nano-dispersion technology, analysis technology and process technology nurtured through the photographic film business in order to incorporate the existing water-soluble anti-cancer agent gemcitabine*1 into liposomes.

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Liposomes are artificially constructed vesicles made from the same organic phospholipids that make up cell membranes and bio membranes. As one of a variety of drug delivery system (DDS) technologies, liposomes are used to deliver the required amount of a drug to the specified part of the body on the necessary schedule. Certain anti-cancer agents act on healthy tissue in addition to the tumor that can result in severe adverse effects. Liposomes are currently attracting significant attention as an effective means of avoiding these adverse effects on healthy tissue. Preparing pharmaceuticals in the form of liposomes allows the pharmaceutical to be delivered selectively to the tumor, which can be expected to improve pharmacological efficacy and suppress adverse effects. In order to achieve this, the following conditions must all be met: (1) improve the stability of the pharmaceutical agent in the blood (2) the achievement of the Enhanced Permeability and Retention (EPR) effect*2 (namely the long-term, sustainable concentration of the agent within the tumor as a result of ensuring that the agent does not leak from healthy blood vessels) and (3) the release of the agent within the tumor. Generally, it is difficult to simultaneously achieve both (1) the improved stability of the pharmaceutical agent in the blood and (3) the release of the agent within the tumor. This is particularly the case with water-soluble drugs, where the technical barriers are very high, and these considerations have been an issue affecting the production of effective liposomes.

FF-10832 harnesses Fujifilm’s expertise including nano-dispersion technology, analysis technology and process technology in order to incorporate gemcitabine, a drug with a short half-life*3 in blood, into liposomes, which is expected to lead to a significant increase in the stability of the agent within the blood. Furthermore, to achieve EPR benefits, the liposomes are designed to have a uniform size of approximately 80 nm, raising the concentration of the agent within the tumor. In experiments on mice transplanting human-derived pancreatic cancer cells, concentrations of FF-10832 within the pancreatic cancer cells reach higher levels than with the original preparation of gemcitabine – confirming the long-term sustainable presence of the agent within the tumor (in mice experiments).

Furthermore, the same experiments on mice also demonstrate that when FF-10832 is administered, it is possible to obtain a pharmacological benefit in excess of that produced by the original preparation of gemcitabine with only 1/60th of the dose. In addition, the release of the agent within the tumor was confirmed by demonstrating the efficacy including in the case of human-derived pancreatic cancer cells, which included a subtype that does not usually respond well to the original gemcitabine treatment, as well as in other mice experiments involving the transplantation of cancer cells other than pancreatic cancer cells. From these results, it can be expected that FF-10832 fulfills the conditions required of liposome preparations for human, and provides effective treatment not only for pancreatic cancer, a condition for which the number of promising treatments is currently limited, but also potentially in further applications for the treatment of other solid tumors.

Fujifilm plans to submit an investigational new drug (IND) application for FF-10832 in the US before the end of 2017 and plans to start clinical trials in 2018.

[Schematic diagram showing how FF-10832 is released into tumor]

Fujifilm is defining oncology as its focal area and the company is actively engaged in the research and development of pharmaceuticals by combining the technologies and knowledge accumulated in the photographic film business in fields including the synthesis and design of compounds in addition to nano-dispersion technology and analysis technology. Going forward, the company is committed not only to the development of new drugs, but also to the development of new Drug Delivery Systems, as the company works to address social issues through the provision of innovative pharmaceutical products.

*1 Gemcitabine (Gemzar) is an anti-cancer agent developed by the US company Eli Lilly and Company. It is used as a drug of first choice for the treatment of pancreatic cancer, and is also indicated for the treatment of a wide range of other cancers including lung cancer and ovarian cancer.

