Aandelen in “Fabricage van farmaceutische preparaten”

Aandeel Datum Koers Evolutie
vlag Nature's Sunshine Products, Inc. 12/12 22,740 USD
+2,57% 		+2,57%
vlag Navidea Biopharmaceuticals Inc 12/12 0,000 USD
0,00% 		0,00%
vlag Nektar Therapeutics 15/12 53,300 USD
-2,56% 		-2,56%
vlag Nkarta Inc 12/12 1,880 USD
+0,53% 		+0,53%
vlag Novabay Pharmaceuticals Inc 12/12 2,800 USD
-0,36% 		-0,36%
vlag NuCana plc 12/12 3,720 USD
-8,15% 		-8,15%
vlag Nurix Therapeutics Inc 12/12 19,070 USD
0,00% 		0,00%

Nieuws over “Fabricage van farmaceutische preparaten”

00:00 · Nektar to Hold Conference Call to Discuss Topline Results from the 36-Week Induction Treatment Period for its REZOLVE-AA Phase 2b Study of Rezpegaldesleukin in Alopecia Areata on December 16, 2025 · Persbericht

00:00 · Nektar to Hold Conference Call to Discuss Topline Results from the 36-Week Induction Treatment Period for its REZOLVE-AA Phase 2b Study of Rezpegaldesleukin in Alopecia Areata on December 16, 2025 · Persbericht

15/12 · Vanda Announces Submission of Biologics License Application to the FDA for Imsidolimab for the Treatment of Generalized Pustular Psoriasis · Persbericht

15/12 · Vanda Announces Submission of Biologics License Application to the FDA for Imsidolimab for the Treatment of Generalized Pustular Psoriasis · Persbericht

15/12 · RedHill Biopharma's Positive Opaganib Results Indicate Reduction in Venetoclax Resistant Cells · Persbericht

15/12 · Johnson & Johnson krijgt boete van 40 miljoen dollar in zaak rond kankerverwekkend talkpoeder · Business AM

Key takeaways Twee Californische vrouwen krijgen een schadevergoeding van in totaal 40 miljoen dollar (34 miljoen euro) van Johnson & Johnson. De jury achtte het bedrijf verantwoordelijk voor de diagnose van hun eierstokkanker....

15/12 · Press Release: Sanofi provides update on tolebrutinib in primary progressive multiple sclerosis · Persbericht

15/12 · Press Release : Sanofi provides update on tolebrutinib regulatory submission in non-relapsing secondary progressive multiple sclerosis · Persbericht

13/12 · U.S. FDA approves AKEEGA® as the first precision therapy for BRCA2-mutated metastatic castration-sensitive prostate cancer with 54% reduction in disease progression vs standard of care* · Persbericht

12/12 · Teva Releases Q4 2025 Aide Memoire · Persbericht

12/12 · Teva to Host Conference Call to Discuss Fourth Quarter 2025 Financial Results at 8 a.m. ET on January 28, 2026 · Persbericht

12/12 · Updated data for Lilly's Inluriyo™ (imlunestrant) reinforce efficacy results as monotherapy and in combination with Verzenio® (abemaciclib) in ER+, HER2- advanced breast cancer · Persbericht

12/12 · Abbott increases quarterly dividend for 54th consecutive year · Persbericht

12/12 · AI Diagnostics Hit Critical Mass as Hospitals Race to Cut Costs · Persbericht

12/12 · Levi & Korsinsky Notifies Shareholders of Perrigo Company plc(PRGO) of a Class Action Lawsuit and an Upcoming Deadline · Persbericht

11/12 · Vanda Pharmaceuticals Announces Participation in the J.P. Morgan Healthcare Conference · Persbericht

11/12 · Biohaven Presents Clinical Safety and Efficacy Data for BHV-1510, a Next-Generation Trop2 Antibody Drug Conjugate in Combination with Cemiplimab at the 2025 European Society for Medical Oncology (ESMO) Immuno-Oncology Congress · Persbericht

11/12 · AC Immune Positive Interim Phase 2 Data on ACI-7104.056 Support Potential Slowing of Progression of Parkinson’s Disease · Persbericht

11/12 · Lilly's triple agonist, retatrutide, delivered weight loss of up to an average of 71.2 lbs along with substantial relief from osteoarthritis pain in first successful Phase 3 trial · Persbericht

11/12 · Press Release: Sanofi’s Qfitlia and Cablivi approved in China, expanding care for rare diseases · Persbericht

11/12 · Addex Amends its at the Market Offering Agreement With H.C. Wainwright & Co. · Persbericht

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