Accelera and CROSS: an integrated solution for Pre-clinical to Clinical transition
Nerviano, 17 May 2021 The relationship between Accelera and CROss Alliance® started a decade ago and since then we have renewed our collaboration during the years. Our specializations, preclinical and early phase clinical development respectively, our shared values...
NerPharMa and ICROM sealed Partnership Agreement
Nerviano, 6 May 2021 NerPharMa, a veteran CDMO with a specialization in oncology small molecule drug manufacture and a member of NMS Group, has announced today a Partnership Agreement with ICROM srl, aiming for collaboration on commercial production of High Potent...
NMS Group wins China Awards for creating concrete values
Nerviano, 9 February 2021 NMS Group has been named the winner of the “Value creators' category at the prestigious 'China Awards 2021' during the online event held by the Italy China Foundation on Monday 8 February 2021. The “Value creators' award is a recognition for...
NERVIANO MEDICAL SCIENCES ANNOUNCED CLINICAL TRIAL APPROVAL IN CHINA OF THE PARP INHIBITOR NMS-293 IN PATIENTS WITH ADVANCED SOLID TUMORS TODAY.
Nerviano, 01.12.2020 Nerviano Medical Science Srl, the NMS Group subsidiary specialized in research and development of innovative oncological drugs, today announced the recent approval of a phase I clinical study for its PARP...
DMED SUCCESSFULLY ASSISTED ITALIAN NMS GROUP’S PARP INHIBITOR TO OBTAIN CLINICAL TRIAL APPROVAL
Nerviano, 30.11.2020 dMed Company (Shanghai) Ltd. congratulated the recent approval of a PARP inhibitor (NMS-03305293 capsules) of its collaborator NMS Group, an Italian oncology drug discovery and development company, by the National Medical Products Administration...
NANDING ZHAO APPOINTED CEO OF NMS GROUP TO ACCELERATE THE DEVELOPMENT OF THE GROUP’S STRATEGY
Nerviano, 02.10.2020 NMS Group announces today that its board of directors has accepted the resignation of Ying Shao as CEO, effective October 1, 2020. The Board has contextually appointed as CEO Dr. Nanding Zhao. Dr. Nanding Zhao, PhD and MBA, is an executive leader...
ROZLYTREK, ROCHE’S FIRST TUMOUR-AGNOSTIC THERAPY, APPROVED IN EUROPE FOR PEOPLE WITH NTRK FUSION-POSITIVE SOLID TUMOURS AND FOR PEOPLE WITH ROS1-POSITIVE ADVANCED NON-SMALL CELL LUNG CANCER
Basel, 03.08.2020 Roche (SIX: RO, ROG; OTCQX: RHHBY) today announced that the European Commission has granted conditional marketing authorisation for Rozlytrek® (entrectinib) for the treatment of adult and paediatric patients 12 years of age and older with solid...
THERMO FISHER SCIENTIFIC SIGNS COMPANION DIAGNOSTIC AGREEMENT WITH CHUGAI PHARMACEUTICAL
Calif, 08.07.2020 Thermo Fisher Scientific has signed a companion diagnostic (CDx) agreement with Chugai Pharmaceutical Co., Ltd., a member of the Roche Group, and has applied to the Ministry of Health, Labour and Welfare (MHLW) to expand the use of the Oncomine Dx...
CANCER PATIENTS TO BENEFIT FROM NEW HISTOLOGY INDEPENDENT TREATMENT
25.06.2020 Entrectinib (Rozlytrek, Roche), a revolutionary treatment for a range of cancers, is the second histology independent drug to be recommended by NICE for use on the Cancer Drugs Fund (CDF). As a histology independent treatment, entrectinib targets all solid...
CARDIFF ONCOLOGY DATA CONTINUES TO DEMONSTRATE EFFICACY, DURABILITY AND SAFETY OF ONVANSERTIB IN PATIENTS WITH DIFFICULT-TO-TREAT RELAPSED/REFRACTORY AML
San Diego, 15.06.2020 Cardiff Oncology, Inc. (Nasdaq: CRDF), a clinical-stage oncology therapeutics company developing drugs to treat cancers with the greatest medical need for new treatment options, including KRAS-mutated colorectal cancer, Zytiga®-resistant prostate...
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