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Jubilant Pharmova Limited (530019) investor relations material
Jubilant Pharmova Limited Q1 25/26 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
Executive summary
Achieved 10% year-over-year revenue growth in Q1'FY26, with EBITDA and PAT margin expansion across all business units.
Vision 2030 targets doubling revenues, 23–25% EBITDA margin, zero net debt, and high teens ROCE by FY30.
Board approved unaudited standalone and consolidated financial results for the quarter ended June 30, 2025, with results reviewed by the Audit Committee and limited review by statutory auditors.
API business classified as discontinued operations following approval of its sale to a wholly-owned subsidiary; continuing operations now comprise management and support services.
Major growth drivers include expansion in radiopharma, allergy immunotherapy, CDMO sterile injectables, CRDMO, and generics.
Financial highlights
Q1'FY26 revenue: Rs. 1,901 Cr, up 10% year-over-year; EBITDA: Rs. 302 Cr, up 14% year-over-year; EBITDA margin: 15.8%.
Consolidated revenue from operations was ₹18,789 million, up from ₹17,204 million year-over-year.
Normalized PAT: Rs. 103 Cr, up 48% year-over-year; Normalized PAT margin: 5.4%.
Consolidated net profit for the quarter was ₹1,025 million, compared to ₹4,818 million in the same quarter last year.
All business segments reported year-over-year revenue growth, with notable EBITDA margin improvements in generics and CRDMO.
Outlook and guidance
On track to double revenues by FY30, with EBITDA margin guidance of 23–25% and zero net debt.
API business sale expected to complete by September 1, 2025, with no impact on consolidated results as the transaction is with a wholly-owned subsidiary.
Radiopharma and CDMO sterile injectables to drive margin expansion through new product launches and capacity doubling.
Generics and API businesses targeting top quartile profitability and margin improvement.
Proprietary novel drugs to explore monetization via licensing or external funding, with clinical data readouts expected in CY2026.
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