ViroCell Biologics has manufactured a GMP-grade lentiviral vector for a University College London (UCL) clinical trial aimed at tackling relapse …

Qlucore has announced that it has entered into an agreement with Sahlgrenska Hospital, in Gothenberg, Sweden. This agreement means the …

Eli Lilly has announced that the US Food and Drug Administration (FDA) has approved Jaypirca (pirtobrutinib, 100mg and 50mg tablets) …

Japanese pharmaceutical company Astellas Pharma and the Blood and Marrow Transplant Clinical Trials Network (BMT CTN) have presented their phase …

The National Institute for Health and Care Excellence (NICE) has recommended that AstraZenecaโs Calquence (acalabrutinib) be used on the NHS in …

NICE has recommended venetoclax in combination with obinutuzumab under final draft guidance for the first-line treatment of untreated chronic lymphocytic …

AbbVie have announced positive results from its latest Phase 3 clinical trial where Venclexta plus azacitidine improved survival and remission …

Gilead took the opportunity at this yearโs American Society of Clinical Oncology (ASCO) Annual Meeting to unveil new Phase 1b …

The leukemia drug nilotinib has shown promise in reducing the effects of Alzheimerโs disease and while having safe and minimal …

AbbVieโs Imbruvica (ibrutinib) has scored its 11th FDA approval, this time in combination with rituximab for the treatment of chronic …

Scientists from the Childrenโs Hospital of Los Angeles have engineered T-cells to identify and target multiple sites on acute lymphoblastic …

AstraZeneca confirmed it had recorded positive results from its Phase 3 trial of Calquence plus obinutuzumab in leukaemia. The trial …

Sanofi has agreed to buy California-based biotechnology firm Synthrox, in a deal worth about $2.5 billion (ยฃ1.95 billion). Paul Hudson, …

The FDA has approved AstraZenecaโs BTK inhibitor Calquence (acalabrutinib) in the treatment of chronic lymphocytic leukaemia (CLL) and small lymphocytic …

Astellas has revealed that the European Commission has awarded marketing approval for Xospata (gilteritinib) as an oral, once-daily monotherapy for …