Logo

Nurix Therapeutics Receives the US FDA’s IND Clearance for NX-1607 to Treat Advanced Malignancies

Share this
Nurix Therapeutics Receives the US FDA’s IND Clearance for NX-1607 to Treat Advanced Malignancies

Nurix Therapeutics Receives the US FDA’s IND Clearance for NX-1607 to Treat Advanced Malignancies

Shots:

  • The company has received the US FDA’s clearance for the IND application to expand an ongoing P-I dose escalation and expansion trial to evaluate the safety and tolerability of NX-1607 in adults with advanced malignancies incl. a range of solid tumor indications
  • Patients are now being enrolled in the trial in the UK with clinical sites in the US being added later. The result from initial biomarker data from the P-I trial are expected in H1’22
  • NX-1607 is an orally bioavailable inhibitor of CBL-B for immuno-oncology indications incl. a range of solid tumor types. Additionally, the therapy showed single-agent anti-tumor activity in multiple tumor models

Ref: Nurix | Image: Nurix

Click here to­ read the full press release 

Neha

Neha is a Senior Editor at PharmaShots. She is passionate and very enthusiastic about recent updates and developments in the life sciences and pharma industry. She covers Biopharma, MedTech, and Digital health segments along with different reports at PharmaShots. She can be contacted at connect@pharmashots.com.

Share this article on WhatsApp, LinkedIn and Twitter

Join the PharmaShots family of 12000+ subscribers

I accept the Terms and Conditions