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250-511 Administration of Symantec(TM) Data Loss(R) Prevention 11

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250-511 exam Dumps Source : Administration of Symantec(TM) Data Loss(R) Prevention 11

Test Code : 250-511
Test name : Administration of Symantec(TM) Data Loss(R) Prevention 11
Vendor name : Symantec
: 176 actual Questions

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Symantec Administration of Symantec(TM) Data

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First identify: ultimate name: electronic mail tackle: Password: ascertain Password: Username:

Title: C-level/President manager VP corpse of workers (associate/Analyst/and many others.) Director

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Google Chrome 70 is coming. Are your safety certificates so as? | killexams.com actual Questions and Pass4sure dumps

previous this yr, I wrote about what security professionals should execute to keep together for the upcoming Google distrust time limit. I illustrious that DigiCert had taken a number of steps that ended in a smooth process this spring for the first of two distrust dates. they now own yet another date drawing near when Google Chrome 70 will distrust outright TLS certificates issued from the Symantec PKI.

Given what I’ve discovered from DigiCert, I suppose confident that DigiCert is managing the Chrome 70 process easily this time round, too.

Plan to allotment out Symantec certificates

For those unfamiliar with the particulars of this, in 2017 Google and Mozilla decided to deprecate outright Symantec-issued digital certificates according to their assessment that Symantec didn't as it should exist validate its SSL certificates previous to issuing them to shoppers.

Google and Mozilla then decided to dwelling in location a multi-step diagram to mistrust any certificates issued from the Symantec PKI. This diagram phased out Symantec certificates over the subsequent yr and a half. as an alternative of following the Google plan, Symantec elected to promote its certificates enterprise to DigiCert. regardless of the transaction, the requirement to replace outright certificates issued from the Symantec PKI remained intact, requiring hundreds of thousands of certificates to bag replaced during 2018. To aid valued clientele in changing their certificates, DigiCert contacted every certificates holder, providing free replacement certificates chained to the trusted DigiCert roots.

the first most notable mistrust date changed into on December 1, 2017, when no extra TLS certificates can exist issued during the Symantec PKI. earlier than that date, DigiCert lop over outright issuance techniques to its PKI and validation methods. The next predominant mistrust date changed into March 15, 2018, when Chrome 66 beta distrusted outright Symantec TLS certificates issued earlier than June 1, 2016. 

The final predominant step in this distrust event is scheduled for Oct. sixteen, 2018, when Chrome 70 righteous will mistrust outright TLS certificates issued from the Symantec PKI. (This date might too alternate in accordance with Google’s release time table.) Upon release of Chrome 70, any web page nevertheless the exercise of a Symantec certificates may own an interstitial warning a yoke of non-private connection.

HTTPS is now in outright places, making certificates compliance obligatory

regularly occurring scholarship was once that handiest sites that deal with economic or other sensitive facts required certificates, however instances own changed. today over 80 p.c of net site visitors is “https”, which contains many ground pages. there has been a speedy pressure to https outright over the place, and it won’t exist long when basically every page is comfortable.

Google is ushering that along. Chrome now marks outright HTTP net pages as “now not comfy” in the browser address bar. also, notwithstanding the web site is monitor handiest, the warning clients will contemplate may scare them off and reason them talk over with a competitor, so it’s something outright safety specialists that manage sites may noiseless exist concerned about. 

different platforms additionally crack down on Symantec certificates

It’s crucial to note that despite the fact Chrome 70 is the dwelling the instant challenge is, other platforms will exist doing the same issue with Symantec-issued certificates. Mozilla's date is across the equal time as Chrome's, however the user ground is a righteous deal smaller. Apple has not issued a final date, however the primary phase has been accomplished, so older certificates won’t work. Microsoft nonetheless has no introduced date, however the trade has incredible controls for the mistrust difficulty, so there should noiseless no longer exist plenty of an touch in the beginning.

conform to Chrome distrust now

My assistance to safety leaders is to focus on the rigor now, forward of the Chrome date. Google had essentially the most aggressive date, so complying with Chrome mistrust skill the other dates down the street won’t exist of rigor as a result of a compliant certificates will exist in vicinity. I mentioned this before, but it surely’s price reiterating that here is whatever outright businesses should noiseless conform to inspite of the objective of the web page. 

companies that own a immense number of websites might locate this a onerous system as a result of changing certificates manually can exist time-drinking, tedious, and filled with error because of the variety of steps involved. DigiCert has keep a yoke of automation paraphernalia in location to upshot the system of checking and upgrading convenient. It is rarely plenary automation, as a yoke of lead steps are required, however the technique of relocating from the non-compliant Symantec certificates to a present one is enormously more convenient than before, so complexity is not any longer a barrier.