*2 Tumors produce new blood vessels for the purpose of nourishing the tumor, but these new blood vessels are immature, with the walls of the vessels containing gaps that do not exist in normal healthy vessels. When a high concentration of liposomes and high-molecular weight drugs is observed in these vessels, there is no leakage from the healthy vessels that do not contain these gaps, with the liposomes and high-molecular-weight drugs leaking only from the blood vessel walls of the tumor. In addition, since the lymphatic tissue within tumor is also immature, it is difficult to remove the liposomes and high-molecular-weight drugs that have permeated the surrounding tissue, causing the drug to accumulate within the tumor. This effect is called Enhanced Permeability and Retention effect. The effect was originally reported in 1986 by Hiroshi Maeda, Professor at the Sojo University DDS research center and Honorary Professor at Kumamoto University, and Yasuhiro Matsumura, Director at Division of Development Therapeutics at the National Cancer Center’s Exploratory Oncology Research & Clinical Trials Center (NCC-EPOC) in the paper " A new concept for macromolecular therapeutics in cancer chemotherapy: mechanism of tumoritropic accumulation of proteins and the antitumor agent smancs." In 2016, Maeda and Matsumura were recognized as Thomson Reuters Citation Laureates, distinction conferred by Thomson Reuters on researchers considered to be likely candidates for future Nobel prizes on the basis of an analysis of research literature and citations.

*3 The half-life is the time taken for the concentration of pharmaceutical in the blood to decrease by half.

On August 30, 2017 Amgen (NASDAQ: AMGN) reported positive results from a post-hoc analysis requested by the U.S. Food and Drug Administration (FDA) of the Phase 3 head-to-head ENDEAVOR trial, which followed patients for at least three years after enrollment (Press release, Amgen, AUG 30, 2017, View Source [SID1234520338]). The analysis evaluated overall survival (OS) and long-term safety of KYPROLIS (carfilzomib) administered at 56 mg/m2 twice weekly and dexamethasone (Kd) versus Velcade (bortezomib) and dexamethasone (Vd) in patients with relapsed or refractory multiple myeloma. Kd reduced the risk of death by 24 percent over Vd (median OS 47.8 months for Kd versus 38.8 months for Vd, HR=0.76, 95 percent CI, 0.63-0.92; p=0.0017). This Kd regimen is currently approved in the U.S., European Union and other countries based on the primary analysis of progression-free survival in the ENDEAVOR study.

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"For physicians making prescribing decisions, long-term follow-up helps to further support the safety and efficacy of a therapy and instills confidence in the treatment," said Robert Orlowski, M.D., Ph.D., Florence Maude Thomas Cancer Research professor and chair, ad interim, Department of Lymphoma & Myeloma at The University of Texas MD Anderson Cancer Center. "The current three-year follow-up analysis demonstrates that this proteasome inhibitor continues to demonstrate a prolonged overall survival benefit and consistent safety profile when combined with dexamethasone for relapsed multiple myeloma patients."

"We are excited about the three-year follow-up of the ENDEAVOR study as the overall survival benefit reflects both the efficacy and the long-term safety of this KYPROLIS regimen in patients with relapsed multiple myeloma," said Sean E. Harper, M.D., executive vice president of Research and Development at Amgen. "These results confirm that when a patient relapses, KYPROLIS should replace Velcade as a standard-of-care."

Adverse events observed in this updated analysis were consistent with those previously reported for ENDEAVOR. The most common adverse events (greater than or equal to 20 percent) in the KYPROLIS arm were anemia, diarrhea, pyrexia, hypertension, dyspnea, fatigue, cough, insomnia, upper respiratory tract infection, nausea, bronchitis, asthenia, back pain, thrombocytopenia, edema peripheral, headache and muscle spasms.

Results from the primary ENDEAVOR OS analysis were recently published online in The Lancet Oncology. Data showed Kd reduced the risk of death by 21 percent over Vd. Patients treated with KYPROLIS lived 7.6 months longer than those treated with Velcade (median OS 47.6 months for Kd versus 40.0 months for Vd, HR=0.79, 95 percent CI, 0.65-0.96). On Aug. 30, 2017, Amgen announced the FDA accepted for review the supplemental New Drug Application (sNDA) for KYPROLIS to include OS data from the Phase 3 head-to-head ENDEAVOR trial in the product information. The FDA has set a Prescription Drug User Fee Act (PDUFA) action date of April 30, 2018.

Since its approval in 2012, more than 50,000 patients worldwide have received KYPROLIS. The KYPROLIS clinical program continues to focus on providing solutions for physicians and patients in treating this frequently relapsing and difficult-to-treat cancer. KYPROLIS is available for patients whose myeloma has relapsed or become resistant to another treatment and continues to be studied in a range of combinations and patient populations.

