Novartis's Entresto Voyage: Hindsight Is 20/20

Total Page:16

File Type:pdf, Size:1020Kb

Novartis's Entresto Voyage: Hindsight Is 20/20 26 May 2017 No. 3855 Scripscrip.pharmamedtechbi.com Pharma intelligence | informa summer or autumn. So, we feel good about that progression.” He is predicting a dramatic acceleration for Entresto this year. Jefferies analysts have joined Novartis’s optimistic bandwagon – a May 15 note from the group highlights that Entresto has seen a recent upturn in the US. They point out that Entresto saw one round of accel- eration in spring 2016 when new treatment guidelines were introduced, but that this was mostly swallowed by a poor launch performance (see box on p10). Now they predict this second wave of acceleration will hold steadfast for Entresto “as payer hur- dles continue to fall and enthusiasm builds among cardiologists.” Still, consensus estimates remain mostly conservative for the drug at $3.1bn by 2021. Shutterstock: samantha cheah samantha Shutterstock: Jefferies now estimates that Entresto rev- enues will reach $4.7bn by that time. Novartis’s Entresto Voyage: WHAT WENT WRONG? First approved in the US in July 2015 as a treatment for CHF, Entresto (valsartan/sacubi- Hindsight Is 20/20 tril) was predicted to be a prominent growth LUCIE ELLIS [email protected] driver for Novartis’s pharmaceutical unit. However, the launch got off to a slow start s a novel treatment for heart failure to piece together why a successful product and sales for its first full year on the market coming into a marketplace that had with a large target market missed the mark missed the big pharma’s own target: Entres- Aseen little innovation in recent years, in its first 18 months post-launch. to’s 2016 sales were $170m, while Novartis with a proven effect on morbidity and mor- Only now, after the close of 2017’s first had forecast $200m for the period. However, tality, Entresto should have been a ground- full quarter, is Entresto beginning to earn the company believes its full year sales target breaking US launch in 2015 for Novartis AG its keep for Novartis. The drug saw sales of for 2017 of $500m is still “very achievable.” – a region where nearly 5 million people are $84m in the first quarter compared with First-in-class Entresto, an angiotensin currently living with congestive heart failure just $17m in the year-ago quarter. Paul Hud- receptor blocker/neutral endopeptidase (CHF) and approximately 550,000 new cases son, who heads Novartis’ pharmaceuticals (ARB/NEP) inhibitor, is a fixed dose combi- are diagnosed each year. But the drug suf- operations, said in the company’s 1Q 2017 nation comprising valsartan (Novartis’s an- fered a slower-than-expected start in its big- earnings call this strong revenue rise is be- giotensin receptor blocker Diovan, a mega- blockbuster franchise that faced generic gest market and missed out on sales targets cause of doctors’ increased familiarity with competition in 2014) and the NEP inhibitor in 2016 despite Novartis introducing new the drug and a stronger sales force. prodrug sacubitril. value-based reimbursement methods to Hudson said the full deployment of the Slow uptake of the drug in the US was tempt US payers. Novartis sales force for the product “hap- unexpected, but is understandable because In light of these unusual circumstances, pened at the beginning of [this] year and Scrip has taken a look back at Entresto’s story the true operational impact will come late CONTINUED ON PAGE 10 BROUGHT TO YOU BY THE EDITORS OF PHARMASIA NEWS, START-UP AND SCRIP INTELLIGENCE Business Strategy Drugs To Watch At ASCO Exclusive Interview The three anchors steadying Pfizer’s Abstracts hint it’s not all about Novo Nordisk CEO to empower regions, oncology ship (p14) I-O Drugs (p16) cut red tape (p18) IN THIS ISSUE from the editor [email protected] If you’re limbering up for the American Society of Clini- to a new contender and from a major cancer to a rare cal Oncology meeting in Chicago, check out Mandy one – we might also see data that could lead to a filing Jackson’s piece on seven drugs to watch at ASCO on for Loxo Oncology’s TRK inhibitor larotrectinib in glio- page 16. Our colleagues at Informa Pharma Intelli- blastoma, bringing the Stamford, Conn.