Dating durect

That's because it has another drug compound known as DUR-928, which is an orally bioavailable small molecule; it is being tested in three different indications, each of which targets large markets." "Durect Corp. In part two of his interview with The Life Sciences Report, Ed Arce, managing director in equity research and senior analyst covering companies in the biopharmaceuticals and specialty pharmaceuticals sectors for H. Wainwright, and organizer of the recent inaugural NASH Investor Conference, says that small companies are rushing to fill the pipeline, with numerous compounds in trials. commercialization agreement with Sandoz AG, as an important validating milestone. positive Phase 3 data in 4Q, DURECT expects to resubmit the NDA in 1Q18, followed by an 8-month Priority Review by FDA leading to a likely product launch by Sandoz in late 2018." "We are especially optimistic about DURECT Corp.'s epigenetic regulator DUR-928, which holds great market potential for multiple indications, including NAFLD/NASH and acute kidney injury. Sandoz has a very strong sales/marketing team and has a great presence in the US. continue to be optimistic about Durect's story and maintain our price target at per share based on the progress the company has made in advancing its candidates. Durect announced on June 22nd that it has completed enrollment the PERSIST Phase III trial ahead of schedule. Company expects to announce topline data in the fourth quarter of 2017.is partnered on two drug development programs (RBP-7000 and Remoxy) that may receive U. "In terms of catalysts, we continue to expect DURECT Corp.'s initiation of Phase 2 for its primary sclerosing cholangitis program before 2017E. Multiple Phase II trials will be initiated in 2017. "Highlights of the second quarter include reaching a commercialization agreement with Sandoz, completing enrollment of a pivotal Phase III trial for this asset, and completing drug-drug interaction studies and a Phase Ib trial for DUR-928. Durect completed drug-drug interaction studies of DUR-928, which showed no evidence of likely drug interactions. .a Phase Ib trial of DUR-928 also demonstrated that the compound is well-tolerated in patients with moderate to severe kidney function impairment." "DURECT Corp.'s Posimir remains front and center, in our opinion, as DRRX was able to execute the US commercialization agreement with Sandoz. continue to see Sandoz as an ideal partner due to their impressive hospital presence and sales expertise. DRRX reiterated their intent to initiate a Phase 2 trial for oral DUR-928 in primary sclerosing cholangitis (PSC) by YE17. DURECT believes the drug qualifies for 5-year statutory exclusivity as a new chemical entity. .anticipate the initiation of a Phase 2b trial in acute kidney injury, and especially a potentially positive Phase 2a readout in an undisclosed chronic cholestatic liver disease, both expected later this year, to attract investor attention and interest in the program and DRRX." "We are especially optimistic about DURECT Corp.'s epigenomic regulator DUR-928, which holds great market potential for multiple indications, including nonalcoholic fatty liver disease/nonalcoholic steatohepatitis and acute kidney injury; multiple Phase 2 trials will be initiated in 2017.Our members choose us in order to find lasting love, and because they are seeking a deeper connection. Understanding your personality is just one of our four core considerations when matching you up with potential partners; your location in the US, your level of education & income, and your own search preferences also decide who we’ll introduce you to.We don’t want to waste your time, so we send you just a handful of new matches daily so you can take the time to really consider each in turn.DURECT's epigenomic regulator program includes the lead molecule DUR-928 in Phase 1 development. company reported net income of .1M in Q3/17, as compared to a net loss of .8M in Q3/16. 30, it had cash and investments of .8M, which compared to .6M at June 30, 2017." -Zacks Small-Cap Research "DURECT Corp.DUR-928 is an endogenous small molecule that modulates lipid homeostasis, inflammation and cell survival. recorded a total revenue of .7M in Q3/17 ended Sept. reported its Q3/17 last night after the close, roughly in line with expectations after adjusting for one-time events. company ended Q3/17 with cash and investments of .8M, which should be sufficient for the next couple years. believe 2018 could prove to be a pivotal year for DURECT." "DURECT Corp. DURECT is also finalizing a study protocol for a Phase 2 proof-of-concept study of topically applied DUR-928." "We are especially optimistic about DURECT Corp.'s epigenetic regulator DUR-928, which holds great market potential for multiple indications, including nonalcoholic fatty liver disease/nonalcoholic steatohepatitis and acute kidney injury; multiple Phase 2 trials will be initiated in 2017.

