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Genmab, de Deense parel

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  1. Juargo 13 november 2017 14:14
    Thnx Sheriff. Bijna alles in Copenhagen in het rood, dus ik hoop dat dit morgen niet doorzet. Anders zitten we zo onder de 1000 ben ik bang.
  2. [verwijderd] 13 november 2017 14:51
    quote:

    sheriff Grover schreef op 13 november 2017 14:08:

    Juargo , dat lijkt mij heel sterk ? (heel!!) simpel gezegd dat zou betekenen nu een deal met Grolsch sluiten omdat volgende maand Heineken toch van ons is ?? maar misschien weten andere het antwoord hierop ?? Globalmacro ? Jeroen ?

    Genoeg mogelijkheden, als het een goed platform is wil je het sowieso uit de handen van je concurrenten houden. Daarnaast kan het platform andere voordelen bieden dan de platformen van Genmab. Who knows, maar zegt niet meteen direct iets over de platformen van Genmab in mijn ogen.
  3. Juargo 13 november 2017 14:59
    Thnx Macro. Denk jij dat we richting de 1000dkk gaan? Met de aankomende warrants kan het hard gaan lijkt mij.
  4. [verwijderd] 13 november 2017 20:32
    quote:

    Juargo schreef op 13 november 2017 14:59:

    Thnx Macro. Denk jij dat we richting de 1000dkk gaan? Met de aankomende warrants kan het hard gaan lijkt mij.
    Geen pijl op te trekken, het zou me echter niets verbazen. Alles is mogelijk want wat er nu gebeurd is verre van reëel, er wordt met de Genmab koers gefucked.
    Het is een gevecht tussen de banken die verdienen aan derivaten (turbo's) en de financiële elite die de echte waarde van Genmab erkennen (Blackrock oa), uiteindelijk is er een niveau waarop de koers zo ver van de realiteit komt te liggen dat het echte opkopen begint, dan sta je binnen no time weer op 1300 - 1400. De vraag is how low can we go, sub 1000 zou me niets verbazen, maar zou wel flink zuur zijn en het vertrouwen in Genmab voor de leek wellicht aantasten, gelukkig maakt de leek geen impact meer en wordt alles door de insituionals bepaald en die weten prima wat Genmab waard is en waar het heen gaat.

    Meestal blijft het bij een drop van 20% - 25%, daar zijn we nu beland.
    Tevens zie ik parallellen met de Actelion situatie net voordat de overname geruchten begonnen, ook die dropte 25%. Laten we hopen dat dit het is. Sub 1000 zou echt bizar zijn, maar niet onmogelijk.
  5. Juargo 14 november 2017 13:23
    De mijlpaal van 1mld moet nu toch ook wel bereikt zijn lijkt mij? Gaat er dan geen persbericht naar buiten?
  6. [verwijderd] 14 november 2017 15:47
    Juargo, je hoeft gelukkig PB niet af te wachten, want dit bericht is al ingeprijsd door de markt. Iedereen weet dat de mijlpaal dit jaar behaald wordt zo niet al is. PB gaat er tzt komen, maar is non-issue voor beleggers dus.
  7. sheriff Grover 14 november 2017 18:23
    Ze houden het beschaafd met de warrants ....

    Company Announcement

    Copenhagen, Denmark; November 14, 2017 — Genmab A/S (Nasdaq Copenhagen: GEN) will increase its share capital by 22,532 shares as a consequence of the exercise of employee warrants.
    The increase is effected without any preemption rights for the existing shareholders of the company or others. The shares are subscribed in cash at the following price per share of nominally DKK 1:
    • 50 shares at DKK 40.41,
    • 750 shares at DKK 210,
    • 1,125 shares at DKK 220.40,
    • 7,687 shares at DKK 225.90,
    • 500 shares at DKK 231.50,
    • 3,450 shares at DKK 254,
    • 6,425 shares at DKK 329,
    • 100 shares at DKK 337.40,
    • 945 shares at DKK 466.20, and
    • 1,500 shares at DKK 636.50.
    Proceeds to the company are approximately DKK 6.68 million. The increase corresponds to approx. 0.04% of the company's share capital.
  8. [verwijderd] 14 november 2017 20:53
    Company Announcement

    First commercial sale of DARZALEX in Japan triggers USD 25 million in milestone payments from Janssen
    Financial guidance updated
    Copenhagen, Denmark; November 14, 2017 — Genmab A/S (Nasdaq Copenhagen: GEN) announced today that the first commercial sale of DARZALEX (daratumumab) in Japan has taken place, triggering USD 25 million in milestone payments from Janssen Biotech, Inc. (Janssen). The milestone was mentioned at the time of the September 2017 announcement of the approval of DARZALEX for the treatment of adults with relapsed or refractory multiple myeloma in Japan. As a result of this milestone, Genmab is updating its 2017 financial guidance.