-based upstart gence’s Biomedtracker analyst service pulled apart the within spitting distance of commercialization. conference abstracts released last week –we’ve taken Back in IO territory, where combination testing is their digest and distilled it further for your delectation. all the rage, indoleamine 2,3-dioxygenase is the rather Immuno-oncology will be a dominant theme, no unlikely name on everyone’s lips. Or rather, IDO is. In- doubt, but progress in other areas of cancer therapy hibiting this immunosuppressive enzyme at the same as is worth watching too. For example, details of Roche’s targeting immune checkpoints like PD-1 and CLTA-4 successful APHINITY trial of Perjeta combined with looks set to drive further advances in therapeutic effica- Herceptin and chemotherapy as an adjuvant therapy for cy. Incyte’s epacadostat is the one to watch; ASCO will breast cancer are expected to enable the triple combo’s provide a chance to see new data on its combination move from a conditional to a full approval. At the op- with Merck & Co’s PD-1 inhibitor Keytruda. NewLink posite end of the spectrum – from a cancer behemoth Genetics will also present IDO inhibitor study data. LEADERSHIP ADVERTISING DESIGN Phil Jarvis, Mike Ward Christopher Keeling Paul Wilkinson SUBSCRIPTIONS DESIGN SUPERVISOR Scrip Daniel Frere Gayle Rembold Furbert EDITORS IN CHIEF Vibha Sharma EDITORIAL OFFICE Eleanor Malone (Europe) Joanne Shorthouse Christchurch Court Denise Peterson (US) Sten Stovall 10-15 Newgate Street Ian Haydock (Asia) Sukaina Virji London, EC1A 7AZ CUSTOMER SERVICES EXECUTIVE EDITORS US Tel: +44 (0)20 7017 5540 COMMERCIAL Michael Cipriano or (US) Toll Free: 1 800 997 3892 Alexandra Shimmings (Europe) Derrick Gingery Email: clientservices@ Mary Jo Laffler (US) Joseph Haas pharmamedtechbi.com Emily Hayes POLICY AND REGULATORY Mandy Jackson TO SUBSCRIBE, VISIT Maureen Kenny (Europe) Cathy Kelly scrip.pharmamedtechbi.com Nielsen Hobbs (US) Jessica Merrill TO ADVERTISE, CONTACT Brenda Sandburg [email protected] EUROPE Bridget Silverman Lubna Ahmed Sue Sutter Neena Brizmohun Francesca Bruce ASIA John Davis Ying Huang Lucie Ellis Anju Ghangurde All stock images in this publication John Hodgson Jung Won Shin courtesy of www.shutterstock.com Ian Schofield Brian Yang unless otherwise stated Scrip is published by Informa UK Limited. ©Informa UK Ltd 2017: All rights reserved. ISSN 0143 7690. 2 | Scrip intelligence | 26 May 2017 © Informa UK Ltd 2017 Real World Changing The ‘Think Global, Evidence? Diversity Narrative Act Local’ 20 9 20 18 exclusive online content inside: COVER / Novartis’s Entresto Voyage: Hindsight Is 20/20 Merck Develops ‘New And Improved’ CRISPR http://bit.ly/2r8SnNU 4 J&J Plots Five-Year Pharma Growth Plan Around Merck of Germany has developed a new genome editing tool Mega-Brands And Launches that it believes improves on the popular, but IP battle-worn, CRISPR technology. How this will affect the existing IP landscape 6 Ipsen’s New CEO Targets At Least One New Drug is as yet unknown. Annually ‘Forever’ 7 Infographic Infant Bacterial Therapeutics Harnesses Microbiome To Treat Preterm Babies 8 More Pressure On Pradaxa? US Payers May Narrow Coverage http://bit.ly/2qOauW4 Of NOACs By harvesting Lactobacillus reuteri from lactating mothers, Infant Bacterial Therapeutics has developed an approach to 9 MedImmune’s Bahija Jallal On Changing The treat necrotizing enterocolitis, a major killer of premature babies. Diversity Narrative 11 Takeda Picks Next Big Thing In Immunotherapy: Gamma Sinergium’s Gateway To Latin American Vaccine & Delta T Cells Biologics Markets http://bit.ly/2q8OrZk 13 AstraZeneca’s Iressa May Pave Way For EGFR Inhibitors In With the Latin American vaccines market forecast to more than Adjuvant Lung Cancer quadruple in size from just over $150m to 2015 to just under $700m in 2020, opportunities abound for both homegrown 14 Pfizer’s Oncology Strategy Centers On Three Anchors To businesses and multinationals looking to tap into local markets. Steady The Ship 15 Humira’s Formulation Patent Loss Boosts Biosimilar Mitochondrial Medicine Focus Drives NeuroVive Manufacturers Orphan Ambitions http://bit.ly/2rKbiuw 16 It’s Not All About IO: Seven Drugs To Watch At ASCO Erik Kinnman, CEO of NeuroVive Pharmaceutical, spoke to Scrip about the company’s work in mitochondrial medicine. 