{"id":514887,"date":"2021-07-20T07:04:12","date_gmt":"2021-07-20T11:04:12","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/redhill-biopharma-significantly-extends-unrestricted-commercial-coverage-for-talicia-with-optumrx\/"},"modified":"2021-07-20T07:04:12","modified_gmt":"2021-07-20T11:04:12","slug":"redhill-biopharma-significantly-extends-unrestricted-commercial-coverage-for-talicia-with-optumrx","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/redhill-biopharma-significantly-extends-unrestricted-commercial-coverage-for-talicia-with-optumrx\/","title":{"rendered":"RedHill Biopharma Significantly Extends Unrestricted Commercial Coverage for Talicia\u00ae with OptumRx"},"content":{"rendered":"
\n

Addition of Talicia\u00ae by OptumRx significantly extends Commercial patient access to Talicia\u00ae through this leader in U.S. healthcare<\/h2>\n

Patient access to Talicia now extends to greater than 8 out of 10 covered U.S. Commercial lives<\/h2>\n

Talicia\u00ae is the first and only FDA-approved rifabutin-based therapy for H. pylori infection, designed as a first-line option to address the high resistance of H. pylori bacteria to standard-of-care therapies<\/h2>\n

H. pylori bacterial infection is a Group 1 carcinogen and the strongest risk factor for gastric cancer; H. pylori affects approximately 35% of the U.S. population<\/h2>\n

PR Newswire<\/p>\n<\/p><\/div>\n

\n

\n TEL-AVIV, Israel<\/span> and RALEIGH, N.C.<\/span>, July 20, 2021<\/span> \/PRNewswire\/ —\u00a0RedHill Biopharma Ltd.<\/a> (Nasdaq: RDHL) (“RedHill” or the “Company”), a specialty biopharmaceutical company, today announced that OptumRx, part of the UnitedHealth Group – a leader in healthcare coverage, partnered with more than 1.3 million healthcare professionals and 6,500 hospitals, has added Talicia\u00ae<\/sup> (omeprazole magnesium, amoxicillin and rifabutin)[1] to its Commercial Formulary as an unrestricted brand for H. pylori<\/i> treatment, effective July 1, 2021<\/span>.<\/p>\n

\u00a0<\/p>\n

\n \"RedHill\n <\/div>\n

\u00a0<\/p>\n

“Momentum with Talicia is growing strongly and the addition of unrestricted Commercial coverage for Talicia by OptumRx, a major operator in U.S. healthcare coverage serving more than 26 million Americans, is an important advance in extending patient access to Talicia, which now extends to greater than 8 out of 10 covered U.S. Commercial lives,” said Rick Scruggs<\/span>, RedHill’s Chief Commercial Officer<\/b>. “Talicia is the first and only FDA-approved rifabutin-based therapy for the treatment of H. pylori<\/i> infection, and this listing represents the understanding within the medical community of the need to combat the high and growing resistance of H. pylori<\/i> to commonly used antibiotics with an effective new first-line treatment.”\u00a0\u00a0\u00a0 <\/p>\n

About Talicia\u00ae\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0
<\/sup><\/b>Talicia\u00ae<\/sup> is the only rifabutin-based therapy approved for the treatment of H. pylori<\/i> infection and is designed to address the high resistance of H. pylori<\/i> bacteria to clarithromycin-based therapies. The high rates of H. pylori<\/i>\u00a0resistance to clarithromycin have led to significant rates of treatment failure with clarithromycin-based therapies and are a strong public health concern, as highlighted by the FDA and the World Health Organization (WHO) in recent years. <\/p>\n