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They also happen to be the people who verify each and every new profile on our site, and who’ll you will contact once you’ve met your perfect match and no longer require our services… Be sure to check out our online magazine – from first date to How To Propose, we’re with you every step of the way! With marriage minded singles from all walks of life, you’re bound to find someone who suits you.We also believe it will be starting Phase 2 trials for DUR-928 in both its acute kidney trial as well as in topical psoriasis in H1/18. look forward to the company's initiation of three Phase 2 trials in the near term followed by potential readout of all three in 2018." "The next expected milestone for DURECT Corp. patent rights to Indivior in exchange for a .5M nonrefundable, upfront fee. .while we view Indivior deal positively as DURECT is able to gain exposure to a late stage asset in a lucrative deal, we remain focused on Phase 3 PERSIST data expected 4Q17. are positive on POSIMIR given the big pharma validation provided by the development and commercialization agreement with Sandoz AG. The deal not only boosts Durect's balance sheet, but also validate the company's long-acting risperidone formulation technology." "DURECT Corp. DURECT has received an upfront payment of .5 million, and is also eligible for million in the event of FDA approval for RBP-7000, and single digit percentage payments based on net sales in the US. .given the realized near-term revenue, and potential recurring, long-term revenues, we view this agreement as a favorable development for DURECT." "DURECT Corp. DURECT announced the completion of enrollment at 296 patients, ahead of schedule and 12% above its 264-patient target. Management still anticipates PERSIST to read out in 4Q17. On the back of a solid deal with Sandoz and with more catalysts to come in 2017 such as Posimir Phase 3 readout in 4Q17 and IND filings for DUR-928, we see potential near-term upside." "There are good reasons to believe DURECT Corp.'s upcoming Phase III PERSIST results will be positive and finally pave the road to approval. Posimirs higher dose of bupivacaine and and longer duration of efficacy relative to Exparel, along with competitive pricing, will enable DURECT to carve a niche with surgeons seeking extended pain relief. .based on our NPV analysis, Posimir contributes

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We also believe it will be starting Phase 2 trials for DUR-928 in both its acute kidney trial as well as in topical psoriasis in H1/18. look forward to the company's initiation of three Phase 2 trials in the near term followed by potential readout of all three in 2018." "The next expected milestone for DURECT Corp. patent rights to Indivior in exchange for a $12.5M nonrefundable, upfront fee. .while we view Indivior deal positively as DURECT is able to gain exposure to a late stage asset in a lucrative deal, we remain focused on Phase 3 PERSIST data expected 4Q17. are positive on POSIMIR given the big pharma validation provided by the development and commercialization agreement with Sandoz AG. The deal not only boosts Durect's balance sheet, but also validate the company's long-acting risperidone formulation technology." "DURECT Corp. DURECT has received an upfront payment of $12.5 million, and is also eligible for $5 million in the event of FDA approval for RBP-7000, and single digit percentage payments based on net sales in the US. .given the realized near-term revenue, and potential recurring, long-term revenues, we view this agreement as a favorable development for DURECT." "DURECT Corp. DURECT announced the completion of enrollment at 296 patients, ahead of schedule and 12% above its 264-patient target. Management still anticipates PERSIST to read out in 4Q17. On the back of a solid deal with Sandoz and with more catalysts to come in 2017 such as Posimir Phase 3 readout in 4Q17 and IND filings for DUR-928, we see potential near-term upside." "There are good reasons to believe DURECT Corp.'s upcoming Phase III PERSIST results will be positive and finally pave the road to approval. Posimirs higher dose of bupivacaine and and longer duration of efficacy relative to Exparel, along with competitive pricing, will enable DURECT to carve a niche with surgeons seeking extended pain relief. .based on our NPV analysis, Posimir contributes $1.18/share to our $3 Target Price valuation." "DURECT Corp. focused on results of a pharmacokinetic study with DUR-928 for the treatment of NASH patients. DURECT provided a 4Q16 earnings update and indicated that they are actively working towards commencing a Phase 2 trial with an oral formulation of DUR-928 for PSC." "Given the clean safety profile and biomarker activity observed in DURECT Corp.'s Phase 1 studies of NASH and renally impaired patients. anticipate continued positive progress with DUR-928 to drive value-creating optionality for DURECT management regarding indications and potential collaborations. We continue to be positive about the company's story." -Zacks Small-Cap Research "Conatus Pharmaceuticals Inc.

