Skip to main content

Day: November 9, 2019

NextCure Presents Updated Clinical Data from NC318 Phase 1/2 Clinical Trial at the 34th Annual Meeting of Society for Immunotherapy of Cancer (SITC) and Announces Initiation of Phase 2 Portion of the Trial

NC318 was well toleratedSingle agent activity observed in multiple tumor types, including a CR and a PR in NSCLCInitiated Phase 2 portion of the Phase 1/2 monotherapy trial and plans for a combo trial with standard of care chemotherapiesBELTSVILLE, Md., Nov. 09, 2019 (GLOBE NEWSWIRE) — NextCure, Inc. (Nasdaq: NXTC), a clinical-stage biopharmaceutical company committed to discovering and developing novel, first-in-class immunomedicines to treat cancer and other immune-related diseases, today announced that updated clinical results from the Phase 1 portion of its ongoing trial with NC318, a monoclonal antibody targeting Siglec-15 (S15), were presented at the SITC annual meeting. S15 is a novel immunomodulatory protein that is expressed on highly immunosuppressive cells called M2 macrophages and on tumor cells. In addition, NextCure...

Continue reading

New Studies Demonstrate the Predictive Value of the Vectra® Test in People Diagnosed with Rheumatoid Arthritis

SALT LAKE CITY, Nov. 09, 2019 (GLOBE NEWSWIRE) — Myriad Genetics, Inc. (NASDAQ: MYGN), a global leader in precision medicine, announced that its Myriad Autoimmune business unit will present new data on the Vectra test at the 2019 ACR/ARP Annual Meeting being held Nov. 8-13, 2019 in Atlanta, GA.  The key findings are that the Vectra test predicts the risk of radiographic progression (RP) within one year, and the Vectra score, in combination with other clinical measures, predicts the risk of a cardiovascular (CV) event in people with rheumatoid arthritis (RA).“A hallmark feature of rheumatoid arthritis is inflammation, which increases the risk of joint damage, cardiovascular disease and other comorbidities,” said Elena Hitraya, M.D., Ph.D., rheumatologist and chief medical officer at Myriad Autoimmune. “The data being presented by...

Continue reading

NEW DATA ON FILGOTINIB IN RHEUMATOID ARTHRITIS (RA) DEMONSTRATE DURABLE EFFICACY AND SAFETY PROFILE

— Pooled Analysis from the FINCH RA Clinical Program with Investigational Filgotinib Reinforces Favorable Safety and Tolerability Profile Alone and in Combination with Methotrexate (MTX) or Conventional Disease Modifying Antirheumatic Drug(s) (csDMARDs) —— Data Demonstrate Efficacy and Safety Across a Wide Range of Patient Populations, Including Those Intolerant or Unresponsive to Biologic Treatment —— Data to be Presented at 2019 ACR/ARP Annual Meeting —Foster City, Calif., and Mechelen, Belgium, November 9, 2019, 22.30 CET – Gilead Sciences, Inc. (Nasdaq: GILD) and Galapagos NV (Euronext & NASDAQ: GLPG) today announced detailed results from the companies’ clinical research program evaluating filgotinib, an investigational, oral, selective JAK1 inhibitor, in adults with moderately-to-severely...

Continue reading

NIEUWE FILGOTINIB-DATA BIJ REUMA (RA) TONEN DUURZAAM WERKZAAMHEIDS- EN VEILIGHEIDSPROFIEL AAN

— Analyse van alle gegevens in het klinische FINCH RA-programma staaft het gunstige veiligheids- en tolerantieprofiel van kandidaatgeneesmiddel filgotinib, zowel in monotherapie als in combinatie met methotrexaat (MTX) of bestaande reumamedicjjnen  (de zgn. DMARD’s) —— Gegevens tonen werkzaamheid en veiligheid aan in een breed scala aan patiëntenpopulaties, inclusief bij patiënten die intolerant zijn voor, of niet reageren op, een behandeling met biologische medicijnen–— Data worden gepresenteerd op jaarvergadering 2019 van ACR/ARP —Foster City, California, en Mechelen, België, 9 november 2019, 22.30 CET – Gilead Sciences, Inc. (Nasdaq: GILD) en Galapagos NV (Euronext & NASDAQ: GLPG) maakten vandaag gedetailleerde resultaten bekend van hun klinische onderzoeksprogramma naar filgotinib, een experimentele,...