Talicia\u00ae<\/sup> is a novel, fixed-dose, all-in-one oral capsule combination of two antibiotics (amoxicillin and rifabutin) and a proton pump inhibitor (PPI) (omeprazole). In November 2019<\/span>, Talicia\u00ae<\/sup> was approved by the U.S. FDA for the treatment of H. pylori<\/i> infection in adults. In the pivotal Phase 3 study, Talicia\u00ae <\/sup>demonstrated 84% eradication of H. pylori<\/i> infection in the intent-to-treat (ITT) group vs. 58% in the active comparator arm (p<0.0001). Minimal to zero resistance to rifabutin, a key component of Talicia\u00ae, was detected in RedHill’s pivotal Phase 3 study. Further, in an analysis of data from this study, it was observed that subjects who were confirmed adherent[2] to their therapy had response rates of 90.3% in the Talicia\u00ae<\/sup> arm vs. 64.7% in the active comparator arm[3]. \u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 <\/p>\n

Talicia\u00ae<\/sup> is eligible for a total of eight years of U.S. market exclusivity under its Qualified Infectious Disease Product (QIDP) designation and is also covered by U.S. patents which extend patent protection until 2034 with additional patents and applications pending and granted in various territories worldwide.<\/p>\n

\n About\u00a0H. pylori\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0
<\/i><\/b>
\n H. pylori<\/i>\u00a0is a bacterial infection that affects approximately 35%[4] of the U.S. population, with an estimated two million patients treated annually[5]. Worldwide, more than 50% of the population has
H. pylori <\/i>infection, which is classified by the WHO as a Group 1 carcinogen. It remains the strongest known risk factor for gastric cancer[6]\u00a0and a major risk factor for peptic ulcer disease[7]\u00a0and gastric mucosa-associated lymphoid tissue (MALT) lymphoma[8]. More than 27,000 Americans are diagnosed with gastric cancer annually[9]. Eradication of\u00a0H. pylori<\/i>\u00a0is becoming increasingly difficult, with current therapies failing in approximately 25-40% of patients who remain\u00a0H. pylori<\/i>-positive due to high resistance of\u00a0H. pylori<\/i>\u00a0to antibiotics commonly used in standard combination therapies[10].<\/p>\n

\n About RedHill Biopharma\u00a0\u00a0
<\/b>RedHill Biopharma Ltd. (Nasdaq: RDHL) is a specialty biopharmaceutical company primarily focused on gastrointestinal and infectious diseases. RedHill promotes the gastrointestinal drugs, Movantik\u00ae <\/sup><\/b>for opioid-induced constipation in adults[11]<\/sup><\/sup>, Talicia\u00ae<\/sup><\/b>for the treatment of Helicobacter pylori (H. pylori)<\/i> infection in adults[12]<\/sup><\/sup>, and Aemcolo\u00ae<\/sup><\/b> for the treatment of travelers’ diarrhea in adults[13]<\/sup><\/sup>. RedHill’s key clinical late-stage development programs include: (i) RHB-204<\/b>,\u00a0with an ongoing Phase 3 study for pulmonary nontuberculous mycobacteria (NTM) disease; (ii) opaganib (<\/b>ABC294640)<\/b>, a first–<\/b>in–<\/b>class SK2 selective inhibitor targeting multiple indications with positive Phase 2 COVID-19 data and an ongoing Phase 2\/3 program for COVID-19 and Phase 2 studies for prostate cancer and cholangiocarcinoma ongoing; (iii) RHB-107 (upamostat)<\/b>, a serine protease inhibitor in a U.S. Phase 2\/3 study as treatment for symptomatic COVID-19, and targeting multiple other cancer and inflammatory gastrointestinal diseases; (iv) RHB-104<\/b>, with positive results from a first Phase 3 study for Crohn’s disease; (v) RHB-102<\/b>(Bekinda\u00ae<\/sup>)<\/b>, with positive results from a Phase 3 study for acute gastroenteritis and gastritis and positive results from a Phase 2 study for IBS-D; and (vi) RHB<\/b>–106<\/b>, an encapsulated bowel preparation. More information about the Company is available at www.redhillbio.com<\/a> \/ https:\/\/twitter.com\/RedHillBio<\/a>.\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 <\/p>\n

