Akums Drugs -
Q2 FY 25 results and concall highlights -
Some extracts from Q2 management commentary -
We are excited to share that as part of our international expansion strategy, we entered into a JV with the Zambian government to set up a pharmaceutical manufacturing plant, having capabilities across multiple dosage forms and therapeutic areas in Zambia. Additionally, over the next two years, we envisage supplying medicines of aggregate value of USD 50 million from Indian facilities to Zambia. The plant also aims to establish Zambia as a pharma export hub by catering to neighboring African countries. Akums will hold 51 pc in this JV. Additionally, GRZ to procure medicines worth USD 25 million per annum from Akums for FY27 and FY28. Capex required from Akums will be aprox 200 cr, rest 200 cr shall be provided by Govt Of Zambia
Another milestone we achieved recently was our first commercial supply of formulations in Europe, with the supply of Dapagliflozin tablets to Switzerland. We will also supply Rivaroxaban in Europe in Q3. The European contract for oral liquid supply is on track with Plant 2 undergoing EU-GMP Audit in October
Our financial position remains healthy with robust cash flows during H1. Our net cash position of over INR 1,600 crore gives us leverage to pursue both organic as well as inorganic growth opportunities
While the performance during Q2 was below our expectations, we remain focused on delivering long term shareholder value by further cementing our leadership position in CDMO business, taking measures to grow our domestic and exports branded business and curtailing losses in API and trade generics
Some comments from Q1 concall -
Company’s top therapeutic areas wrt their domestic branded formulations include - paediatrics, gynaecology, cardiology
Company’s top destinations for their exports business include - Uganda, Nigeria, Philippines, Myanmar, Cambodia. Current export business is around 140 cr / yr. Aim to ramp it upto 900 cr / yr in next 5 yrs
Capex lined up for FY 26 @ 300 cr to set up new lines for Onco drugs, Steroids , LBPs ( live bio-therapeutic products )
Capex required in order to serve the European contract shall be around 200 cr ( to be incurred @ their Baddi plant ). The European contract should be a 320 - 340 cr / yr kind of business for the company, lasting 6 yrs ( starting Mar 2027 ). EBITDA margins should be around 14-15 pc wrt this contract
The API business that the company operates was acquired via IBC proceedings ( where in they acquired Parabolic drugs ). Company got credits against 870 cr of previous losses which they plan to utilise over next 3-4 yrs ( hence their tax rates shall continue to remain on the lower side )
Have received European approvals for 2 molecules - Rivaroxaban and Dapagliflozin. Company doesn’t have a field force in EU. Shall continue to supply / operate in EU mkts as a CMO supplier to other Pharma companies / Big Pharma distributors / participate in Tenders. Company expects their EU business to have better margins than their domestic CMO business. In next 3-4 yrs, company intends to own at least 10 sizeable dossiers in European mkts ( to supply to large distributors / participate in tenders ). This doesn’t include the large CMO contract from EU that the company has won and has got advance payment for
Inorganic areas where the company is looking at includes - acquiring capabilities to make dosage forms that they currently don’t have or an acquisition that gives them ready access to new markets so they can ramp up quickly
Wrt API business, company has global ambitions - to sell in Europe, LatAm and African mkts. Should continue to invest behind this business
The API business that the company operates was acquired via IBC proceedings ( where in they acquired Parabolic drugs ). Company got credits against 870 cr of previous losses which they plan to utilise over next 3-4 yrs ( hence their tax rates shall continue to remain on the lower side )
Q2 outcomes -
Revenues - 1018 vs 1033 cr
Gross margins @ 41.8 vs 42.3 pc
EBITDA - 94 vs 121 cr, down 22 pc ( margins @ 9.3 vs 11.7 pc ) - due operating de-leverage
PAT - 43 vs 67 cr, down 36 pc
Segmental revenues and EBITDA margins for Q2 -
CMO - 804 vs 799 cr, margins @ 10.5 vs 15.4 pc
Domestic branded - 122 vs 116 cr, margins @ 21.6 vs 17.8 pc
International branded - 22 vs 26 cr, margins @ 24.5 vs 13.8 pc
Trade generics - 24 vs 33 cr, margins @ (-) 3 vs (-) 6 pc
APIs - 44 vs 59 cr, margins @ (-)14 vs (-) 14 pc
H1 performance -
Revenues - 2042 vs 2052 cr
EBITDA - 223 vs 245 cr, down 9 pc ( margins @ 11 vs 12 pc )
PAT - 107 vs 124 cr, down 14 pc
Segmental revenues and EBITDA margins for H2 -
CMO - 1618 vs 1581 cr, margins @ 12.6 vs 15.4 pc
Domestic branded - 229 vs 220 cr, margins @ 18.4 vs 15.5
International branded - 57 vs 60 cr, margins @ 23.5 vs 18.3 pc
Trade generics - 48 vs 62 cr, margins @ (-) 6 vs (-) 10 cr
APIs - 89 vs 129 cr, margins @ (-) 20 vs (-) 26 cr
Notes from Q2 concall -
Top 200 APIs used by the company witnessed an avg YoY drop of 8 pc - hence the sluggishness in CMO division’s topline growth. CMO business witnessed a volume growth of 7 pc
CMO margins were hit by slower than expected ramp up of their new facilities and higher overhead costs
International branded business is expected to have a strong H2 led by demand pull from their focussed mkts
Cash on books @ 1650 cr. Enables them to go after both organic and in-organic opportunities
Three of company’s plants are going in for EU GMP certification - due increased filings and launch intentions of the company in Europe ( as brought out in the management commentary above )
Company has filed for 2 Cephalosporin based Formulations in the EU mkts. Should get an approval in next 6 months. GMs in EU are better. This would help the company use its APIs captively and help improve the API business’s operating performance. Also the Cephalosporin API prices should start to recover in next 3-6 months
Depending on the market conditions ( as company sees them today ), H2 should broadly be in line with H1 ie a topline around 2050 cr and bottomline around 105-115 cr ( just like H1 )
The large European contract against which the company has also got > 900 cr in advance is for the supply of an Oral Liquid molecule in various dosage strengths and different packagings, be supplied to one of the largest pharma company globally, starting Apr 27, to be supplied from Haridwar facility ( recently inspected by EU GMP officials ). Company would be supplying goods worth > 300 cr / yr for 6 yrs
Charging notional interest of Rs 19 cr / Qtr to the P&L - against the advance they have got from the European major. Anyways, its a non cash entry
Zambian contract should start going live in next FY. In FY 28, both the Zambian and EU contracts would be online. Plus the organic growth should also pick up wef next FY. Additionally the new set of molecules that the company intends to sell in EU should add to growth going forward
Capex in H1 @ 107 cr. H2 capex should be similar
Disc: holding, biased, not SEBI registered, not a buy/sell recommendation