Pharmaceutical giant Biocon, based in Bangalore, reported a 52% drop in consolidated net profit for the year, amounting to 41 crore rupees for the second financial quarter of 2027. This decline occurred as supplies worth approximately $20 million failed to enter the reporting period, while the company's revenue increased by 2%, reaching 4,389 crore rupees.
The results were announced during the trading session, after which Biocon shares rose by 0.19% and closed at 344 rupees on the BSE exchange. Net profit decreased compared to the previous year (85 crore rupees) and compared to the June quarter (141 crore rupees).
Details on Financial Performance
Shrihas Tambe, Managing Director of Biocon, explained that supply delays, which account for about 5% of biopharmaceutical revenue, are caused by ongoing geopolitical turmoil, and the goods only reached customers after September. According to accounting rules, the revenue could not be recognized in the second quarter, although the corresponding costs were accounted for. Since the products were sold in October, the revenue will appear in the third quarter.
Tambe emphasized that there are 'no fundamental problems in the business,' calling the situation a matter of revenue recognition. Furthermore, EBITDA fell by 7% to 865 crore rupees, and the margin decreased from 22% to 20%. Nevertheless, Tambe predicted that the margin would remain in the mid-twenties range, although he did not provide specific targets for the second half of the year.
Revenue from biopharmaceutical operations grew by 5% to 3,583 crore rupees, with biosimilars increasing by 3% and generics by 10%. Revenue from services, mainly Syngene, decreased by 9% year-on-year but consistently grew by 13%. For the first half of the year, biopharma revenue grew by 11%, and net profit increased by 57% to 182 crore rupees.
Growth Prospects and New Contracts
Tambe stated that the second half of the year would be stronger, citing four growth factors. The company's biosimilar of ustekinumab, Yesintek, holds 34% of the US market, and its aflibercept biosimilar, Yesafili, is increasing production volumes. The company signed a 10-year contract to supply pertuzumab in Brazil worth approximately $400 million, with deliveries starting in the fourth quarter. The launch of pertuzumab in Europe is expected in the same quarter in a market valued at $600–700 million, where Biocon and Organon are the only approved players.
Additionally, a second insulin filling line is now operational in Malaysia, expanding production capacity to meet demand in the US. Regarding semaglutide, Biocon has transferred the technology of its product to the Brazilian partner Biomm, which is seeking approval from the Anvisa regulator. Tambe noted that the approval process could take between 12 and 24 months and declined to disclose the regulatory status in Canada.
Responding to questions about the US midterm elections, Tambe stated that both political parties are focused on reducing healthcare costs, and Biocon expects to remain protected from these changes. He added: 'We are part of the solution.'