\n About OptumRx
<\/b>OptumRx provides a full spectrum of pharmacy care services through its network of more than 67,000 retail pharmacies, multiple home delivery, specialty and community health pharmacies and through the provision of in-home and pharmacy infusion services. OptumRx manages limited and ultra-limited distribution drugs in oncology, HIV, pain management and ophthalmology and serves the growing pharmacy needs of people with behavioral health and substance use disorders, particularly Medicare and Medicaid beneficiaries.<\/p>\n

OptumRx’s comprehensive whole-person approach to pharmacy care services integrates demographic, medical, laboratory, pharmaceutical and other clinical data and applies analytics to drive clinical care insight to support care treatments and compliance, benefiting clients and individual consumers through enhanced services, elevated clinical quality and cost trend management.<\/p>\n

\n About Talicia\u00ae<\/sup>\u00a0(omeprazole magnesium, amoxicillin and rifabutin)<\/b>\n <\/p>\n

\n INDICATION AND USAGE\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0
<\/b>Talicia is a three-drug combination of omeprazole, a proton pump inhibitor, amoxicillin, a penicillin-class antibacterial, and rifabutin, a rifamycin antibacterial\u00ad\u00ad, indicated for the treatment of\u00a0Helicobacter pylori\u00a0<\/i>infection in adults.\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0
\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0
To reduce the development of drug-resistant bacteria and maintain the effectiveness of Talicia and other antibacterial drugs, Talicia should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria.\u00a0<\/p>\n

\n IMPORTANT SAFETY INFORMATION <\/b>\n <\/p>\n

Talicia contains omeprazole, a proton pump inhibitor (PPI), amoxicillin, a penicillin-class antibacterial and rifabutin, a rifamycin antibacterial. It is contraindicated in patients with known hypersensitivity to any of these medications, any other components of the formulation, any other beta-lactams or any other rifamycin.<\/p>\n

Talicia is contraindicated in patients receiving rilpivirine-containing products.<\/p>\n

Talicia is contraindicated in patients receiving delavirdine or voriconazole.<\/p>\n

Serious and occasionally fatal hypersensitivity reactions have been reported with omeprazole, amoxicillin and rifabutin.<\/p>\n

\n Clostridioides difficile<\/i>-associated diarrhea (CDAD) has been reported with use of nearly all antibacterial agents and may range from mild diarrhea to fatal colitis.
Talicia may cause fetal harm. Talicia is not recommended for use in pregnancy.<\/p>\n

Talicia may reduce the efficacy of hormonal contraceptives. An additional non-hormonal method of contraception is recommended when taking Talicia.<\/p>\n

Talicia should not be used in patients with hepatic impairment or severe renal impairment.<\/p>\n

Acute Interstitial Nephritis has been observed in patients taking PPIs and penicillins.<\/p>\n

Cutaneous lupus erythematosus (CLE) and systemic lupus erythematosus (SLE) have been reported in patients taking PPIs. These events have occurred as both new onset and exacerbation of existing autoimmune disease.<\/p>\n

The most common adverse reactions (\u22651%) were diarrhea, headache, nausea, abdominal pain, chromaturia, rash, dyspepsia, oropharyngeal pain, vomiting, and vulvovaginal candidiasis.<\/p>\n

To report SUSPECTED ADVERSE REACTIONS, contact RedHill Biopharma INC. at
1-833-ADRHILL (1-833-237-4455) or FDA at 1-800-FDA-1088 or www.fda.gov\/medwatch<\/a>. \u00a0 <\/p>\n

Full prescribing information for Talicia\u00a0is available at\u00a0www.Talicia.com<\/a><\/p>\n

