News

Lilly embraces gene editing

Country
United States

Eli Lilly and Co has signed a collaboration agreement with Verve Therapeutics Inc,  a clinical stage US genetic medicines company, to develop a product that can treat atherosclerotic cardiovascular disease. This is a disorder arising from a thickening of the arteries, restricting the flow of blood to organs and tissues. An increase in a specific type of lipoprotein can cause the disease. The amount of this protein in individuals is congenital.

Columvi approved for DLBCL

Country
Switzerland

A bispecific T cell engaging antibody developed by Roche for diffuse large B-cell lymphoma (DLBCL) received an accelerated US approval on 16 June, the second authorisation this year for the Swiss multinational in this indication. The drug, Columvi (glofitamab) was authorised by the Food and Drug Administration based on response rate and durability of response in a Phase 1/2 trial. In April the FDA approved Polivy, an antibody drug conjugate from Roche in combination with other drugs, also for DLBCL.

Chikungunya vaccine effective

Country
France

A candidate vaccine designed to protect against chikungunya virus infection has met its primary endpoint in a Phase 3 study paving the way for a regulatory review and possible launch in geographies where the disease is prevalent. The results of the study were published in The Lancet on 12 June 2023. The vaccine, VLA1553, has been developed by Valneva SE of France.

Novartis to acquire Chinook

Country
Switzerland

Novartis is to pay $3.2 billion upfront to acquire Chinook Therapeutics Inc of Seattle, Washington, US, in a bid to strengthen its renal portfolio with two Phase 3 assets for immunoglobulin A nephropathy (IgAN), a rare, progressive kidney disease. The transaction, which has been approved by the boards of both companies, is expected to close in the second half of 2023. It will take the form of a merger of Chinook into a newly formed Novartis subsidiary.

Beacon Therapeutics is launched

Country
United Kingdom

Syncona Ltd, the UK investment group, has launched its third gene therapy company directed against retinal diseases, including an inherited monogenic disorder that leads to progressive vision loss in males. The launch of Beacon Therapeutics Holdings Ltd was announced on 12 June and follows the UK group’s acquisition and restructuring of Applied Genetic Technologies Corp (AGTC) of the US. Beacon’s assets include a late-stage programme from AGTC in X-linked retinitis pigmentosa, the inherited monogenic disorder, and two proprietary pre-clinical assets identified by Syncona.

ITM secures investment

Country
Germany

ITM Isotope Technologies Munich SE (ITM) has secured €255 million from an investor syndicate led by Temasek of Singapore to advance its pipeline of radiopharmaceuticals for the treatment of cancer. The round, which was also supported by BlackRock Alternatives and the Qatar Investment Authority, will help advance the company’s lead product for neuroendocrine tumours and expand capacity for the production of targeted radionuclide therapies. These are a type of radiation therapy in which a radioactive chemical is linked to a cell-targeting molecule such as a peptide or small molecule.

Quell and AZ team up

Country
United Kingdom

Quell Therapeutics Ltd has secured its first major partnership for the development of its regulatory T cell technology for the treatment of autoimmune diseases. An agreement with AstraZeneca Plc, announced on 9 June, will bring the two parties together to research and develop potential therapies for Type 1 diabetes and inflammatory bowel disease. AstraZeneca is to make an $85 million upfront payment to Quell comprising cash and equity. If the collaboration is successful, with the commercialistion of new products, milestone payments could exceed $2 billion.

Advisory body backs Leqembi

Country
United States

An advisory committee that reviews drug applications for the US Food and Drug Administration has concluded that the Alzheimer’s disease treatment Leqembi (lecanemab) has shown clinical benefit for patients and should be approved. The Peripheral and Central Nervous System Drugs Advisory Committee voted unanimously to recommend full approval on 9 June. A decision by the FDA is expected on 6 July.

Second lawsuit against IRA

Country
United States

A lawsuit has been filed by the US Chamber of Commerce against the American government seeking to revoke part of the Inflation Reduction Act that gives the government powers to negotiate the prices of some drugs directly with industry. The suit was filed on 9 June in the US District Court in Dayton, Ohio saying the legislation violates constitutional protections for free enterprise. Merck & Co Inc registered a similar complaint in the US District Court in Washington DC on 6 June.

New deal for BC Platforms

Country
Switzerland

Switzerland-based BC Platforms AG is to strengthen its position as a provider of real world data for clinical research with the acquisition of 4Pharma Ltd, a contract research organisation located in Turku Finland. The acquisition, announced on 1 June, will bring the Finnish company’s research capabilities, which include medical writing and data collection, into BC Platform’s global service offering. The financial terms of the transaction were not disclosed.