DigiCert has completed a righteous job disposing of any obstacles to doing a free alternative with them. They’ve managed to simplify the process prerogative down to a pair clicks in a client internet portal, akin to how an administrator would renew a certificate about to sprint out.

I checked in with DigiCert, the brand current owner of the Symantec CA company, on how the upgrade of the Symantec consumer ground has gone. to this point, about ninety nine % of the Alexa 1 million (which makes up the huge majority of web traffic) ground domains own been changed devoid of difficulty. the majority of outright impacted certificates are reissued or in technique. The past dates own Come and gone devoid of concern, and i anticipate an analogous outcomes with the remaining step developing in mid-October.


Symantec warns of China-based mostly espionage crusade concentrated on satellites | killexams.com actual Questions and Pass4sure dumps

A China-based cyber community is accomplishing an in depth hacking crusade by means of concentrated on satellite tv for pc, telecom and defense companies within the u.s. and Southeast Asia, a U.S. cybersecurity difficult warned this week.

The purpose of the hacking community, referred to as "Thrip," is likely national cyber espionage, security researchers at Symantec Corp. spoke of on Tuesday.

"Thrip’s assault on telecoms and satellite tv for pc operators exposes the opportunity that the attackers may intercept and even alter communications site visitors from agencies and consumers," Symantec observed in a statement, including that the most stressful discovery is an try and manage satellites via infecting linked computers with malware.

commercial

"The assault group seemed to exist notably interested in the operational facet of the company, hunting for and infecting computer systems operating utility that displays and controls satellites. this suggests to us that Thrip’s motives Go past spying and may additionally include disruption," Symantec wrote in a separate blog publish.

Satellites play a primary position in telecommunications, receiving and transmitting phone and cyber web alerts in addition to mapping and geolocation information.

Symantec said in Tuesday's remark that it has tracked Thrip seeing that 2013 and currently accompanied that the cyber community seems to own "discovered current tools and innovations used by the community during this most simultaneous set of attacks."

The possibility of the more advantageous hacking toolbox is further compounded via Thrip's means to reside smartly hidden.

"They duty very quietly, mixing in to networks, and are handiest organize out using simulated intelligence that may determine and flag their movements," Symantec Chief executive Greg Clark referred to in a press release.

The trade says it organize out the current assaults through its simulated intelligence-primarily based targeted storm Analytics, which helped the researchers spot the malicious conduct that was hiding in legitimate IT administration tools.


250-511 Administration of Symantec(TM) Data Loss(R) Prevention 11

Study lead Prepared by Killexams.com Symantec Dumps Experts


Killexams.com 250-511 Dumps and actual Questions

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250-511 exam Dumps Source : Administration of Symantec(TM) Data Loss(R) Prevention 11

Test Code : 250-511
Test name : Administration of Symantec(TM) Data Loss(R) Prevention 11
Vendor name : Symantec
: 176 actual Questions

actual 250-511 examination inquiries to bypass exam in the beginning try.
I used killexams.com cloth which affords enough expertise to attain my purpose. I constantly usually memorize the things before going for any exam, but that is the handiest one exam, which I took without without a doubt memorizing the wanted things. I thanks without a doubt from the bottom of my coronary heart. i will Come to you for my subsequent examination.


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I own cleared 250-511 exam in a solitary try with ninety eight% marks. Killexams.Com is the character medium to smooth this examination. Thanks, your case research and material had been well. I want the timer might sprint too whilst they offer the practice exams. Thank you again.


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Before I stroll to the testing middle, I was so assured about my training for the 250-511 examination due to the fact I knew I became going to ace it and this self assurance came to me after the usage of this killexams.Com for my help. It is superb at supporting college students similar to it assisted me and I became capable of bag suitable scores in my 250-511 test.


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I should admit, i was at my wits quit and knew after failing the 250-511 check the primary time that i used to exist on my own. Until I searched the internet for my check. Many web sites had the sample wait on checks and some for spherical $2 hundred. I discovered this internet site and it become the bottom price spherical and that i certainly couldnt manage to pay for it but bit the bullet and purchased it prerogative here. I recognize I sound like a salesperson for this organisation but I can not confidence that I exceeded my cert exam with a ninety eight!!!!!! I opened the exam most efficient to scrutinize almost each query on it emerge as covered on this sample! You guys rock huge time! In case you need me, convene me for a testimonial cuz this works oldsters!


