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Protalix BioTherapeutics, Inc. (PLX)

NYSE American - NYSE American Delayed Price. Currency in USD
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4.9000+0.0700 (+1.45%)
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Previous Close4.8300
Bid4.8800 x 1100
Ask4.9000 x 900
Day's Range4.7000 - 5.0400
52 Week Range2.0400 - 7.0200
Avg. Volume692,118
Market Cap222.376M
Beta (5Y Monthly)2.83
PE Ratio (TTM)N/A
EPS (TTM)-0.2700
Earnings DateOct 30, 2020
Forward Dividend & YieldN/A (N/A)
Ex-Dividend DateN/A
1y Target Est13.00
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.
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  • PLX: A Busy Month
    Zacks Small Cap Research

    PLX: A Busy Month

    By John Vandermosten, CFA NYSE:PLX READ THE FULL PLX RESEARCH REPORT Over the last few weeks, Protalix Biotherapeutics, Inc. (NYSE:PLX) has posted several updates includ-ing the announcement of pricing and closing of its ~$40 million financing. The company has also con-summated an exclusive partnership with SarcoMed USA, presented BRIDGE data at the 17th Annual WORLDSymposium and reported topline

  • Benzinga

    Protalix's PRX–102 Monthly Treatment Shows Benefit In Fabry Disease

    Protalix BioTherapeutics Inc (NYSE: PLX) and its collaborating partner Chiesi Farmaceutici S.p.A. announced positive topline results from the BRIGHT Phase 3 trial evaluating pegunigalsidase alfa (PRX–102) for the potential treatment of Fabry disease. It is a genetic disorder in which the body cannot make an enzyme called alpha-galactosidase A, which is essential to breaking down globotriaosylceramide (Gb3 or GL-3), a type of fat that cells can use as building blocks. PRX–102 is a plant cell-expressed recombinant, PEGylated, cross-linked α–galactosidase–A product candidate that is, administered every four weeks. Results indicated that intravenous infusion of PRX–102 was well-tolerated, and stable clinical presentation was maintained. No new patients developed treatment-induced anti-drug antibodies following the switch to PRX–102 treatment. Study outcome measures showed plasma lyso–Gb3 concentrations remained stable during the study with a mean change of 3.01 nM from baseline to Week 52. Mean absolute change of eGFR values were stable during the 52–week treatment period, with a mean change from baseline of –1.27 mL/min/1.73 m2. The company will report final data from the study in the second half of 2021 Price Action: PLX increased 7.2% at $5.54 in premarket trading on the last check Tuesday. See more from BenzingaClick here for options trades from BenzingaProtalix BioTherapeutics Raises M Via Equity At 21% DiscountProtalix BioTherapeutics Perks Up On Alidornase Alfa Licensing Pact In Respiratory Conditions© 2021 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.

  • The Daily Biotech Pulse: Aridis To Study Antibody Cocktail For Coronavirus Variants, Revance & Protalix Data Readouts

    The Daily Biotech Pulse: Aridis To Study Antibody Cocktail For Coronavirus Variants, Revance & Protalix Data Readouts