About ENDEAVOR

The randomized ENDEAVOR (RandomizEd, OpeN Label, Phase 3 Study of Carfilzomib Plus DExamethAsone Vs Bortezomib Plus DexamethasOne in Patients With Relapsed Multiple Myeloma) trial of 929 patients evaluated Kd versus Vd in patients whose multiple myeloma has relapsed after at least one, but not more than three prior therapeutic regimens. The primary endpoint of the trial was PFS, defined as the time from treatment initiation to disease progression or death. The primary analysis was published in The Lancet Oncology and is described in the Prescribing Information.

Patients received treatment until progression with KYPROLIS as a 30-minute infusion on days 1, 2, 8, 9, 15 and 16 of 28 day treatment cycles, along with low-dose dexamethasone (20 mg). For cycle one only, KYPROLIS was administered at 20 mg/m2 on days 1 and 2, and if tolerated was escalated to 56 mg/m2 from day 8 cycle one onwards. Patients who received bortezomib (1.3 mg/m2) with low-dose dexamethasone (20 mg) were treated with bortezomib administered subcutaneously or intravenously at the discretion of the investigator and in accordance with regional regulatory approval of bortezomib. More than 75 percent of the patients in the control arm received bortezomib subcutaneously. This study was conducted at 235 sites worldwide.

For information about this trial, please visit www.clinicaltrials.gov under trial identification number NCT01568866.

About Multiple Myeloma

Multiple myeloma is an incurable blood cancer, characterized by a recurring pattern of remission and relapse.1 It is a rare and very aggressive disease that accounts for approximately one percent of all cancers.2,3 In the U.S., there are nearly 95,000 people living with, or in remission from, multiple myeloma.4 Approximately 30,330 Americans are diagnosed with multiple myeloma each year and 12,650 patient deaths are reported on an annual basis.4

About KYPROLIS (carfilzomib)

Proteasomes play an important role in cell function and growth by breaking down proteins that are damaged or no longer needed.5 KYPROLIS has been shown to block proteasomes, leading to an excessive build-up of proteins within cells.5 In some cells, KYPROLIS can cause cell death, especially in myeloma cells because they are more likely to contain a higher amount of abnormal proteins.5,6

KYPROLIS is approved in the U.S. for the following:

In combination with dexamethasone or with lenalidomide plus dexamethasone for the treatment of patients with relapsed or refractory multiple myeloma who have received one to three lines of therapy.
As a single agent for the treatment of patients with relapsed or refractory multiple myeloma who have received one or more lines of therapy.
KYPROLIS is also approved in Argentina, Australia, Bahrain, Canada, Hong Kong, Israel, Japan, Kuwait, Lebanon, Macao, Mexico, Thailand, Colombia, S. Korea, Canada, Qatar, Switzerland, United Arab Emirates, Turkey, Russia, Brazil, India, Oman and the European Union. Additional regulatory applications for KYPROLIS are underway and have been submitted to health authorities worldwide.

IMPORTANT SAFETY INFORMATION

Cardiac Toxicities

New onset or worsening of pre-existing cardiac failure (e.g., congestive heart failure, pulmonary edema, decreased ejection fraction), restrictive cardiomyopathy, myocardial ischemia, and myocardial infarction including fatalities have occurred following administration of KYPROLIS. Some events occurred in patients with normal baseline ventricular function. Death due to cardiac arrest has occurred within one day of KYPROLIS administration.
Monitor patients for clinical signs or symptoms of cardiac failure or cardiac ischemia. Evaluate promptly if cardiac toxicity is suspected. Withhold KYPROLIS for Grade 3 or 4 cardiac adverse events until recovery, and consider whether to restart KYPROLIS at 1 dose level reduction based on a benefit/risk assessment.
While adequate hydration is required prior to each dose in Cycle 1, monitor all patients for evidence of volume overload, especially patients at risk for cardiac failure. Adjust total fluid intake as clinically appropriate in patients with baseline cardiac failure or who are at risk for cardiac failure.
Patients ≥ 75 years, the risk of cardiac failure is increased. Patients with New York Heart Association Class III and IV heart failure, recent myocardial infarction, conduction abnormalities, angina, or arrhythmias may be at greater risk for cardiac complications and should have a comprehensive medical assessment (including blood pressure and fluid management) prior to starting treatment with KYPROLIS and remain under close follow-up.
Acute Renal Failure

Cases of acute renal failure and renal insufficiency adverse events (including renal failure) have occurred in patients receiving KYPROLIS. Acute renal failure was reported more frequently in patients with advanced relapsed and refractory multiple myeloma who received KYPROLIS monotherapy. Monitor renal function with regular measurement of the serum creatinine and/or estimated creatinine clearance. Reduce or withhold dose as appropriate.
Tumor Lysis Syndrome

