Evotec SE has expanded a partnership with Celgene Corp to identify new treatments for neurodegenerative diseases using induced pluripotent stem (iPS) cells. This has triggering a milestone payment to the German company of $9 million.
Genmab A/S, one of Europe’s oldest antibody companies, has registered to make a public offering of American Depositary Shares on the US Nasdaq market of up to $500 million. The plans were disclosed on 28 May but as of 6 June the final size of the offering had not been decided. The company is currently listed on Nasdaq Copenhagen and is proposing the US listing to broaden its shareholder base.
Denmark-based Abacus Medicine A/S announced on 29 May that it was postponing an initial public offering planned for the Frankfurt Stock Exchange because of unfavourable market conditions. The parallel trade company was reportedly planning to raise €50 million to finance expansion.
The company’s biggest market is Germany where it sells drugs purchased at cheaper prices in other European markets.
It is estimated that up to 7% of patients with pancreatic cancer have a mutation in the tumour suppressor genes BRCA1 and BRCA2, impairing the body's ability to repair damaged DNA and allowing tumours to grow. BRCA mutations also drive ovarian and breast cancers, but they can be particularly lethal in pancreatic tumours because this cancer is difficult to detect at an early stage.
Novo Holdings A/S is to make an equity investment of up to £53.5 million in Oxford Biomedica Plc which has grown a business around the supply of lentiviral vectors for third parties including Novartis, the developer of Kymriah, the first gene therapy for cancer to be approved by the US Food and Drug Administration. Following the transaction Novo will have a stake of up to 10.1% in the UK company.
Novartis has decided to price its new gene therapy for spinal muscular atrophy using a formula that measures the performance of the drug over five years. The therapy, Zolgensma (onasemnogene abeparvovec-xioi), is a one-time treatment for a genetic disease that affects a child’s ability to swallow and breath, frequently leading to death.
The US Food and Drug Administration has approved a gene therapy to treat children under the age of two years who have spinal muscular atrophy, a rare genetic disease that affects a child’s ability to swallow and breath, frequently leading to death.
Evotec SE is to expand its pharmaceutical services business into biologics with the acquisition of Just Biotherapeutics Inc of Seattle, Washington, US. The deal will give the Germany-based company a capacity to discover and develop protein therapeutics in addition to its existing small molecule business. Evotec will pay an initial $60 million for the company, a figure that could rise to $90 million depending on the achievement of certain milestones within the next three years.
Syncona Ltd, an active investor in cell and gene therapy, has launched a new company, Quell Therapeutics Ltd, which will develop cell therapies to treat autoimmune conditions based on engineered T regulatory (Treg) cells. Tregs are a subset of T cells with the potential to down-regulate the immune system.
Rinri Therapeutics Ltd, a spin-out of Sheffield University in the UK, has received £1.4 million in seed funding from a European syndicate in order to advance a prospective stem cell therapy to restore hearing. The company aims to reverse neuropathic sensorineural hearing loss by repairing the damaged cytoarchitecture of the inner ear.