Pharmaceutical company Dr Reddy's Laboratories Ltd (BSE:500124)(NSE:DRREDDY) (NYSE:RDY) on Wednesday announced the availability of Bortezomib for Injection 3.5 mg/vial for intravenous use only in the US cancer market.
The company added that the Bortezomib for Injection 3.5 mg/vial has been approved by the US Food and Drug Administration (USFDA) via a 505(b)(2) new drug application (NDA) pathway.
In addition, the US FDA has approved the company's Bortezomib for Injection 3.5 mg/vial for the treatment of adult patients with multiple myeloma as well as for the treatment of adult patients with mantle cell lymphoma who have received at least one prior therapy.
Dr Reddy's Laboratories stated that it is committed to providing affordable and innovative medicines for healthier lives. It operates through three businesses: Pharmaceutical Services & Active Ingredients, Global Generics and Proprietary Products.
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Astrazeneca Imfinzi perioperative regimen gains positive EU CHMP opinion in early gastric cancer
I Peace generates human iPS cells from NKT cells and offers them for research use
Frontage expands early phase clinical research capabilities across US and China
Summit Therapeutics' BLA for ivonescimab in EGFR-mutated NSCLC accepted by FDA
InSysBio agrees new collaborative project with BeOne Medicines
Physiomics secures new modelling contract with Numab Therapeutics
Mabwell reports first patient dosed with 7MW4911 in US trial
Atossa Therapeutics' founder and CEO named one of The Top 50 Healthcare Technology CEOs of 2025
Avacta secures FDA clearance for second pre|CISION oncology programme
Guardant Health and Merck enter multi-year oncology diagnostics collaboration
Akeso secures NMPA review acceptance for gumokimab in ankylosing spondylitis