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Thanks lots killexams.Com group, for getting ready outstanding practice checks for the 250-511 examination. It is pellucid that without killexamss examination engine, college students cannot even regard taking the 250-511 exam. I tried many different assets for my exam coaching, however I couldnt find myself assured sufficient for taking the 250-511 examination. Killexamss examination manual makes immaculate examination instruction, and offers self credit to the scholars for taking examination without problems.


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hi, I had symptom up for 250-511. even though I had read outright chapters extensive, however your question bank furnished enough preparation. I cleared this examination with ninety nine % the day before today, thanks a lot for to the factor question bank. Even my doubts had been clarified in minimum time. I want to exercise your carrier in destiny as properly. You guys are doing a terrific job. thanks and Regards.


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Administration of Symantec(TM) Data Loss(R) Prevention 11

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Cyber Security Market in Depth Professional Survey Report 2018-2022 | killexams.com actual questions and Pass4sure dumps

(MENAFN Editorial) iCrowdNewswire - Sep 18, 2018

The Global Cyber Security Market was worth USD 58.13 billion in the year 2012 and is expected to achieve approximately USD 173.57 billion by 2022, while registering itself at a compound annual growth rate (CAGR) of 10.35% during the forecast period.

Cyber Security - Top Major Market Players:

The major players in the market are Symantec Software Solutions Private Limited, Trend Micro, Cisco Systems, Check Point Software Technologies and Fortinet Inc.

Sample Copy of the Report here @ www.crystalmarketresearch.com/report-sample/IC10289 .

Cyber security is the group of practices, technologies and procedures intended to ensure data, networks, programs and computers from attacks, unauthorized access or damage. Security incorporates both cyber security and physical security in computing context. Guaranteeing cyber security requires composed endeavors outright through a data framework. A standout amongst the trickiest components of cyber security is the constantly and rapidly developing nature of security dangers. The conventional approach has been to concentrate most assets on the most vital framework segments and secure against the greatest known dangers, which required abandoning some less essential framework parts undefended and some less unsafe dangers not ensured against. Such an approach is deficient in the present condition.

The emergence of cloud storage has increased the chances of data breaches and cybercrimes. The institution of Internet of Things (IoT) is opening up storm surfaces, using vulnerabilities for network frameworks. This is bringing about the adoption of remote and endpoint security being one of the prime factors that influence the progress of the cyber security market. The emerging economies, for example, China, India, Hong Kong, South Korea, and, own high motivating forces in consolidating their IT structures.

The Global Cyber Security market is segmented as follows:

Cyber Security - By Region:

North America - U.S, Canada, MexicoEurope - Germany, France, UK, Italy, Spain, leisure of EuropeAsia-Pacific - Japan, China, Australia, India, South Korea, leisure of Asia PacificRest of the World - Brazil, South Africa, Saudi Arabia, United Arab Emirates, Others

Cyber Security - Regional Outlook and Trend Analysis:

In 2015 Asia Pacific represented more than 21 percent partake of the global industry. The expanding dependence on the Internet has expanded vulnerabilities, giving chances to programmers and assailants. South Korea, Singapore, and Singapore own expanded the extent of their cyber policy structure and the viability of their execution. Nonetheless, nations, for example, Australia, India, and China are concentrating on bringing together the organization of the cyber policy under the government divisions. Latin America is expected to exist a developing locale over the gauge time frame. The area has one of the most elevated penetrations of cell phones prompting vulnerabilities for digital assaults as these gadgets are a simple focus for malware attack, stressing the requirement for the advancement of compelling cybercrime security and policies.

Cyber Security - Service Outlook and Trend Analysis

Security models are being outsourced by associations to third party suppliers inferable from lacking security experts in-house, hence boosting the progress of security benefits over the evaluate time frame. Rising claim for cloud-based security administrations to diminish costs and enhance profitability is anticipated to drive the progress of security services over the figure time frame. Managed services are anticipated to own a high progress attributable to the expanding dangers from regular extremist exercises. The rising government expenditure for the usage of cyber security arrangements in India and China is boosting the progress of security services.

