KARYOPHARM THERAPEUTICS WKN: A1W77U ISIN: US48576U1060 Kürzel: 25K Forum: Aktien Thema: Hauptdiskussion

👁️👁️

Wahnsinn, wo ist der Boden, bei 0, oder was?

Meines Erachtens wurde die Aktie zu Unrecht abgestraft. Hab mal angefangen im unteren 3er-Bereich Aktien aufzusammeln und werde bei fortlaufender Kursschwäche nachlegen!

👀

👁👁

so, ich bin mal mit dem ersten bein rein. Ich finde die sehr vielversprechend und kann warten. Beim Kurs von 5,65 Euro kann man das versuchen

ich würde gern, aber warum fällt das Ding heute wie ein Stein?

Steigt jemand nochmal ein?

9. Februar 2022, 06:39 Karyopharm Therapeutics stellte Ergebnisse des abgelaufenen Quartals vor Karyopharm Therapeutics hat am 08.02.2022 das Zahlenwerk zum am 31.12.2021 abgelaufenen Jahresviertel vorgestellt. Es stand ein EPS von 0,460 USD je Aktie in den Büchern. Ein Jahr zuvor hatte bei Karyopharm Therapeutics noch ein Gewinn pro Aktie von -0,590 USD in den Büchern gestanden. Den Umsatz betreffend wurde ein Zuwachs von 259,74 Prozent gegenüber dem Vorjahresquartal erwirtschaftet. Zuletzt wurden 126,3 Millionen USD umgesetzt, gegenüber 35,1 Millionen USD im Vorjahreszeitraum. Der Verlust je Aktie wurde für das Gesamtjahr auf 1,650 USD beziffert. Im Vorjahr hatte Karyopharm Therapeutics ein Ergebnis je Aktie von -2,720 USD vermeldet. Der Umsatz lag bei 209,82 Millionen USD – das entspricht einem Zuwachs von 94,12 Prozent gegenüber dem Vorjahr. Damals waren 108,09 Millionen USD erwirtschaftet worden. Die Erwartungen der Analysten für das abgelaufene Gesamtjahr hatten bei einem Verlust von 2,616 USD je Aktie gelegen. Die Umsatzschätzung für das Gesamtjahr hatten sie auf 133,12 Millionen USD beziffert. https://www.google.com/amp/s/www.finanzen.at/nachrichten/amp/karyopharm-therapeutics-stellte-ergebnisse-des-abgelaufenen-quartals-vor-1031174932

08/02/2022 | 08:18am KARYOPHARM THERAPEUTICS INC. : Results of Operations and Financial Condition, Other Events, Financial Statements and Exhibits (form 8-K) On February 8, 2022, Karyopharm Therapeutics Inc. (the "Company") reported financial results for the fourth quarter and full year ended December 31, 2021 and highlighted select corporate milestones, including details regarding the ongoing U.S. commercialization of XPOVIO® (selinexor), and provided an overview of its key clinical development programs. The full text of the press release issued in connection with the announcement is furnished as Exhibit 99.1 to this Current Report on Form 8-K. The information in this Item 2.02 and Exhibit 99.1 attached hereto shall not be deemed "filed" for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the "Exchange Act"), or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended, or the Exchange Act, except as expressly set forth by specific reference in such a filing. https://www.google.com/amp/s/www.marketscreener.com/amp/quote/stock/KARYOPHARM-THERAPEUTICS-I-14825950/news/KARYOPHARM-THERAPEUTICS-INC-Results-of-Operations-and-Financial-Condition-Other-Events-Financia-37813661/