\n This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Such statements may be preceded by the words “intends,” “may,” “will,” “plans,” “expects,” “anticipates,” “projects,” “predicts,” “estimates,” “aims,” “believes,” “hopes,” “potential” or similar words. Forward-looking statements are based on certain assumptions and are subject to various known and unknown risks and uncertainties, many of which are beyond the Company’s control and cannot be predicted or quantified, and consequently, actual results may differ materially from those expressed or implied by such forward-looking statements. Such risks and uncertainties include, without limitation, the risk that Company will be unable to secure additional Pharmacy Benefit Management formulary coverage for Talicia\u00ae<\/sup>, as well as risks and uncertainties associated with (i) the initiation, timing, progress and results of the Company’s research, manufacturing, pre-clinical studies, clinical trials, and other therapeutic candidate development efforts, and the timing of the commercial launch of its commercial products and ones it may acquire or develop in the future; (ii) the Company’s ability to advance its therapeutic candidates into clinical trials or to successfully complete its pre-clinical studies or clinical trials or the development of a commercial companion diagnostic for the detection of MAP; (iii) the extent and number and type of additional studies that the Company may be required to conduct and the Company’s receipt of regulatory approvals for its therapeutic candidates, and the timing of other regulatory filings, approvals and feedback; (iv) the manufacturing, clinical development, commercialization, and market acceptance of the Company’s therapeutic candidates and Talicia\u00ae<\/sup>; (v) the Company’s ability to successfully commercialize and promote Talicia\u00ae<\/sup>, and Aemcolo\u00ae <\/sup>and Movantik\u00ae<\/sup><\/i>; (vi) the Company’s ability to establish and maintain corporate collaborations; (vii) the Company’s ability to acquire products approved for marketing in the U.S. that achieve commercial success and build its own marketing and commercialization capabilities; (viii) the interpretation of the properties and characteristics of the Company’s therapeutic candidates and the results obtained with its therapeutic candidates in research, pre-clinical studies or clinical trials; (ix) the implementation of the Company’s business model, strategic plans for its business and therapeutic candidates; (x) the scope of protection the Company is able to establish and maintain for intellectual property rights covering its therapeutic candidates and its ability to operate its business without infringing the intellectual property rights of others; (xi) parties from whom the Company licenses its intellectual property defaulting in their obligations to the Company; (xii) estimates of the Company’s expenses, future revenues, capital requirements and needs for additional financing; (xiii) the effect of patients suffering adverse experiences using investigative drugs under the Company’s Expanded Access Program; (xiv) competition from other companies and technologies within the Company’s industry; and (xv) the hiring and employment commencement date of executive managers. More detailed information about the Company and the risk factors that may affect the realization of forward-looking statements is set forth in the Company’s filings with the Securities and Exchange Commission (SEC), including the Company’s Annual Report on Form 20-F filed with the SEC <\/i>
\n on March 18, 2021. All forward-looking statements included in this press release are made only as of the date of this press release. The Company assumes no obligation to update any written or oral forward-looking statement, whether as a result of new information, future events or otherwise unless required by law.<\/i>\n <\/p>\n

\n\n\n
\n

\u00a0<\/p>\n

\n
\n Company contact:<\/b>
\n <\/span>\n <\/p>\n

\n Adi Frish<\/span>\n <\/p>\n

\n Chief Corporate & Business Development Officer<\/span>\n <\/p>\n

\n RedHill Biopharma<\/span>\n <\/p>\n

\n +972-54-6543-112<\/span>\n <\/p>\n

\n
\n adi@redhillbio.com<\/a>
\n
\n <\/span>\n <\/p>\n<\/td>\n

\n

\u00a0<\/p>\n

\n
\n Media contacts:<\/b>
\n <\/span>\n <\/p>\n

\n
\n U.S.:<\/b> Bryan Gibbs, Finn Partners<\/span>\n <\/p>\n

\n +1 212 529 2236<\/span>\n <\/p>\n

\n
\n bryan.gibbs@finnpartners.com<\/a>
\n <\/span>\n <\/p>\n

\n
\n UK:<\/b> Amber Fennell, Consilium<\/span>\n <\/p>\n

\n +44 (0) 7739 658 783 \u00a0<\/span>\n <\/p>\n

\n
\n fennell@consilium-comms.com<\/a>
\n <\/span>\n <\/p>\n<\/td>\n<\/tr>\n<\/table><\/div>\n

