Mode of action of allosteric modulation, © Addex Therapeutics Ltd.

Following a private placement worth CHF3m in February, Swiss allosteric modulator specialist Addex Therapeutics has increased its capital to finance clinical studies of dipraglurant in Parkinson’s and ADX71441.

Mark Vossenaar

Gyros Protein Technologies has appointed Mark Vossenaar as Vice President, European Sales.

© Eppendorf

Eppendorf extends its range of accessories and consumables for the epMotion® 5070, 5053 and 5075 automated Liquid Handling systems to facilitate pipetting of small volumes from 10 µL down to 200 nL.

A variation of type 1 myotonic dystrophy, called congenital myotonic dystrophy, is apparent at birth. Characteristic features include weak muscle tone (hypotonia), an inward- and upward-turning foot (clubfoot, see photo), breathing problems, delayed development, and intellectual disability. © NIH Genetics home reference

London-based orphan drug developer AMO Pharma’s drug AMO-02 has been granted FDA fast track status as treatment for congenital myotonic dystrophy, a sub-indication muscular dystrophy.

Easylog was voted Best Innovation Exhibitor at the Pharmapack Awards in February 2016, © Biocorp

French drug delivery specialist Biocorp S.A. (Issoire) has signed an industrialisation contract with Virbac, one of the top-ten vet-med makers. 

Paris-based biopharma GenSight Biologics SA named Mohamed Genead as Chief Medical Officer in early May. Most recently, Genead was Vice President & Global Therapeutic Area Head for Ophthalmology/Retina Gene Therapy at Biogen.

New HQ of Morphosys, which developed guselkumab, © MorphoSys AG

Janssen speeds up US approval of psoriasis antibody guselkumab and targets further indications.

Abzena plc shares are traded at AIM market of the London Stock Exchange under the ticker ABZA, © LSE

British Abzena plc has announced that True North Therapeutics (TNT) will be taken over by Bioverativ Inc. Bioverativ will further develop TNT’s complement factor C1-blocking antibody TNT009, developed using technology, which was licenced from Abzenawhich was licenced from Abzena.

Following the EMA’s recommendation for EU approval of sarilumab as second-line treatment for rheumatoid arthritis, French drug giant Sanofi and partner Regeneron have also been given the green light from the US FDA.

UCB headquarters. © Assar architects

Top-Line Phase 3 data of Amgen’s/UCB’s osteoporosis antibody romosozumab in postmenopausal women suggest efficacy but uncover a new safety signal.