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SecteurRecherche biotechnologique et médicale

Développement et fabrication de produits pharmaceutiques

Spectrum Pharmaceuticals, Inc. est une société de biotechnologie spécialisée dans l'acquisition, le développement et la commercialisation de produits cliniques et commerciaux à un stade avancé.

Elle opère à travers les marques suivantes: FOLOTYN, ZEVALIN, MARQIBO, BELEODAQ et EVOMELA.

La société a été fondée en décembre 1987 et son siège est à Henderson, NV.

Einstiegschance

Ich denke nicht, dass die Reaktion auf die gestrige Präsentation (-22%) gerechtfertigt war. Ich wollte schon geraume Zeit auf den Zug aufspringen und sehe jetzt eine gute Einstiegschance…Kurserholung hat heute bereits begonnen. Ich halte die Daten für gar nicht schlecht und sehe weiter gewaltiges Potential in den beiden Hauptprodukten POZIOTINIB in Phase 2 und noch mehr in ROLONTIS zur Behandlung von durch Chemotherapy verursachte Neutropenie in Phase 3.

Spectrum Pharmaceuticals Announces Release of Updated Poziotinib Data From MD Anderson Phase 2 Study in Non-Small Cell Lung Cancer Patients Nachrichtenquelle: Business Wire (engl.)  24.09.2018, 17:40  

Spectrum Pharmaceuticals, Inc. (NasdaqGS: SPPI), a biotechnology company with fully integrated commercial and drug development operations with a primary focus in hematology and oncology, today announced preliminary poziotinib data from the University of Texas, MD Anderson Cancer Center Phase 2 non-small cell lung cancer (NSCLC) study which were released today during an oral presentation at the IASLC 19th World Conference on Lung Cancer hosted by the International Association for the Study of Lung Cancer. The MD Anderson study is the single largest data set of patients with an exon 20 mutation in EGFR or HER2.

 “There are currently no approved targeted therapies for this hard-to-treat population,” said John Heymach, M.D., Ph.D., Chairman and Professor, Department of Thoracic/Head and Neck Medical Oncology, University of Texas, MD Anderson Cancer Center. “For this reason, it is especially exciting to observe that poziotinib is highly active, with a manageable safety profile, in these heavily pre-treated patients. The study is ongoing with nineteen EGFR patients remaining on treatment, six of which have been on drug for longer than a year. Poziotinib may offer a much needed option to NSCLC patients with exon 20 mutations in EGFR or HER2.”

In the interim analysis presented at the WCLC, the following observations were made:

• This phase II study demonstrates high anti-tumor activity for poziotinib in metastatic, heavily pretreated EGFR exon 20 mutant NSCLC, a group for which no targeted agents have proven effective to date (other than patients bearing T790M or S768I mutations) with best response of PR in 55% of evaluable patients (43% confirmed ORR to date; 19 patients remain on treatment).
• Median PFS 5.5m; durable responses observed with 6 treated for >1year thus far.
• Compares favorably to historical ORR rates of <8% approved TKIs and <19% for standard of care 2L agents (docetaxel, PD-1/PD-L1 inhibitors).
• Significant activity also observed in HER2 exon 20-mutant NSCLC with initial responses observed in 50% (6/12) evaluable patients and median PFS 5.1m.
• EGFR-related toxicities (including rash, diarrhea, & paronychia) were manageable and required dose reductions in 60%. Discontinuation due to poor tolerance was rare (3%).
• Encouraging activity has prompted a confirmatory, international, multicenter study in EGFR and HER2 exon 20 mutant NSCLC patients which is currently enrolling (NCT03318939), including a first-line cohort, and development of a separate pan-tumor basket study.

The poziotinib NSCLC clinical program for patients with EGFR or HER2 exon 20 insertion mutations currently consists of a Phase 2 investigator-initiated study at The University of Texas, MD Anderson Cancer Center and a Phase 2 pivotal, Spectrum-sponsored, multi-center, global study (ZENITH20) with active sites in the United States and future centers planned in Canada and Europe. The overall poziotinib clinical development program is focused on four pillars, including previously treated NSCLC, first-line treatment of NSCLC, combination therapy and treatment of other solid tumors.

About Poziotinib Poziotinib is a novel, orally available Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor (EGFR TKI) that inhibits the tyrosine kinase activity of EGFR as well as HER2 and HER4. Importantly this, in turn, leads to the inhibition of the proliferation of tumor cells that overexpress these receptors. Mutations or overexpression/amplification of EGFR family receptors have been associated with a number of different cancers, including non-small cell lung cancer (NSCLC), breast cancer, and gastric cancer. Spectrum received an exclusive license from Hanmi Pharmaceuticals to develop, manufacture, and commercialize worldwide, excluding Korea and China. Poziotinib is currently being investigated by Spectrum and Hanmi in several mid-stage trials in multiple solid tumor indications.

SecteurRecherche biotechnologique et médicale Agenda 13/11 Publication de résultats

Développement et fabrication de produits pharmaceutiques

Spectrum Pharmaceuticals, Inc. est une société de biotechnologie spécialisée dans l'acquisition, le développement et la commercialisation de produits cliniques et commerciaux à un stade avancé.

Il opère sous les marques suivantes: FOLOTYN, ZEVALIN, MARQIBO, BELEODAQ et EVOMELA.

La société a été fondée en décembre 1987 et son siège est à Henderson, NV.

Kaufen

Kaufen

16$

könnte möglich sein.

14$

möglich.

Boden

erneut erreicht.?

Zweiter Versuch

Habe die ja schon einmal Empfohlen...und musst seit dem ganz schön bluten. Ich glaube jedoch weiterhin an ein gewaltiges Potential in den beiden Hauptprodukten POZIOTINIB in Phase 2 und noch mehr in ROLONTIS zur Behandlung von durch Chemotherapy verursachte Neutropenie in Phase 3.

 Seit Februar haben einige institutionelle ganz schön aufgesattelt (SG Americas, Los Angeles Capital Mgt,BNP Paribas und Tibra Equities). Am 09. Mai kommen die Zahlen für das erste Quartal, bin mal gespannt...zu Jahresbeginn hatten die noch 200 Mio$ cash, im März haben Sie ihre 6 fertigen Medikamente für 150 Mio $ verkauft, also gehe ich mal davon aus, das die jetzt über 300 Mio $ cash haben dürften... denke hier noch vor dem 9. Mai wieder einzusteigen könnte eine gute Idee sein...

Boden

endlich bald erreicht?