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MannKind Corporation (MNKD)

NasdaqGS - NasdaqGS Real Time Price. Currency in USD
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2.9500-0.1100 (-3.59%)
At close: 4:00PM EST

2.9800 +0.03 (1.02%)
After hours: 6:23PM EST

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Previous Close3.0600
Bid2.9400 x 47300
Ask2.9600 x 3200
Day's Range2.9200 - 3.0850
52 Week Range0.8000 - 3.2000
Avg. Volume2,582,889
Market Cap686.173M
Beta (5Y Monthly)2.10
PE Ratio (TTM)N/A
Earnings DateN/A
Forward Dividend & YieldN/A (N/A)
Ex-Dividend DateN/A
1y Target EstN/A
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    The Daily Biotech Pulse: Amarin Surges On Vascepa Data, Mesoblast Rallies On Novartis Deal, Decision Day For Eiger

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(RTRX) * Trillium Therapeutics Inc (NASDAQ: TRIL) * Twist Bioscience Corp (NASDAQ: TWST) * Urovant Sciences Ltd (NASDAQ: UROV) * Veracyte Inc (NASDAQ: VCYT)Down In The Dumps (Biotech Stocks Hitting 52-week Lows Nov. 19) * Benitec Biopharma Inc (NASDAQ: BNTC) * Kiromic Biopharma Inc (NASDAQ: KRBP) * Polypid Ltd (NASDAQ: PYPD)Stocks In Focus Amarin's Late-Stage Vascepa Trial In China Meets Study Goals Amarin Corporation plc (NASDAQ: AMRN) announced positive, statistically significant top-line results from a Phase 3 clinical trial of its fish oil pill Vascepa conducted in China by its partner, Edding. The study, which investigated Vascepa as a treatment for patients with very high triglycerides, met its primary efficacy endpoint as defined in the clinical trial protocol and demonstrated a safety profile similar to placebo, the company said.The company said the findings are being prepared to support Edding's dossier for seeking regulatory approval of Vascepa in mainland China.Amarin shares were jumping 18.06% to $5.36 premarket Friday.Mesoblast Strikes Stem Cell Therapy Collaboration Agreement With Novartis Mesoblast limited (NASDAQ: MESO) announced an exclusive worldwide license and collaboration agreement with Novartis AG (NYSE: NVSP) for the development of its mesenchymal stromal cell product remestemcel-L, with an initial focus on the development of the treatment of acute respiratory distress syndrome, including that associated with COVID-19.The agreement provides for Novartis making a $50-million upfront payment, including $25 million in equity. Mesoblast may also receive a total of $505 million pending achievement of precommercialization milestones for ARDS indications. It could also receive additional payments post-commercialization of up to $750 million based on achieving certain sales milestones and tiered double-digit royalties on product sales.Separately, Mesoblast reported first-quarter revenue of $1.3 million, down from $17 million in the year-ago quarter, which included $15 million in upfront milestone payment received for the strategic partnership with Grunenthal GmbH.The net loss per share widened from 1.10 cents to 4.21 cents.The stock jumped 17.73% premarket to $13.88. Lilly's Drug Combo Issued Emergency Use Authorization For COVID-19 Eli Lilly And Co (NYSE: LLY) and Incyte Corporation (NASDAQ: INCY) said the FDA issued an emergency use authorization for the distribution and emergency use of baricitinib to be used in combination with Gilead Sciences, Inc.'s (NASDAQ: GILD) remdesivir in hospitalized adult and pediatric patients two years of age or older with suspected or laboratory confirmed COVID-19 who require supplemental oxygen, invasive mechanical ventilation or extracorporeal membrane oxygenation.Baricitinib, discovered by Incyte, has been licensed to Lilly.Separately, Lilly announced a R&D and exclusive license agreement to utilize Precision BioSciences Inc's (NASDAQ: DTIL) proprietary ARCUS genome editing platform for the R&D of potential in vivo therapies for genetic disorders, with an initial focus on Duchenne muscular dystrophy and two other undisclosed gene targets.Lilly shares were up 0.7% premarket at $144.41, while Gilead shares were down 1.62% at $59.65.Precision BioSciences shares were jumping 28.1% to $12.40 in premarket trading Friday.Pfizer, BioNTech To Submit EUA For Coronavirus Vaccine Friday Pfizer Inc. (NYSE: PFE) and BioNTech SE - ADR (NASDAQ: BNTX) confirmed that they would submit emergency use application for their coronavirus vaccine candidate to the FDA on Friday.In premarket trading Friday, Pfizer was adding 1.6% to $36.77 and BioNTech shares were rallying 6.99% to $101.57.Related Link: The Week Ahead In Biotech: The Vaccine Updates, Drug Presentations, And FDA Decisions That Will Move The MarketsBeiGene's In-Licensed Osteoporosis Drug Gets Label Expansion In China Beigene Ltd (NASDAQ: BGNE) said the China National Medical Products Administration has approved Xgeva for the prevention of skeletal-related events in patients with bone metastases from solid tumors and in patients with multiple myeloma.Developed by Amgen, Inc. (NASDAQ: AMGN) and licensed to BeiGene in China under a strategic collaboration commenced earlier this year, Xgeva is also approved and marketed in China for the treatment of adults and skeletally mature adolescents with giant cell tumor of the bone that is unresectable or where surgical resection is likely to result in severe morbidity.MannKind Gets Final Development Milestone Payment Of $12.5M For Hypertension Drug MannKind Corporation (NASDAQ: MNKD) said it has achieved the final development milestone under its licensing and collaboration agreement with United Therapeutics Corporation (NASDAQ: UTHR) for the development and commercialization of a dry powder formulation of treprostinil. The fourth milestone payment fetched MannKind $12.5 million.View more earnings on IBBTreprostinil Technosphere is an investigational product currently being evaluated in clinical trials for the treatment of pulmonary arterial hypertension."We are looking forward to working with United Therapeutics during the first part of 2021 to prepare an FDA submission for TreT," said MannKind CEO Michael Castagna.In after-hours trading, MannKind shares were up 2.54% to $2.83.AstraZeneca's Imfinzi Approved For Additional Dosage In Lung, Bladder Cancers AstraZeneca plc (NASDAQ: AZN) said its Imfinzi has been approved in the U.S. for an additional dosing option, a 1,500mg fixed dose every four weeks in the approved indications of unresectable Stage 3 non-small cell lung cancer after chemoradiation therapy and previously treated advanced bladder cancer.In premarket trading Friday, the shares were up 2.07% to $55.15.Aptevo Confirms Takeover Interest For $50/Share In Cash Aptevo Therapeutics Inc (NASDAQ: APVO) confirmed it has received an unsolicited non-binding indication of interest from Tang Capital Partners, LP expressing its interest in acquiring all of the outstanding shares of Aptevo that it does not already own for $50 per share in cash.While recommending that shareholders take no action at this juncture, the company said its board will carefully evaluate and consider this indication of interest in due course in the context of Aptevo's strategic plans, and its ongoing review of a broad range of opportunities to enhance stockholder value.After jumping 29.10% to $45.69 in regular trading on the speculation, the stock was down slightly premarket at $45.65.Affimed Reports Positive Phase 1 Results For Cancer Drug Combo Affimed NV (NASDAQ: AFMD) announced the publication in Blood of positive results for the Phase 1b study of AFM13, a CD30/CD16A innate cell engager, in combination with Merck & Co., Inc.'s (NYSE: MRK) Keytruda.The results demonstrate promising signs of efficacy including an objective response rate of 88% at the highest treatment dose, as well as a complete response of 46% in patients with relapsed/refractory Hodgkin lymphoma. 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The shares of the Broadview Heights, Ohio-based company will be listed on the Nasdaq under the ticker symbol "SHC."Related Link: Attention Biotech Investors: Mark Your Calendar For These November PDUFA Dates See more from Benzinga * Click here for options trades from Benzinga * The Daily Biotech Pulse: Aquestive's Positive FDA Meeting, Prevail Awarded Patent, Neuro-Oncology Conference Gets Underway * The Daily Biotech Pulse: Kazia Jumps On Data Readout, Clinical Hold On Cellectis' Blood Cancer Study Lifted(C) 2020 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.

