APPROVALS

Mirum’s CTEXLI tablets receives FDA approval for cerebrotendinous xanthomatosis

The U.S. Food and Drug Administration (FDA) has approved Mirum Pharmaceuticals' CTEXLI (chenodiol) tablets, a bile acid, for the treatment of adults with cerebrotendinous xanthomatosis (CTX). CTEXLI is the...

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Ultra-Hygienic mixing at small-scale

Introducing the new 150 UHS Ultra-Hygienic Small-Scale In-Line mixer from Silverson Machines. The 150 UHS In-Line is designed for Ultra Hygienic applications typically encountered in...

Pioneer Group drives AI innovation in healthcare through industry and academic collaboration

Pioneer Group, the life science infrastructure and venture building specialist, has joined forces with Innovate UK, The Medical Research Council (MRC) and AstraZeneca, to...

New SWLP laboratory at Croydon Hospital transforms the diagnostic facility into one of the most advanced and innovative in the UK

South West London Pathology (SWLP) introduces cutting-edge technologies to its laboratories to create one of the most modern, innovative, and efficient clinical blood science...

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Supply Chain

Pharmanovia signs exclusive distribution agreement with Er-Kim for Sunosi in Eastern Europe

Pharmanovia has signed an exclusive distribution agreement with Er-Kim, to enhance the availability of Sunosi (Solriamfetol), a first-in-class treatment for Excessive Daytime Sleepiness (EDS),...

Dr. Reddy’s enters into collaboration with Henlius for commercialization of HLX15, a biosimilar candidate to Darzalex & Darzalex Faspro in the U.S. and Europe

Dr. Reddy’s Laboratories has entered into a license agreement with Shanghai Henlius Biotech for the commercialization of HLX15, Henlius’ investigational daratumumab biosimilar candidate to...

Er-Kim signs distribution agreement with the MEDICE Health Family for Vafseo in Central & Eastern Europe

Er-Kim, an international company specializing in the commercialization of novel therapies for pharmaceutical and biopharmaceutical companies, has signed a distribution agreement with the MEDICE...

Er-Kim extends exclusive distribution agreement with Ascendis to expand commercialization of endocrinology portfolio

Er-Kim, an international pharmaceutical company specializing in the commercialization of novel therapies, has extended its exclusive agreement with Danish biopharmaceutical company Ascendis Pharma to commercialize...

Approvals

Mirum’s CTEXLI tablets receives FDA approval for cerebrotendinous xanthomatosis

The U.S. Food and Drug Administration (FDA) has approved Mirum Pharmaceuticals' CTEXLI (chenodiol) tablets, a bile acid, for the treatment of adults with cerebrotendinous...

Bavarian Nordic’s Chikungunya vaccine receives U.S. FDA approval for those aged 12 and older

The U.S. Food and Drug Administration (FDA) has approved Bavarian Nordic's VIMKUNYA (Chikungunya Vaccine, Recombinant) for injection, the first virus-like particle (VLP) single-dose chikungunya...

European Commission approves CSL’s ANDEMBRY for the prevention of recurrent attacks of hereditary angioedema

GSK’s 5-in-1 meningococcal vaccine approved by US FDA

BridgeBio’s BEYONTTRA approved by European Commission to treat ATTR-CM

U.S. FDA approves SpringWorks Therapeutics’ GOMEKLI for patients with NF1-PN

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R&D

U.S. FDA grants Breakthrough Therapy Designation to Innate Pharma’s lacutamab for relapsed or refractory Sézary syndrome

The U.S. Food and Drug Administration (FDA) has granted Breakthrough Therapy Designation (BTD) to Innate Pharma's lacutamab, an anti-KIR3DL2 cytotoxicity-inducing antibody, for the treatment...
R&D

AbbVie and Xilio Therapeutics to develop novel tumor-activated immunotherapies

AbbVie and Xilio Therapeutics, a clinical-stage biotechnology company discovering and developing tumor-activated immuno-oncology therapies for people living with cancer, have announced a collaboration and...
R&D

Royalty Pharma to provide $250m R&D funding in Biogen lupus collaboration

Royalty Pharma has entered into an agreement with Biogen to provide research and development (R&D) funding of up to $250 million for litifilimab, a...
R&D

FDA orphan drug and rare pediatric disease designations granted to Arbor Biotechnologies’ primary hyperoxaluria type 1 treatment

The U.S. Food and Drug Administration (FDA) has granted orphan drug designation (ODD) and rare pediatric disease designation (RPDD) to Arbor Biotechnologies' ABO-101 for...
R&D

Relmada Therapeutics acquires potential Tourette syndrome therapy from Asarina Pharma

Relmada Therapeutics, a clinical-stage biotechnology company, has acquired Sepranolone, a Phase 2b ready neurosteroid, from Asarina Pharma, being developed for the potential treatment of...

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