Zydus Lifesciences posts 6% revenue growth in Q1 FY26, Net profit rises to Rs 14,668 Million

Strong performance in chronic therapies, robust international growth, and strategic acquisitions bolster the company’s innovation pipeline and global presence

0
75
New Delhi: Zydus Lifesciences Limited announced its unaudited consolidated financial results for the quarter ended June 30, 2025, reporting a revenue from operations of Rs 65,737 million, a 6% year-on-year growth. Research and development investments stood at Rs 4,856 million, representing 7.4% of revenues.
EBITDA was Rs 20,885 million, remaining flat compared to the previous year, with a margin of 31.8%. Net profit rose 3% year-on-year to ₹14,668 million, while organic capex for the quarter was Rs 4,020 million.
The India geography business, contributing 37% to consolidated revenues, generated Rs 23,744 million, a 6% rise from the previous year. The formulations segment posted Rs 15,195 million, growing 8% year-on-year, driven by robust performance in chronic therapies such as cardiology, respiratory, anti-infectives, pain management, and oncology, where the company retained its leadership position. The consumer wellness business recorded Rs 8,549 million, a 2% increase, with strong double-digit growth in non-seasonal brands and a rising share of organized trade and e-commerce sales.
The US formulations business contributed 49% of revenues at Rs 31,817 million, growing 3% year-on-year, with three new product launches, three ANDA filings, and six product approvals. The international markets formulations segment rose sharply by 37% to Rs 7,265 million, while the API business grew 11% to Rs 1,575 million. Revenues from alliances and others declined 28% to ₹269 million. The company’s API facilities at Ankleshwar and Dabhasa received Establishment Inspection Reports from the USFDA.
On the innovation front, Zydus initiated Phase II(b) clinical trials of Usnoflast, a novel NLRP3 inflammasome inhibitor for ALS, which also received USFDA Fast Track designation and holds Orphan Drug Designation. Its biotech R&D received marketing authorization for Rituximab and Aflibercept biosimilars and Phase III trial approval for a second antibody drug conjugate. In vaccines, the company completed Phase II trials of a Hepatitis E vaccine and began Phase IV trials of its rabies vaccine.
Strategic moves included entering the global biologics CDMO space with the planned acquisition of Agenus Inc.’s US-based manufacturing facilities and completing a stake acquisition in France’s Amplitude Surgical SA, a leader in lower-limb orthopedic technologies. The company remains optimistic about achieving its FY26 goals and sees upcoming innovations as key to sustainable growth.