Cyber Security - By Component:

SolutionsUnified threat managementIDS/IPSData Loss Prevention (DLP)

Identity Access Management (IAM)Security Information and Event Management (SIEM)Distributed Denial of Service (DDoS)Risk and compliance managementOther Solutions

ServicesProfessional servicesManaged services

Cyber Security - By Security Type:

Enterprise securityCloud securityNetwork securityApplication securityOther Security Types

Cyber Security - By Deployment:

CloudOn-premise

Cyber Security - By Organization:

Small and medium enterprisesLarge enterprises

Cyber Security - By Application:

IT & TelecomBFSIRetailHealthcareAutomotiveDefense/governmentOther Applications

For more information, click on the below link @ www.crystalmarketresearch.com/report/cyber-security-market .

Cyber Security - Application Outlook and trend Analysis

The BFSI section is anticipated to encounter a solid progress in the cyber security market in the upcoming years. The segment is expanding its cyber security expenditure in light of the developing breaches and risks. The expanded utilization of versatility channels for monetary transactions and correspondence is expanding the susceptibility for cyberattacks. Banks own actualized a two-factor confirmation for online and mobile banking, which has a high exposure to threats because of the risks like loss of gadget and frail passwords. The defense/government segment is changing progressively as dangers from regular exercises are not any more the main concerns. The assignment of resources for growing investment and research and progress of defense programs are foreseen to remain the key patterns in the cyber security industry. For example, the United States President proposed a monetary diagram of USD 14 billion for 2016 for the digital security endeavors over the administration to shield the private and government systems from cyber assaults.

Read Premium advice from OpenPR of 'Cyber Security Market @ https://www.openpr.com/news/1244743/Cyber-Security-Market-Development-Strategy-CAGR-10-35-forecasted-period-2018-2022-Symantec-Software-Solutions-Private-Limited-Trend-Micro-Cisco-Systems-Check-Point-Software-Technologies-and-Fortinet-Inc.html .

Cyber Security - Table of Contents:

1.Introduction

2.Executive Summary

3.Market Overview

4.Cyber Security Market, By Component4.1.Introduction4.2.The Cyber Security Market Assessment and Forecast, By Component, 2012-20224.3.Solutions4.4.Services5.Cyber Security Market, By Security Type5.1.Introduction5.2.The Cyber Security Market Assessment and Forecast, By Security sort 2012-20225.3.Enterprise security5.4.Cloud security5.5.Network security5.6.Application security5.7.Other Security Types…

Key findings of the Cyber Security Market:

The healthcare segment is anticipated to encounter significant progress in the upcoming years. The health insurers are the prime focus of the cyber assaults like spear phishing and Advanced Persistent Threats (APTs). The violations and breaks in this area are ascending as the cost of stolen medical record is expanding.

The rising requirement for Security-as-a-Service (SaaS) and cloud-based solutions is anticipated to render growth opportunities to the service segment.

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TherapeuticsMD Announces Multiple Presentations Related to Imvexxy™ and TX-001HR at the 2018 Annual Meeting of the North American Menopause Society | killexams.com actual questions and Pass4sure dumps

BOCA RATON, Fla.--(Business Wire)--TherapeuticsMD, Inc. (NASDAQ: TXMD), an innovative women’s healthcare company, today announced the schedule of ten oral presentations and posters at NAMS 2018, the annual meeting of the North American Menopause Society being held in San Diego, California on October 3-6, 2018, related to ImvexxyTM (estradiol vaginal inserts) and TX-001HR, the Company’s investigational bio-identical hormone therapy combination of estradiol and progesterone in a single, oral softgel for the treatment of moderate-to-severe vasomotor symptoms due to menopause.

There will exist three oral presentations reviewing the findings of the phase 3 Replenish visitation of TX-001HR and the systemic profile of Imvexxy (TX-004HR).

“We are pleased to present additional data from the Replenish visitation that further advocate the safety and efficacy of TX-001HR as the first bio-identical combination hormone therapy of estradiol and progesterone,” said TherapeuticsMD Chief Medical Officer Sebastian Mirkin, M.D. “The FDA PDUFA target action date for TX-001HR is October 28, 2018. If approved, TX-001HR would provide an FDA-approved treatment option for the millions of postmenopausal women who are currently seeking treatment for moderate to severe vasomotor symptoms using unapproved compounded hormones.”

The posters and presentations will exist made available on the Investors & Media section of the company’s website at www.therapeuticsmd.com.

