
Mumbai, July 2, 2025 —
In a landmark moment that has electrified both the medical and investment worlds, shares of NovaCure Biopharma Ltd. skyrocketed 14% in early morning trade after the company announced it had received final approval from the U.S. Food and Drug Administration (USFDA) for its breakthrough oncology drug — OncoRelix, a first-in-class therapy targeting aggressive metastatic tumors.
This isn’t just another drug approval — it’s a watershed moment that could redefine cancer care, while giving a massive jolt of energy to India’s pharmaceutical landscape.
🧬 What is OncoRelix?
OncoRelix is a next-generation immuno-oncology treatment that targets cancer cells using a dual-action approach: it boosts the immune system’s natural killer cells while simultaneously suppressing tumor-shielding proteins. Early trials reported an 82% improvement in patient survival rates over existing chemotherapy standards, especially in late-stage liver and pancreatic cancers.
“This is not just a win for us as a company, but a win for humanity. The FDA’s nod proves that innovation knows no borders,” said Dr. Meera Jain, Chief Medical Officer at NovaCure.
📈 Stock Market Frenzy
Following the approval, NovaCure’s stock on the NSE surged by 14.02%, hitting a 52-week high of ₹1,137, with trading volumes spiking 5x the daily average. Market analysts are already raising target prices and upgrading their ratings to “Strong Buy.”
“This is the kind of FDA approval that transforms a mid-cap pharma player into a global powerhouse,” said Rahul Mehta, Senior Analyst at Axis Equities.
💡 What This Means for India’s Pharma Sector
India has long been known as the “pharmacy of the world,” but OncoRelix’s approval places it on a whole new pedestal. It’s not just about generics anymore — Indian firms are now creating pathbreaking, patented solutions that are globally competitive.
The development is also expected to accelerate clinical research investments and raise investor confidence across the healthcare sector.
🌍 Global Reach & Market Impact
With FDA approval secured, NovaCure plans to launch OncoRelix across the U.S. within the next quarter, followed by Europe, Canada, and key Asian markets. Analysts predict the drug could generate over $850 million in revenue annually within its first two years of launch.
Moreover, partnerships with leading oncology centers such as MD Anderson Cancer Center and Tata Memorial could fast-track real-world case studies and cement OncoRelix as a frontline cancer treatment globally.