AmacaThera and Pacira sign agreement for AMT-143
AmacaThera has entered into an exclusive worldwide licensing agreement with Pacira BioSciences for up to $230m for AMT-143, an investigational long-acting non-opioid anaesthetic.
AmacaThera has entered into an exclusive worldwide licensing agreement with Pacira BioSciences for up to $230m for AMT-143, an investigational long-acting non-opioid anaesthetic.
Myrio Therapeutics has announced a collaborative partnership with NYU Langone Health and the University of Pennsylvania Perelman School of Medicine to expedite next-generation T cell immunotherapeutics development for solid tumours.
Naobios and Tokyo Metropolitan Institute of Medical Science (TMIMS) have announced a partnership for the development of a new mpox vaccine using a live-attenuated approach.
Tempus has entered into a collaboration with Whitehawk to enhance biomarker-driven research and facilitate the development of Whitehawk's oncology pipeline.
iQure has formed a research partnership with University of Padova associate professor Laura Civiero to investigate iQ-007, the company's lead programme targeting EAAT2, the transporter responsible for glutamate uptake.
AeroRx Therapeutics has secured $21m in Series A financing, led by Avalon BioVentures, with participation from Alexandria Venture Investments, Correlation Ventures, and other investors.
The US Food and Drug Administration (FDA) has awarded Fast Track designation to Alto Neuroscience’s ALTO-101, a novel small molecule phosphodiesterase-4 (PDE4) inhibitor for the treatment of cognitive impairment linked to schizophrenia (CIAS).
BioLineRx and Hemispherian have formed a joint venture to advance the development of GLIX1, an oral small molecule aimed at targeting DNA damage response in glioblastoma (GBM) and other types of cancer.
Sandoz has launched a generic iron sucrose injection in the US, aimed at treating iron deficiency anaemia in patients with chronic kidney disease.
Argo Biopharmaceutical has received investigational new drug (IND) approval from the National Medical Products Administration (NMPA) of China for a Phase II clinical trial of BW-40202 for the treatment of paroxysmal nocturnal haemoglobinuria (PNH).