 

Oral Presentations

  Date:         October 4, 2018 Time: 4:45-5:00 pm Title:

Effects of Single-Capsule 17β-Estradiol/Progesterone (TX-001HR) on Metabolic Parameters and Cardiovascular Outcomes in Menopausal Women of the REPLENISH Trial

  Date: October 5, 2018 Time: 4:15-4:30 pm Title: 17β-Estradiol/Progesterone in a Single, Oral, Softgel Capsule (TX-001HR) Significantly Increased the Number of Symptom-free Days in the REPLENISH Trial   Date: October 5, 2018 Time: 5:00-5:15 pm Title:

Evaluation of Systemic Effects of a Vaginal Estradiol Softgel Capsule (TX-004HR) in Menopausal Women with Moderate-to-Severe Dyspareunia

 

Posters

Date: October 4, 2018 Time: 6:00-7:00 pm   Title: Physical Characteristics of TX-004HR: An Ultra-Low-Dose (4- and 10-µg) Estradiol Softgel Capsule Vaginal Insert   Title: A 17β-Estradiol, Softgel, Vaginal Capsule (TX-004HR) Demonstrated an Early Onset of Action for Treating Vulvar and Vaginal Atrophy (VVA) and Moderate-to-Severe Dyspareunia   Title: Systemic Estradiol Levels with Low-Dose Vaginal Estrogens May disagree by Dose and by Product   Title: Correlations of Serum Estradiol and Estrone Concentrations with Menopausal Outcomes and Bleeding   Title: Effects of Single-Capsule 17β-Estradiol/Progesterone (TX-001HR) on Weight and Blood Pressure in Menopausal Women of the REPLENISH Trial   Title: Estradiol and Progesterone Bioavailability for Moderate-to-Severe Vasomotor Symptom Treatment and Endometrial Protection with the Continuous-Combined Regimen of TX-001HR (Oral Estradiol and Micronized Progesterone Capsules)   Title: TX-001HR is Associated with a Clinically Meaningful upshot on Severity of Moderate-to-Severe Vasomotor Symptoms in the REPLENISH Trial  

About Imvexxy

Imvexxy (estradiol vaginal inserts) is approved in the U.S. for the treatment of moderate-to-severe dyspareunia (vaginal throe associated with sexual activity), a symptom of vulvar and vaginal atrophy (VVA), due to menopause. Imvexxy is the only product in its therapeutic class to offer a 4 mcg and 10 mcg dose, the 4 mcg dose representing the lowest approved dose of vaginal estradiol available. The plenary prescribing information may exist viewed by visiting www.Imvexxy.com.

IMPORTANT SAFETY INFORMATION FOR IMVEXXY

  WARNING: ENDOMETRIAL CANCER, CARDIOVASCULAR DISORDERS, BREAST CANCER and PROBABLE DEMENTIA

See plenary prescribing information for complete boxed warning.

Estrogen-Alone Therapy

• There is an increased risk of endometrial cancer in a woman with a uterus who uses unopposed estrogens

• Estrogen-alone therapy should not exist used for the prevention of cardiovascular disease or dementia

• The Women’s Health Initiative (WHI) estrogen-alone substudy reported increased risks of stroke and abysmal vein thrombosis (DVT)

• The WHI memory Study (WHIMS) estrogen-alone ancillary study of WHI reported an increased risk of probable dementia in postmenopausal women 65 years of age and older

 

Estrogen Plus Progestin Therapy

• Estrogen plus progestin therapy should not exist used for the prevention of cardiovascular disease or dementia

• The WHI estrogen plus progestin substudy reported increased risks of stroke, DVT, pulmonary embolism (PE) and myocardial infarction (MI)

• The WHI estrogen plus progestin substudy reported increased risks of invasive breast cancer

• The WHIMS estrogen plus progestin ancillary study of WHI reported an increased risk of probable dementia in postmenopausal women 65 years of age and older

 

CONTRAINDICATIONS

  • Imvexxy™ is contraindicated in women with any of the following conditions: undiagnosed abnormal genital bleeding; known, suspected, or history of breast cancer; known or suspected estrogen-dependent neoplasia; energetic DVT, PE, or history of these conditions; energetic arterial thromboembolic disease or a history of these conditions; known anaphylactic reaction or angioedema to Imvexxy; known liver impairment or disease; known protein C, protein S, or antithrombin deficiency, or other known thrombophilic disorders.
  • WARNINGS AND PRECAUTIONS

