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ABLYNX Juli 2016

261 Posts
Pagina: «« 1 2 3 4 5 6 ... 14 »» | Laatste | Omlaag ↓
  1. forum rang 6 de tuinman 7 juli 2016 10:00
    Zomaar een gedachte/verklaring over de heftige daling van Ablynx de afgelopen periode.
    (Ik ben blij dat ik dit niet eerder zag)

    Ablynx heeft vlak voor q3 nog een flink aantal aandelen uitgebracht op 13,40.
    Waarom wacht Ablynx hier niet mee tot na de uitslagen van het Reuma-onderzoek?
    Hieruit zou je kunnen concluderen dat Ablynx weinig vertrouwen heeft in hun eigen Reuma medicijn.
    Ik kan mij voorstellen dat er beleggers zijn die daarom even op de zijlijn zijn gaan staan.

    Gelukkig bleek deze theorie niet juist en kunnen we weer richting ATH.

  2. forum rang 6 de tuinman 7 juli 2016 10:10
    Subjects were evaluated for efficacy and safety up to week 12 and eligible subjects on vobarilizumab were then invited to enroll in an open-label extension study, with 91% accepting. Subjects who were not eligible to roll over or who did not elect to do so were followed for safety for an additional 12 weeks after the last dosing. Evaluation is ongoing for a minority of these subjects.
  3. [verwijderd] 7 juli 2016 11:11
    zijn inderdaad mooie data en zou wel eens kunnen doorzetten dat nanobodies daadwerkelijk geregisstreerd kunnen gaan worden. Zie ook dat Edje wat minder zijn aandelen-opties verzilverd en dan toch blij dat ik er wat had opgepikt op 11 euro. Blijf nu zitten want wil wel eens zien of deze nanobodies nu geaccepteerd gaan worden. Dit is ook belangrijk voor de andere antibody players in mijn mandje als argenix en merus die simple bodies en bispecifieke antibodies ontwikkelen, die kunnen komende jaren ook enorm gaan stijgen.
  4. [verwijderd] 7 juli 2016 13:08
    Een must read...(beursig)

    Blockbuster hopes grow for Ablynx drug backed by AbbVie

    By Ben Hirschler

    (Reuters) - Ablynx's hopes for a potential multibillion-dollar drug were boosted on Thursday by strong clinical trial results in rheumatoid arthritis, vindicating a $175 million bet placed on the product by U.S. pharma group AbbVie in 2013.

    Belgian drugmaker Ablynx, which produces so-called nanobody medicines derived from camel and llama antibodies, said that a 12-week Phase IIb trial showed that its experimental drug vobarilizumab produced clinical remission from disease in up to 41 percent of patients.

    Those results compared well with Roche's established product Actemra, which has to be given more frequently and has more side-effects.

    Shares in Ablynx jumped 15.1 percent to 13.27 euros by 0448 ET.

    "We're getting really stand-out data, which is great, and it is the first step for us in providing a data package to AbbVie, who will decide later in the year whether to take up their option and license the product," Ablynx CEO Edwin Moses told Reuters.

    Both the Roche and Ablynx drugs target a protein called interleukin 6, which is involved in the inflammation underlying rheumatoid arthritis (RA).

    Actemra had sales last year of $1.5 billion and Moses said that vobarilizumab also has blockbuster potential, assuming other clinical trials are positive.

    "If you look at the size of the opportunity, not just in RA but also in lupus and other possible inflammatory indications, you have to begin to think in the billions (of dollars) in terms of the sales opportunity," Moses said.

    AbbVie currently sells the RA treatment Humira, which is the world's top-selling prescription drug, but it is looking for new medicines to expand its portfolio to counter the impact of cut-price competition from biosimilar copies of Humira in the coming years.

    Ablynx's product could help to underpin the U.S. company's market-leading position in RA, though analysts at Jefferies said it is not yet clear if AbbVie viewed vobarilizumab as a must-have product.

    AbbVie signed a partnership deal worth up to $840 million for the Ablynx medicine three years ago, including a $175 million upfront payment. The remaining $665 million is payable in future milestones if AbbVie opts to license the drug and it proves successful.

    Ablynx will also be eligible to receive royalties on sales, assuming the drug makes it to market.

    Moses said that he expects AbbVie to decide whether to license vobarilizumab -- triggering a $75 million payment -- after it sees results from a second RA trial slated for August.

    duke.fm/news/articles/2016/jul/0 ... by-abbvie/
  5. Lauwry 7 juli 2016 13:18
    www.fiercebiotech.com/biotech/ablynx-...

    While the ACR results fall short of making a clear-cut case for vobarilizumab, Ablynx thinks other aspects of its dataset show why a physician may prescribe its drug over Actemra. Most patients in the Actemra arm received the drug every week. Vobarilizumab achieved similar levels of efficacy when given every two weeks. Ablynx’s drug may also have the edge in terms of safety. Fewer patients in the vobarilizumab arms dropped out of the trial or experienced treatment-related adverse events.
  6. Lauwry 7 juli 2016 13:23
    Ik denk dat Ablynx daar een goed punt heeft. Minder belasting van de patiënt gecombineerd met zelfde of beter effect. Die ruim 90% rollover rate zegt daarin ook veel, patiënt heeft ook zijn/haar wensen.

    Dan nog de kosten. Zijn nanobodies ook niet veel goedkoper te produceren? Geen idee hoeveel invloed dat heeft op de kostprijs, maar productieproces wordt vaak wel benadrukt door ablynx.
261 Posts
Pagina: «« 1 2 3 4 5 6 ... 14 »» | Laatste |Omhoog ↑

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