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Gufic Biosciences (509079) Q2 24/25 earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for Gufic Biosciences Limited

Q2 24/25 earnings summary

13 Jan, 2026

Executive summary

  • Indore facility commissioned and operational, marking a transformative milestone with phased production ramp-up and regulatory alignment for domestic and international markets.

  • Strategic business units expanded, including Critical Care, Ferticare, Aesthaderm, Neuro Care, Sparsh, Spark, Stellar, and Healthcare, each targeting specific therapeutic areas and market needs.

  • International business growth driven by new market approvals, including a UK NHS tender and expansion in Thailand, Sri Lanka, Cambodia, and Lithuania.

  • Focus on high-barrier products, clinician engagement, and innovative launches across divisions to drive growth and market positioning.

  • Revenue and net profit for H1 FY25 remained stable year-over-year, reflecting consistent performance.

Financial highlights

  • H1 FY25 revenue at ₹407 crore, nearly flat versus ₹409.9 crore in H1 FY24; Q2 FY25 revenue at ₹204.2 crore, down from ₹214.9 crore in Q2 FY24.

  • H1 FY25 EBITDA at ₹79.8 crore (margin 18.62%), up from ₹76.1 crore (18.57%) in H1 FY24.

  • H1 FY25 PAT at ₹42.6 crore (margin 10.47%), slightly lower than ₹43.8 crore (10.69%) in H1 FY24.

  • Cash generated from operations for H1 FY25 was ₹8,940.77 lakhs, a significant increase from ₹1,229.55 lakhs year-over-year.

  • FY24 revenue was ₹808.8 crore, EBITDA ₹148.0 crore (18.3% margin), and PAT ₹86.1 crore (10.6% margin).

Outlook and guidance

  • Indore facility expected to contribute minimally to revenue in FY25, with significant impact anticipated over the next two to three years.

  • EU and US regulatory approvals targeted, with EU audit expected by late 2024 and USFDA action anticipated in 2026.

  • CMO/CDMO business to commence in late 2024, supporting long-term international growth.

  • Plans to increase market share in botulinum toxin, expand contract manufacturing, and commercialize immuno-oncology therapy.

  • Continued investment in international registrations and manufacturing scale-up to support global expansion.

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