18 ‘Think Global, Act Local’ – Novo Nordisk CEO To Empower The company aims to develop orphan drugs to treat rare Regions, Cut Red Tape genetic conditions and seek partners for its NASH and liver cancer projects. 19 Novo Nordisk CEO Puts Pricing On The Line Avir BD Execs On Innovative Meds For Canadians 20 Real World Evidence Is Critical To Pharma’s Future: Can We Agree On What It Is? http://bit.ly/2q2MLo7 Avir Pharma’s business development associate Vanessa 22 Pipeline Watch Fortin and VP of business development Kaled Kadri talk to Scrip about the company’s business model and strategy for bringing innovative medicines to Canada 23 Henri Termeer Dies Aged 71 23 Appointments @PharmaScrip /scripintelligence /scripintelligence /scripintelligence scrip.pharmamedtechbi.com 26 May 2017 | Scrip intelligence | 3 COMPANY STRATEGY J&J Plots Five-Year Pharma Growth Plan Around Mega-Brands And Launches JESSICA MERRILL [email protected] ohnson & Johnson’s strategy to outpace its branded pharma- Drugs On Track For Filing By 2021 ceutical peers by achieving above-market compound annual • apalutamide (ARN-509) for pre-metastatic prostate cancer Jgrowth over the five-year period from 2016 to 2021 will require • esketamine for treatment-resistant depression building several blockbuster brands into “mega-blockbusters” and • talacotuzumab (CSL362) for acute myeloid leukemia launching new commercial successes, worldwide chair-pharmaceu- • erdafitinib (FGFR Inhibitor) for solid tumors ticals Joaquin Duato said during an R&D briefing on May 17.
Recommended publications
  • BIOWORLD TODAY Inquiry
    BIOWORLDTM TODAY THE DAILY BIOPHARMACEUTICAL NEWS SOURCE JUNE 30 , 2016 BIOTECH’S MOST RESPECTED NEWS SOURCE FOR MORE THAN 20 YEARS VOLUME 27, NO. 126 LIPID JAM NOT OVER EASILY STOPPED FOR FUTILITY Waffle house? FDA Galena Biopharma implodes as PRESENT review fidgets endpoint, puts cancer vaccine Neuvax future in doubt outcome details; By Jennifer Boggs, Managing Editor Esperion grilled on holdup With the bulk of Galena Biopharma Inc.’s value riding on cancer vaccine Neuvax By Randy Osborne, Staff Writer (nelipepimut-S), the firm’s shares predictably plunged to a new 52-week low Wednesday as an independent data monitoring committee (IDMC) recommended the Analysts had plenty of questions but PRESENT phase III study in breast cancer be stopped for futility following a planned Esperion Therapeutics Inc. offered few interim analysis. But it’s the troubling language in the IDMC’s letter, suggesting the answers regarding the FDA’s stalling on placebo arm might actually have bested the treatment arm, that could signal the end oral, once-daily bempedoic acid (ETC- of the road for Neuvax. 1002) for lipid lowering, after the agency See Galena, page 3 See Esperion, page 4 CHINA DEALS AND M&A IN THE CLINIC Pfizer invests in Asia Merck strikes cancer SUPER ‘NOVA’ with $350M biotech vaccines deal with Tesaro shares blast plant in Hangzhou Moderna, delivering off as niraparib hits By Haky Moon, Staff Writer $200M up front PFS in ovarian cancer HONG KONG – China’s economy may By Michael Fitzhugh, Staff Writer By Marie Powers, News Editor be slowing down, but multinationals Findings from the phase III NOVA trial are positioning themselves to leverage Cancer vaccines tailored to fit tumor- specific profiles are at the heart of a new of niraparib in women with recurrent it as best they can while navigating a ovarian cancer blasted shares of still-complex regulatory environment.
