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Πέμπτη 4 Ιουλίου 2019

Janssen riceve il parere positivo del CHMP per l'estensione dell'utilizzo di Imbruvica®▼(ibrutinib) per due indicazioni in Europa
BEERSE, Belgio--(BUSINESS WIRE)--Le aziende farmaceutiche Janssen di Johnson & Johnson hanno oggi annunciato che il Comitato per i medicinali per uso umano (CHMP) dell'Agenzia europea per i medicinali (EMA) ha emesso un parere positivo sull'estensione dell'autorizzazione alla commercializzazione di Imbruvica® (ibrutinib) per due indicazioni. Una è per l'uso di ibrutinib in combinazione con obinutuzumab per il trattamento dei pazienti adulti affetti da leucemia linfocitica cronica (LLC) non
Business Wire Health: Clinical Trials News
Mon Jul 01, 2019 16:40
Amphivena’s Human Proof-of-Concept Data for AMV564 in Relapsed/Refractory AML Updated at the European Hematology Association Annual Meeting
SOUTH SAN FRANCISCO, Calif.--(BUSINESS WIRE)--AMPHIVENA DATA AT EHA
Business Wire Health: Clinical Trials News
Mon Jul 01, 2019 16:15
Instem Awarded EU Horizon 2020 Research Grant
CONSHOHOCKEN, Pa.--(BUSINESS WIRE)--Instem is pleased to announce that NOTOCORD, an Instem Company, has been awarded an EU Horizon 2020 Research Grant.
Business Wire Health: Clinical Trials News
Mon Jul 01, 2019 16:06
Janssen recibe opinión positiva del CHMP recomendando el uso ampliado de Imbruvica®▼(ibrutinib) en dos indicaciones en Europa
BEERSE, Bélgica--(BUSINESS WIRE)--Las compañías farmacéuticas Janssen de Johnson & Johnson han anunciado que el Comité de Medicamentos de Uso Humano (CHMP) de la Agencia Europea de Medicamentos (EMA) ha recomendado ampliar la autorización de comercialización existente para Imbruvica® (ibrutinib) en dos indicaciones. Una recomendación es para el uso de ibrutinib en combinación con obinutuzumab en pacientes adultos con leucemia linfocítica crónica (LLC) no tratada previamente.1 La segunda es
Business Wire Health: Clinical Trials News
Mon Jul 01, 2019 16:06
Puma Biotechnology Submits a Supplemental New Drug Application to U.S. FDA for Neratinib to Treat HER2-Positive Metastatic Breast Cancer
LOS ANGELES--(BUSINESS WIRE)--Puma Biotechnology has submitted a supplemental NDA to the U.S. FDA for neratinib in combination with capecitabine for the treatment of breast cancer
Business Wire Health: Clinical Trials News
Mon Jul 01, 2019 15:00
Boehringer Ingelheim Expands Nonalcoholic Steatohepatitis (NASH) R&D Pipeline With New First-in-Class Compound from Yuhan Corporation
INGELHEIM, Germany & SEOUL, South Korea--(BUSINESS WIRE)--Boehringer Ingelheim and Yuhan Corporation today announced a collaboration and license agreement for the development of a first-in-class dual agonist for the treatment of NASH and related liver diseases that combines GLP-1 and FGF21 activity in one molecule. The collaboration brings together Yuhan Corporation’s expertise in FGF21 biology, obesity and NASH with Boehringer Ingelheim’s pharmaceutical expertise and commitment to bringing inn
Business Wire Health: Clinical Trials News
Mon Jul 01, 2019 15:00
Semma Therapeutics Announces Pre-Clinical Proof-of-Concept in Two Lead Programs in Type 1 Diabetes
CAMBRIDGE, Mass.--(BUSINESS WIRE)--Semma Therapeutics, Inc., a biotechnology company pioneering the curative use of stem cells in regenerative medicine, today announced the achievement of pre-clinical proof-of-concept based on data from its two lead programs for type 1 diabetes testing stem cell-derived islets (SC-islets) in both non-human primates and pigs. The data were presented by Felicia Pagliuca, Ph.D., Vice President of Cell Biology Research and Development, on Saturday, June 29th in a p
Business Wire Health: Clinical Trials News
Mon Jul 01, 2019 15:00
Synergys Announces Second Phase 1 SBIR Funding From National Institutes of Health
WALNUT CREEK, Calif.--(BUSINESS WIRE)--Synergys announces second Phase 1 SBIR funding from NIH for development of vasculogenic mimicry-blocking antibody fusion product for ovarian cancer.
Business Wire Health: Clinical Trials News
Mon Jul 01, 2019 15:00
UroGen Pharma Joins Russell 3000® Index
NEW YORK--(BUSINESS WIRE)--UroGen Pharma Ltd. (Nasdaq:URGN), a clinical-stage biopharmaceutical company developing treatments to address unmet needs in uro-oncology, today announced that it joined the broad-market Russell 3000® Index at the conclusion of the 2019 Russell indexes annual reconstitution, effective after the close of the US market on June 28, 2019. Annual Russell indexes reconstitution captures the 4,000 largest US stocks as of May 10, ranking them by total market capitalization. M
Business Wire Health: Clinical Trials News
Mon Jul 01, 2019 15:00
Bicycle Therapeutics Announces Positive Topline Results from Oxurion’s Phase I Trial Using a Novel Bicycle-based Plasma Kallikrein Inhibitor for the Treatment of Diabetic Macular Edema
CAMBRIDGE, U.K., & BOSTON--(BUSINESS WIRE)--Bicycle Therapeutics announces the successful completion of Oxurion’s Phase I clinical trial evaluating the safety and tolerability of THR-149.
Business Wire Health: Clinical Trials News
Mon Jul 01, 2019 14:30
Viela Bio Appoints Mitchell Chan as Chief Financial Officer
GAITHERSBURG, Md.--(BUSINESS WIRE)--Viela Bio today announced the appointment of Mitchell Chan as Chief Financial Officer, effective July 1. In this role, he will be responsible for leading corporate financing, financial operations, treasury, investor relations, corporate communications and corporate strategy. Previously, Mr. Chan served as Viela’s Vice President, Head of Finance & Corporate Strategy. “We are pleased to announce Mitch’s appointment to the CFO position,” said Bing Yao, Ph.D.
Business Wire Health: Clinical Trials News
Mon Jul 01, 2019 14:00

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