Cases of Tumor Lysis Syndrome (TLS), including fatal outcomes, have occurred in patients receiving KYPROLIS. Patients with multiple myeloma and a high tumor burden should be considered at greater risk for TLS. Adequate hydration is required prior to each dose in Cycle 1, and in subsequent cycles as needed. Consider uric acid lowering drugs in patients at risk for TLS. Monitor for evidence of TLS during treatment and manage promptly. Withhold KYPROLIS until TLS is resolved.
Pulmonary Toxicity

Acute Respiratory Distress Syndrome (ARDS), acute respiratory failure, and acute diffuse infiltrative pulmonary disease such as pneumonitis and interstitial lung disease have occurred in patients receiving KYPROLIS. Some events have been fatal. In the event of drug-induced pulmonary toxicity, discontinue KYPROLIS.
Pulmonary Hypertension

Pulmonary arterial hypertension (PAH) was reported in patients treated with KYPROLIS. Evaluate with cardiac imaging and/or other tests as indicated. Withhold KYPROLIS for PAH until resolved or returned to baseline and consider whether to restart KYPROLIS based on a benefit/risk assessment.
Dyspnea

Dyspnea was reported in patients treated with KYPROLIS. Evaluate dyspnea to exclude cardiopulmonary conditions including cardiac failure and pulmonary syndromes. Stop KYPROLIS for Grade 3 or 4 dyspnea until resolved or returned to baseline. Consider whether to restart KYPROLIS based on a benefit/risk assessment.
Hypertension

Hypertension, including hypertensive crisis and hypertensive emergency, has been observed with KYPROLIS. Some of these events have been fatal. Monitor blood pressure regularly in all patients. If hypertension cannot be adequately controlled, withhold KYPROLIS and evaluate. Consider whether to restart KYPROLIS based on a benefit/risk assessment.
Venous Thrombosis

Venous thromboembolic events (including deep venous thrombosis and pulmonary embolism) have been observed with KYPROLIS. Thromboprophylaxis is recommended for patients being treated with the combination of KYPROLIS with dexamethasone or with lenalidomide plus dexamethasone. The thromboprophylaxis regimen should be based on an assessment of the patient’s underlying risks.
Patients using oral contraceptives or a hormonal method of contraception associated with a risk of thrombosis should consider an alternative method of effective contraception during treatment with KYPROLIS in combination with dexamethasone or lenalidomide plus dexamethasone.
Infusion Reactions

Infusion reactions, including life-threatening reactions, have occurred in patients receiving KYPROLIS.
Symptoms include fever, chills, arthralgia, myalgia, facial flushing, facial edema, vomiting, weakness, shortness of breath, hypotension, syncope, chest tightness, or angina. These reactions can occur immediately following or up to 24 hours after administration of KYPROLIS. Premedicate with dexamethasone to reduce the incidence and severity of infusion reactions. Inform patients of the risk and of symptoms of an infusion reaction and to contact a physician immediately if they occur.
Hemorrhage

Fatal or serious cases of hemorrhage have been reported in patients receiving KYPROLIS. Hemorrhagic events have included gastrointestinal, pulmonary, and intracranial hemorrhage and epistaxis. Promptly evaluate signs and symptoms of blood loss. Reduce or withhold dose as appropriate.
Thrombocytopenia

KYPROLIS causes thrombocytopenia with recovery to baseline platelet count usually by the start of the next cycle. Thrombocytopenia was reported in patients receiving KYPROLIS. Monitor platelet counts frequently during treatment with KYPROLIS. Reduce or withhold dose as appropriate.
Hepatic Toxicity and Hepatic Failure

Cases of hepatic failure, including fatal cases, have been reported during treatment with KYPROLIS. KYPROLIS can cause increased serum transaminases. Monitor liver enzymes regularly regardless of baseline values. Reduce or withhold dose as appropriate.
Thrombotic Microangiopathy

Cases of thrombotic microangiopathy, including thrombotic thrombocytopenic purpura/hemolytic uremic syndrome (TTP/HUS), including fatal outcome have occurred in patients receiving KYPROLIS. Monitor for signs and symptoms of TTP/HUS. Discontinue KYPROLIS if diagnosis is suspected. If the diagnosis of TTP/HUS is excluded, KYPROLIS may be restarted. The safety of reinitiating KYPROLIS therapy in patients previously experiencing TTP/HUS is not known.
Posterior Reversible Encephalopathy Syndrome (PRES)