    Here's a roundup of top developments in the biotech space over the last 24 hours. Scaling The Peaks (Biotech Stocks Hitting 52-week Highs Feb. 22) Acceleron Pharma Inc (NASDAQ: XLRN) Akari Therapeutics PLC (NASDAQ: AKTX) Annexon Inc (NASDAQ: ANNX) Applied Molecular Transport Inc. (NASDAQ: AMTI) AxoGen, Inc (NASDAQ: AXGN) Burning Rock Biotech Ltd (NASDAQ: BNR) Celcuity Inc (NASDAQ: CELC) (announced a $20 million common stock offering) Celldex Therapeutics, Inc. (NASDAQ: CLDX) Cerecor Inc (NASDAQ: CERC) Citius Pharmaceuticals Inc (NASDAQ: CTXR) DermTech Inc (NASDAQ: DMTK) Gemini Therapeutics Inc (NASDAQ: GMTX) Intra-Cellular Therapies Inc (NASDAQ: ITCI) (announced NDA submissions for two indications for Caplyta - as monotherapy and as adjunctive therapy with lithium or valproate for the treatment of depressive episodes associated with bipolar I or II disorder) iTeos Therapeutics Inc (NASDAQ: ITOS) Mereo BioPharma Group plc – ADR (NASDAQ: MREO) Nantkwest Inc (NASDAQ: NK) Orthofix Medical Inc (NASDAQ: OFIX) PAVmed Inc (NASDAQ: PAVM) (reacted to its fourth-quarter results) Pharvaris BV (NASDAQ: PHVS) Pliant Therapeutics Inc (NASDAQ: PLRX) RedHill Biopharma Ltd (NASDAQ: RDHL) Silence Therapeutics ADR Representing 3 Ord Shs (NASDAQ: SLN) United Therapeutics Corporation (NASDAQ: UTHR) Vistagen Therapeutics Inc (NASDAQ: VTGN) Down In The Dumps (Biotech Stocks Hitting 52-week Lows Feb. 22) bluebird bio Inc (NASDAQ: BLUE) Pharming Group (NASDAQ: PHAR) Talis Biomedical Corp (NASDAQ: TLIS) Vallon Pharmaceuticals Inc (NASDAQ: VLON) Stocks In Focus Surface Oncology Exercises Option to License Vaccinex Platform-discovered Anti-CCR8 Antibody Vaccinex Inc (NASDAQ: VCNX) announced that Surface Oncology Inc (NASDAQ: SURF) will be exercising its option to license the anti-CCR8 antibody discovered via Vaccinex's ActivMAb antibody discovery and novel viral display platform. The antibody, SRF114, is a fully human IgG1 anti-CCR8 antibody that selectively depletes immuno-suppressive tumor T regulatory cells while sparing peripheral Tregs. The terms of agreement with Surface Oncology provided that Surface Oncology pay technology access and licensing fees in addition to research funding, and that Vaccinex will qualify for development milestone payments and royalties. In after-hours trading, Vaccinex shares were down 3.91% to $4.91, while Surface Oncology was up 12.33% to $10.20. Aridis to Study Inhaled Antibody Cocktail For Neutralizing Emerging Variants of The Novel Coronavirus Aridis Pharmaceuticals Inc (NASDAQ: ARDS) said it has augmented its inhaled AR-711 monoclonal antibody to COVID-19 with a second mAb, AR-713, that is designed to neutralize newly emerging COVID-19 mutated variants including those from South Africa, Brazil and Japan. Together, the enhanced dual antibody cocktail will be delivered as an inhaled treatment and is expected to provide broad coverage of all known high-risk strains, the company said. In addition, Aridis announced preclinical development services support from NIAID. The preclinical development services support is also provided by the Coronavirus Immunotherapy Consortium. Aridis said it is on track to initiate the program's Phase 1/2/3 clinical trial in second half of 2021. In premarket trading Tuesday, the stock was up 11:45% to $8.08. Celldex to Expand The Study of CDX-0159 For Additional Dermatologic Indication Celldex said it will expand clinical development of CDX-0159 into prurigo nodularis, a chronic skin disease characterized by the development of hard, intensely itchy nodules on the skin. CDX-0159 is a humanized monoclonal antibody developed by Celldex that binds the KIT receptor with high specificity and potently inhibits its activity. Frequency Therapeutics Announces Publication of Positive Phase 1/2 Study Data For Drug to Treat Hearing Loss Frequency Therapeutics Inc (NASDAQ: FREQ) announced the publication in Otology & Neurotology, results of its FX-322 Phase 1/2 study, showing hearing improvements in adults with acquired sensorineural hearing loss and the first-known linkage of pharmacokinetics and pharmacodynamics for a potential hearing restoration therapy. Findings from the Phase 1/2 study of FX-322, the company's lead product candidate to treat SNHL, showed statistically significant increases in word recognition and words-in-noise scores, the company added. View more earnings on IBB In after-hours trading, the stock was up 5.59% to $55. Related Link: The Week Ahead In Biotech: J&J Vaccine Adcom Meeting, Sarepta FDA Decision And Plenty Of Earnings Revance's DaxibotulinumtoxinA Injection Shows Mixed Results In Mid-stage Study In Upper Limb Spasticity Revance