    [Show full text]
  • Initiation of Francis Trial
    August 25‚ 2008 ANTHERA PHARMACEUTICALS ADVANCES GLOBAL DEVELOPMENT STRATEGY FOR VARESPLADIB IN PATIENTS WITH ACUTE CORONARY SYNDROME WITH THE INITIATION OF FRANCIS TRIAL SAN MATEO, CA – August 25, 2008 – Anthera Pharmaceuticals Inc., a privately held biopharmaceutical company developing anti-inflammatory drugs, today announced the initiation of the FRANCIS (Fewer Recurrent Acute coronary events with Near-term Cardiovascular Inflammation Suppression) clinical trial designed to examine the impact of varespladib when administered to patients within 96 hours of an Acute Coronary Syndrome (ACS) event. The FRANCIS trial is designed to assess the impact of oral varespladib on known biological markers of cardiovascular risk. It will enroll up to 500 patients that will be treated for a minimum of six months. The study will be conducted at sites in North America and Europe. FRANCIS will provide insight into the prevention of secondary Major Adverse Cardiovascular Events (MACE) over the duration of the trial. In this study, MACE is defined as a composite endpoint consisting of cardiovascular death, non-fatal stroke, non-fatal myocardial infarction, unstable angina, and a subset of revascularization following the initial event. During the course of the study, patients will receive therapeutic standard of care in addition to high dose Lipitor ® (atorvastatin). In previous clinical trials, varespladib, a potent and highly selective inhibitor of secretory phospholipase A 2 (sPLA 2), has demonstrated marked improvements in independent markers of cardiovascular risk including, a near complete suppression of the target enzyme sPLA 2, a clinically meaningful and statistically significant reduction in “bad” LDL cholesterol, and a reduction in C-reactive protein, a known marker of inflammation.
    [Show full text]
  • Boston University Journal of Science & Technology
    4 B.U. J. SCI. & TECH. L. 1 January 23, 1997 Boston University Journal of Science & Technology Law Symposium Financing the Biotech Industry: Can the Risks Be Reduced? Ronald Cass, Joshua Lerner, Farah H. Champsi, Stanley C. Erck, Jonathan R. Beckwith, Leslie E. Davis, Henri A. Termeer Table of Contents Speeches..........................................................................................................................[1] Dean Ronald Cass.............................................................................................[1] Joshua Lerner....................................................................................................[2] Farah Champsi..................................................................................................[8] Stanley Erck.....................................................................................................[18] Jonathan Beckwith.........................................................................................[24] Leslie Davis......................................................................................................[37] Henri Termeer.................................................................................................[47] Question and Answer Session..................................................................................[60] Financing the Biotech Industry: Can the Risks Be Reduced?† Jonathan R. Beckwith, Farah H. Champsi, Leslie E. Davis,* Stanley C. Erck, Joshua Lerner, Henri A. Termeer Dean Ronald Cass: 1. The biotechnology
    [Show full text]
  • Schedule 14A
    QuickLinks -- Click here to rapidly navigate through this document UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 SCHEDULE 14A Proxy Statement Pursuant to Section 14(a) of the Securities Exchange Act of 1934 (Amendment No. ) Filed by the Registrant ý Filed by a Party other than the Registrant o Check the appropriate box: o Preliminary Proxy Statement o Confidential, for Use of the Commission Only (as permitted by Rule 14a-6(e)(2)) ý Definitive Proxy Statement o Definitive Additional Materials o Soliciting Material under §240.14a-12 Verastem, Inc. (Name of Registrant as Specified In Its Charter) (Name of Person(s) Filing Proxy Statement, if other than the Registrant) Payment of Filing Fee (Check the appropriate box): ý No fee required. o Fee computed on table below per Exchange Act Rules 14a-6(i)(1) and 0-11. (1) Title of each class of securities to which transaction applies: (2) Aggregate number of securities to which transaction applies: (3) Per unit price or other underlying value of transaction computed pursuant to Exchange Act Rule 0-11 (set forth the amount on which the filing fee is calculated and state how it was determined): (4) Proposed maximum aggregate value of transaction: (5) Total fee paid: o Fee paid previously with preliminary materials. o Check box if any part of the fee is offset as provided by Exchange Act Rule 0-11(a)(2) and identify the filing for which the offsetting fee was paid previously. Identify the previous filing by registration statement number, or the Form or Schedule and the date of its filing.