Cases of PRES have occurred in patients receiving KYPROLIS. PRES was formerly known as Reversible Posterior Leukoencephalopathy Syndrome. Consider a neuro-radiological imaging (MRI) for onset of visual or neurological symptoms. Discontinue KYPROLIS if PRES is suspected and evaluate. The safety of reinitiating KYPROLIS therapy in patients previously experiencing PRES is not known.
Increased Fatal and Serious Toxicities in Combination with Melphalan and Prednisone in Newly Diagnosed Transplant‐ineligible Patients

In a clinical trial of transplant‐ineligible patients with newly diagnosed multiple myeloma comparing KYPROLIS, melphalan, and prednisone (KMP) vs bortezomib, melphalan, and prednisone (VMP), a higher incidence of serious and fatal adverse events was observed in patients in the KMP arm. KYPROLIS in combination with melphalan and prednisone is not indicated for transplant‐ineligible patients with newly diagnosed multiple myeloma.
Embryo-fetal Toxicity

KYPROLIS can cause fetal harm when administered to a pregnant woman based on its mechanism of action and findings in animals.
Females of reproductive potential should be advised to avoid becoming pregnant while being treated with KYPROLIS. Males of reproductive potential should be advised to avoid fathering a child while being treated with KYPROLIS. If this drug is used during pregnancy, or if pregnancy occurs while taking this drug, the patient should be apprised of the potential hazard to the fetus.
ADVERSE REACTIONS

The most common adverse reactions occurring in at least 20% of patients treated with KYPROLIS in the combination therapy trials: anemia, neutropenia, diarrhea, dyspnea, fatigue, thrombocytopenia, pyrexia, insomnia, muscle spasm, cough, upper respiratory tract infection, hypokalemia.
The most common adverse reactions occurring in at least 20% of patients treated with KYPROLIS in monotherapy trials: anemia, fatigue, thrombocytopenia, nausea, pyrexia, dyspnea, diarrhea, headache, cough, edema peripheral.
Please see full prescribing information at www.kyprolis.com.

On August 30, 2017 Clovis Oncology, Inc. (NASDAQ: CLVS) reported that abstracts highlighting progress in the rucaparib clinical development program will be presented at the 2017 European Society for Medical Oncology (ESMO) (Free ESMO Whitepaper) Congress taking place September 8-12, 2017 in Madrid, Spain (Press release, Clovis Oncology, AUG 30, 2017, View Source [SID1234520335]). These abstracts include a late breaker oral presentation that serves as the first academic presentation of an expanded dataset from the ARIEL3 clinical study.

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ARIEL3 is a double-blind, placebo-controlled, phase 3 trial of rucaparib that enrolled 564 women with platinum-sensitive, high-grade ovarian, fallopian tube, or primary peritoneal cancer. Topline data announced in June 2017 demonstrate that ARIEL3 successfully achieved the primary endpoint of improved progression free survival by investigator review and blinded independent central review (BICR) in each of the three populations studied: tumor BRCA-mutant, HRD-positive and overall intent-to-treat populations. The safety of rucaparib observed in ARIEL3 was highly consistent with the U.S. treatment label for rucaparib. The September 8 ESMO (Free ESMO Whitepaper) presentation will provide comprehensive, detailed results of each ARIEL3 endpoint, along with a summary of safety data.

Additionally, two abstracts will provide an overview of the background and clinical trial design for the ongoing ARIEL4 study of rucaparib in ovarian cancer and the TRITON2 and TRITON3 studies of rucaparib in prostate cancer. These studies are evaluating rucaparib in germline and somatic BRCA-mutated, relapsed, high-grade ovarian cancer, and in metastatic castration-resistant prostate cancer associated with homologous recombination deficiency, respectively.

"We look forward to presenting the comprehensive dataset from our ARIEL3 clinical trial, which demonstrates rucaparib’s clinically meaningful benefit in the maintenance setting for women with platinum-sensitive, advanced ovarian cancer," said Patrick J. Mahaffy, President and CEO of Clovis Oncology. "It has become increasingly clear that PARP inhibitors have a significant role to play in the current and future cancer-treatment paradigm, as monotherapy and potentially in combination with other therapeutic agents. The abstracts being presented at ESMO (Free ESMO Whitepaper) 2017 highlight our commitment to leveraging the very exciting potential of rucaparib in the fight against prostate and ovarian cancer, both devastating diseases for which we hope rucaparib may be able to offer new hope to patients and physicians."