Continue reading

Genocea Preclinical Data at SITC Demonstrate that Inhibitory Neoantigens in an Otherwise Protective Vaccine Reverse Anti-Tumor Responses

ATLAS™ identifies naturally occurring neoantigen-specific inhibitory T cell responses that are augmented after vaccinationInhibitory T cell responses exacerbate tumor growthCAMBRIDGE, Mass., Nov. 09, 2019 (GLOBE NEWSWIRE) — Genocea Biosciences, Inc. (NASDAQ: GNCA), a biopharmaceutical company developing next-generation neoantigen immunotherapies, today presented clinical and preclinical data demonstrating the potential of Genocea’s unique, biology-driven ATLAS platform to select neoantigens for inclusion in anti-tumor immunotherapies. Striking clinical evidence shows that the presence of inhibitory neoantigens in an otherwise protective therapeutic vaccine completely suppressed anti-tumor immune responses and promoted tumor growth in pre-clinical models. These data were presented at the 34th Annual Meeting of the Society for Immunotherapy...

Continue reading

Vaccinex Presents Updated Interim Data from a Phase 1b/2 Study of Pepinemab (VX15/2503) in Combination with Avelumab (BAVENCIO®) in Non-Small Cell Lung Cancer at the 34th Annual Meeting of the Society for Immunotherapy of Cancer (SITC)

ROCHESTER, N.Y., Nov. 09, 2019 (GLOBE NEWSWIRE) — Vaccinex, Inc. (Nasdaq: VCNX), a clinical-stage biotechnology company pioneering novel investigational antibody therapies in cancer and Huntington’s disease, today announced that updated interim data of the Phase 1b/2 study of pepinemab in combination with anti-PD-L1 checkpoint inhibitor, BAVENCIO® (avelumab), in non-small cell lung cancer (NSCLC) is being reported during a poster presentation on Saturday, November 9 at the 34th Annual Meeting of The Society for Immunotherapy of Cancer (“SITC”).   Below is a summary of updated interim data from the poster presentation.Updated Interim DataThe CLASSICAL-Lung trial is being conducted in collaboration with Merck KGaA, Darmstadt, Germany.  It is a multi-center, open-label study designed to evaluate the safety and potential efficacy of...

Continue reading

Autolus Therapeutics Presents Preclinical Data on AUT06NG at the SITC Annual Meeting

LONDON, Nov. 09, 2019 (GLOBE NEWSWIRE) — Autolus Therapeutics plc (Nasdaq: AUTL), a clinical-stage biopharmaceutical company developing next-generation programmed T cell therapies for the treatment of cancer, today presented pre-clinical data on AUTO6NG, the company’s next generation GD2-targeting CAR (chimeric antigen receptor) T cell therapy, at the 34th Annual Meeting of the Society for Immunotherapy of Cancer (SITC) being held November 6-10, 2019, in Washington, D.C.“Autolus’ growing set of programming modules ​addresses a range of inhibitory factors within the highly complex and dynamic solid tumor microenvironment​.  This presentation demonstrates the utility of three modules added to the clinically active and validated AUTO6 GD-2 targeting CAR that not only improve CAR T persistence but also combat the immunosuppressive environment,”...

Continue reading

ERYTECH veröffentlicht Business Update und gibt die Finanzergebnisse für das dritte Quartal 2019 bekannt

Telefonkonferenz und Webcast am Freitag, den 8. November um 14:30 Uhr MEZ 20:30 Uhr ETTRYbeCA1, Phase-3-Studie mit Eryaspase als Zweitlinienbehandlung bei Bauchspeicheldrüsenkrebs:positive Sicherheitsüberprüfung durch ein unabhängiges Datenüberwachungskomiteefür Patienteneinschreibung in den USA eröffneterste klinische Standorte in den USA aktiviertProduktionsstätte in Princeton bereit für die Herstellung von klinischen ChargenCash-Position von 81,9 Mio. € (89,2 Mio. USD) per Ende SeptemberLYON, Frankreich und CAMBRIDGE, Massachusetts, Nov. 09, 2019 (GLOBE NEWSWIRE) — ERYTECH Pharma (Nasdaq & Euronext: ERYP), ist ein in der klinischen Entwicklungsphase tätiges Biopharma-Unternehmen, das innovative Therapien entwickelt, indem es therapeutische Wirkstoffe in rote Blutkörperchen einkapselt, hat heute ein Business Update vorgelegt...