    [Show full text]
  • February 11-12, 2013 the Waldorf Astoria New York
    February 11-12, 2013 The Waldorf Astoria New York 15th ANNU AL EVENT Now in its fifteenth year, the BIO CEO & Investor Conference is the largest independent investor conference focused on leading publicly-traded biotech companies. The meeting provides a neutral forum where institutional investors, industry analysts, and senior biotechnology executives have the opportunity to shape the future investment landscape of the biotechnology industry. Reasons Top 10 to attend 1 Present your company story to an audience of targeted investors. 2 Hear the Washington perspective on the Affordable Care Act, debt ceiling, and other timely policy developments affecting the industry. 3 Evaluate fresh investment opportunities including compatible, complementary and competitive companies. 4 Learn about the hottest clinical developments and industry catalysts by attending the conference’s therapeutic workshops and business roundtables. 5 Attend fireside chats with CEOs who will share their recent company successes, what keeps the C-suite up at night, and where the industry’s leading companies are headed in 2013. 6 Gain access to BIO’s 1x1 Partnering System for scouting potential deal partners and optimizing your time at the event. 7 Access presentations from more than 140 established public and private biotech companies and non-profit funding organizations, including many you won’t hear from at other investor conferences. 8 Get the pulse on the current and proposed investment trends in biotechnology. 9 Network with peers, investors and potential partners attending the conference. 10 It’s the first NYC biotech conference of the year, kicking off a week of key industry events that you don’t want to miss.
    [Show full text]
  • Example of Corresponding Structure of Excel Report, for E
    CDDW™ Faculty Conflict of Interest Disclosure The Canadian Association of Gastroenterology (CAG) must ensure balance, independence, objectivity, and scientific rigour in all educational and scientific activities. Accordingly, CDDW™ faculty members are expected to disclose to the audience any potential, apparent or actual interests or connections that appear to influence their ability to act with integrity, objectivity, and independence on the assigned task. The intent of this disclosure summary is to provide the audience with information on the faculty interests/relationships that could influence interpretations, recommendations, and conclusions. The following faculty have indicated that they do have relevant relationships of commercial interest Afif, Waqqas Janssen (Consultant) (Company Advisory Board); Abbvie (Company Advisory Board) (Research Support); Takeda (Company Advisory Board) (Consultant); Pfizer (Company Advisory Board); Merck (Company Advisory Board); Ferring (Company Advisory Board); Shire (Company Advisory Board); Prometheus (Research Support); Theradiag (Research Support) (Consultant); Buhlmann (Research Support) Anderson, John Olympus (Other); Norgine (Speaker's Bureau) Andrews, Christopher Newstrike Inc. (Research Support) (Stockholder); Newstrike Inc. (Company Advisory Board); Allergan (Research Support) (Speaker's Bureau); Allergan (Company Advisory Board); Pendopharm (Speaker's Bureau); Lupin (Company Advisory Board); Jannsen (Research Support); Medtronic (Company Advisory Board); M Pharma Inc. (Company Advisory Board)
    [Show full text]
  • Board of Director Candidates
    2021 Annual General Meeting Board of Director Candidates James I. Healy, M.D., Ph.D. (Current Board Member) James I. Healy, M.D., Ph.D. has served as a member of our board of directors since November 2014. Dr. Healy has been a General Partner of Sofinnova Investments, Inc. (formerly Sofinnova Ventures), a venture capital firm, since June 2000. Prior to June 2000, Dr. Healy held various positions at Sanderling Ventures, Bayer Healthcare Pharmaceuticals (as successor to Miles Laboratories) and ISTA Pharmaceuticals, Inc. Dr. Healy is currently on the board of directors of Bolt Therapeutics, Inc. (Nasdaq: BOLT), Coherus BioSciences, Inc. (Nasdaq: CHRS), Karuna Therapeutics, Inc. (Nasdaq: KRTX), Natera, Inc. (Nasdaq: NTRA), NuCana plc (Nasdaq: NCNA), ObsEva SA (Nasdaq: OBSV) and Y-mAbs Therapeutics, Inc. (Nasdaq: YMAB) and two private companies. Previously, he served as a board member of Amarin Corporation, Auris Medical Holding AG, Edge Therapeutics, Inc., Hyperion Therapeutics, Inc., InterMune, Inc., Iterum Therapeutics PLC, Anthera Pharmaceuticals, Inc., Durata Therapeutics, Inc., CoTherix, Inc., Movetis NV and several private companies. Dr. Healy holds an M.D. and a Ph.D. in Immunology from Stanford University School of Medicine and holds a B.A. in Molecular Biology and a B.A. in Scandinavian Studies from the University of California, Berkeley. Jan Møller Mikkelsen (Current Board Member) Jan Møller Mikkelsen founded Ascendis Pharma and has served as President and Chief Executive Officer as well as Board member since December 2007 and currently serves on the board of Visen. From 2002 to 2006, Mr. Mikkelsen served as President and Chief Executive Officer of LifeCycle Pharma A/S, now Veloxis Pharmaceuticals A/S, which was a publicly traded biotechnology company.