The three rucaparib abstracts accepted for presentation at the 2017 ESMO (Free ESMO Whitepaper) congress comprise:

Abstract LBA40– ARIEL3: A Phase 3, Randomised, Double-Blind Study of Rucaparib vs Placebo Following Response to Platinum-Based Chemotherapy for Recurrent Ovarian Carcinoma (OC)
Presenter: Professor Jonathan A. Ledermann, MD, University College London Cancer Institute and University College London Hospitals, UK
Session: Proffered paper session, Gynecological Cancers
Date/Time: Friday, September 8, 16:12-16:24 CEST
Location: Cordoba Auditorium
This abstract will also be featured in the ESMO (Free ESMO Whitepaper) press program from 08:15–09:00 CEST on Sunday, 10 September in Hall 10.

Abstract 988TIP – ARIEL4: An International, Randomised Phase 3 Study of the PARP Inhibitor Rucaparib vs Chemotherapy for the Treatment of BRCA-Mutated, Relapsed, High-Grade Ovarian Cancer
Presenter: Dr. Rebecca S. Kristeleit, MD, University College London Cancer Institute, UK
Session: Poster session
Date/Time: Saturday, September 9, 13:15-14:15 CEST
Location: Hall 8

Abstract 836TIP – The TRITON Clinical Trial Program: Evaluation of the PARP Inhibitor Rucaparib in Patients (Pts) with Metastatic Castration-Resistant Prostate Cancer (mCRPC) Associated with Homologous Recombination Deficiency (HRD)
Presenter: Dr. Simon Chowdhury, MD, Guy’s Hospital & Sarah Cannon Research Institute, UK
Session: Poster session
Date/Time: Sunday, September 10, 13:15-14:15 CEST
Location: Hall 8

Clovis’ rucaparib presentations and posters will be available online at View Source as of the time they are presented at the meeting.

Investor/Analyst Briefing and Webcast

Clovis Oncology, Inc. will webcast an investor and analyst briefing in Madrid on Saturday, September 9 at 6:00 PM CEST in conjunction with the ESMO (Free ESMO Whitepaper) annual meeting. At this briefing, Clovis Oncology management will review the rucaparib development program and data presented at ESMO (Free ESMO Whitepaper) and answer questions from investors and analysts. This event will be webcast live and archived for 30 days, and may be accessed from the Clovis Oncology Investor Events and Presentations webpage at www.clovisoncology.com. The presentation will begin at 6:00 PM CEST for those institutional investors and analysts attending this event in Madrid; please RSVP to [email protected] to attend.

About Rucaparib

Rucaparib is an oral, small molecule inhibitor of PARP1, PARP2 and PARP3 being developed in ovarian cancer as well as several additional solid tumor indications. In December 2016, rucaparib became the first PARP inhibitor approved by the U.S. Food and Drug Administration (FDA) as monotherapy for treatment of patients with deleterious BRCA mutation (germline and/or somatic) associated advanced ovarian cancer who have been treated with two or more prior chemotherapies. During the fourth quarter of 2016, the Marketing Authorization Application (MAA) submission in Europe for rucaparib in the same ovarian cancer treatment indication was submitted and accepted for review. By the end of October 2017, Clovis Oncology intends to submit a supplemental New Drug Application (sNDA) in the U.S. for a second line or later maintenance treatment indication in ovarian cancer based on the ARIEL3 data, and in early 2018, plans to file an MAA in Europe for the maintenance treatment indication upon receipt of a potential approval for the treatment indication. Studies open for enrollment or under consideration include ovarian, prostate, breast, pancreatic, gastroesophageal, bladder, lung and urothelial cancers. Clovis is also developing rucaparib in patients with mutant BRCA tumors and other DNA repair deficiencies beyond BRCA – commonly referred to as homologous recombination deficiencies, or HRD. Clovis holds worldwide rights for rucaparib.