  • Imvexxy is intended only for vaginal administration. Systemic absorption may occur with the exercise of Imvexxy.
  • The exercise of estrogen-alone and estrogen plus progestin therapy has been reported to result in an expand in abnormal mammograms requiring further evaluation.
  • The WHI estrogen plus progestin substudy reported a statistically non-significant increased risk of ovarian cancer. A meta-analysis of 17 prospective and 35 retrospective epidemiology studies organize that women who used hormonal therapy for menopausal symptoms had an increased risk for ovarian cancer. The exact duration of hormone therapy exercise associated with an increased risk of ovarian cancer, however, is unknown.
  • Other warnings include: gallbladder disease; severe hypercalcemia, loss of vision, severe hypertriglyceridemia or cholestatic jaundice.
  • Estrogen therapy may reason an exacerbation of asthma, diabetes mellitus, epilepsy, migraine, porphyria, systemic lupus erythematosus, and hepatic hemangiomas and should exist used with caution in women with these conditions.
  • Women on thyroid replacement therapy should own their thyroid duty monitored.
  • ADVERSE REACTIONS

  • The most common adverse reaction with Imvexxy (incidence ≥ 3 percent) and greater than placebo was headache.
  • Please note that this information is not comprehensive. gladden visit www.Imvexxy.com for the plenary Prescribing Information, including the Boxed WARNING.

    About TherapeuticsMD, Inc.

    TherapeuticsMD, Inc. is an innovative healthcare company focused on developing and commercializing novel products exclusively for women. Their products are designed to address the unique changes and challenges women sustain through the various stages of their lives with a therapeutic focus in family planning, reproductive health, and menopause management. The company is committed to advancing the health of women and championing awareness of their healthcare issues. To learn more about TherapeuticsMD, gladden visit www.therapeuticsmd.com or follow us on Twitter: @TherapeuticsMD and on Facebook: TherapeuticsMD.

    Forward-Looking Statements

    This press release by TherapeuticsMD, Inc. may accommodate forward-looking statements. Forward-looking statements may include, but are not limited to, statements relating to TherapeuticsMD’s objectives, plans and strategies as well as statements, other than historical facts, that address activities, events or developments that the company intends, expects, projects, believes or anticipates will or may occur in the future. These statements are often characterized by terminology such as “believes,” “hopes,” “may,” “anticipates,” “should,” “intends,” “plans,” “will,” “expects,” “estimates,” “projects,” “positioned,” “strategy” and similar expressions and are based on assumptions and assessments made in light of management’s sustain and perception of historical trends, current conditions, expected future developments and other factors believed to exist appropriate. Forward-looking statements in this press release are made as of the date of this press release, and the company undertakes no duty to update or revise any such statements, whether as a result of current information, future events or otherwise. Forward-looking statements are not guarantees of future performance and are topic to risks and uncertainties, many of which are outside of the company’s control. notable factors that could reason actual results, developments and trade decisions to disagree materially from forward-looking statements are described in the sections titled “Risk Factors” in the company’s filings with the Securities and Exchange Commission, including its most recent Annual Report on figure 10-K and Quarterly Reports on figure 10-Q, as well as reports on figure 8-K, and include the following: whether the FDA will ratify the NDA for the company’s TX-001HR product candidate and whether such approval will occur by the PDUFA target action date; the company’s competence to maintain or expand sales of its products; the company’s competence to develop and commercialize IMVEXXYTM, ANNOVERATM and its hormone therapy drug candidates and obtain additional financing necessary therefor; whether the company will exist able to comply with the covenants and conditions under its term loan agreement; the length, cost and uncertain results of the company’s clinical trials; the potential of adverse side effects or other safety risks that could preclude the approval of the company’s hormone therapy drug candidates or adversely touch the commercialization of the company’s current or future approved products; the company’s reliance on third parties to conduct its clinical trials, research and progress and manufacturing; the availability of reimbursement from government authorities and health insurance companies for the company’s products; the repercussion of product liability lawsuits; the influence of extensive and costly government regulation; the volatility of the trading price of the company’s common stock and the concentration of power in its stock ownership. PDF copies of the company’s historical press releases and monetary tables can exist viewed and downloaded at its website: www.therapeuticsmd.com/pressreleases.aspx.

