Para movimientos locos las ACST que habla Zoka...Rango diario de 1,20 a 3,05!Ahora estan “halt t1, news pending” Así que supongo seguirán nuevos meneos locosACST
Para mi no es lo normal/habitual. Es bueno no porque sea un solo inversor (eso me parece irrelevante), si no porque el offering es a petición del comprador y no de la empresa (eso es lo que no es habitual):“We are excited to have completed this unsolicited financing with a premier biotechnology investor and believe it represents a major vote of confidence in our drug candidates and current pivotal programs."TGTX
CBIOAna!!! Partnership con BIIB. Saltó la liebre...+30% ahora. O igual le puedes meter un cortoCatalyst Biosciences Announces Global License and Collaboration Agreement to Develop Pegylated CB 2782 for the Treatment of Dry Age-Related Macular DegenerationCatalyst to receive $15 million upfront and is eligible to receive an additional $340 million in milestones and tiered royalties up to low double digitshttps://www.globenewswire.com/news-release/2019/12/19/1962743/0/en/Catalyst-Biosciences-Announces-Global-License-and-Collaboration-Agreement-to-Develop-Pegylated-CB-2782-for-the-Treatment-of-Dry-Age-Related-Macular-Degeneration.html
EXELPartnership con Roche Exelixis Enters into a Clinical Collaboration for Three Phase 3 Combination Trials for Patients with Advanced Solid Tumors– New pivotal trials will evaluate the combination of cabozantinib and atezolizumab in patients with advanced non-small cell lung cancer, castration-resistant prostate cancer and renal cell carcinoma – – Collaboration based on data from phase 1b COSMIC-021 trial – https://ir.exelixis.com/news-releases/news-release-details/exelixis-enters-clinical-collaboration-three-phase-3-combination
SGMOPues lo que comenté, promedio en los 8. Media en 9 bajos y a esperar sentado los 11 o comérmelas.MEIPOffering a 1,60 con mucho descuento (un 30%), si llega a esa zona estos días le meto un tirito
Sí, le ha metido un pedazo de upgrade inimaginable! Me partoOppenheimer analyst Leland Gershell raised his price target for Amarin to $8 from $7 following Friday's FDA approval of Vascepa to reduce cardiovascular event risk that came roughly two weeks ahead of its December 28 PDUFA date.AMRN
AMRNPues ahí estáAMARIN WINS EXPANDED USE OF VASCEPA FROM FDAFDA approved Vascepa as an adjunctive (secondary) therapy to reduce the risk of CV events among adults with elevated TG of 150 mg/dL or higher. Patients must also have either established CV disease or diabetes and two or more additional risk factors for CV disease.