Jan. 24, 2022 Press Releases Karyopharm Receives Orphan Drug Designation from FDA for Eltanexor for the Treatment of Myelodysplastic Syndromes Karyopharm Therapeutics Inc. (Nasdaq: KPTI), a commercial-stage pharmaceutical company pioneering novel cancer therapies, today announced that the U.S. Food and Drug Administration (FDA) has granted orphan drug designation for eltanexor, a novel oral, Selective Inhibitor of Nuclear Export (SINE) compound, for the treatment of myelodysplastic syndromes (MDS). MDS are a group of diseases characterized by ineffective production of the components of the blood due to poor bone marrow function with a risk of progression to acute myeloid leukemia. Karyopharm is currently investigating eltanexor in an ongoing open-label Phase 1/2 study as a single-agent or in combination with approved and investigational agents in patients with several types of hematologic and solid tumor cancers (KCP-8602-801; NCT02649790). Previously, Karyopharm reported positive data from an investigator-sponsored Phase 1 study evaluating single-agent eltanexor in patients with hypomethylating agent (HMA)-refractory MDS, where eltanexor demonstrated a 53% overall response rate and median overall survival of 9.9 months. This compares favorably to historical survival of four to six months for HMA-refractory MDS patients. Approximately 15,000 people are diagnosed with intermediate-to-high risk MDS each year in the U.S.1 HMAs are the current standard of care for newly diagnosed, higher-risk MDS patients. However, only 40-60% of patients respond, with these responses typically lasting less than two years.2 The prognosis in HMA-refractory disease is poor, with a median overall survival of four to six months.3,4 There are currently no approved therapies for HMA- refractory MDS. "We are pleased to receive the FDA's orphan drug designation for eltanexor in MDS and believe it reinforces eltanexor's potential to improve clinical outcomes for patients with HMA-refractory MDS," said Richard Paulson, President and Chief Executive Officer of Karyopharm. "We are focused on advancing our ongoing clinical trials and remain steadfast in our commitment to bringing this new treatment option to patients and their families." Orphan drug designation by the FDA is granted to promote the development of drugs that target conditions affecting 200,000 or fewer U.S. patients annually and are expected to provide a significant therapeutic advantage over existing treatments. Orphan designation qualifies a company for certain incentives that apply across all stages of drug development, including the potential for seven years of market exclusivity following marketing approval, tax credits on qualified U.S. clinical trials, eligibility for orphan drug grants, and exemption from certain administrative fees. [...] https://investors.karyopharm.com/2022-01-24-Karyopharm-Receives-Orphan-Drug-Designation-from-FDA-for-Eltanexor-for-the-Treatment-of-Myelodysplastic-Syndromes

Press Releases https://investors.karyopharm.com/press-releases Jan 24, 2022 Karyopharm Receives Orphan Drug Designation from FDA for Eltanexor for the Treatment of Myelodysplastic Syndromes Jan 21, 2022 Karyopharm to Present at B. Riley Securities Oncology Investor Conference Jan 10, 2022 Karyopharm Promotes Sohanya Cheng to Chief Commercial Officer Jan 10, 2022 Karyopharm Announces Preliminary Unaudited Fourth Quarter and Full Year 2021 Net Product Revenues and Outlines 2022 Objectives Jan 4, 2022 Karyopharm to Present at 40th Annual J.P. Morgan Healthcare Conference Jan 3, 2022 Karyopharm Therapeutics Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4) Dec 21, 2021 Karyopharm and Menarini Group Enter into Exclusive License Agreement to Commercialize NEXPOVIO® (selinexor) in Europe and Other Key Global Territories Dec 17, 2021 Karyopharm's Partner Antengene Receives Approval in China for XPOVIO® (selinexor) for the Treatment of Patients with Relapsed or Refractory Multiple Myeloma Dec 11, 2021 Karyopharm Announces Presentation of Updated Phase 2 Selinexor Data in Patients with Myelofibrosis at the American Society of Hematology 2021 Annual Meeting and Exposition Dec 6, 2021 Karyopharm Announces the Appointment of Peter K Honig, MD, MPH to its Board of Directors

Published: Nov 09, 2021 Antengene to Release Preliminary Results of Selinexor for the Treatment of Peripheral T-Cell Lymphoma and NK/T-Cell Lymphoma at the 2021 ASH Annual Meeting SHANGHAI and HONG KONG,  Nov. 9, 2021 /PRNewswire/ --  Antengene Corporation Limited ("Antengene", SEHK: 6996.HK), a leading innovative global biopharmaceutical company dedicated to discovering, developing and commercializing first-in-class and/or best-in-class therapeutics in hematology and oncology, today announced the acceptance of an abstract at the upcoming 2021 American Society of Hematology (ASH) Annual Meeting, which will be held from December 11-14, 2021, both in Atlanta, Georgia, and virtually at https://www.hematology.org/meetings/annual-meeting. Antengene will release preliminary results of this Company-sponsored open-label Phase 1b study with selinexor (ATG-010) for the treatment of peripheral T-cell lymphoma and NK/T-cell lymphoma, in an offline poster presentation (full text of the abstract available at: https://ash.confex.com/ash/2021/webprogram/Paper147100.html). Meanwhile, another seventeen abstracts related to selinexor and eltanexor will be presented at the 2021 ASH Annual Meeting as announced by Antengene's partner, Karyopharm Therapeutics, Inc. (Karyopharm) (see below for details of these abstracts). "We are very pleased that the poster related to Antengene's selinexor (ATG-010) T-Cell Lymphoma program has been accepted at the 2021 ASH Annual Meeting," said Jay Mei, M.D., Ph.D., Founder, Chairman and Chief Executive Officer of Antengene. "Selinexor is Antengene's first commercial stage product. We look forward to sharing more about this program following the poster session." https://www.biospace.com/article/releases/antengene-to-release-preliminary-results-of-selinexor-for-the-treatment-of-peripheral-t-cell-lymphoma-and-nk-t-cell-lymphoma-at-the-2021-ash-annual-meeting/