is the initiation of a Phase 2 study during Q4/17 using oral DUR-928 for primary sclerosing cholangitis. company also intends to conduct a Phase 2 study with an injectable formulation of DUR-928 in the near term, and DURECT also has formulated topical versions of DUR-928 that have potential to treat inflammatory skin disorders." "DURECT Corp. We view the $20M upfront payment as a signal of confidence for near-term approval prospects, and the lucrative back-end milestone/royalty payment structure as testament to the drug's significant longterm market potential." "DURECT Corp. This assignment may provide further intellectual property protection for RBP-7000, Indivior's investigational once-monthly injectable risperidone product for the treatment of schizophrenia. announced that they have come to an agreement to sell a family of US patents to Indivior, which pertain to the intellectual protection of Indivior's once-monthly, injectable risperidone treatment RBP-7000 in development for schizophrenia. confirmed that it expects to complete patient follow-up visits this quarter, and announce top-line results from the Phase 3 PERSIST study in 4Q17. We forecast Posimir approval/launch in 1H/19 and project FY25 peak unadjusted sales of $381M, yielding $65M in royalties to Durect. We assume a price point of ~$285/treatment, in-line with Exparel. is a biopharmaceutical company with a rich development pipeline that includes an epigenetic regulator program and a portfolio of 505(b)(2) programs. Company is focused on the development of DUR-928, an endogenous epigenetic regulator with potential in chronic liver diseases, acute organ injury, and inflammatory conditions. DURECT Corporation announced it has completed patient enrollment into its pivotal Phase 3 trial of Posimir, an investigational extended-release depot utilizing DURECT's patented SABER technology intended to continuously deliver bupivacaine to the surgical site for continuous pain relief for up to three days post surgery. This was an open-label Phase 1b study that assessed DUR-928 in NASH patients and matched control subjects (MCS). indicate that NASH patients had 10-30% greater drug exposure as compared to MCS, and DUR-928 was well tolerated overall. .preliminary biomarker data indicate reductions from baseline following dosing of DUR-928 in f CK-18, c CK-18, IL-18, and bilirubin. Beyond NASH, DURECT disclosed its Phase 2 development plans in an orphan disease, primary sclerosing cholangitis (PSC). is the third recent deal in the NASH space and points to the potential value of drugs in development for this disease.

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They also happen to be the people who verify each and every new profile on our site, and who’ll you will contact once you’ve met your perfect match and no longer require our services… Be sure to check out our online magazine – from first date to How To Propose, we’re with you every step of the way! With marriage minded singles from all walks of life, you’re bound to find someone who suits you.We also believe it will be starting Phase 2 trials for DUR-928 in both its acute kidney trial as well as in topical psoriasis in H1/18. look forward to the company's initiation of three Phase 2 trials in the near term followed by potential readout of all three in 2018." "The next expected milestone for DURECT Corp. patent rights to Indivior in exchange for a $12.5M nonrefundable, upfront fee. .while we view Indivior deal positively as DURECT is able to gain exposure to a late stage asset in a lucrative deal, we remain focused on Phase 3 PERSIST data expected 4Q17. are positive on POSIMIR given the big pharma validation provided by the development and commercialization agreement with Sandoz AG. The deal not only boosts Durect's balance sheet, but also validate the company's long-acting risperidone formulation technology." "DURECT Corp. DURECT has received an upfront payment of $12.5 million, and is also eligible for $5 million in the event of FDA approval for RBP-7000, and single digit percentage payments based on net sales in the US. .given the realized near-term revenue, and potential recurring, long-term revenues, we view this agreement as a favorable development for DURECT." "DURECT Corp. DURECT announced the completion of enrollment at 296 patients, ahead of schedule and 12% above its 264-patient target. Management still anticipates PERSIST to read out in 4Q17. On the back of a solid deal with Sandoz and with more catalysts to come in 2017 such as Posimir Phase 3 readout in 4Q17 and IND filings for DUR-928, we see potential near-term upside." "There are good reasons to believe DURECT Corp.'s upcoming Phase III PERSIST results will be positive and finally pave the road to approval. Posimirs higher dose of bupivacaine and and longer duration of efficacy relative to Exparel, along with competitive pricing, will enable DURECT to carve a niche with surgeons seeking extended pain relief. .based on our NPV analysis, Posimir contributes $1.18/share to our $3 Target Price valuation." "DURECT Corp. focused on results of a pharmacokinetic study with DUR-928 for the treatment of NASH patients. DURECT provided a 4Q16 earnings update and indicated that they are actively working towards commencing a Phase 2 trial with an oral formulation of DUR-928 for PSC." "Given the clean safety profile and biomarker activity observed in DURECT Corp.'s Phase 1 studies of NASH and renally impaired patients. anticipate continued positive progress with DUR-928 to drive value-creating optionality for DURECT management regarding indications and potential collaborations. We continue to be positive about the company's story." -Zacks Small-Cap Research "Conatus Pharmaceuticals Inc.is the initiation of a Phase 2 study during Q4/17 using oral DUR-928 for primary sclerosing cholangitis. company also intends to conduct a Phase 2 study with an injectable formulation of DUR-928 in the near term, and DURECT also has formulated topical versions of DUR-928 that have potential to treat inflammatory skin disorders." "DURECT Corp. We view the $20M upfront payment as a signal of confidence for near-term approval prospects, and the lucrative back-end milestone/royalty payment structure as testament to the drug's significant longterm market potential." "DURECT Corp. This assignment may provide further intellectual property protection for RBP-7000, Indivior's investigational once-monthly injectable risperidone product for the treatment of schizophrenia. announced that they have come to an agreement to sell a family of US patents to Indivior, which pertain to the intellectual protection of Indivior's once-monthly, injectable risperidone treatment RBP-7000 in development for schizophrenia. confirmed that it expects to complete patient follow-up visits this quarter, and announce top-line results from the Phase 3 PERSIST study in 4Q17. We forecast Posimir approval/launch in 1H/19 and project FY25 peak unadjusted sales of $381M, yielding $65M in royalties to Durect. We assume a price point of ~$285/treatment, in-line with Exparel. is a biopharmaceutical company with a rich development pipeline that includes an epigenetic regulator program and a portfolio of 505(b)(2) programs. Company is focused on the development of DUR-928, an endogenous epigenetic regulator with potential in chronic liver diseases, acute organ injury, and inflammatory conditions. DURECT Corporation announced it has completed patient enrollment into its pivotal Phase 3 trial of Posimir, an investigational extended-release depot utilizing DURECT's patented SABER technology intended to continuously deliver bupivacaine to the surgical site for continuous pain relief for up to three days post surgery. This was an open-label Phase 1b study that assessed DUR-928 in NASH patients and matched control subjects (MCS). indicate that NASH patients had 10-30% greater drug exposure as compared to MCS, and DUR-928 was well tolerated overall. .preliminary biomarker data indicate reductions from baseline following dosing of DUR-928 in f CK-18, c CK-18, IL-18, and bilirubin. Beyond NASH, DURECT disclosed its Phase 2 development plans in an orphan disease, primary sclerosing cholangitis (PSC). is the third recent deal in the NASH space and points to the potential value of drugs in development for this disease.The trouble is, there are plenty of frivolous dating sites out there and choosing the wrong one will cost you time and energy, and won’t get you any closer to the altar either!

