Regenerative Medicine

ReNeuron receives clearance for stem cell trial

Country
United Kingdom

The ReNeuron Group Plc has received final regulatory clearance to start its ground-breaking first-in-man study of a stem cell therapy for stroke. The therapy will be administered to patients who have been left disabled by an ischaemic stroke.

First patient treated in US stem cell trial

Country
United States

A patient in the US has become the first person with the neurodegenerative disease, amyotrophic lateral sclerosis (ALS), to be treated with stem cells. The cells were directly injected into the spinal cord of the patient on 20 January 2010.

FDA puts hold on ACT trial

Country
United States

The US Food and Drug Administration has put a ‘clinical hold’ on a proposed first-in-man study of a new embryonic stem cell treatment for eye disease, according to the developer.

Cell Medica links up with US medical centre

Country
United Kingdom

Cell Medica Ltd of London, UK has signed a research and development agreement with a medical research center in Texas to help it commercialise clinically-proven cell therapies which have been pioneered by the US researchers.

Geron sees trial start in 2010 third quarter

Country
United States

Geron Corporation of Menlo Park California, US expects to begin its first-in-man study of a new embryonic stem cell therapy for spinal cord injury in the third quarter of 2010. This follows discussions with the Food and Drug Administration during which a strategy was outlined for lifting the trial hold.

UK regenerative medicines company receives £1.2 million

Country
United Kingdom

BioCeramic Therapeutics, a privately-owned company that is developing bioactive materials for orthopaedic and dental applications has received £1.2 million to support its operations ahead of the commercialisation of its lead product in 2010.

Cell Medica receives £1.95 million to commercialise cell therapy

Country
United Kingdom

Cell Medica Ltd, an early-stage cellular therapeutics company, has received £1.95 million in new funding in order to commercialise its lead product, a cell therapy technique which protects patients from infection following a bone marrow transplant.