Biocon (BIOCON) Q4 07/08 earnings summary
Event summary combining transcript, slides, and related documents.
Q4 07/08 earnings summary
25 Oct, 2026Executive summary
FY08 consolidated total income rose 10% to Rs 10,902m; EBITDA increased 17% to Rs 3,350m and PAT before exceptional items and minority interest rose 12% to Rs 2,180m.
Portfolio shift toward biopharmaceuticals accelerated after the October 2007 enzyme-business divestment; licensing income, research services and branded formulations supported the growth mix.
Enzyme-sale gain lifted consolidated PAT after exceptional items to Rs 4,639m; excluding exceptional items, PAT after minority interest was Rs 2,245m.
Financial highlights
Consolidated total income was Rs 10,902m versus Rs 9,896m; net sales were Rs 8,334m and contract research revenue was Rs 1,755m.
Consolidated EBITDA was Rs 3,350m versus Rs 2,873m; PBT before exceptional items was Rs 2,309m versus Rs 2,110m.
PAT before exceptional items was Rs 2,180m, up from Rs 1,941m; after minority interest, PAT was Rs 2,245m versus Rs 2,003m.
Exceptional items net of tax were Rs 2,394m; reported consolidated PAT after exceptional items was Rs 4,639m.
Recommended dividend totaled 100%, or Rs 5/share, including a special Rs 2/share dividend following the enzyme-business sale.
Outlook and guidance
Four biosimilars—GCSF, Reteplase, Streptokinase and insulin analogs—were targeted for launch within two years, subject to partnerships and market approvals.
Insulin capacity expansion was underway, with the new facility expected to be commissioned later in 2008; EU and multiple Asian, Latin American and African registrations were progressing.
Oral insulin IN-105 entered Phase II in India; Anti-CD6 T1h Phase II studies for rheumatoid arthritis and psoriasis were expected to complete in 2009.
Management expected pipeline programs to deliver significant upside over the next 2–3 years; global Phase III development and commercialization would require substantial investment and partnerships.
Clinigene planned 40% manpower growth, expansion of its human pharmacology unit to 86 beds and a six-bed Phase I glucose-clamp unit.
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