.18/share to our Target Price valuation." "DURECT Corp. focused on results of a pharmacokinetic study with DUR-928 for the treatment of NASH patients. DURECT provided a 4Q16 earnings update and indicated that they are actively working towards commencing a Phase 2 trial with an oral formulation of DUR-928 for PSC." "Given the clean safety profile and biomarker activity observed in DURECT Corp.'s Phase 1 studies of NASH and renally impaired patients. anticipate continued positive progress with DUR-928 to drive value-creating optionality for DURECT management regarding indications and potential collaborations. We continue to be positive about the company's story." -Zacks Small-Cap Research "Conatus Pharmaceuticals Inc.is the initiation of a Phase 2 study during Q4/17 using oral DUR-928 for primary sclerosing cholangitis. company also intends to conduct a Phase 2 study with an injectable formulation of DUR-928 in the near term, and DURECT also has formulated topical versions of DUR-928 that have potential to treat inflammatory skin disorders." "DURECT Corp. We view the M upfront payment as a signal of confidence for near-term approval prospects, and the lucrative back-end milestone/royalty payment structure as testament to the drug's significant longterm market potential." "DURECT Corp. This assignment may provide further intellectual property protection for RBP-7000, Indivior's investigational once-monthly injectable risperidone product for the treatment of schizophrenia. announced that they have come to an agreement to sell a family of US patents to Indivior, which pertain to the intellectual protection of Indivior's once-monthly, injectable risperidone treatment RBP-7000 in development for schizophrenia. confirmed that it expects to complete patient follow-up visits this quarter, and announce top-line results from the Phase 3 PERSIST study in 4Q17. We forecast Posimir approval/launch in 1H/19 and project FY25 peak unadjusted sales of 1M, yielding M in royalties to Durect. We assume a price point of ~5/treatment, in-line with Exparel. is a biopharmaceutical company with a rich development pipeline that includes an epigenetic regulator program and a portfolio of 505(b)(2) programs. Company is focused on the development of DUR-928, an endogenous epigenetic regulator with potential in chronic liver diseases, acute organ injury, and inflammatory conditions. DURECT Corporation announced it has completed patient enrollment into its pivotal Phase 3 trial of Posimir, an investigational extended-release depot utilizing DURECT's patented SABER technology intended to continuously deliver bupivacaine to the surgical site for continuous pain relief for up to three days post surgery. This was an open-label Phase 1b study that assessed DUR-928 in NASH patients and matched control subjects (MCS). indicate that NASH patients had 10-30% greater drug exposure as compared to MCS, and DUR-928 was well tolerated overall. .preliminary biomarker data indicate reductions from baseline following dosing of DUR-928 in f CK-18, c CK-18, IL-18, and bilirubin. Beyond NASH, DURECT disclosed its Phase 2 development plans in an orphan disease, primary sclerosing cholangitis (PSC). is the third recent deal in the NASH space and points to the potential value of drugs in development for this disease.The trouble is, there are plenty of frivolous dating sites out there and choosing the wrong one will cost you time and energy, and won’t get you any closer to the altar either!

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