All Updates

All Updates

icon
Filter
Product updates
Janssen receives European Commission approval for BALVERSA treatment for metastatic urothelial cancer
Precision Medicine
Aug 26, 2024
This week:
Funding
Slingshot Aerospace secures USD 30 million in growth capital from Trinity Capital
Digital Twin
Sep 12, 2024
Product updates
Akselos introduces software for FPSO monitoring
Digital Twin
Sep 12, 2024
Product updates
Vertical Aerospace completes first phase of VX4 flight testing
Passenger eVTOL Aircraft
Sep 12, 2024
Partnerships
Turbine and Ono Pharmaceutical reach developmental milestone in oncology research collaboration
AI Drug Discovery
Sep 12, 2024
Partnerships
Sino Biological and BioGeometry partner to optimize protein design using GenAI technology
AI Drug Discovery
Sep 12, 2024
Funding
Sinopia Biosciences raises USD 2.2 million in Phase II SBIR grant funding to accelerate oral mucositis program
AI Drug Discovery
Sep 12, 2024
Regulation/policy
eToro settles for USD 1.5 million with SEC over unregistered trading of certain crypto assets
Retail Trading Infrastructure
Sep 12, 2024
Funding
Amprion raises USD 100,000 in research grant funding from ALS Network to support ALS research and therapy development
Longevity Tech
Sep 12, 2024
Funding
Amprion raises USD 100,000 in research grant funding from ALS Network to support ALS research and therapy development
Precision Medicine
Sep 12, 2024
Funding
Epitopea raises GBP 500,000 in grant funding to develop vaccines and TCR-based therapies
Precision Medicine
Sep 12, 2024
Precision Medicine

Precision Medicine

Aug 26, 2024

Janssen receives European Commission approval for BALVERSA treatment for metastatic urothelial cancer

Product updates

  • Johnson & Johnson's subsidiary, Janssen-Cilag International, has received European Commission approval for its oncology drug, BALVERSA (erdafitinib). It is designed to treat adults suffering from urothelial carcinoma (mUC) that cannot be removed via surgery or has metastasized.

  • BALVERSA is an oral monotherapy designed to be taken once daily. It's formulated for patients with mUC who have certain FGFR3 genetic alterations and have undergone at least one treatment that involved either a PD-1 or PD-L1 inhibitor. The company claims that according to trial data, patients on erdafitinib had a median overall survival of over a year, with disease progression-free survival of 5.6 months compared to 2.7 months with chemotherapy.

Contact us

Gain access to all industry hubs, market maps, research tools, and more
Get a demo
arrow
menuarrow

By using this site, you agree to allow SPEEDA Edge and our partners to use cookies for analytics and personalization. Visit our privacy policy for more information about our data collection practices.