On January 10, 2020 Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) reported that it will report its fourth quarter and full year 2019 financial and operating results on Thursday, February 6, 2020, before the U.S. financial markets open (Press release, Regeneron, JAN 10, 2020, https://www.prnewswire.com/news-releases/regeneron-to-report-fourth-quarter-and-full-year-2019-financial-and-operating-results-and-host-conference-call-and-webcast-on-february-6-2020-300984444.html [SID1234553002]). The Company will host a conference call and simultaneous webcast at 8:00 AM Eastern Time that day.

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Conference Call Information
To access this call, dial (800) 708-4540 (U.S.) or (847) 619-6397 (International). A link to the webcast may be accessed from the ‘Investors and Media’ page of Regeneron’s website at View Source A replay of the conference call and webcast will be archived on the Company’s website for at least 30 days.

On January 10, 2020 RhoVac AB ("RhoVac") reported, on 10th January 2020, that the company has received approval from Beligian FAMHP (Federal Agency for Medicines and Health Products) and German Federal Institute for Vaccines and Biomedicines for starting the clinical phase IIb study in prostate cancer, a multicenter study entitled RhoVac-002 ("BRaVac") (Press release, RhoVac, JAN 10, 2020, View Source [SID1234553001]). The phase IIb study is an international, multicenter study, which is expected to recruit more than 175 patients in EU, as well as in the United States. RhoVac has previously received approval Denmark and Finland.

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BRaVac is a randomized, placebo-controlled and double-blind study, with the primary objective of evaluating if and to what extent treatment with the drug candidate RV001 can prevent or limit the development of advanced prostate cancer after curative intent therapy measured as a limited development of PSA (Prostate Specific Antigen) in actively treated patients compared to the control group (placebo group). The Phase IIb study is an international multicenter study, which is expected to recruit more than 175 patients in EU, as well as in the United States. The ambition is for all patients to be recruited by end Q3 2020. The results reporting on the primary objective of the study is expected during H2 2021. RhoVac has previously received CTA approval in Denmark and Finland.

On January 10, 2020 Seneca Biopharma, Inc., (NASDAQ: SNCA), a clinical-stage biopharmaceutical company developing novel treatments for diseases of unmet medical need, reported that Seneca’s Executive Chairman, Ken Carter, will present at both Sachs Associates 3rd Annual Neuroscience Innovation Forum, January 12, 2020 at the Marines Memorial Club, San Francisco, and Biotech Showcase 2020, being held January 13–15, 2020 at the Hilton San Francisco Union Square (Press release, Seneca Biopharma, JAN 10, 2020, View Source;biotech-showcase-2020-300984762.html [SID1234553000]).

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The details of Seneca’s presentations are as follows:

Event: Sachs Associates 3rd Annual Neuroscience Innovation Forum
Date: Sunday, January 12 2020
Time: 4:35 p.m. PST
Room: Room Heritage
Venue: Marines Memorial Club, San Francisco, CA (United States)

Event: Biotech Showcase
Date: Tuesday, January 14 2020
Time: 10:30 a.m. PST
Room: Franciscan A (Ballroom Level)
Venue: Hilton San Francisco Union Square Hotel, 333 O’Farrell Street, San
Francisco, CA (United States)

Sachs Associates 3rd Annual Neuroscience Innovation Forum, back for its 3rd annual edition, addresses through its conference programme the main challenges for 2020 in investment, partnering and alliance management. The program will cover BioPartnering for CNS, with industry keynotes and panels on AD, PD, Neuropsychiatry and Pain Management. Moreover, there are panels on innovation in neurotech covering banking, device, diagnostics and software.

Biotech Showcase, produced by Demy-Colton and EBD Group, is an investor conference focused on driving advances in therapeutic development by providing a sophisticated networking platform for executives and investors that fosters investment and partnership opportunities. The conference takes place each year during the course of one of the industry’s largest gatherings and busiest weeks.

On January 10, 2020 IDEXX Laboratories, Inc. (NASDAQ: IDXX), a global leader in veterinary diagnostics, veterinary practice software and water microbiology testing, has reported of its 2019 fourth quarter and full-year financial results for Friday, January 31, 2020 before the market opens (Press release, IDEXX Laboratories, JAN 10, 2020, View Source [SID1234552999]). The Company will host a conference call beginning at 8:30 a.m. ET on that day.

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Individuals can access a live webcast of the conference call through a link on the IDEXX website, www.idexx.com/investors. An archived edition of the webcast will be available after 1:00 p.m. ET on that day via the same link and will remain available for one year.

The live call also will be accessible by telephone. To listen to the live conference call, please dial 1- 844-767-5679 or 1- 409-207-6967 and reference access code 176532. Replay of the conference call will be available through Friday, February 7, 2020 by dialing 1-866-207-1041 or 1- 402-970-0847 and referencing access code 8036553.

On January 10, 2020 Paradigm Diagnostics, Inc. reported that Palmetto GBA, the Medicare Administrative Contractor (MAC) for the Molecular Diagnostics MolDX program, has reviewed the technical dossier and broadly approved the Paradigm Cancer Diagnostic (PCDx) assay under the Local Coverage Determination for next-generation sequencing for solid tumors (Press release, Paradigm Diagnostics, JAN 10, 2020, View Source [SID1234552998]).

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The PCDx test provides physicians and their patients with a blueprint of the underlying mechanisms of a patient’s disease, potential treatment approaches, and inventory of relevant clinical trials. The test gets results back to physicians in three to five business days, rather than weeks. The PCDx assay detects substitutions, insertion and deletion alterations (indels), and copy number alterations in 234 genes and select gene rearrangements. PCDx also detects genomic signatures, including micro satellite instability (MSI) and tumor mutational burden (TMB) using DNA isolated from formalin-fixed paraffin embedded (FFPE) tumor tissue specimens in addition to select immunohistochemistry tests.

"After an extensive technical review, the expanded Medicare coverage significantly enhances Paradigm’s ability to enable broader and earlier access to biomarker-driven treatments that may improve survival for cancer patients," said David Mallery, CEO.