MONTREAL, July 28, 2020 /PRNewswire/ -
Valeo Pharma Inc. (CSE: VPH) ("Valeo" or the "Company"), a Canadian specialty pharmaceutical company, announced today that it will be presenting at Wall Street Reporter's livestream conference on Wednesday July 29, 2020.
Mr. Steve Saviuk, CEO of Valeo will share an overview of the depth and diversity of Valeo's growing product portfolio, the four products scheduled for launch this summer and how these launches and the upcoming Redesca approval expected for late summer will help the Company move towards profitability.
Valeo presentation will take place at 1 pm EST on Wednesday, July 29, 2020.
Following the 20-minute presentation, Mr Saviuk will take questions from the audience.
To sign up for the event, https://www.wallstreetreporter.com/next-superstock-onlineinvestor-conference/
Recent company highlights include:
Notice of Compliance received from Health Canada authorizing the transfer of the AmetopTM commercial rights to Valeo.
The approval for its Abbreviated New Drug Application ("ANDA") received from the U.S. Food and Drug Administration ("FDA") for Ethacrynate Sodium 50 mg.
The Notice of Compliance received from Health Canada authorizing the transfer of the commercial rights of Yondelis® (trabectedin), a novel marine-derived antitumor agent manufactured by PharmaMar S.A., to Valeo.
The notice of a positive recommendation received from Quebec's Institut national d'excellence en santé et en services sociaux ("INESSS") to the Health Minister for the inclusion of Onstryv® on the list of medications covered by the Régie de l'assurance maladie du Québec (RAMQ).
The acceptance for review of its New Drug Submission filed for a low molecular weight heparin biosimilar by Health Canada.
DESPUES DE 18 AÑOS CON SOLO TOPOTECAN CON FULL APPROVAL EN EEUU COMO TREATMENT 2a LÍNE SCLC-ES ... LA USFDA ACABA DE APROBAR AL TARLATAMAB CON FULL APPROVAL ... POR LO QUE ES YA EL NEW TREATMENT STÁNDARD EN EEUU . TIENE APROBACIÓNES ACELERADAS EN CANADA , UK, COREA ... Y EN DÍAS PODRÍA ALCANZAR LA APROBACIÓN TAMBIÉN EN CHINA QUE EN JULIO 2025, LA NMPA ACEPTÓ LA SOLICITUD DE REGISTRO (NDA) PARA TARLA OTORGÁNDOLE ADEMAS LA REVISIÓN PRIORITARIA . LA EMA TAMBIÉN LO ESTÁ YA EVALUANDO .