\n

\n

\n

[1] Talicia\u00ae<\/sup> (omeprazole magnesium, amoxicillin and rifabutin) delayed-release capsules 10 mg\/250 mg\/12.5 mg is indicated for the treatment of Helicobacter pylori<\/i> (H. pylori<\/i>) infection in adults. For full prescribing information see: www.Talicia.com<\/a>.<\/p>\n

[2] Defined as the PK population which included those subjects in the ITT population who had demonstrated presence of any component of investigational drug at visit 3 (approx. day 13) or had undetected levels drawn >250 hours after the last dose.<\/p>\n

[3] The pivotal Phase 3 study with Talicia\u00ae<\/sup> demonstrated 84% eradication of H. pylori<\/i> infection with Talicia\u00ae<\/sup> vs. 58% in the active comparator arm (ITT analysis, p<0.0001).<\/p>\n

[4] Hooi JKY et al. Global Prevalence of Helicobacter pylori<\/i> Infection: Systematic Review and Meta-Analysis. Gastroenterology 2017; 153:420-429.<\/p>\n

[5] IQVIA Custom Study for RedHill Biopharma, 2019<\/p>\n

[6] Lamb A et al. Role of the Helicobacter pylori<\/i>\u2013Induced inflammatory response in the development of gastric cancer. J Cell Biochem 2013;114.3:491-497.<\/p>\n

[7] NIH \u2013 Helicobacter pylori<\/i> and Cancer, September 2013<\/span>.<\/p>\n

[8] Hu Q et al. Gastric mucosa-associated lymphoid tissue lymphoma and Helicobacter pylori<\/i> infection: a review of current diagnosis and management. Biomarker research 2016;4.1:15.<\/p>\n

[9] National Cancer Institute, Surveillance, Epidemiology, and End Results Program (SEER).<\/p>\n

[10] Malfertheiner P. et al. Management of\u00a0Helicobacter pylori<\/i>\u00a0infection – the Maastricht IV\/ Florence Consensus Report, Gut 2012;61:646-664; O’Connor A. et al. Treatment of\u00a0Helicobacter pylori\u00a0<\/i>Infection 2015, Helicobacter 20 (S1) 54-61; Venerito M. et al. Meta-analysis of bismuth quadruple therapy versus clarithromycin triple therapy for empiric primary treatment of\u00a0Helicobacter pylori<\/i>\u00a0infection. Digestion 2013;88(1):33-45.<\/p>\n

[11] Full prescribing information for Movantik\u00ae<\/sup> (naloxegol) is available at: www.Movantik.com<\/a>.\u00a0\u00a0 <\/p>\n

[12] Full prescribing information for Talicia\u00ae<\/sup> (omeprazole magnesium, amoxicillin and rifabutin) is available at: www.Talicia.com<\/a>. \u00a0\u00a0\u00a0\u00a0\u00a0\u00a0<\/p>\n

[13] Full prescribing information for Aemcolo\u00ae<\/sup> (rifamycin) is available at: www.Aemcolo.com<\/a>.<\/p>\n

\n \"Cision\" View original content:https:\/\/www.prnewswire.com\/news-releases\/redhill-biopharma-significantly-extends-unrestricted-commercial-coverage-for-talicia-with-optumrx-301337226.html<\/a><\/p>\n

SOURCE RedHill Biopharma Ltd.<\/p>\n<\/p><\/div>\n

\"\"<\/p>\n","protected":false},"excerpt":{"rendered":"

Addition of Talicia\u00ae by OptumRx significantly extends Commercial patient access to Talicia\u00ae through this leader in U.S. healthcare Patient access to Talicia now extends to greater than 8 out of 10 covered U.S. Commercial lives Talicia\u00ae is the first and only FDA-approved rifabutin-based therapy for H. pylori infection, designed as a first-line option to address the high resistance of H. pylori bacteria to standard-of-care therapies H. pylori bacterial infection is a Group 1 carcinogen and the strongest risk factor for gastric cancer; H. pylori affects approximately 35% of the U.S. population PR Newswire TEL-AVIV, Israel and RALEIGH, N.C., July 20, 2021 \/PRNewswire\/ —\u00a0RedHill Biopharma Ltd. (Nasdaq: RDHL) (“RedHill” or the “Company”), a specialty biopharmaceutical company, today announced that OptumRx, part … <\/p>\n