Therapeutics Inc (NASDAQ: RVNC) announced topline data from its JUNIPER Phase 2 study of DaxibotulinumtoxinA for Injection for the treatment of adults with moderate to severe upper limb spasticity, showing mixed results. The company said the data validated efficacy and safety, while also achieving key co-primary endpoint on efficacy, with the 500-unit dose showing statistically significant difference from placebo in the Modified Ashworth Score improvement from baseline. On the Physician Global Impression Change assessment, all the three evaluated doses showed numerical improvement compared to placebo but did not reach statistical significance. Separately, the company reported a sharp increase in its fourth-quarter revenues to $11.1 million, with the increase primarily due to the commercial launch of the RHA Collection of dermal fillers and the HintMD fintech platform. The loss per share widened from 99 cents to $1.24, in line with the consensus. Protalix Reports Positive Late-stage Data For Drug to Treat Inherited Lysosomal Storage Disease Protalix Biotherapeutics Inc (NYSE: PLX) and Chiesi Global Rare Diseases, announced positive topline results from the BRIGHT Phase 3 clinical trial evaluating pegunigalsidase alfa, 2 mg/kg, administered every four weeks, for the potential treatment of Fabry disease. PRX–102 is Protalix' cell-expressed recombinant, PEGylated, cross-linked α–galactosidase–A product candidate. The stock was climbing 10.64% to $5.72 in premarket trading Tuesday. Oncolytics Presents Pre-clinical Data Showing Synergistic Effect of Pelareorep Combination With CART T Cells In Treating Cancer Oncolytics Biotech, Inc. (NASDAQ: ONCY) announced publication of an e-poster at the CAR-TCR Summit Europe 2021, which showed that loading CAR T cells with pelareorep vastly improved their persistence and efficacy in a murine solid tumor model, in stark contrast to preclinical studies using intratumoral infection with the VSV oncolytic virus that weakened CAR T cells. The stock was gaining 13.94% to $3.76 in premarket trading Tuesday. Earnings ImmuCell Corporation's (NASDAQ: ICCC) product sales rose modestly from $3.63 million in the fourth quarter of 2019 to $3.74 million in the fourth quarter of 2020. The company reversed to a profit of 3 cents from a loss of 4 cents, while analysts, on average, estimated a loss of 4 cents per share. The company also said it has recently submitted the last of five significant technical sections required to achieve FDA approval to market Re-Tain, its mastitis product under development. A response from the FDA to this chemistry, manufacturing and controls technical section is expected during the third quarter of 2021 after the statutory six-month review period. The stock declined 12.61% to $10.26 in after-hours trading. Offerings PAVmed said it's commencing an underwritten public offering of its common stock. All of the shares to be sold in the offering will be sold by the company, subject to customary closing conditions. PAVmed said it intends to use the net proceeds to repay all of its outstanding debt, including all outstanding convertible notes, with the balance to be used for working capital and general corporate purposes. The stock slipped 12.43% to $4.86 in after-hours trading. On The Radar Earnings Rubius Therapeutics Inc (NASDAQ: RUBY) (before the market open) Epizyme Inc (NASDAQ: EPZM) (before the market open) Clovis Oncology Inc (NASDAQ: CLVS) (before the market open) Epizyme Inc (NASDAQ: EPZM) (before the market open) Adamas Pharmaceuticals Inc (NASDAQ: ADMS) (after the close) Arena Pharmaceuticals, Inc. (NASDAQ: ARNA) (after the close) AtriCure Inc. (NASDAQ: ATRC) (after the close) Theravance Biopharma Inc (NASDAQ: TBPH) (after the close) Masimo Corporation (NASDAQ: MASI) (after the close) Insulet Corporation (NASDAQ: PODD) (after the close) Esperion Therapeutics Inc (NASDAQ: ESPR) (after the close) Myriad Genetics, Inc. (NASDAQ: MYGN) (after the close) Halozyme Therapeutics, Inc. (NASDAQ: HALO) (after the close) Inspire Medical Systems Inc (NYSE: INSP) (after the close) Penumbra Inc (NYSE: PEN) (after the close) Xencor Inc (NASDAQ: XNCR) (after the close) Jazz Pharmaceuticals PLC (NASDAQ: JAZZ) (after the close) MacroGenics Inc (NASDAQ: MGNX) (after the close) Medtronic PLC(NYSE: MDT) (after the close) See more from BenzingaClick here for options trades from BenzingaThe Week Ahead In Biotech: J&J Vaccine Adcom Meeting, Sarepta FDA Decision And Plenty Of EarningsThe Daily Biotech Pulse: Novavax Vaccine Supply Deal, Orphan Drug Designation For Travere, COVID-19 Boost For Quidel, Opko© 2021 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.