    [Show full text]
  • AVEO PHARMACEUTICALS, INC. (Name of Registrant As Specified in Its Charter)
    Table of Contents UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 SCHEDULE 14A (Rule 14a-101) INFORMATION REQUIRED IN PROXY STATEMENT SCHEDULE 14A INFORMATION Proxy Statement Pursuant to Section 14(a) of the Securities Exchange Act of 1934 Filed by the Registrant x Filed by a party other than the Registrant ¨ Check the appropriate box: ¨ Preliminary Proxy Statement ¨ Confidential, for Use of the Commission Only (as permitted by Rule 14a-6(e)(2)) x Definitive Proxy Statement ¨ Definitive Additional Materials ¨ Soliciting Material Pursuant to §240.14a-12 AVEO PHARMACEUTICALS, INC. (Name of Registrant as Specified In Its Charter) (Name of Person(s) Filing Proxy Statement, if Other Than The Registrant) Payment of Filing Fee (Check the appropriate box): x No fee required. ¨ Fee computed on table below per Exchange Act Rules 14a-6(i)(1) and 0-11. (1) Title of each class of securities to which transaction applies: (2) Aggregate number of securities to which transaction applies: (3) Per unit price or other underlying value of transaction computed pursuant to Exchange Act Rule 0-11 (set forth the amount on which the filing fee is calculated and state how it was determined): (4) Proposed maximum aggregate value of transaction: (5) Total fee paid: ¨ Fee paid previously with preliminary materials: ¨ Check box if any part of the fee is offset as provided by Exchange Act Rule 0-11(a)(2) and identify the filing for which the offsetting fee was paid previously. Identify the previous filing by registration statement number, or the Form or Schedule and the date of its filing.
    [Show full text]
  • Guidelines with Regard to the Composition, Calculation and Management of the Index
    INDEX METHODOLOGY Solactive Pharma Breakthrough Value Index Version 2.1 dated September 03, 2020 Contents Important Information 1. Index specifications 1.1 Short Name and ISIN 1.2 Initial Value 1.3 Distribution 1.4 Prices and Calculation Frequency 1.5 Weighting 1.6 Index Committee 1.7 Publication 1.8 Historical Data 1.9 Licensing 2. Composition of the Index 2.1 Selection of the Index Components 2.2 Ordinary Adjustment 2.3 Extraordinary Adjustment 3. Calculation of the Index 3.1 Index Formula 3.2 Accuracy 3.3 Adjustments 3.4 Dividends and other Distributions 3.5 Corporate Actions 3.6 Correction Policy 3.7 Market Disruption 3.8 Consequences of an Extraordinary Event 4. Definitions 5. Appendix 5.1 Contact Details 5.2 Calculation of the Index – Change in Calculation Method 2 Important Information This document (“Index Methodology Document”) contains the underlying principles and regulations regarding the structure and the operating of the Solactive Pharma Breakthrough Value Index. Solactive AG shall make every effort to implement regulations. Solactive AG does not offer any explicit or tacit guarantee or assurance, neither pertaining to the results from the use of the Index nor the Index value at any certain point in time nor in any other respect. The Index is merely calculated and published by Solactive AG and it strives to the best of its ability to ensure the correctness of the calculation. There is no obligation for Solactive AG – irrespective of possible obligations to issuers – to advise third parties, including investors and/or financial intermediaries, of any errors in the Index.
