News

Verona in pact with Nuance Pharma

Country
United Kingdom

Verona Pharma Plc has agreed to grant exclusive rights to Nuance Pharma Ltd of Shanghai, China for its respiratory treatment ensifentrine in exchange for an upfront payment of $25 million in cash and other considerations. The rights relate to the development and commercialisation of ensifentrine in mainland China and adjacent territories. Ensifentrine is an investigational therapy, currently in a global Phase 3 programme for the treatment of chronic obstructive pulmonary disease (COPD). Late-stage clinical trials are currently underway at sites in the US, Europe and South Korea.

Launch of Transine Therapeutics

Country
United Kingdom

A new application for therapeutic RNA is being explored by the UK start-up company Transine Therapeutics Ltd. On 2 June, Transine announced receipt of an extended £9.1 million in seed financing. The funding round was co-led by Takeda Ventures Inc and the Dementia Discovery Fund (DDF), a specialist venture capital fund supported by private industry, charities, and the UK government.

Antifungal treatment receives funding

Country
United Kingdom

The developer of a new antifungal agent designed as an inhaled therapy for invasive pulmonary aspergillosis, has received $92 million in new capital. UK-based Pulmocide Ltd will use the Series C financing to carry out a Phase 3 registration trial for the drug PC945, which is a triazole antifungal agent.

Call for exemption from GMO rules

Country
Belgium

Three industry associations have issued an appeal to the European Commission to exempt advanced therapy medicinal products (ATMPs) from the EU’s genetically modified organism (GMO) legislation. This is to make the region more competitive as a site for clinical trials. The appeal was issued in a statement from the Alliance for Regenerative Medicine; the European Federation of Pharmaceutical Industries and Associations; and the European Association of Bioindustries. A paper was also published online on 24 May in the journal Human Gene Therapy.

Innovative Molecules gets funding for viral treatment

Country
Germany

Innovative Molecules GmbH of Germany has raised €20 million from a Series A financing round to progress a treatment for herpes simplex virus, a microbe that jumped from chimpanzees to humans more than 1.6 million years ago and now infects around two-thirds of the global population. There are two forms of the virus, type 1 and type 2, which can present either as cold sores on the mouth or blisters on the genitals. Once infected, an individual has the virus for life, though in many people it remains latent.

Aspirin doesn’t work for Covid-19

Country
United Kingdom

Aspirin has been eliminated as a possible treatment for patients hospitalised with Covid-19. This follows a large randomised clinical trial in the UK that assessed the effects of the compound on the survival of Covid-19 patients and their risk of developing a rare type of blood clot. Aspirin is widely used to reduce blood clotting in other diseases.

Iksuda Therapeutics raises $47 million for ADCs

Country
United Kingdom

The UK-based oncology company Iksuda Therapeutics Ltd has completed a $47 million financing round to progress a pipeline of antibody-drug conjugates (ADCs), a drug class that is seeing renewed interest from investors because of advances in conjugation technologies. The financing was co-led by the South Korean entities Mirae Asset Financial Group and Celltrion Inc.

argenx takes back cusatuzumab

Country
Netherlands

argenx SE is to take back rights to the antibody therapeutic cusatuzumab after its partner Cilag GmbH International, one of the Janssen Pharmaceutical Companies of Johnson & Johnson Inc, announced plans to quit the three-year-old collaboration. Cusatuzumab is in a Phase 1b study in newly-diagnosed, elderly patients with acute myeloid leukaemia (AML). It is being tested with venetoclax and the chemotherapy azacitidine.

Alzheimer’s drug approved

Country
United States

A new treatment for Alzheimer’s disease was approved by the US Food and Drug Administration on 7 June using a surrogate end point for clinical benefit: a reduction of amyloid beta plaque in the brain. Aduhelm (aducanumab) was given an accelerated approval. It is the first new treatment approved for Alzheimer's disease in the US since 2003.

Semaglutide approved for obesity

Country
United States

Novo Nordisk A/S has received US Food and Drug Administration approval for its drug Wegovy (semaglutide) for the treatment of obesity – the first weight management drug to be approved by the agency since 2014. More than one-third of US adults are estimated to be obese with the highest prevalence among those in middle age. Obesity is a risk factor for multiple disorders including heart disease, stroke and diabetes.