ROG - Rogers Corporation

NYSE - Nasdaq Real Time Price. Currency in USD
110.33
+5.45 (+5.20%)
As of 10:17AM EDT. Market open.
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Momentum

Momentum

Performance Outlook
  • Short Term
    2W - 6W
  • Mid Term
    6W - 9M
  • Long Term
    9M+
Previous Close104.88
Open108.67
Bid108.99 x 1000
Ask109.97 x 1000
Day's Range108.72 - 110.36
52 Week Range75.72 - 183.34
Volume5,555
Avg. Volume169,830
Market Cap2.059B
Beta (5Y Monthly)1.80
PE Ratio (TTM)64.11
EPS (TTM)1.72
Earnings DateJul 29, 2020 - Aug 03, 2020
Forward Dividend & YieldN/A (N/A)
Ex-Dividend DateJan 09, 1992
1y Target Est136.67
Fair Value is the appropriate price for the shares of a company, based on its earnings and growth rate also interpreted as when P/E Ratio = Growth Rate. Estimated return represents the projected annual return you might expect after purchasing shares in the company and holding them over the default time horizon of 5 years, based on the EPS growth rate that we have projected.
Fair Value
XX.XX
Overvalued
-6% Est. Return
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    The National Institute of Allergy and Infectious Diseases (NIAID) said Friday it is testing Gilead Sciences Inc.'s remdesivir in combination with Eli Lilly & Co.'s rheumatoid arthritis drug Olumiant in COVID-19 patients as part of the next phase of the randomized, controlled clinical trial that led to the authorization of remdesivir. This study will enroll 1,000 people at more than 100 sites in the U.S. and abroad, to "examine if adding an anti-inflammatory agent to the remdesivir regimen can provide additional benefit for patients," NIAID director Dr. Anthony Fauci said in a statement. The topline results from the remdesivir trial helped make up the basis of the Food and Drug Administration's (FDA) emergency use authorization for the drug last week. A number of medicines that have been previously approved by the FDA to treat rheumatoid arthritis have been proposed as possible COVID-19 treatments, including Regeneron Pharmaceuticals Inc. and Sanofi's Kevzara and Roche Holding AG's Actemra. Olumiant, which was developed by Incyte Corp. and is licensed to Lilly, brought in $427 million in sales in 2019 for the Indianapolis-based drugmaker. Only two types of therapies - remdesivir and hydroxycholorquine and chlorquine - are authorized by the FDA as COVID-19 treatments. Year-to-date, Gilead's stock has gained 18.6%, while shares of Lilly are up 16.6%. The S&P 500 is down 10.8%.

  • Thomson Reuters StreetEvents

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  • MarketWatch

    FDA: Antibody test makers must seek EUA, noting 'unscrupulous actors'

    The Food and Drug Administration (FDA) on Monday changed its emergency-use policy for antibody tests, saying that manufacturers now have to seek regulatory authorization. The tests identify COVID-19 antibodies, which indicate a past infection with the novel coronavirus and are believed to provide some level of immunity to future infections; some experts say that widespread antibody testing is needed to reopen the economy. The FDA had announced on March 16 that antibody tests could be performed in some labs without an emergency use authorization (EUA), which is a type of regulatory OK granted during the pandemic. It is not an FDA approval. The makers of more than 200 tests have sought an EUA, and at least 12 have been granted one, including Abbott Laboratories Inc. and Roche Holding AG . But concerns about the quality and marketing claims for some tests that have not received an EUA created concern at the FDA. "The careful balancing of risks and benefits has shifted from where it was in mid-March," the regulator said. Test developers must now submit an EUA request with validation data within 10 days of an FDA notification, and these developers will follow a different submission template than the labs that are also developing antibody tests for authorization. "Flexibility never meant we would allow fraud," the FDA said Monday. "We, unfortunately, see unscrupulous actors marketing fraudulent test kits and using the pandemic as an opportunity to take advantage of Americans' anxiety." This includes claiming the tests are FDA approved or authorized, that they can be conducted at home, or can be used to diagnose COVID-19, according to the FDA. The regulator noted that all forms of antibody tests can produce false results, based on their "inherent limitations," and in some cases at least two antibody tests may need to be performed for one patient.

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  • Roche backs 2020 view as first-quarter sales rise
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    Roche backs 2020 view as first-quarter sales rise

    Roche Holding AG said Wednesday that sales rose in the first quarter and backed its full-year outlook.

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    Rogers Corporation (NYSE:ROG) plans to announce first quarter 2020 results on April 30 after market close, which will be followed by a conference call at 5:00 pm ET. The call will be hosted by Bruce Hoechner, President and CEO, who will be joined by Mike Ludwig, SVP and CFO, and Bob Daigle, SVP and CTO.

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    BMO downgrades Gilead over concerns about commercial promise of remdesivir

    Shares of Gilead Sciences Inc. gained 0.4% in trading on Monday after BMO Capital Markets downgraded the stock to market perform from outperform. Analysts there believe that despite [l: investor excitement about remdesivir, an experimental drug being tested as a treatment for COVID-19 patients, they "no longer see favorable risk/reward in shares given continued uncertainty around the remdesivir commercial opportunity." They wrote that progression of vaccines in development, which would prevent infection with the virus, raise questions about the durability of a post-infection treatment, noting that Roche AG's Tamiflu flu treatment generated more than $3 billion in revenue in 2009 during the H1N1 pandemic but sales of that drug brought in an average of $670 million annually after that. Year-to-date, Gilead's stock is up 29.6%, while the S&P 500 is down 11.0%.

