All content on this site is intended for healthcare professionals only. By acknowledging this message and accessing the information on this website you are confirming that you are a Healthcare Professional.

  TRANSLATE

The lupus Hub website uses a third-party service provided by Google that dynamically translates web content. Translations are machine generated, so may not be an exact or complete translation, and the lupus Hub cannot guarantee the accuracy of translated content. The lupus and its employees will not be liable for any direct, indirect, or consequential damages (even if foreseeable) resulting from use of the Google Translate feature. For further support with Google Translate, visit Google Translate Help.

The Lupus Hub is an independent medical education platform, supported through a grant from AstraZeneca. The funders are allowed no direct influence on our content. The levels of sponsorship listed are reflective of the amount of funding given. View funders

Now you can support HCPs in making informed decisions for their patients

Your contribution helps us continuously deliver expertly curated content to HCPs worldwide. You will also have the opportunity to make a content suggestion for consideration and receive updates on the impact contributions are making to our content.

Find out more

Important announcement

@US_FDA grants breakthrough device designation to an extracorporeal therapeutic apheresis column, a blood purification device designed to selectively remove cfDNA and NETs from patient plasma, for the treatment of severe, treatment-refractory #SLE.
Read more 👉 https://loom.ly/BZDFTTg

More drug updates

VIEW ALL
Positive CHMP opinion for anifrolumab subcutaneous self-administration for adult patients with SLE

Positive CHMP opinion for anifrolumab subcutaneous self-administration for adult patients with SLE

The CHMP of the @EMA_News has recommended approval of anifrolumab as a self-administered once-weekly pre-filled pen for adult patients with #SLE, on top of standard therapy. Read more: loom.ly/budKpD4

Obinutuzumab receives U.S. FDA approval for the treatment of lupus nephritis

Obinutuzumab receives U.S. FDA approval for the treatment of lupus nephritis

@US_FDA approves obinutuzumab for the treatment of adult patients with active #LupusNephritis, who are receiving standard therapy, as well as a shorter 90-minute infusion time after the first infusion, for eligible patients. Read more: loom.ly/EXKLaUA

Important announcement

@US_FDA clears IND application for QT-019B, an off-the-shelf CD19/BCMA dual-target CAR T-cell therapy, for the treatment of refractory #SLE. This clearance enables the initiation of a phase I/II trial in the US. 👉 https://loom.ly/vsyMZN0