Aurobindo Pharma shares jump 2% after UK arm secures regulatory approval for cancer drug
Aurobindo Pharma's stock rose after its subsidiary got approval for a cancer drug. CuraTeQ Biologics received the UK's MHRA approval for Bevgolva. This biosimilar treats various cancers. The company also saw recent USFDA observations and EMA app...

Bevgolva, a 25 mg/mL concentrate for infusion, will be available in 4 mL (100 mg) and 16 mL (400 mg) single-use vials for intravenous administration. The drug is also indicated for non-squamous non-small cell lung cancer, advanced renal cell carcinoma, cervical cancer, and ovarian-related cancers.
The approval comes amid other notable updates for Aurobindo Pharma. Last week, the USFDA issued two observations following an inspection of its Unit-V API manufacturing facility at Apitoria Pharma in Telangana.
Earlier this month, the European Medicines Agency (EMA) recommended marketing authorization for Zefylti, a filgrastim biosimilar developed by CuraTeQ Biologics.
In another development, Aurobindo’s subsidiary, Eugia Pharma Specialities, secured USFDA approval to produce and market Pazopanib Tablets, 200 mg. The drug, a bioequivalent to Novartis’ Votrient Tablets, is expected to launch in Q4FY25.
In Q2 FY25, Aurobindo Pharma reported an 8.6% year-on-year (YoY) rise in net profit to Rs 817 crore, driven by strong sales in Europe and growth markets. The company posted a net profit of Rs 752 crore in the corresponding quarter of the previous year. On a quarter-on-quarter (QoQ) basis, net profit declined by 11%.
Meanwhile, its revenue from operations increased by 8% YoY to Rs 7,796 crore in Q2 FY25. The earnings before interest, tax, depreciation, and amortization (EBITDA) before forex and other income rose 11.6% to Rs 1,566 crore. The EBITDA margin for the quarter increased by 65 basis points YoY to 20.1%.
On Friday, Aurobindo Pharma’s shares closed at Rs 1,240.70, marking a decline of 1.17%, on the BSE.
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