    TherapeuticsMD, Inc.Investor Contact:Nichol Ochsner, 561-961-1900, ext. 2088Vice President Investor RelationsNochsner@TherapeuticsMD.com


    ARCA biopharma Announces Second Quarter 2018 monetary Results and Provides Corporate Update | killexams.com actual questions and Pass4sure dumps

    WESTMINSTER, Colo., Aug. 09, 2018 (GLOBE NEWSWIRE) -- ARCA biopharma, Inc. (ABIO), a biopharmaceutical company applying a precision medicine approach to developing genetically-targeted therapies for cardiovascular diseases, today reported monetary results for the quarter ended June 30, 2018.

    “The second quarter of this year saw an notable milestone for the Gencaro progress program with the completion of an End-of-Phase 2 FDA meeting that provided notable guidance for the next steps in their progress of Gencaro as potentially the first genetically-targeted treatment for atrial fibrillation,” commented Dr. Michael Bristow, ARCA’s President and Chief Executive Officer.  “With labor underway on completing the Gencaro phase 3 visitation protocol and continued progress with IND enabling activities for AB171 in PAD and HF, they believe ARCA is advancing their pipeline of genetically-targeted therapeutics to address the unmet medical needs of patients with cardiovascular disease.”

    Pipeline Update

    Gencaro (bucindolol hydrochloride) - a pharmacologically unique beta-blocker and mild vasodilator being developed for the potential treatment of patients with atrial fibrillation (AF) and confirmed heart failure with reduced left ventricular ejection fraction (HFrEF).

  • In April 2018, Medtronic, Inc. and ARCA agreed to extend their current U.S., Canadian and European Clinical visitation Collaboration Agreement for one additional year.
  • In May 2018, results from ARCA’s GENETIC-AF phase 2B clinical visitation were presented in a “Late Breaking Clinical Trials” oral presentation at the European Society of Cardiology (ESC) Heart Failure 2018 World Congress.
  • In June 2018, ARCA held an End-of-Phase 2 meeting with the U.S. Food and Drug Administration (FDA) to review the GENETIC-AF data and potential future Gencaro progress plans.
  • FDA concurrence to proceed into phase 3 was reached. ARCA anticipates submitting a Special Protocol Assessment (SPA) application for the proposed Gencaro phase 3 clinical visitation in the third quarter of 2018. Progress to phase 3 is topic on the Company receiving additional funding.
  • AB171 – a thiol-substituted isosorbide mononitrate being developed as a potential genetically-targeted treatment for heart failure (HF) and peripheral arterial disease (PAD).

  • Chemistry, manufacturing and controls (CMC) activities were continued in the second quarter.
  • IND-enabling non-clinical studies are anticipated to start in the first half of 2019.
  • Second Quarter 2018 Summary monetary Results

    Cash, cash equivalents and marketable securities totaled $9.6 million as of June 30, 2018, compared to $11.8 million as of December 31, 2017. ARCA believes that its current cash, cash equivalents and marketable securities will exist sufficient to fund its operations, at its projected cost structure, through the discontinuance of the first quarter of 2019.

    Research and progress (R&D) expenses for the quarter ended June 30, 2018 totaled $1.2 million compared to $4.5 million for the corresponding age of 2017.  The $3.3 million subside in research and progress expenses in the second quarter of 2018 as compared to the second quarter 2017 was primarily due to decreased clinical expenses following the completion of the GENETIC-AF clinical trial.  The Company expects R&D expenses in 2018 to exist lower than 2017 as the GENETIC-AF clinical visitation has been completed.

    General and administrative (G&A) expenses for the quarter ended June 30, 2018 were $1.0 million, relatively unchanged compared to the $1.1 million in the second quarter of 2017.  ARCA expects G&A expenses in 2018 to exist consistent with those in 2017 as it maintains administrative activities to advocate ongoing operations.

    Total operating expenses for the quarter ended June 30, 2018 were $2.2 million compared to $5.6 million for the second quarter of 2017.  The subside in total operating expenses for the second quarter of 2018 was primarily due to the subside in R&D expense due to the completion of the GENETIC-AF clinical trial.

    Net loss was $2.1 million, or $0.15 per share, for the second quarter of 2018 compared to $5.5 million, or $0.59 per share, for the second quarter of 2017.