    [Show full text]
  • Proqr Therapeutics N.V
    ANNUAL REPORT 2017 Meaningful progress - Excited about the future PAGE I PAGE II ANNUAL MAGAZINE 2017 ANNUAL MAGAZINE 2017 our courage to do things differently University of Colorado and during his ACCOMPLISHMENTS – and challenge the status quo. career has earned a global reputation A QUICK GLANCE We can and will make a meaningful for translating cutting-edge science impact – changing the lives of into transformational new therapies Eluforsen (formely known as QR-010) for CF patients. Be it in a small way – for rare diseases including cystic fibro- • Completed second trial for eluforsen by improving one’s quality of life. sis, pulmonary fibrosis, pulmonary • Announced positive data from Or in a big way – by stopping artery hypertension, severe immuno- Phase 1b safety and tolerability study a disease or by curing patients. logic, and inflammatory diseases. • Received FDA Fast Track designation and Orphan Drug Designation (ODD) CREATING MEANINGFUL IMPACT At ProQR, we do it all in the interest Dave is excited to be part of ProQR’s in US and Europe of patients. We’re driven, deter- management team: “ProQR has • Granted two key patents mined, excited to make this differ- a patient-centric culture committed ence. Today, tomorrow and more to transforming lives. Applying our QR-110 for LCA 10 days to come, until we get it right. RNA editing platform to precision • IND clearance from FDA and IN THE INTEREST medicine in hereditary forms of commenced Phase 1/2 safety and Building ProQR blindness, dystrophic epidermolysis efficacy trial In 2017, we made important strides bullosa, cystic fibrosis and other • First patient in trial dosed in late 2017 in ProQR’s growth.
    [Show full text]
  • The Weekly Shot Biotech Issue a Weekly Summary of Healthcare Industry Valuation and Near-Term Catalysts June 17, 2010
    Small Cap The Weekly Shot Biotech Issue June 17, 2010 A weekly summary of healthcare industry valuation and near-term catalysts The Weekly Shot: Overview and Comment - Small Cap Biotechnology Next week's sector highlights include LGND’s Thursday analyst event at the Eventi - Pharmaceuticals and Large Cap Biotech Hotel in NYC. The company on 6/15 announced updated 2010 revenue guidance of approx $25M, op ex of approx $30M, and expects to finish the year with $30M - Generics and Specialty Pharmaceuticals in cash (vs approx $43M as of 1Q10). Management will likely focus on partner GSK’s progress with add’l trials of Promacta (for ITP), which could potentially expand the drug’s label to Hep C, AML, and MDS (LGND receives <10% royalty from GSK). Investors should focus on pipeline plans following LGND’s opportunistic 2008/09 M&A activity. Key pipeline programs include LGD-4033 (ph.I, SARM candidate from PCOP) and RG7348, partnered with Roche (ph.I, Hep C candidate from MBRX). We do not expect major data announcements at the event. FDA’s Pediatric Drugs Advisory Committee will meet Monday to discuss pediatric safety reviews of multiple approved drugs, including Kogenate, Casodex, Apidra, NovoLog, Arimidex, Desmopressin, Prevacid, Nexium, Aciphex, Priolex, OraVerse, Zemuron, and Suprane . While important from a public safety perspective, we do not anticipate regulatory activity to be announced. Brian Lian, Ph.D. Small caps biotechs rebounded mid-week as elevated volatility continued across 212.500.6646 [email protected] the broader market. Investors are struggling to balance economic data supporting a modest recovery against concerns on EU debt loads, financial reform legislation, and aggressive govt rhetoric on BP’s oil spill.
    [Show full text]
  • Orphan Drug Letters
    November 18, 2010 Kent Lieginger Senior Vice President, Managed Care and Customer Operations Genentech 1 DNA Way South San Franciso, CA 94080 Dear Dr. Lieginger: We are writing on behalf of a broad coalition of hospitals participating in the federal 340B drug discount program. We have been advised that Genentech has begun to withhold 340B pricing for orphan drugs purchased by a subset of our membership, primarily children’s and rural hospitals. We are aware that, under the Health Care and Education Reconciliation Act (HCERA), Congress established a statutory exclusion with respect to orphan drugs purchased by hospitals specifically added by the Patient Protection and Affordable Care Act (PPACA) to the 340B program under the Public Health Service Act, including freestanding cancer hospitals, children’s hospitals, sole community rural referral centers, and critical access hospitals. 1 However, we are deeply concerned with Genentech’s broad interpretation of the orphan drug exclusion, which Genentech has stated extends to all drugs that have been designated “orphan” by the FDA, regardless of the intended use of the drugs. We believe that, absent guidance from the Health Resources and Services Administration (HRSA) regarding the scope of the orphan drug exclusion, it is premature to withhold 340B pricing on orphan drugs. Accordingly, we request that Genentech resume its sale of orphan drugs to hospitals identified in PPACA at 340B prices until directed otherwise by HRSA. We understand that several manufacturers have decided to delay implementation until they receive further guidance from the government and ask that you follow their lead. Our concerns regarding your company’s interpretation are two-fold.
    [Show full text]