    "We're pleased that DARZALEX is now commercially available for patients with relapsed or refractory multiple myeloma who are living in Japan," said Jan van de Winkel, Ph.D., Chief Executive Officer of Genmab.

    OUTLOOK

    MDKK Revised Guidance Previous Guidance
    Revenue 2,110 — 2,310 1,950 — 2,150
    Operating expenses (1,000) — 1,100) (1,000) — (1,100)
    Operating income 1,060 — 1,260 900 — 1,100
    Cash position at end of year* >4,900 >4,500
    *Cash, cash equivalents, and marketable securities
    Genmab is improving its 2017 financial guidance last published on November 8, 2017 due to the inclusion of the DARZALEX milestones totaling USD 25 million associated with first commercial sale of DARZALEX in Japan.

    Operating Result
    We expect our 2017 revenue to be in the range of DKK 2,110 — 2,310 million, an increase of DKK 160 million compared to the previous guidance. We have increased our projected daratumumab milestones to DKK 960 million (previously DKK 800 million) due to inclusion of USD 25 million in milestone payments triggered by the first commercial sale of DARZALEX in Japan. We expect DARZALEX royalties to remain in the range of DKK 930 — 1,100 million, which are based on an estimated USD 1,100 — 1,300 million of DARZALEX sales in 2017. The remainder of the revenue mainly consists of Arzerra® royalties, DuoBody® milestones, and non-cash amortization of deferred revenue.

    We anticipate that our 2017 operating expenses will remain in the range of DKK 1,000 —1,100 million.

    As a result of the increased revenue, we now expect the operating income for 2017 to be approximately DKK 1,060 — 1,260 million, compared to DKK 900 — 1,100 million in the previous guidance.

    Cash Position
    As a result of the above and proceeds from the exercise of warrants during the year, we are now projecting a cash position at the end of 2017 of greater than DKK 4,900 million.

    Outlook: Risks and Assumptions
    In addition to factors already mentioned, the estimates above are subject to change due to numerous reasons, including but not limited to the achievement of certain milestones associated with our collaboration agreements; the timing and variation of development activities (including activities carried out by our collaboration partners) and related income and costs; DARZALEX and Arzerra sales and corresponding royalties to Genmab; fluctuations in the value of our marketable securities; and currency exchange rates. The financial guidance does not include any potential proceeds from future warrant exercises and also assumes that no significant agreements are entered into during 2017 that could materially affect the results.

    About DARZALEX® (daratumumab)
    DARZALEX® (daratumumab) injection for intravenous infusion is indicated in the United States in combination with lenalidomide and dexamethasone, or bortezomib and dexamethasone, for the treatment of patients with multiple myeloma who have received at least one prior therapy; in combination with pomalidomide and dexamethasone for the treatment of patients with multiple myeloma who have received at least two prior therapies, including lenalidomide and a proteasome inhibitor (PI); and as a monotherapy for the treatment of patients with multiple myeloma who have received at least three prior lines of therapy, including a PI and an immunomodulatory agent, or who are double-refractory to a PI and an immunomodulatory agent.1 DARZALEX is the first monoclonal antibody (mAb) to receive U.S. Food and Drug Administration (FDA) approval to treat multiple myeloma. DARZALEX is indicated in Europe for use in combination with lenalidomide and dexamethasone, or bortezomib and dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least one prior therapy and as monotherapy for the treatment of adult patients with relapsed and refractory multiple myeloma, whose prior therapy included a PI and an immunomodulatory agent and who have demonstrated disease progression on the last therapy. In Japan, DARZALEX is approved in combination with lenalidomide and dexamethasone, or bortezomib and dexamethasone, for treatment of adults with relapsed or refractory multiple myeloma. DARZALEX is the first human CD38 monoclonal antibody to reach the market. For more information, visit www.DARZALEX.com.

    Daratumumab is a human IgG1k monoclonal antibody (mAb) that binds with high affinity to the CD38 molecule, which is highly expressed on the surface of multiple myeloma cells. Daratumumab triggers a person's own immune system to attack the cancer cells, resulting in rapid tumor cell death through multiple immune-mediated mechanisms of action and through immunomodulatory effects, in addition to direct tumor cell death, via apoptosis (programmed cell death).1,2,3,4,5

    Daratumumab is being developed by Janssen Biotech, Inc. under an exclusive worldwide license to develop, manufacture and commercialize daratumumab from Genmab. A comprehensive clinical development program, including multiple Phase III studies, is ongoing with daratumumab in relapsed and frontline multiple myeloma settings, and additional studies are ongoing or planned to assess its potential in other malignant and pre-malignant diseases on which CD38 is expressed, such as smoldering myeloma, NKT-cell lymphoma, amyloidosis, myelodysplastic syndromes and solid tumors. Daratumumab has received two Breakthrough Therapy Designations from the U.S. FDA, for multiple myeloma, as both a monotherapy and in combination with other therapies.
  9. sheriff Grover 14 november 2017 20:54