  • Bearish: Analysts Just Cut Their MannKind Corporation (NASDAQ:MNKD) Revenue and EPS estimates
    Simply Wall St.

    Bearish: Analysts Just Cut Their MannKind Corporation (NASDAQ:MNKD) Revenue and EPS estimates

    The analysts covering MannKind Corporation (NASDAQ:MNKD) delivered a dose of negativity to shareholders today, by...

  • MannKind Stock: Next Stop, $4?

    MannKind Stock: Next Stop, $4?

    2020 has provided a reversal of fortune for MannKind (MNKD). After several difficult years, the diabetes focused biotech’s stock has been on the mend and is up by 77% year-to-date.However, according to BTIG analyst Robert Hazlett, there’s plenty of upside yet to come. The 5-star analyst has a Buy rating on MNKD shares along with a $4 price target. Investors could be pocketing gains of a hefty 75%, should Hazlett’s thesis play out over the coming months. (To watch Hazlett’s track record, click here)Hazlett’s confidence in MannKind is based on 2 main drivers; The first is the increasing sales of the company's flagship product, Afrezza -- a portable inhaling device consisting of a dry powder formulation of human insulin for diabetes management.In Q3, Afrezza’s US net revenue increased by 27% year-over-year to $7.3 million. Hazlett puts Afrezza’s strong performance down to “increased pricing, favorable mix shift toward larger cartridges, and steady Afrezza script demand of +8% yr/yr.”The analyst paints an optimistic picture regarding its future: “We believe Afrezza's 3Q performance bodes well for MannKind and its long term commercialization efforts, as the company has stepped on the accelerator a bit in terms of marketing, with more reps to get the Afrezza message out, as it can rely on published data that show good glycemic control for ultrarapid acting Afrezza, among other favorable considerations.”The other catalyst concerns the company’s partnership with United Therapeutics on the development of Treprostinil Technosphere, a dry powder formulation of the already approved treprostinil (TreT). The medication is currently in a Phase 3 study for the treatment of pulmonary arterial hypertension (PAH), which is expected to wrap before the end of the year. An FDA filing is mooted for early 2021.MannKind should see a development milestone payment of $12.5 million in Q4, while Hazlett estimates there could be a huge market for the treatment once approved.“We continue to believe TreT is transformative for MannKind. We model a 2021 launch and peak revenues of ~$1B with a double-digit royalty to MannKind,” Hazlett noted.Over the past 3 months, only two other analysts have thrown the hat in with a view on the inhaled insulin maker. The two additional Buy ratings provide MNKD with a Strong Buy consensus rating. With an average price target of $3.17, investors stand to take home an 39% gain, should the target be met over the next 12 months. (See MNKD stock analysis on TipRanks)To find good ideas for stocks trading at attractive valuations, visit TipRanks’ Best Stocks to Buy, a newly launched tool that unites all of TipRanks’ equity insights.Disclaimer: The opinions expressed in this article are solely those of the featured analyst. The content is intended to be used for informational purposes only. It is very important to do your own analysis before making any investment.