    About ARCA biopharma

    ARCA biopharma is dedicated to developing genetically-targeted therapies for cardiovascular diseases through a precision medicine approach to drug development. ARCA’s lead product candidate, GencaroTM (bucindolol hydrochloride), is an investigational, pharmacologically unique beta-blocker and mild vasodilator being developed for the potential treatment of patients with atrial fibrillation (AF) and confirmed heart failure with reduced left ventricular ejection fraction (HFrEF) which recently completed a phase 2B clinical trial. ARCA has identified common genetic variations that it believes foretell individual patient response to Gencaro, giving it the potential to exist the first genetically-targeted AF prevention treatment. ARCA has a collaboration with Medtronic, Inc. for advocate of the GENETIC-AF trial. The Gencaro progress program has been granted lickety-split Track designation by FDA. ARCA is too developing AB171, a thiol-substituted isosorbide mononitrate, as a potential genetically-targeted treatment for peripheral arterial disease (PAD) and for heart failure (HF). For more information, gladden visit www.arcabio.com.

    Story Continues

    Safe Harbor Statement

    This press release contains "forward-looking statements" for purposes of the safe harbor provided by the Private Securities Litigation Reform Act of 1995. These statements include, but are not limited to, statements regarding the competence of ARCA’s monetary resources to advocate its operations through the discontinuance of the first quarter of 2019, potential future progress plans for Gencaro, the expected features and characteristics of Gencaro or AB171, including the potential for genetic variations to foretell individual patient response to Gencaro, Gencaro’s potential to treat AF, AB171’s potential to treat HF, future treatment options for patients with AF, and the potential for Gencaro to exist the first genetically-targeted AF prevention treatment. Such statements are based on management's current expectations and involve risks and uncertainties.  Actual results and performance could disagree materially from those projected in the forward-looking statements as a result of many factors, including, without limitation, the risks and uncertainties associated with: ARCA’s monetary resources and whether they will exist sufficient to meet its trade objectives and operational requirements; ARCA may not exist able to raise sufficient capital on acceptable terms, or at all, to continue progress of Gencaro or to otherwise continue operations in the future; results of earlier clinical trials may not exist confirmed in future trials; the protection and market exclusivity provided by ARCA’s intellectual property; risks related to the drug discovery and the regulatory approval process; and, the repercussion of competitive products and technological changes.  These and other factors are identified and described in more detail in ARCA’s filings with the Securities and Exchange Commission, including without limitation ARCA’s annual report on figure 10-K for the year ended December 31, 2017, and subsequent filings. ARCA disclaims any intent or obligation to update these forward-looking statements.

    Investor & Media Contact:Derek Cole720.940.2163derek.cole@arcabio.com

    (Tables follow)

      ARCA BIOPHARMA, INC.   BALANCE SHEET DATA  (in thousands)  (unaudited)     June 30, 2018   December 31, 2017 Cash, cash equivalents & marketable securities $9,635   $11,752 Working capital $8,950   $10,229 Total assets $10,067   $12,365 Total stockholders’ equity $8,998   $10,275        

     

        ARCA BIOPHARMA, INC.       STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS   (unaudited)         Three Months Ended     Six Months Ended     June 30,     June 30,     2018     2017     2018     2017                                     (in thousands, except partake and per partake amounts)   Costs and expenses:                               Research and development $ 1,154     $ 4,508     $ 2,874     $ 7,754   General and administrative   1,002       1,051       2,055       2,186   Total costs and expenses   2,156       5,559       4,929       9,940   Loss from operations   (2,156 )     (5,559 )     (4,929 )     (9,940 )                                 Interest and other income   43       39       84       84   Interest expense   (3 )     (2 )     (6 )     (4 ) Net loss $ (2,116 )   $ (5,522 )   $ (4,851 )   $ (9,860 )                                 Change in unrealized loss on marketable securities   —       4       2       14   Comprehensive loss $ (2,116 )   $ (5,518 )   $ (4,849 )   $ (9,846 )                                 Net loss per share:                               Basic and diluted $ (0.15 )   $ (0.59 )   $ (0.35 )   $ (1.07 ) Weighted medium shares outstanding:                               Basic and diluted   13,923,512       9,324,822       13,772,947       9,210,186                                  

    A photo accompanying this announcement is available at http://www.globenewswire.com/NewsRoom/AttachmentNg/af496e97-20da-420a-bf93-e51b3a3ed740



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    References :


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    Box.net : https://app.box.com/s/5r2u6vfx48ncpeh44ywv1cpc3xntdr9g
    publitas.com : https://view.publitas.com/trutrainers-inc/pass4sure-250-511-dumps-and-practice-tests-with-real-questions
    zoho.com : https://docs.zoho.com/file/5r1nh86271bcfec424501bd6f46d4184572be
    Calameo : http://en.calameo.com/books/004923526e89f6a9daa22






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