Biocon Reports Strong Q2 FY26 Results: 20% Revenue Growth Led by Biosimilars
Biocon Limited reported robust Q2 FY26 results with operating revenue up 20% YoY to INR 4,296 crores. Core EBITDA grew 23% to INR 1,218 crores, while EBITDA margin reached 21%. Biosimilars segment led growth with 25% revenue increase. The company reduced debt, launched new biosimilars, and expanded its generics and CRDMO businesses. Biocon expects continued margin improvement and growth across segments.

*this image is generated using AI for illustrative purposes only.
Biocon Limited , a leading biopharmaceutical company, has reported robust financial results for the second quarter of fiscal year 2026, demonstrating significant growth across its key business segments.
Financial Highlights
| Metric | Q2 FY26 | YoY Growth |
|---|---|---|
| Operating Revenue | 4,296.00 | 20% |
| Core EBITDA | 1,218.00 | 23% |
| EBITDA | 928.00 | 29% |
| EBITDA Margin | 21.00% | - |
| Profit Before Tax (excluding exceptionals) | 183.00 | 153% |
| Net Profit (after tax and minority interest) | 85.00 | - |
All financial figures in INR crores
Segment Performance
Biosimilars
- Revenue: INR 2,721.00 crores (25% YoY growth)
- EBITDA: INR 669.00 crores (over 40% growth)
- EBITDA Margin: 25% (up approximately 400 basis points)
Generics
- Revenue: INR 774.00 crores (24% YoY growth)
- R&D Investment: INR 71.00 crores (9% of segment revenues)
CRDMO (Contract Research, Development, and Manufacturing Organization)
- Revenue: INR 911.00 crores (2% YoY growth)
- Reported EBITDA: INR 215.00 crores (23% margin)
Key Developments
Debt Reduction: Biocon has strengthened its balance sheet by settling structured debt obligations with Goldman Sachs and Kotak using QIP proceeds. The company expects annual savings of around INR 300.00 crores in interest costs from FY27.
Biosimilars Progress:
- Successful launches of biosimilar Ustekinumab, Aspart, Bevacizumab, and Aflibercept across geographies.
- U.S. FDA approval for biosimilar Denosumab and a license agreement with Amgen for U.S. commercialization.
- Strong market traction for Yesintek (biosimilar Ustekinumab) in the U.S., with over 70% commercial formulary coverage.
Insulin Partnership: Entered a partnership with the California government through Civica Inc. to supply affordable insulin glargine under the CalRx initiative.
ESG Performance: Improved S&P Global Corporate Sustainability Assessment score to 71, up 3 points from the previous year.
Generics Expansion: Inaugurated an oral solid dosage manufacturing facility in Cranbury, New Jersey, expanding capacity for the U.S. market.
CRDMO Advancements: Syngene secured its first global Phase III clinical trial from a U.S.-based biotech company and expanded its clinical trials footprint globally.
Kiran Mazumdar-Shaw, Executive Chairperson of Biocon, commented on the results, stating, "We've already started to see margin improvement in Q2 following the Goldman Sachs exit, and we expect this trend to continue through quarters 3 and 4 as we see the impact of both Kotak and Edelweiss exits."
Shreehas Tambe, CEO of Biocon Biologics, highlighted the company's strong position in the insulin market, saying, "The only other player outside of that which is a biosimilar insulin player and is in a position to bring in GLP-1s is Biocon. So, it does place us in a very unique position."
Outlook
With a strong pipeline of biosimilars, ongoing expansion in generics, and a growing CRDMO business, Biocon is poised for continued growth. The company's focus on debt reduction and improved profitability is expected to further strengthen its financial position in the coming quarters.
Historical Stock Returns for Biocon
| 1 Day | 5 Days | 1 Month | 6 Months | 1 Year | 5 Years |
|---|---|---|---|---|---|
| +0.15% | +9.48% | +15.73% | +23.42% | +29.58% | -0.33% |
















































