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    Akums Drugs

    AKUMS
    Healthcare·7 Feb 2025
    Management Summary

    Akums Drugs reported a mixed Q3 FY25 with total income declining to INR1,025 crores, but EBITDA and PAT showed growth, reaching INR136 crores and INR66 crores respectively. A significant highlight was securing a EUR 200 million CDMO contract for European markets, with an upfront payment of EUR 100 million expected. The API segment saw reduced losses, and the company continued to invest in R&D and capacity expansion, though overall capacity utilization remains low at 40%.

    Highlights

    5
    • EBITDA grew 1% QoQ to INR136 crores and 12% YoY to INR136 crores.

    • PAT grew 15% YoY to INR66 crores, up from INR57 crores in Q3 last year.

    • Secured a EUR 200 million CDMO contract for European markets, including an upfront payment of EUR 100 million.

    • API business losses significantly reduced to INR11 crores in Q3 FY25 from INR14 crores in Q2 FY25.

    • Received DCGI approvals for 7 products in Q3, including Empagliflozin combination.

    Concerns

    3
    • Total income declined 2% QoQ to INR1,025 crores and 6% YoY.

    • CDMO volume growth was subdued at 0.6% QoQ and 1% for 9 months FY25.

    • Overall capacity utilization is low at around 40%.

    What Changed2

    vs Q4 FY25

    Guidance items8 → 6 (-2)Risks discussed4 → 3 (-1)
    Key financials

    Metrics

    6

    Periods

    2

    Headline

    5
    • Total Income
      ₹1,025 Cr
      YoY-6%QoQ-2%
    • EBITDA
      ₹136 Cr
      YoY+12%QoQ+1%
    • PAT
      ₹66 Cr
      YoY+15%QoQ-1.5%
    • Cash Flow from Operations
      ₹91 Cr
      QoQ+3.8%
    • Free Cash Flow
      ₹50 Cr

    9M FY25

    1
    • R&D Investment
      ₹94 Cr

    Segment breakdown

    • CDMO₹787 Cr78.0%
    • Branded Generics₹182 Cr18.0%
    • API₹40 Cr4.0%
    Donut· Share of Revenue

    Order Book

    high confidence

    Total Value

    EUR 200 million

    as of 2024-12-31

    quantified

    Inflow this qtr

    EUR 200 million

    Execution

    commercial supply will commence from 2027 and will continue until 2032

    Composition

    Oral liquid formulations(product)

    "This is the first of many such contracts and partnerships we will undertake to serve the European markets in the years ahead."

    Source:
    Prepared remarks

    Capital allocation

    3
    high confidence
    CategoryHeadline
    Capex

    ₹175 crores

    Debt

    Debt disclosed

    Liquidity

    Cash ₹340 crores

    Cash flow for the Group stands at surplus.

    Guidance & targets

    6
    CategoryTargetPriority
    Capex
    R&D Capex
    INR 32 crores
    High
    Capex
    New Plants and Production Lines Capex
    INR 175-200 crores annually
    High
    Profitability
    API Business Breakeven
    Breakeven
    Medium
    Volume
    CDMO Volume Growth
    4-5%
    Medium
    Revenue
    CDMO Revenue Growth
    12-13%
    Medium
    Capacity
    Capacity Utilization for Breakeven
    60-65%
    High

    API business breakeven

    Next 1-2 years
    CurrentINR11 crores EBITDA loss in Q3 FY25
    TargetBreakeven (EBITDA)

    Why it matters

    API is a loss-making segment; achieving breakeven will significantly improve overall profitability.

    So we are progressing well. I think this is in a ZIP code of 1 to 2 years when we'll be in a breakeven.