Continue reading

ERYTECH presenta business update e risultati finanziari del terzo trimestre 2019

TRYbeCA1, trial clinico di fase 3 relativo all’eryaspase per il trattamento di seconda linea del carcinoma pancreatico:valutazione positiva della sicurezza da parte di un comitato indipendente per il monitoraggio dei datiiniziato il reclutamento dei pazienti negli Stati Unitiattivati i primi siti clinici negli Stati UnitiLo stabilimento di produzione di Princeton è pronto per la produzione di lotti cliniciPosizione finanziaria di €81,9 milioni ($89,2 milioni) alla fine di settembreLIONE, Francia e CAMBRIDGE, Mass., Nov. 09, 2019 (GLOBE NEWSWIRE) — ERYTECH Pharma (Nasdaq & Euronext: ERYP), un’azienda biofarmaceutica in fase clinica che sviluppa terapie innovative incapsulando sostanze farmacologiche all’interno dei globuli rossi, ha presentato oggi un business update e i risultati finanziari relativi al trimestre...

Continue reading

Top Cannabis Products of 2019 Announced at the Sixth Annual Canadian Cannabis Awards

Following the first full year of legalization, over 31,000 consumer votes on lift.co determined the top cannabis flower and oil products of 2019Innovation of the Year goes to Solei Renew CBN Oil7ACRES wins Brand of the Year for the second year in a rowSuperette sweeps the newly added retail categories winning Top Retail Store—Single Location and Top Budtender, as well as Startup of the Year; Co-founder and CEO Mimi Lam wins Womxn in Weed-TrailblazerTORONTO, Nov. 08, 2019 (GLOBE NEWSWIRE) — Three weeks following the first anniversary of legalization, Lift & Co. (the “Company”) (TSXV: LIFT) (OTCQB: LFCOF) tonight announced the top cannabis people, brands, organizations and products of 2019 at the sixth annual Canadian Cannabis Awards (“CCAs”) as selected by consumers and industry experts. A total of 32 awards were...

Continue reading

Disclaimer & Cookie Notice

Welcome to GOLDEA services for Professionals

Before you continue, please confirm the following:

Professional advisers only

I am a professional adviser and would like to visit the GOLDEA CAPITAL for Professionals website.

Important Notice for Investors:

The services and products offered by Goldalea Capital Ltd. are intended exclusively for professional market participants as defined by applicable laws and regulations. This typically includes institutional investors, qualified investors, and high-net-worth individuals who have sufficient knowledge, experience, resources, and independence to assess the risks of trading on their own.

No Investment Advice:

The information, analyses, and market data provided are for general information purposes only and do not constitute individual investment advice. They should not be construed as a basis for investment decisions and do not take into account the specific investment objectives, financial situation, or individual needs of any recipient.

High Risks:

Trading in financial instruments is associated with significant risks and may result in the complete loss of the invested capital. Goldalea Capital Ltd. accepts no liability for losses incurred as a result of the use of the information provided or the execution of transactions.

Sole Responsibility:

The decision to invest or not to invest is solely the responsibility of the investor. Investors should obtain comprehensive information about the risks involved before making any investment decision and, if necessary, seek independent advice.

No Guarantees:

Goldalea Capital Ltd. makes no warranties or representations as to the accuracy, completeness, or timeliness of the information provided. Markets are subject to constant change, and past performance is not a reliable indicator of future results.

Regional Restrictions:

The services offered by Goldalea Capital Ltd. may not be available to all persons or in all countries. It is the responsibility of the investor to ensure that they are authorized to use the services offered.

Please note: This disclaimer is for general information purposes only and does not replace individual legal or tax advice.