Continue reading “RedHill Biopharma Significantly Extends Unrestricted Commercial Coverage for Talicia\u00ae with OptumRx”<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-514887","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"\nRedHill Biopharma Significantly Extends Unrestricted Commercial Coverage for Talicia\u00ae with OptumRx - Market Newsdesk<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.marketnewsdesk.com\/index.php\/redhill-biopharma-significantly-extends-unrestricted-commercial-coverage-for-talicia-with-optumrx\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"RedHill Biopharma Significantly Extends Unrestricted Commercial Coverage for Talicia\u00ae with OptumRx - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"Addition of Talicia\u00ae by OptumRx significantly extends Commercial patient access to Talicia\u00ae through this leader in U.S. healthcare Patient access to Talicia now extends to greater than 8 out of 10 covered U.S. Commercial lives Talicia\u00ae is the first and only FDA-approved rifabutin-based therapy for H. pylori infection, designed as a first-line option to address the high resistance of H. pylori bacteria to standard-of-care therapies H. pylori bacterial infection is a Group 1 carcinogen and the strongest risk factor for gastric cancer; H. pylori affects approximately 35% of the U.S. population PR Newswire TEL-AVIV, Israel and RALEIGH, N.C., July 20, 2021 \/PRNewswire\/ —\u00a0RedHill Biopharma Ltd. (Nasdaq: RDHL) (“RedHill” or the “Company”), a specialty biopharmaceutical company, today announced that OptumRx, part … Continue reading "RedHill Biopharma Significantly Extends Unrestricted Commercial Coverage for Talicia\u00ae with OptumRx"\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.marketnewsdesk.com\/index.php\/redhill-biopharma-significantly-extends-unrestricted-commercial-coverage-for-talicia-with-optumrx\/\" \/>\n<meta property=\"og:site_name\" content=\"Market Newsdesk\" \/>\n<meta property=\"article:published_time\" content=\"2021-07-20T11:04:12+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/mma.prnewswire.com\/media\/1334141\/RedHill_Biopharma_Logo.jpg\" \/>\n<meta name=\"author\" content=\"Newsdesk\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Newsdesk\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"11 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/redhill-biopharma-significantly-extends-unrestricted-commercial-coverage-for-talicia-with-optumrx\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/redhill-biopharma-significantly-extends-unrestricted-commercial-coverage-for-talicia-with-optumrx\\\/\"},\"author\":{\"name\":\"Newsdesk\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/#\\\/schema\\\/person\\\/482f27a394d4fda80ecb5499e519d979\"},\"headline\":\"RedHill Biopharma Significantly Extends Unrestricted Commercial Coverage for Talicia\u00ae with OptumRx\",\"datePublished\":\"2021-07-20T11:04:12+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/redhill-biopharma-significantly-extends-unrestricted-commercial-coverage-for-talicia-with-optumrx\\\/\"},\"wordCount\":2153,\"image\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/redhill-biopharma-significantly-extends-unrestricted-commercial-coverage-for-talicia-with-optumrx\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/mma.prnewswire.com\\\/media\\\/1334141\\\/RedHill_Biopharma_Logo.jpg\",\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/redhill-biopharma-significantly-extends-unrestricted-commercial-coverage-for-talicia-with-optumrx\\\/\",\"url\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/redhill-biopharma-significantly-extends-unrestricted-commercial-coverage-for-talicia-with-optumrx\\\/\",\"name\":\"RedHill Biopharma Significantly Extends Unrestricted Commercial Coverage for Talicia\u00ae with OptumRx - 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