    How to verify

    key_financials.segment_breakdown[name='API'].metrics[label='EBITDA Loss']

    Risks & concerns

    3
    RiskSeverity

    API Segment Losses

    The API business is currently loss-making (INR11 crores in Q3 FY25) due to low prices of cephalosporin APIs, but management is rationalizing the portfolio and targeting breakeven in 1-2 years.Management acknowledged

    medium

    Subdued CDMO Volume Growth

    CDMO volume growth was 0.6% QoQ and 1% for 9 months FY25, lower than historical rates, but management attributes this to a transient period and expects recovery, seeing 'green shoots' in Q4 and Q1 FY26.Management acknowledged

    medium

    Low Capacity Utilization

    Overall capacity utilization stands at around 40%, impacting operational leverage, but management is commissioning new facilities and expects utilization to improve as new orders come in.Management acknowledged

    medium

    Q&A highlights

    8

    “So we are progressing well. I think this is in a ZIP code of 1 to 2 years when we'll be in a breakeven.”

    Management provides a specific timeline for the loss-making API segment to achieve profitability.

    asked by Darshil Jhaveri

    2 min read6 chapters

    Detailed Narrative

    01

    Q3 FY25 Financial Performance Overview

    Akums Drugs reported a total income of INR1,025 crores in Q3 FY25, marking a 2% QoQ and 6% YoY decline. Despite this, adjusted EBITDA grew 1% QoQ to INR136 crores and 12% YoY, while PAT increased 15% YoY to INR66 crores. Cash flow from operations significantly improved to INR91 crores from INR19 crores QoQ, and free cash flow turned positive at INR50 crores from negative INR73 crores.

    02

    CDMO Business Performance and European Contract

    The CDMO segment, contributing 78% of revenue (INR787 crores), saw its EBITDA grow 9% YoY, with overall CDMO EBITDA margins close to 15.4%. Volume growth in CDMO was subdued at 0.6% QoQ and 1% for the 9 months of FY25, though management expects recovery. A major highlight was securing a EUR 200 million CDMO contract for oral liquid formulations in European markets, with commercial supply commencing in 2027 and an upfront payment of EUR 100 million already transferred.

    03

    API Business Rationalization

    The API segment, representing 4% of revenue (INR40 crores), continued to incur losses, though these significantly reduced to INR11 crores in Q3 FY25 from INR14 crores in Q2 FY25. This improvement was a result of rationalizing the portfolio, discontinuing lower-margin cephalosporin APIs due to a 20-30% price drop. Management aims for the API business to reach breakeven within 1 to 2 years by focusing on higher-margin products, general APIs, and exports.

    04

    R&D and New Product Development

    Akums invested INR94 crores in R&D over the first 9 months of FY25, securing 7 DCGI approvals in Q3, including for Empagliflozin combination. The company plans to incur an additional INR32 crores in capex over the next two quarters to upgrade R&D capabilities for regulated markets and niche dosage forms. DSIR accreditation was received for the Barwala R&D facility for APIs.

    05

    Strategic Partnerships

    Akums entered into several strategic partnerships, including an exclusive master sales agreement with Caregen (South Korea) for nutraceuticals in India and a licensing deal with Triple Hair (Canada) for a patented topical solution for alopecia in India, valid until 2035. They also partnered with Jagdale Industries for aseptic carton technology products in wellness and sports nutrition. These are primarily in-licensing deals for the Indian market, not global CDMO, and are expected to contribute to the P&L from 2027.

    06

    Capacity Expansion and Utilization

    The company incurred INR191 crores in capex over 9 months FY25, primarily in the CDMO vertical, and plans to spend INR175-200 crores annually over the next two years for new plants and production lines. Current overall capacity utilization stands at around 40%. The new injectable facility, which recently started operations and received WHO GMP approval in January, has insignificant utilization currently but is expected to ramp up over the next 6 months. Management targets 60-65% utilization for operational breakeven.

    This is an AI-generated summary of a publicly available earnings call transcript. It is for informational purposes only and does not constitute investment advice, a recommendation, or an endorsement. inve.money is not a SEBI-registered investment advisor. Please consult a qualified financial advisor before making any investment decisions.