On August 30, 2017 Array BioPharma Inc. (Nasdaq: ARRY), a biopharmaceutical company focused on the discovery, development and commercialization of targeted small molecule cancer therapies, reported that results from the Phase 3 BEACON CRC safety lead-in study in BRAF-mutant colorectal cancer and the Phase 3 COLUMBUS Part 2 study in BRAF-mutant melanoma will be presented at the 2017 European Society for Medical Oncology Congress in Madrid, Spain on September 9 (Press release, Array BioPharma, AUG 30, 2017, View Source [SID1234520334]). In addition, Array will host an investor reception and webcast on September 9.

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BEACON CRC SAFETY LEAD-IN DATA

A presentation of data from the safety lead-in will take place on Saturday, September 9 from 1:15 – 2:15 pm CEST (7:15 – 8:15 am EDT). The presentation will include details on the safety and tolerability profile of the triplet therapy, encorafenib + binimetinib + cetuximab, as well as preliminary measures of efficacy including overall response rate and available durability results.

Abstract #517P: BEACON CRC: Safety Lead-In (SLI) for the Combination of Binimetinib (BINI), Encorafenib (ENCO), and Cetuximab (CTX) in Patients (Pts) with BRAFV600E Metastatic Colorectal Cancer (mCRC)
COLUMBUS PART 2 TRIAL DATA

Data from Part 2 of the Phase 3 study will be featured as an oral presentation on Saturday, September 9 at 2:45 pm Central European Summer Time (CEST) (8:45 am EDT). The presentation will include progression free survival, objective response rate, dose intensity, safety and tolerability.

Abstract #1215O: Results of COLUMBUS Part 2: A Phase 3 Trial of Encorafenib (ENCO) Plus Binimetinib (BINI) Versus ENCO in BRAF-Mutant Melanoma
ARRAY INVESTOR RECEPTION AND WEBCAST: Array will host an investor reception during ESMO (Free ESMO Whitepaper) 2017 where key opinion leaders in the colorectal cancer field, including Dr. Scott Kopetz, M.D. Anderson and Dr. Axel Grothey, Mayo Clinic will give presentations covering the BRAF-mutant colorectal cancer landscape and data from the BEACON CRC safety lead-in. The presentations will be webcast (live and replay), for those who wish to participate remotely.

Date:
Saturday, September 9, 2017
Time:
4:00-6:00 PM CEST (10:00 am – 12-noon EDT)
Location:
Neuvo Boston Hotel, Madrid, Spain
RSVP:
View Source

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08000288438
Pass Code:
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Webcast:
View Source
Additional data from Array BioPharma and partner compounds will also be presented at ESMO (Free ESMO Whitepaper).

All abstracts can be accessed on August 30, 2017 at 6:05 pm EDT through the ESMO (Free ESMO Whitepaper) website, View Source After the presentation and poster are public, they will be available as PDFs on Array’s website at www.arraybiopharma.com.

About Binimetinib and Encorafenib
MEK and BRAF are key protein kinases in the MAPK signaling pathway (RAS-RAF-MEK-ERK). Research has shown this pathway regulates several key cellular activities including proliferation, differentiation, survival and angiogenesis. Inappropriate activation of proteins in this pathway has been shown to occur in many cancers, such as melanoma, colorectal and thyroid cancers. Binimetinib is a late-stage small molecule MEK inhibitor and encorafenib is a late-stage small molecule BRAF inhibitor, both of which target key enzymes in this pathway. Binimetinib and encorafenib are being studied in clinical trials in advanced cancer patients, including the Phase 3 BEACON CRC trial with encorafenib in combination with cetuximab with or without binimetinib in patients with BRAF V600E-mutant colorectal cancer. On July 5, 2017, Array announced that it submitted two NDAs to the Food and Drug Administration (FDA) to support use of the combination of binimetinib 45 mg twice daily and encorafenib 450 mg once daily (COMBO450) for the treatment of patients with BRAF-mutant advanced, unresectable or metastatic melanoma. The submissions are supported by data from the pivotal Phase 3 COLUMBUS study. In addition, Array’s European partner, Pierre Fabre, announced on August 28, 2017, that the European Medicines Agency (EMA) has validated the review of the Marketing Authorization Applications (MAAs) for binimetininb and encorafenib.

Binimetinib and encorafenib are investigational medicines and are not currently approved in any country.

Array BioPharma retains exclusive rights to binimetinib and encorafenib in key markets including the U.S., Canada and Israel. Array has granted Ono Pharmaceutical exclusive rights to commercialize both products in Japan and South Korea and Pierre Fabre exclusive rights to commercialize both products in all other countries, including Europe, Asia and Latin America.