Autres langues Clinuvel Pharmaceuticals Limited Deutsche Boerse AG

Actions

UR9

AU000000CUV3

Produits pharmaceutiques

Marché Fermé - Deutsche Boerse AG 08:04:35 31/07/2026 Varia. 5j. Varia. 1 janv.
5,500 EUR -4,84% Graphique intraday de Clinuvel Pharmaceuticals Limited -8,33% -21,43%

Autres langues

30/07 Clinuvel Pharmaceuticals Strengthens Supply Chain as Part of Commercial Preparations for North American Vitiligo Market
28/07 Clinuvel Pharmaceuticals Ltd Provides Update On SCENESSE In Vitiligo
28/07 Clinuvel Pharmaceuticals Plans to Report Late-Stage Vitiligo Study Topline Results in December
23/07 Clinuvel Pharmaceuticals Limited to Reduce Global Workforce by Approximately 10%-20%
23/07 Clinuvel Pharmaceuticals Limited Announces Relocation of Corporate Headquarters to the United States
23/07 CLINUVEL implements strategic reorganisation to refocus on U.S. markets
23/07 Clinuvel Pharmaceuticals to Move Headquarters to US, Plan Workforce Reduction of Up to 20%
23/07 Australian Shares Open Higher as Oil, Gold Rally on Middle East Tensions; Santos Posts Higher Q2 Total Production
21/07 Clinuvel Pharmaceuticals Confirms ADS Start Trading on Nasdaq
21/07 Clinuvel Pharmaceuticals Limited(NasdaqGS:CUVL) added to NASDAQ Composite Index
20/07 CLINUVEL’s ADS to commence trading on Nasdaq
20/07 Clinuvel Pharmaceuticals' ADS to Begin Trading on Nasdaq
13/07 Clinuvel Pharmaceuticals Limited Receives Health Canada Notice of Compliance for Scenesse for Prevention of Phototoxicity in Adult Patients with Erythropoietic Protoporphyria
13/07 SCENESSE® approved for EPP in Canada
13/07 Clinuvel Pharmaceuticals' Photoprotection Drug Candidate Receives Health Canada Approval
02/07 Clinuvel Pharmaceuticals Extends CEO Philippe Wolgen's Term of Employment
16/06 Clinuvel Pharmaceuticals Advances US Listing Plan With SEC Filing for Nasdaq ADS Upgrade
28/04 Clinuvel Pharmaceuticals plans level II ADR upgrade and Nasdaq listing as CUVL
28/04 Clinuvel Pharmaceuticals Advances Nasdaq ADR Uplisting With US SEC Review Underway
27/04 Clinuvel Pharmaceuticals says FDA relaxes Scenesse postmarketing requirement
27/04 Clinuvel Pharmaceuticals Says FDA Removes Post-Authorization Requirement for Implant
27/04 Clinuvel Unlikely to Seek Scenesse's Vitiligo Approval Before Phase 3 Completion, Says Jefferies
24/04 Clinuvel Pharmaceuticals Limited Receives Final European Scientific Advice for Pivotal Phase III Vitiligo Study
24/04 CLINUVEL receives final EMA scientific advice for pivotal Phase III vitiligo study
24/04 Clinuvel Pharmaceuticals receives final EMA scientific advice for pivotal phase III vitiligo study
Aucun résultat pour cette recherche