  • Roche developing coronavirus serology test
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    We hate to say this but, we told you so. On February 27th we published an article with the title Recession is Imminent: We Need A Travel Ban NOW and predicted a US recession when the S&P 500 Index was trading at the 3150 level. We also told you to short the market and buy […]

  • MarketWatch

    Roche gets go-ahead from FDA for COVID-19 clinical trial

    Shares of Roche Holding AG are down 3% in trading on Monday after the drugmaker said it had received regulatory approval to begin a late-stage clinical trial examining the safety and effectiveness of Actemra, its rheumatoid arthritis treatment, in hospitalized patients with COVID-19 pneumonia. The randomized, double-blind, placebo-controlled Phase 3 clinical trial will be conducted in partnership with the Biomedical Advanced Research and Development Authority. Actemra was first approved by the Food and Drug Administration in 2010; however, it has not been approved by the regulator for a COVID-19 indication. Roche also said it will provide 10,000 vials of the drug to the U.S. Strategic National Stockpile for potential future use. Roche's stock is down 11% year-to-date, while the S&P 500 has tumbled 28%.

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    CDC, public health labs have tested at least 54,205 Americans for coronavirus

    At least 54,205 tests for COVID-19 have been conducted by public health organizations in the U.S., as of March 18, according to the Centers for Disease Control and Prevention (CDC). This includes 4,524 tests performed by the CDC and 49,681 tests by public health laboratories. At least four major diagnostics makers including Abbott Laboratories , Hologic Inc. , Roche Holding AG and Thermo Fisher Scientific Inc. have made tests for the novel coronavirus. As those tests become available, it is expected to expand testing access in the U.S.

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    CDC, public health labs performed at least 44,000 COVID-19 tests

    At least 44,872 tests for COVID-19 have been conducted by public health organizations in the U.S., as of March 18, according to the Centers for Disease Control and Prevention (CDC). This includes 4,505 tests performed by the CDC and 40,367 tests by public health laboratories. At least four major diagnostics makers including Abbott Laboratories , Hologic Inc. , Roche Holding AG and Thermo Fisher Scientific Inc. have said they are now making tests for the novel coronavirus. As those tests become available, it is expected to expand testing access in the U.S.

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    Roche to test Actemra as a treatment for COVID-19

    Shares of Roche Holding AG gained 3.7% in premarket trading on Thursday after the Swiss drugmaker said it plans to run a Phase 3 clinical testing Actemra, its rheumatoid arthritis drug, as a treatment for patients with COVID-19 who have been hospitalized with severe pneumonia. Roche said Thursday it is in talks with the Food and Drug Administration to set up the trial in partnership with the Biomedical Advanced Research and Development Authority. The trial is expected to begin enrolling around 330 patients in early April, in the U.S. and elsewhere in the world. The company plans to examine patient mortality and need for mechanical ventilation or an intensive care unit stay among other primary and secondary endpoints. Roche is also manufacturing COVID-19 tests for the U.S. Roche's stock is down 7.7% year-to-date, while the S&P 500 has dropped 25.7%.

  • MarketWatch

    CDC, public labs have conducted 37,824 COVID-19 tests

    At least 37,824 tests for COVID-19 have been conducted in the U.S. by the Centers for Disease Control and Prevention (CDC) and public health laboratories, as of March 17, according to the CDC. This includes a total of 4,484 tests conducted by the CDC and 33,340 tests conducted by public labs. The Trump administration has been criticized for the botched rollout of the tests and complaints about access to testing by those who are sick. At least four commercial diagnostics companies have received emergency use authorization from the Food and Drug Administration for their COVID-19 tests. This includes Hologic Inc. , Roche Holding AG , and Thermo Fisher Scientific Inc. , and most recently Abbott Laboratories , which announced Wednesday that it had shipped 150,000 tests, with a plan of providing up to 1 million tests per week. The U.S. has more than 9,400 confirmed cases of the novel coronavirus and at least 150 people have died.

  • MarketWatch

    Abbott Labs gets FDA green light to ship coronavirus tests

    Abbott Laboratories said late Wednesday that it received an emergency authorization from the Food and Drug Administration to ship 150,000 tests for COVID-19, or infection from the SARS-CoV-2 coronavirus. The tests use Abbott's m2000 system, which is in use at more than 175 hospitals and labs in the U.S., and can run up to 470 tests in 24 hours, the company said. "Abbott is immediately distributing 150,000 tests and will continue ramping up production to the highest levels possible, with the goal of providing up to 1 million tests per week," the company said in a statement. Abbott shares were up 1.6% after hours, following a 0.3% decline to finish the regular session at $79.26. Recently, Hologic Inc. , Roche Holding AG and Thermo Fisher Scientific Inc. said they received similar FDA authorizations for their COVID-19 tests.

  • MarketWatch

    CDC, public health labs have conducted at least 31,000 tests

    At least 31,878‬ tests have been conducted for people suspected of having COVID-19, as of March 17, according to the most recent data provided by the Centers for Disease Control and Prevention (CDC). This includes specimens tested by public health laboratories (27,623) and by the CDC (4,255). That's up from Tuesday's tally of 25,162 COVID-19 tests. That said, the jump in test counts doesn't mean that more than 6,000 tests were conducted Tuesday. The tally could include lag times, the CDC has said. However, now that large diagnostics makers like Hologic Inc. , Roche Holding and Thermo Fisher Scientific Inc. have received emergency use authorization from the Food and Drug Administration to begin COVID-19 testing, case counts in the U.S. are expected to significantly increase. There are currently 6,510 confirmed cases of COVID-19 in the U.S.; 114 people in 18 states have died.