    Genmab Achieves USD 25 Million Milestone for First Commercial Sale of DARZALEX® (daratumumab) in Japan and Updates Financial Guidance

    Company Announcement
    • First commercial sale of DARZALEX in Japan triggers USD 25 million in milestone payments from Janssen
    • Financial guidance updated
    Copenhagen, Denmark; November 14, 2017 — Genmab A/S (Nasdaq Copenhagen: GEN) announced today that the first commercial sale of DARZALEX (daratumumab) in Japan has taken place, triggering USD 25 million in milestone payments from Janssen Biotech, Inc. (Janssen). The milestone was mentioned at the time of the September 2017 announcement of the approval of DARZALEX for the treatment of adults with relapsed or refractory multiple myeloma in Japan. As a result of this milestone, Genmab is updating its 2017 financial guidance.
    "We're pleased that DARZALEX is now commercially available for patients with relapsed or refractory multiple myeloma who are living in Japan," said Jan van de Winkel, Ph.D., Chief Executive Officer of Genmab.
    OUTLOOK
    MDKK Revised Guidance Previous Guidance
    Revenue 2,110 — 2,310 1,950 — 2,150
    Operating expenses (1,000) — 1,100) (1,000) — (1,100)
    Operating income 1,060 — 1,260 900 — 1,100
    Cash position at end of year* >4,900 >4,500
    *Cash, cash equivalents, and marketable securities
    Genmab is improving its 2017 financial guidance last published on November 8, 2017 due to the inclusion of the DARZALEX milestones totaling USD 25 million associated with first commercial sale of DARZALEX in Japan.
    Operating Result
    We expect our 2017 revenue to be in the range of DKK 2,110 — 2,310 million, an increase of DKK 160 million compared to the previous guidance. We have increased our projected daratumumab milestones to DKK 960 million (previously DKK 800 million) due to inclusion of USD 25 million in milestone payments triggered by the first commercial sale of DARZALEX in Japan. We expect DARZALEX royalties to remain in the range of DKK 930 — 1,100 million, which are based on an estimated USD 1,100 — 1,300 million of DARZALEX sales in 2017. The remainder of the revenue mainly consists of Arzerra® royalties, DuoBody® milestones, and non-cash amortization of deferred revenue.
    We anticipate that our 2017 operating expenses will remain in the range of DKK 1,000 —1,100 million.
    As a result of the increased revenue, we now expect the operating income for 2017 to be approximately DKK 1,060 — 1,260 million, compared to DKK 900 — 1,100 million in the previous guidance.
    Cash Position
    As a result of the above and proceeds from the exercise of warrants during the year, we are now projecting a cash position at the end of 2017 of greater than DKK 4,900 million.

    Misschien kan dit de boel keren ......
  10. Juargo 15 november 2017 12:56
    Veel fondsen in Copenhagen in het rood. Dus de echte stijging zou ook morgen pas kunnen plaatsvinden.
  11. forum rang 10 DeZwarteRidder 16 november 2017 10:45
    quote:

    HansGarrincha schreef op 16 november 2017 10:01:

    DKK 1182, 4.3% up in eerste uur, bodem gezet?
    Het dieptepunt is pas bereikt als de grote verkoper klaar is.
  12. Genmob 16 november 2017 11:28
    quote:

    DeZwarteRidder schreef op 16 november 2017 10:45:

    [...]
    Het dieptepunt is pas bereikt als de grote verkoper klaar is.
    Nadenkertje...
  13. [verwijderd] 16 november 2017 12:29
    quote:

    DeZwarteRidder schreef op 16 november 2017 10:45:

    [...]
    Het dieptepunt is pas bereikt als de grote verkoper klaar is.
    Onzin: een grote verkoper kan verkopen in opgaande koers. Koers is kopers maal verkopers..
  14. forum rang 10 DeZwarteRidder 16 november 2017 12:30
    quote:

    GenTrap schreef op 16 november 2017 12:29:

    [...]Onzin: een grote verkoper kan verkopen in opgaande koers. Koers is kopers maal verkopers..
    Jij weet alles....
  15. sheriff Grover 16 november 2017 17:48
    ZO eindelijk weer eens een redelijk dagje na 1 maand ellende . Nog 3 van zulke dagen en we staan weer op ons oude niveau !

    Viel me op dat er een grote speler zit (100K) in de 933 turbo's dan praten we toch over een klein half miljoen als gokje ............ Of hij is zo zeker van zijn zaak dat ... het zal toch niet @Globalmacro zijn he ;o)
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